<?xml version="1.0" encoding="utf-8" standalone="yes"?>
<source>
  <publisher>Regeneron Pharmaceuticals Inc.</publisher>
  <publisherUrl>https://www.regeneron.com/</publisherUrl>
  <lastBuildDate>Mon, 06 Jul 2026 05:05:06 GMT</lastBuildDate>
  <job>
    <title><![CDATA[Associate Director, Digital Lab Orchestration]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45569]]></requisitionid>
    <referencenumber><![CDATA[R45569]]></referencenumber>
    <apijobid><![CDATA[r45569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45569/associate-director-digital-lab-orchestration/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Associate Director of Digital Lab Orchestration you will be responsible for leading designing, integrating, and deploying the orchestration layer that connects QC laboratory systems into a cohesive, compliant, and automated ecosystem. This role bridges QC operations, IT/OT, automation, and data governance to enable end-to-end digital QC workflows.</p></div><div><div><div><div><p>As an Associate Director, a typical day might include the following:</p><ul><li>Lead the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across all Laboratory instruments and middleware.</li><li>Define integration patterns (APIs, event-driven, message queues, file-based where needed).</li><li>Ensure scalability, resilience, and performance of lab integrations.</li><li>Translate QC business processes into orchestrated digital workflows.</li><li>Enable automated sample lifecycle management, test execution, result capture, review, and release.</li><li>Support real-time and near-real-time data flow from lab instruments to enterprise systems.</li><li>Assist in annual IT budgeting, vendor negotiations, and resource allocation.</li><li>Ensure integrations comply with GxP, ALCOA+, 21 CFR Part 11, Annex 11 and data integrity requirements.</li><li>Partner with Quality and CSV teams to support validation strategies (risk-based, CSA where applicable).</li><li>Ensure auditability, traceability, and controlled change management.</li><li>Act as the primary integration point between QC, IT, automation, and external vendors.</li><li>Evaluate vendor platforms and integration tools for orchestration capabilities.</li><li>Lead technical discussions with system integrators and software suppliers.</li><li>Support incident resolution, root cause analysis, and continuous improvement.</li><li>Make decisions on integration patterns and drive a connected lab progression in 2026 and beyond</li><li>Ensure resiliency is incorporated into our architecture- as we move into a connected lab platform.</li></ul><p>This role may be for you if you have:</p><ul><li>Knowledge of integration technologies: REST APIs, middleware/iPaaS, message brokers, ETL.</li><li>Familiarity with orchestration/workflow engines.</li><li>Understanding of lab instrument connectivity and data flows.</li><li>Experience with cloud and/or hybrid architectures (AWS, Azure, or similar).</li><li>Industry experience implementing Lab orchestration including Scitara, Tetra Science, or any other emerging tools.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field and </p><ul><li>Senior Manager: 8+ years industry experience in Information Systems and Technology or equivalent combination of education and experience. 6 of those years should be in managing employees and budgets, with 5+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment.</li><li>Associate Director: 10+ years industry experience in Information Systems and Technology or equivalent combination of education and experience. 8 of those years should be in managing employees and budgets, with 7+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment. </li><li>Experience with IT Compliance guidelines including PICS, CFR21 Part 11, Annex 11 and GAMP preferred.</li></ul></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Oncology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45863]]></requisitionid>
    <referencenumber><![CDATA[R45863]]></referencenumber>
    <apijobid><![CDATA[r45863]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45863/associate-director-clinical-scientist-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p><strong>As an Associate Director a typical day may include the following:</strong></p><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape as well as maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Possesses proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature.</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements.</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><p>To be considered for this role, you must have a Bachelor’s Degree, Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc) is preferred. ≥ 10 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking proven leadership experience and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Strong cross-functional management, interpersonal and problem-solving skills. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Dermatology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46330]]></requisitionid>
    <referencenumber><![CDATA[R46330]]></referencenumber>
    <apijobid><![CDATA[r46330]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46330/medical-director-clinical-development-dermatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>The Medical Director, Clinical Sciences is responsible for facilitating assigned dermatology studies, providing investigator support of Regeneron driven studies, and may serve as a resource to anticipate and/or resolve study clinical and conduct issues. This role reports into an Executive Medical Director, Clinical Sciences and is expected to have proficient knowledge of the drug development process, good clinical practice, study design and research methodology as well as understand Regulatory and compliance landscape in the pharmaceutical industry. This role utilizes scientific and clinical expertise to initiate, propose, design and execute research and development programs for early and/or late stage assets. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research. Some industry experience preferred.</div><div><div><div><div><div><div><div><div><div><p>A typical day in the life may include the following responsibilities:</p><ul><li><p>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program. Clinical deliverables may include individual protocols; clinical components of regulatory documents/registration dossier and brand related medical information, clinical communication and publications</p></li><li><p>Advanced analytical skills and ability to communicate concise and clear messages</p></li><li><p>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts</p></li><li><p>Ability to lead activities within a matrix environment</p></li><li><p>Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally</p></li></ul><p>This role may be for you if:</p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p>In order to be considered for this role, a M.D. degree or equivalent is required. Specialized clinical fellowship training in Dermatology is strongly preferred. A minimum of 2-4 years of clinical development experience in industry is preferred, but academic research experience will be considered.</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor, Integrated Product Development Laboratories]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46489]]></requisitionid>
    <referencenumber><![CDATA[R46489]]></referencenumber>
    <apijobid><![CDATA[r46489]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46489/supervisor-integrated-product-development-laboratories/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently seeking a Supervisor for the Integrated Product Development Laboratories to join our Process Sciences Drug Product Engineering department. They will oversee the packaging and labeling development laboratory spaces and equipment, drive commissioning and qualification efforts, and coordinate equipment activities to achieve organizational and regulatory objectives while leading a team of Engineering Technicians.</p><p>As a Supervisor, Integrated Product Development Laboratories, a typical day might include the following:</p><ul><li>Lead, coach, and develop a team of technicians supporting laboratory operations</li><li>Ensure laboratory compliance with Regeneron training requirements and GxP standards</li><li>Maintain laboratory infrastructure (facilities, utilities) and operational assets (equipment, instruments, software, documentation)</li><li>Drive continuous process improvement to enhance performance, reliability, and throughput</li><li>Manage relationships with internal stakeholders and external vendors/service providers</li><li>Help shape strategy and establish KPIs/metrics to measure effectiveness and compliance</li><li>Provide day-to-day leadership, direction, and performance management to direct reports</li><li>Develop equipment commissioning related documentation </li></ul><p>This role might be for you if you :</p><ul><li>Have experience with packaging equipment (vibration tables, drop testers, shakers etc.)</li><li>Excel at technical writing and clear, concise verbal communication</li><li>Manage projects and timelines, including coordination with external vendors</li><li>Demonstrate unwavering integrity, honesty, and transparency</li><li>Lead teams and take accountability for performance and results</li><li>Navigate ambiguity and translate it into clear, actionable plans</li></ul><p>To be considered for the Supervisor Integrated Product Development you must have willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS in Life Sciences, packaging science/engineering is preferred and 5+ years of relevant experience; or equivalent combination of education and experience. Previous people leadership/supervisory experience is required. Experience in combination products or medical devices is preferred. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Government Pricing]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46609]]></requisitionid>
    <referencenumber><![CDATA[R46609]]></referencenumber>
    <apijobid><![CDATA[r46609]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46609/associate-director-government-pricing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Government Pricing (GP) position is a key member of Regeneron’s government pricing team, which includes supporting the accurate calculation and timely submission of all required government price reporting.</p><p>Included in this role is responsibility for assuring compliance with all pricing and reporting requirements legislated by the Centers for Medicare & Medicaid Services (CMS), the Department of Veterans Affairs and any state legislation required price reporting. This includes a full understanding of all current legislation and staying abreast of pending legislation. Government Pricing Calculations include: Medicaid, Medicare Part B, Public Health Service (PHS)/340B, and Federal Supply Schedule (FSS), which includes: TriCare and the Industrial Funding Fee (IFF). The Associate Director will work collaboratively with Contracting Strategy supporting the overall strategy, contracting and/or payment activities.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Ability to calculate, validate and report accurate monthly, quarterly, and annual government pricing.</p></li><li><p>Submit and monitor State Price Transparency regulations.</p></li><li><p>Complete understanding of calculation reasonable assumptions and methodologies and ability to research and communicate cause of variances of results when comparing current period to prior periods.</p></li><li><p>Perform all necessary processes needed to ensure compliant submissions including, but not limited to G/L reconciliations, Class of Trade (COT) review, and PHS/340b eligibility review.</p></li><li><p>Associate Director will review calculations with Senior Management and obtain approval signoff (and executes any other required Standard Operating Procedures (SOPs)) before communicating prices to the appropriate government agencies (Center for Medicare and Medicare (CMS), Veterans Affairs (VA)/Department of Defense (DOD), etc.) or internally.</p></li><li><p>Responsible for maintaining and updating SOP’s and reasonable assumptions, on a quarterly basis, as related to Government Programs/Pricing.</p></li><li><p>Monitor policies, procedures and processes supporting Government Pricing submissions and related areas to ensure ongoing compliance with external and internal requirements and guidance.</p></li><li><p>Understand and estimate impact of pricing and policy changes regarding government pricing.</p></li><li><p>Perform pricing research and analysis on special projects as assigned.</p></li><li><p>Ability to review and understand commercial contract language as pertaining to Best Price (BP), Average Sales Price (ASP) and FSS Tracking Customers.</p></li><li><p>Investigate Government pricing trends and cross channel impact. Also provide Government price inputs to the Gross to Net (GTN) team.</p></li><li><p>Monitor for Tracking customer violations, Bona Fide Service Fee treatments & Customer COT assignment.</p></li><li><p>Participate on cross-functional teams as a subject matter expert representing the Government Pricing and Contract Operations as required to evaluate and implement business strategies and initiatives.</p></li><li><p>Serve as a liaison with Commercial Leadership, Pricing, Trade, Brand and Accounting/Finance teams regarding a variety of issues impacting government pricing.</p></li><li><p>Familiar with Fair Market Value methodology while determining bona fide service fees paid to Wholesaler, Pharmacy Benefit Manager (PBM) and Group Purchasing Organizations (GPOs).</p></li></ul><p><strong>The role may be for you if:</strong></p><ul><li><p>Understanding of current government pricing rules, regulations, and calculations</p></li><li><p>Must be able to identify potential problems, conduct analysis and use judgment to determine if problem exists as well as offer up potential solutions.</p></li><li><p>Highly analytical, able to analyze, interpret, and convey data and its commercial impact</p></li><li><p>Ability to decipher calculations to determine key causes of variances.</p></li><li><p>Strong communication skills and ability to communicate effectively to all levels of the organization.</p></li><li><p>Process oriented</p></li><li><p>Proven ability to successfully manage competing priorities, meet challenging deadlines, and work independently and across organizations</p></li><li><p>Demonstrated track record of strong attention to detail; accountability and ownership of results; flexibility and adaptability in a rapidly changing environment</p></li></ul><p>To be consider for this role, we expect you to have a bachelors degree and 7+ years prior experience in Government Pricing OR a related field such as finance, accounting, Medicare/Medicaid (with strong analytical skills). We also will need you to be open to traveling at times.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician (Nights)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46924]]></requisitionid>
    <referencenumber><![CDATA[R46924]]></referencenumber>
    <apijobid><![CDATA[r46924]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46924/hvac-technician-nights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an HVAC Technician to join our Facilities Maintenance team. In this role, you will be responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Working hours: Wednesday-Saturday 2:00pm-12:30am</li><li>Training hours: Monday-Friday 8:00am-4:30pm</li><li>Rensselaer, NY</li></ul><br><h3>Discover your role:</h3><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers.</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work.</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC equipment</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Coordinating with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li></ul><br><h3>This role requires:</h3><ul><li>AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level:</li><li>HVAC Technician II: AAS with 2+ years or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years or equivalent combination of education and experience</li><li>HVAC Technician IV: AAS with 8+ years or equivalent combination of education</li><li>Solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>EPA certified for refrigeration gases</li><li>Able to become fully gown qualified to work in production areas</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs (Standard Operating Procedures, cGMPs (current Good Manufacturing Processes), GDPs (Good Documentation Practices) and quality standards</li><li>Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Pulmonology, Marketing (HCP)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47356]]></requisitionid>
    <referencenumber><![CDATA[R47356]]></referencenumber>
    <apijobid><![CDATA[r47356]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47356/associate-director-pulmonology-marketing-hcp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of HCP Marketing will lead healthcare professional marketing strategy and execution for Asthma indications in the U.S. This highly visible role requires a forward-looking individual with deep marketing expertise and the ability to navigate complex alliance partnerships. The Associate Director will partner closely with cross-functional and alliance teams to advance the products growth, contribute to the brand's financial success, and strengthen its leadership position in Pulmonology. This position reports to the Director, Pulmonology HCP Marketing.</p><p><strong>A Typical Day Might Look Like:</strong></p><ul><li><p>Leading the HCP marketing strategy for the Asthma indication, ensuring full integration with the broader brand strategy.</p></li><li><p>Acting as a key advocate for the brand strategy, clearly articulating priorities and ensuring alignment across Regeneron, Sanofi, and other critical stakeholders.</p></li><li><p>Overseeing the development of HCP engagement strategies, messages, and tactical campaigns tailored to Pulmonologists and Advanced Practice Providers.</p></li><li><p>Building and deploying a competitive market strategy that proactively addresses evolving competitors and market dynamics.</p></li><li><p>Driving strong cross-functional and alliance collaboration, partnering with Sales, Medical Affairs, TLLs, Market Research, Market Access, Regulatory, Legal, Clinical, and HEOR to deliver cohesive, compliant, and impactful initiatives.</p></li><li><p>Ensuring all marketing programs comply with corporate policies, regulatory/ethical frameworks, and alliance standards.</p></li><li><p>Tracking and managing marketing spend, timelines, and deliverables to meet budget, scope, and performance expectations.</p></li></ul><p><strong> </strong></p><p><strong>This Role Might Be For You If You:</strong></p><ul><li><p>Combine strategic and scientific acumen with an ability to translate insights into actionable marketing strategies.</p></li><li><p>Have a proven track record of leadership and influence across organizational levels.</p></li><li><p>Bring exceptional communication and presentation skills, with the ability to simplify and convey complex strategies to diverse audiences—both technical and non-technical, including senior executives.</p></li><li><p>Excel in execution and project management within a fast-paced, dynamic, and competitive marketplace.</p></li><li><p>Demonstrate organizational agility, adapting priorities and strategies to external market shifts or internal dynamics.</p></li><li><p>Thrive in cross-functional and alliance settings, effectively shaping collaboration, alignment, and decision-making.</p></li><li><p>Possess strong experience in managing agencies and external partners, ensuring creative excellence and accountability.</p></li><li><p>Are disciplined in managing budgets and resources aligned to strategic objectives.</p></li></ul><p><strong> </strong></p><p>To be considered for the role, we expect you to have a Bachelor’s degree required; MBA strongly preferred. We are also seeking 10+ years of progressive experience in the pharmaceutical/biotech industry or related field and 8+ years of U.S. commercial experience in pharmaceutical/biotech marketing, product management, or related areas. It is preferred to have Respiratory and/or Immunology experience strongly preferred. Lastly, we expect you to be onsite in Sleepy Hollow, NY 4 days a week and willing to travel 30% of the time.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Pharmacovigilance Hub]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47624]]></requisitionid>
    <referencenumber><![CDATA[R47624]]></referencenumber>
    <apijobid><![CDATA[r47624]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47624/director-pharmacovigilance-hub/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director, Pharmacovigilance Hub</strong> to join our <strong>Global Patient Safety Operations</strong> team. The Director, PV Hub oversees country and/or regional level PV execution within their assigned region and ensures that local safety activities are performed in accordance with global standards, local regulatory requirements are met, and all country-generated safety data are accurately and timely integrated into the global PV system. This role serves as the escalation point for local execution issues and as the conduit between local operations and global oversight functions. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Maintain a comprehensive understanding of local legislation and Health Authority requirements and keep Worldwide Operations Office (WWOO) leadership informed of updates or changes to local requirements or processes (e.g., SOP addenda, safety communications, labeling updates, and local submission requirements) in alignment with country-specific regulatory requirements </p></li><li><p>Track local process status, changes, and risks to drive consistency and continuous improvement for hub’s geographic markets, including maintaining and monitoring via common tool (e.g., tracker, dashboard) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li><li><p>Ensure country compliance with the global PV quality system, supporting inspections, audits, CAPAs, and timely resolution of deviations or non-compliance </p></li><li><p>Serve as local safety PoC to coordinate with global GPS (e.g., PV Enablement, CER, SS) and non-GPS (e.g., Med Affairs, Regulatory) teams to: </p></li><li><p>Guide and inform global teams on local requirements and ensure compliance with local legislations </p></li><li><p>Coordinate with other PV hub(s) as needed for contributions to activities and/or local documentation </p></li><li><p>Shape compliant programs that provide high quality adverse event reports </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum Bachelor’s Degree (Advanced Degree preferred) with 12+ years of PV experience and demonstrated achievements in patient safety</p></li><li><p>Experience supporting regulatory inspections, audits, and quality issue management at the country or regional level </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Ability to coordinate across functions and cultures, operating effectively as an execution and escalation lead rather than a policy owner </p></li><li><p>Strong organizational and communication skills, with the ability to surface local risks early and drive resolution through global governance channels </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Patent Attorney (Immunology & Inflammation)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47665]]></requisitionid>
    <referencenumber><![CDATA[R47665]]></referencenumber>
    <apijobid><![CDATA[r47665]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47665/director-patent-attorney-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Patent Attorney will work collaboratively with our research and development teams to develop, protect, and manage Regeneron’s valuable intellectual property pertaining to therapeutic molecules. This role will be responsible for patent activities relating to approved and pipeline therapeutic molecules in our Immunology & Inflammation (I&I) therapeutic area.</p><p><strong>This role is based 4 days onsite at Regeneron’s headquarters in Tarrytown, NY and is not open to fully remote work arrangements.</strong></p><p><strong>As a Director, Patent Attorney, a typical day might include:</strong></p><ul><li><p>Identifying and capturing new inventions relating to therapeutic antibodies, formulations of therapeutic antibodies, or methods of treatment based on preclinical or clinical research</p></li><li><p>Working with outside counsel to prepare and prosecute US and international patent applications</p></li><li><p>Managing the implementation of coordinated global patent strategies</p></li><li><p>Assisting in US or foreign patent administrative actions (e.g., post-grant oppositions, post grant reviews)</p></li><li><p>Monitoring clinical programs and continued research and development efforts, including reviewing related planned publications or disclosures</p></li><li><p>Conducting or assisting in patent landscape, freedom-to-operate, or competitive intelligence assessments relating to Regeneron’s therapeutic molecules</p></li><li><p>Assisting in litigation or transactional activities as needed.</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Strong organizational skills and the ability to effectively manage multiple projects and competing priorities</p></li><li><p>Ability to work independently and handle a large and complex docket with minimal supervision</p></li><li><p>Excellent oral and written communication skills, including the ability to present complex information accurately and concisely</p></li><li><p>Strong interpersonal skills, including the ability to work effectively and build trust with colleagues and clients at all levels of the organization.</p></li></ul><p><strong>To be considered for this opportunity, you must:</strong></p><ul><li><p>Have a Ph.D. in the life sciences (e.g., molecular biology, cell biology, immunology, biochemistry, or related fields)</p></li><li><p>Have a J.D. from an accredited law school</p></li><li><p>Be admitted to practice before the USPTO and licensed to practice law in at least one state (member of the NY bar or eligible for in-house licensure in NY)</p></li><li><p>Have at least 4-5 years of experience in a law firm and/or corporate law department preparing and prosecuting patent applications in the life sciences</p></li><li><p>Have experience preparing and prosecuting patent applications related to large molecule biologics, especially antibodies.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Applications Analyst – Oracle Fusion]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47859]]></requisitionid>
    <referencenumber><![CDATA[R47859]]></referencenumber>
    <apijobid><![CDATA[r47859]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47859/principal-it-applications-analyst-oracle-fusion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal IT Applications Analyst is a business-facing role supporting Regeneron's Digital Fusion program — the global transformation moving the organization from Oracle EBS to Oracle Fusion. The role is responsible for the configuration, implementation, maintenance, and ongoing project delivery of Fusion and adjacent IT applications. The successful candidate will partner closely with Business Process Owners in Supply Chain, Manufacturing, Quality, Finance, and Procurement, and external implementation partners to translate business needs into working solutions, drive process design, and deliver enhancements that support the future-state operating model.</p><p>As a Principal IT Applications Analyst – Oracle Fusion, a typical day might include the following:</p><ul><li>Acts as a Technical SME and delivery lead on Digital Fusion workstreams, partnering with Business Process Owners, system integrators, and other implementation partners to deliver functional and technical solutions.</li><li>Coordinates across business departments and stakeholders — Supply Chain, Manufacturing, Quality, Finance, Procurement — gathering, challenging, and shaping enhancement requests and design decisions.</li><li>Leads business analysis activities: requirements elicitation, current-state and future-state process mapping, gap analysis, fit-gap workshops, and translation of business needs into functional specifications.</li><li>Drives process flow thinking across cross-functional workstreams — identifying upstream dependencies, downstream impacts, integration touchpoints, and opportunities for harmonization across sites.</li><li>Owns system documentation, including conversion of User Requirement Specifications into Detailed Design Specifications, configuration test plans, traceability matrices, and summary reports.</li><li>Configures reports and supports the design and delivery of Fusion reporting, dashboards, and analytics aligned to business needs.</li><li>Processes IT Applications change control requests, ensuring full traceability, impact assessment, and stakeholder alignment.</li><li>Works with Validation and Quality departments to ensure IT Applications are implemented following Computer Software Assurance (CSA) and development life cycle approaches, in line with GxP and 21 CFR Part 11 expectations.</li><li>Supports integration design and delivery between Oracle Fusion and adjacent systems (e.g. Kinaxis, Maximo, MES, LIMS) using enterprise middleware (e.g. BOOMI, Kong, IBM MQ), partnering with technical architects and integration leads.</li><li>Trains other IT Applications team members and contributes to building team capability across the Fusion footprint.</li><li>Coordinates with other IT Applications team members to implement systems in an efficient, repeatable manner.</li><li>Provides end-user support for IT Applications during hypercare and post-go-live phases, including troubleshooting at the application and integration layer.</li><li>Facilitate solution hand over to operations team and managed service providers.</li><li>Leads IT Applications systems security access reviews and periodic audit trail reviews.</li><li>Supports day-to-day project activities, including RAID log maintenance, status reporting, and cross-functional coordination.</li><li>Prioritizes day-to-day work assignments to support delivery milestones and application troubleshooting activities.</li><li>Maintains up-to-date training records for self and, where applicable, direct reports.</li><li>Other duties as assigned.</li></ul><p>This role may be for you if you have:</p><ul><li>Demonstrated experience delivering enterprise IT applications in a project environment — full lifecycle from requirements through deployment and hypercare.</li><li>Hands-on experience with Oracle Fusion or Oracle EBS strongly preferred; experience supporting an EBS-to-Fusion transformation is highly desirable.</li><li>Previous experience in pharmaceutical, biotech, medical device, or other regulated GxP environment strongly preferred — familiarity with GMP, 21 CFR Part 11, ALCOA+, and CSA/CSV practices.</li><li>Experience working with implementation partners and managing vendor deliverables.</li><li>Project Management experience; professional qualification (PMP, PRINCE2, or equivalent) preferred.</li><li>Exposure to adjacent platforms (Kinaxis, Maximo, MES, Veeva, Boomi, Databricks) is an advantage.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology, Engineering, Business, or a related field, and</p><ul><li>Senior IT Applications Analyst: 5 years of relevant experience.</li><li>Principal IT Applications Analyst: 8 years of relevant experience.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HCP Marketing (Neuro)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47880]]></requisitionid>
    <referencenumber><![CDATA[R47880]]></referencenumber>
    <apijobid><![CDATA[r47880]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47880/associate-director-hcp-marketing-neuro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of HCP Marketing will lead healthcare professional marketing strategy and execution for the Rare Neurology product in the U.S. This highly visible role requires a forward-looking individual with deep marketing expertise and the ability to navigate a competitive landscape. The Associate Director will partner closely with cross-functional teams to advance the products growth, contribute to the brand's financial success, and help support the launch of the first neurology product at Regeneron.</p><p><strong>A Typical Day Might Look Like:</strong></p><ul><li>Contributing and supporting the HCP marketing strategy, ensuring full integration with the broader brand strategy.</li><li>Acting as a key advocate for the brand strategy, clearly articulating priorities and ensuring alignment across Regeneron teams.</li><li>Overseeing the development of HCP engagement strategies, messages, and tactical campaigns tailored to Neurologist.</li><li>Building and deploying a competitive market strategy that proactively addresses evolving competitors and market dynamics.</li><li>Driving strong cross-functional and alliance collaboration, partnering with Sales, Medical Affairs, TLLs, Market Research, Market Access, Regulatory, Legal, Clinical, and HEOR to deliver cohesive, compliant, and impactful initiatives.</li><li>Ensuring all marketing programs comply with corporate policies, regulatory/ethical frameworks, and alliance standards.</li><li>Tracking and managing marketing spend, timelines, and deliverables to meet budget, scope, and performance expectations.</li></ul><p><strong> </strong></p><p><strong>This Role Might Be For You If You:</strong></p><ul><li>Combine strategic and scientific acumen with an ability to translate insights into actionable marketing strategies.</li><li>Have a proven track record of leadership and influence across organizational levels.</li><li>Bring exceptional communication and presentation skills, with the ability to simplify and convey complex strategies to diverse audiences—both technical and non-technical, including senior executives.</li><li>Excel in execution and project management within a fast-paced, dynamic, and competitive marketplace.</li><li>Demonstrate organizational agility, adapting priorities and strategies to external market shifts or internal dynamics.</li><li>Thrive in cross-functional and alliance settings, effectively shaping collaboration, alignment, and decision-making.</li><li>Possess strong experience in managing agencies and external partners, ensuring creative excellence and accountability.</li><li>Are disciplined in managing budgets and resources aligned to strategic objectives.</li></ul><p><strong> </strong></p><p>To be considered for the role, we expect you to have a Bachelor’s degree required; MBA strongly preferred. We are also seeking 10+ years of progressive experience in the pharmaceutical/biotech industry or related field and 8+ years of U.S. commercial experience in pharmaceutical/biotech marketing, product management, or related areas. It is preferred to have Rare Neurology experience strongly preferred. Lastly, we expect you to be onsite in Sleepy Hollow, NY 4 days a week and willing to travel 30% of the time.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, HCP Marketing (Neuro)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47882]]></requisitionid>
    <referencenumber><![CDATA[R47882]]></referencenumber>
    <apijobid><![CDATA[r47882]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47882/senior-director-hcp-marketing-neuro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Director of Neurology HCP Marketing is responsible for developing and implementing marketing strategies for the Neurology portfolio in the United States. This involves understanding the evolving competitive landscape, aligning with broader franchise strategies, and customizing approaches for specific healthcare providers like Neurologist. The Senior Director of will contribute to the financial success of the products and will report to the Executive Director Marketing Lead. </p><p><strong>A Typical Day Might Look Like This:</strong></p><ul><li>Leading the development of the Rare Neurology strategy and ensuring it aligns with the overall brand strategy.</li><li>Effectively conveying and advocating for the Neurology portfolio strategy among key internal stakeholders.</li><li>Overseeing the development of focused messages and tactics for Neurologists.</li><li>Leading the development of competitive strategy to address current and future competitors.</li><li>Developing and fostering strong partnerships with Sales, Medical Affairs, TLLs, Market Research, Market Access, Regulatory, Legal, Clinical, HEOR and other cross functional partners to ensure aligned objectives at Regeneron and across the alliance.</li><li>Ensuring that marketing processes and programs align with corporate guidance, as well as regulatory, legal, and ethical guidelines.</li><li>Leading and providing development opportunities for direct reports.</li><li>Monitoring spending against budget and managing projects to agreed-upon timelines, budgets, and scope.</li></ul><p><strong>This Position Might Be for You If:</strong></p><ul><li>You successfully demonstrate strategic and scientific acumen.</li><li>You have leadership and experience managing teams.</li><li>You bring strong communication and presentation skills, capable of articulating complex strategies to stakeholders of all levels, including Senior Leaders, regardless of their technical background.</li><li>You can focus on execution and manage multiple projects in a fast-paced environment.</li><li>You demonstrate the ability to work effectively and efficiently with team members, and across departments, to ensure consistency and collaboration in strategy development and implementation of programs.</li></ul><p>To be considered for this opportunity you must have a bachelor’s degree is required; an MBA is a plus. 15+ years of progressive industry or relevant professional experience. 8+ years of experience in pharmaceutical/biotech marketing, product management, or a related industry. Rare Neurology experience is preferred. Must be willing to travel 25-30% of the time, including weekend travel as needed. Willingness to work in a hybrid environment with a minimum of 4 days on-site at Sleepy Hollow, NY (Westchester County).</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Study Inspection Readiness]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47671]]></requisitionid>
    <referencenumber><![CDATA[R47671]]></referencenumber>
    <apijobid><![CDATA[r47671]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47671/senior-manager-clinical-study-inspection-readiness/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Senior Manager, Clinical Study Inspection Readiness</strong>, leads all Good Clinical Practice (GCP) inspection readiness activities for one or more assigned clinical programs within Clinical Trial Management (CTM). Reporting to senior leadership and partnering closely with Program Operations Leaders (POLs) and Clinical Study Leads (CSLs), this role owns the preparation, organization, and execution of inspection readiness strategy in accordance with International Council for Harmonization (ICH)/GCP guidelines, Regeneron Standard Operating Procedures (SOPs), Work Instructions (WIs), and Business Practice Tools (BPTs). The role provides inspection readiness leadership across both internally sourced studies and those outsourced to Clinical Research Organizations (CROs), serving as the primary CTM point of contact for all inspection-related activities. This role is expected to leverage Artificial Intelligence (AI)-powered tools — including large language model (LLM) applications such as Claude — to accelerate deliverable production, strengthen documentation quality, and drive continuous improvement in inspection readiness operations, with all AI-assisted outputs subject to human review and full GCP compliance</p><p><strong>A typical day in this role looks like:</strong></p><p><strong>Serve as:</strong></p><ul><li>CTM Inspection Readiness point of contact leading GCP inspection readiness programs across complex, multi-program clinical portfolios involving both internal teams including CRO partners, and Inspection Management.</li><li>Project manager during the inspection process (mock, dry run and/or actual) and assist, and/or lead (as needed) the CTM team with follow up requests from the inspector/inspection management team during mock and actual inspection(s).</li></ul><p><strong>Provide guidance and support to Clinical Trial Management as follows:</strong></p><ul><li>Work with Clinical Study Team (CST) and functional areas to support CTM in providing responses to the Q&A sessions held by Inspection Management for Inspection Readiness, support action item follow up as needed.</li><li>Support ongoing CTM activities related to TMF health and oversight</li><li>Provide guidance on compliance and regulations and ensure CTM staff study teams are following targeted SOPs during study, Business Practice Tools and Working Instructions during the study</li><li>Track inspection readiness meetings, CTM Inspection action items, questions and answers, storyboards, and presentation requests with key stakeholders (internal/CRO) until closure</li><li>Manage CTM inspection action items throughout the inspection lifecycle, from pre-inspection activities (readiness meetings, Q&As, storyboards, presentation requests with internal/CRO stakeholders) to post-inspection tasks (remediation plans, timelines, documentation, closure updates), ensuring prompt resolution and a complete audit trail.</li><li>Support the CTM processes related to Inspection Readiness to ensure that appropriate documentation is produced/maintained in the TMF, including frequently requested documents and early identification of Sites of Interest (SOI).</li><li>Work with the Clinical Study Leads, CRO and/or Vendor team(s) to obtain all the necessary essential and regulatory documents for all study/sites as part of the IRR activities.</li><li>Track CTM action items assigned following inspections to ensure action plans are in place for remediation, as needed, with timelines for completion. Ensure supportive documentation is available to support resolution of the action items and provides updates to as needed on the resolution</li><li>May lead and participate in internal process improvement projects/initiatives to continuously improve operational excellence to support inspection readiness</li><li>Utilize AI-powered applications (e.g., Claude, Microsoft Copilot) to draft, refine, and quality-check executive summaries, inspection storyboards, response documents, and Corrective and Preventive Action (CAPA) narratives, TMF gap analysis, action item tracking, and executive communication.</li><li>Establishing goals, expectations, and accountabilities for direct reports. Regularly reviews performance in respect to quality and timeliness standards according to Regeneron SOPs and working procedures.</li><li>Responsible for coaching, managing training and leading the direct reports.</li><li>May require up to 25% travel</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a BS/BA Degree and 8+years relevant clinical experience. Clinical Inspection experience heavily preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Environmental Sustainability]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48087]]></requisitionid>
    <referencenumber><![CDATA[R48087]]></referencenumber>
    <apijobid><![CDATA[r48087]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48087/associate-director-environmental-sustainability/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we believe that protecting ecosystems essential to human health is inseparable from our mission to improve lives. Guided by Regeneron’s philosophy of “Doing Well by Doing Good,” “Planet” is a pillar of our responsibility strategy — and this role is at the center of it.</p><p>As Associate Director, Environmental Sustainability, you will lead cross-functional efforts to develop and drive enterprise-wide climate and nature strategies. You will translate strategy into action, including by: assessing and addressing risks and opportunities, driving cross-functional strategic initiatives, overseeing data management, owning key disclosures, engaging stakeholders, and partnering across the organization to achieve our 2030 Planet goals.</p><p>This is a rare opportunity to shape and execute sustainable strategies at a science-led, high-integrity company at the forefront of medical innovation.</p><p><strong>When & where:</strong></p><p><strong>Where</strong>: Sleepy Hollow NY</p><p><strong>When</strong>: 4 days on-site plus one work from home day</p><p><strong>Discover your role:</strong></p><ul><li>Lead enterprise-level efforts to drive progress towards our 2030 Planet goals, including partnering with cross-functional stakeholders to develop and execute strategic action plans</li></ul><ul><li>Work hand-in-hand with subject matter experts to develop and advance strategies on evolving climate and nature topics, such as sustainable packaging, environmental lifecycle assessments, and nature-based solutions</li></ul><ul><li>Lead climate and nature risk assessments, action plans, and reporting in line with TCFD and TNFD frameworks and regulatory requirements</li><li>Lead enterprise-wide data collection, management and validation of environmental data across GHG emissions, energy, water, and waste</li><li>Identify and implement opportunities to enhance environmental performance, including improvements to data quality, integrity and management</li><li>Own Regeneron’s environmental data management system (UL360) and ensure data governance frameworks are robust and audit-ready</li><li>Lead relevant readiness efforts for upcoming regulatory requirements, such as the EU Taxonomy and California Climate Rules</li><li>Engage colleagues and harness their shared passion for sustainability to drive corporate sustainability priorities</li><li>Build relationships with external stakeholders, including industry peers, disclosure frameworks, and ratings agencies</li><li>Oversee cross-functional efforts to develop and maintain environmental disclosures, including our annual Responsibility Report, CDP submission, ESG ratings and rankings, tender applications, and policies and position statements</li></ul><p><strong>This role requires:</strong><br> </p><ul><li>10–15 years of experience in environmental sustainability with a proven track record of developing and implementing strategies</li><li>Deep technical expertise in GHG accounting, environmental data management, and TCFD/TNFD frameworks</li><li>Strong command of international environmental standards (e.g. GHG Protocol) and evolving regulatory requirements (EU CSRD, California SB253/SB261)</li><li>Experience with environmental data systems (e.g. UL360, Workiva, or similar) and a commitment to data quality and integrity</li><li>Exceptional communication skills, including the ability to translate complex environmental topics for executive and non-technical audiences</li><li>Bachelor’s degree in environmental science, sustainability, engineering, or related field; advanced degree preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison  - Neurology (Northeast)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48117]]></requisitionid>
    <referencenumber><![CDATA[R48117]]></referencenumber>
    <apijobid><![CDATA[r48117]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48117/associate-director-thought-leader-liaison-neurology-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Massachusetts]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Neurology Marketing team. It will be focused on enhancing and improving interactions with key external US Neurology thought leaders at academic centers and leading community practices for our neurology product.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Neurology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><p><strong>The typical day may include the following:</strong></p><ul><li>The Neurology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You possess a strong science background with deep knowledge of rare neurology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p><strong>To be considered for this opportunity, you will possess the following:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10 years of relevant work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in Neurology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry. Launch experience preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li><li>Must have a valid driver’s license</li><li>Must be able to travel 60%-80% of time </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison  - Neurology (Mid-South)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48124]]></requisitionid>
    <referencenumber><![CDATA[R48124]]></referencenumber>
    <apijobid><![CDATA[r48124]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48124/associate-director-thought-leader-liaison-neurology-mid-south/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - North Carolina]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Neurology Marketing team. It will be focused on enhancing and improving interactions with key external US Neurology thought leaders at academic centers and leading community practices for our neurology product.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Neurology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><p><strong>The typical day may include the following:</strong></p><ul><li>The Neurology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You possess a strong science background with deep knowledge of rare neurology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p><strong>To be considered for this opportunity, you will possess the following:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10years of relevant work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in Neurology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry. Launch experience preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li><li>Must have a valid driver’s license</li><li>Must be able to travel 60%-80% of time </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Group Quantitative Pharmacology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47831]]></requisitionid>
    <referencenumber><![CDATA[R47831]]></referencenumber>
    <apijobid><![CDATA[r47831]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47831/director-group-quantitative-pharmacology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Director in Pharmacometrics (Quantitative Pharmacology), this individual is accountable for the delivery of support for one or more research & development programs, within their pharmacometrics discipline. In this capacity the Director is accountable for the timely and accurate delivery of needed quantitative analyses, interpretation, and messaging to PMx management, as well as the timely delivery of well-constructed and well-messaged reports for PMx review.</p><p><strong>A day in the life of a Director may look like:</strong></p><ul><li><p>Manages and is accountable for the PK/PD evaluation of a small portfolio of products or projects.</p></li><li><p>Works independently, with guidance in only the most complex situations.</p></li><li><p>Informs PMx management of important program and regulatory developments in a timely manner.</p></li><li><p>Ensures analyses and documentation are of the highest quality and accuracy.</p></li><li><p>Ensures that reports and other documents have the appropriate messaging and that a meaningful “story-line” is developed.</p></li><li><p>Ensures that study reports and other documents have an appropriate functional review and are suitable for review by senior management.</p></li><li><p>Solves complex problems; takes a broad perspective to identify solutions.</p></li><li><p>Has a strong publication record and actively publishes work in scientific literature</p></li><li><p>Makes contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.</p></li><li><p>Has excellent interpersonal and communication skills, both written and oral, and has ability to communicate complex information succinctly.</p></li></ul><p><strong>This may be the right role for you if you:</strong></p><ul><li><p>Are fully knowledgeable of pharmacokinetic /pharmacodynamic principles, pharmacology, biology, and quantitative aspects of drug development as well as having an advanced knowledge of pharmaceutical drug development.</p></li><li><p>Possess a deep understanding of scientific literature and technical skills in a number of PK/PD methods and techniques. Has extensive knowledge base of the work in overall scientific community in own discipline.</p></li><li><p>Recognized as an expert in own area within the organization.</p></li><li><p>Have extensive regulatory experience through authoring of regulatory briefing books, CTD summaries, contribution at HA meetings, HA negotiations through regulatory reviews and approvals of BLA or equivalent.</p></li><li><p>Decisions are guided by policies, procedures and business plan; receives guidance from head of function.</p></li></ul><p><strong>In order to be considered qualified for this role, </strong>you must have a PhD and 10+ years with a degree in Quantitative Pharmacology (Pharmacometrics) or related field.</p><ul><li><p>Hands on usage of a broad range of quantitative tools and systems is required, as is a strong publication record in the field.</p></li><li><p>A proven track record of displaying excellent interpersonal and communication skills both written and oral and ability to communicate complex information succinctly.</p></li><li><p>Proven experience developing QP elements of regulatory strategy and interacting with regulatory agencies without supervision.</p></li></ul><p>#PMx</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Associate Scientist, Drug Product Development and Technology (1 of 3)]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46695]]></requisitionid>
    <referencenumber><![CDATA[R46695]]></referencenumber>
    <apijobid><![CDATA[r46695]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46695/sr-associate-scientist-drug-product-development-and-technology-1-of-3/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Drug Product Development & Technology is seeking a Senior Associate Scientist as we work to support all stages of pre-clinical, clinical, commercial formulation, and drug product development for various drug product modalities. In this role, you will apply biochemical and biophysical methods to carry out developability assessment and formulation development studies on monoclonal antibody-based therapeutics, to support drug substance and drug product development.</p><p><em><strong>Job Duties:</strong></em></p><ul><li><p>Design and independently execute phase-appropriate formulation development studies, such as formulation screening, stability and compatibility studies, to support drug product development for early and late-stage development programs.</p></li><li><p>Conduct pre-formulation studies for monoclonal antibodies, bioconjugates and peptides, using various biophysical and biochemical techniques to identify critical quality attributes for formulation and drug product development.</p></li><li><p>Develop analytical methods for drug products, with primary focus on peptides, and supporting focus on antibody–drug conjugates, siRNA, monoclonal antibodies, and bispecific antibodies </p></li><li><p>Develop and qualify analytical methods for critical quality attributes to support formulation development, DP process development, and stability testing for programs in preclinical and clinical stage. </p></li><li><p>Characterize drug product formulation to support the process development and manufacturing of clinical drug substances and drug products.</p></li><li><p>Document findings and lab records in electronic laboratory notebook by following the organizational best practices and policies.</p></li><li><p>Contribute to formulation development technical reports to provide insights into process development and manufacturing of clinical drug substances and drug products.</p></li><li><p>Participate in meetings and present study results in cross-functional team meetings or department meetings.</p></li><li><p>Author protocols, technical documents for internal use and support regulatory filings.</p></li><li><p>Take part in the general laboratory and instrument maintenance.</p></li></ul><h3><em><strong>Job Requirements:</strong></em></h3><ul><li><p>Take direction and guidance for data-driven decision making, priority setting and technical problem solving.</p></li><li><p>Generate and organize data figures and data tables in a clear and insightful way</p></li><li><p>Communicate critical data in timely manner to supervisor and team</p></li><li><p>Strong ability to prioritize and manage multiple tasks effectively.</p></li><li><p>Highly organized, detail-oriented, self-motivated, effective team player.</p></li><li><p>Excellent oral and written communication skills.</p></li></ul><p>This role requires a B.S or M.S degree in Pharmaceutical Sciences, Chemistry, Biochemistry, Biophysics, Biomedical Engineering, Analytical Chemistry, Chemical Engineering, or a related discipline with at least 3 years of industrial experience. The ability to design and execute experiments, as well as interpret, document, and communicate results with minimal supervision is required. Strong technical knowledge base and relevant experience with protein/peptide chemistry, biophysical/biochemical characterization of proteins, bioanalytical method development and biomolecule product development is desirable. Hands-on experience with biochemical and biophysical techniques for protein characterization, including chromatography (SEC, IEX, RP), viscosity, gel electrophoresis (CE-SDS, MCE, cIEF, iCE), particle size (DLS, HIAC, MFI), spectroscopy (UV-Vis, CD, AUC, fluorescence), and thermostability characterization (DSC, DSF) is desirable.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Pharmacy Support Services]]></title>
    <date><![CDATA[Thu, 14 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44682]]></requisitionid>
    <referencenumber><![CDATA[R44682]]></referencenumber>
    <apijobid><![CDATA[r44682]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44682/senior-manager-pharmacy-support-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Senior Manager, Pharmacy Support Services</strong> (PSS) serves as a high‑impact subject matter expert in investigational product (IP) management and pharmacy operations across our clinical portfolio. In this role, you will guide best practices for IP handling, preparation, and administration; develop high‑quality pharmacy documentation and training; and support global clinical sites to ensure safe, compliant, and streamlined trial execution.</p><p>You will partner closely with Formulation Development Group (FDG), Clinical Operations, and CDSL leadership to shape strategy, improve processes, and directly influence the success of our trials. This is an opportunity to elevate your clinical and scientific expertise in a role that blends technical depth, operational leadership, and cross‑functional collaboration.</p><p><strong>A typical day in this role looks like: </strong></p><p><strong>Lead Pharmacy & Clinical Trial Support</strong></p><ul><li>Act as the primary SME on investigational product preparation, administration, blinding, and pharmacy‑related ancillary supplies.</li><li>Shape the development of pharmacy manuals, clinical study documents, and training materials supporting biologics and gene therapy programs.</li><li>Partner with Clinical Operations, CROs, and site pharmacy teams to ensure IP readiness, compliance with regulatory requirements, and optimal preparation workflows.</li></ul><p><strong>Drive Study Execution Excellence</strong></p><ul><li>Lead or contribute to Kick‑Off Meetings, Site Initiation Visits, Investigator Meetings, and IP‑focused training for global clinical teams.</li><li>Support the review and resolution of IP‑related deviations and practice‑based issues to maintain protocol integrity and patient safety.</li><li>Manage ancillary supply compatibility assessments in collaboration with FDG.</li></ul><p><strong>Uphold Quality, Compliance & Continuous Improvement</strong></p><ul><li>Provide guidance on IP‑related quality assurance issues and support risk mitigation strategies.</li><li>Ensure adherence to GCP, ICH guidelines, and federal/international regulatory standards.</li><li>Identify opportunities to enhance processes and elevate site experience through data‑driven improvements and feedback mechanisms.</li></ul><p><strong>Develop & Mentor Talent</strong></p><ul><li>Create engaging training modules for internal teams, monitors, and research sites.</li><li>Play a key role in onboarding new colleagues and fostering a culture of scientific excellence, collaboration, and shared knowledge.</li></ul><p><strong>This role may be for you if you have: </strong></p><ul><li>Expertise in sterile product preparation and infusion‑based drug administration</li><li>Experience with biologics; cell and gene therapy exposure preferred</li><li>Strong understanding of clinical supply chains and clinical trial execution</li><li>Exceptional communication, documentation, and presentation skills</li><li>Ability to manage complex projects and influence cross‑functional teams</li><li>Adaptability, critical thinking, and a continuous‑improvement mindset</li><li>Familiarity with PCAB, FDA, USP <795>/<797>, NABP/VPP, and EU CTR guidelines</li><li>Strong analytical, decision‑making, and problem‑solving capabilities</li></ul><p><strong>In order to be considered qualified</strong>, a minimum of a bachelor’s degree in pharmacy or nursing with 8+ years of experience in hospital pharmacy, clinical research, or pharma/biotech. Or a PharmD with 6+ years of experience in hospital pharmacy, clinical research, or pharma/biotech.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41999]]></requisitionid>
    <referencenumber><![CDATA[R41999]]></referencenumber>
    <apijobid><![CDATA[r41999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41999/hvac-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add an experienced HVAC Technician to our growing team at our Menands campus with a Monday-Friday 8:00am-4:30pm shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. We perform all tasks necessary for troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><div><p>As an HVAC Technician, a typical day might include the following:</p><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC and facilities related equipment</li></ul><p>This role might be for you if you:</p><ul><li>Follow current good manufacturing practices (cGMPs) and good business practices (G)</li><li>Ensure safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, GDPs and quality standards</li><li>Can communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Are able to coordinate with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Have a solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>Are EPA certified for refrigeration gases</li><li>Have the ability to become fully gown qualified to work in production areas</li></ul><p>To be considered for the HVAC Technician you ideally should have an AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level. Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred.</p><ul><li>HVAC Technician II: AAS with 2+ years of relevant experience or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years of relevant experience or equivalent combination of education and experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Finance & Administration - Netherlands]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46247]]></requisitionid>
    <referencenumber><![CDATA[R46247]]></referencenumber>
    <apijobid><![CDATA[r46247]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46247/associate-director-finance-administration-netherlands/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are hiring an Associate Director, Finance & Administration to partner closely with country leadership and commercial teams, supporting high‑impact business decisions through financial insight, forecasting, and analysis. This role sits at the centre of the country organisation, working across Finance, Accounting, Tax, Treasury, and global CFO functions to shape commercial performance, governance, and long‑term planning.</p><p>If you enjoy combining critical thinking with hands‑on delivery—and value visible ownership at country level—this is a role where your expertise will genuinely influence outcomes.</p><h3>What You’ll Be Doing:</h3><ul><li>Partnering with country leadership on budgeting, forecasting, and financial planning</li><li>Preparing and presenting forecasts, including actuals versus forecast analysis</li><li>Managing resource planning, including FTE utilisation across cost centres</li><li>Supporting commercial teams with P&L ownership and profitability insights</li><li>Translating epidemiology and commercial data into financial forecasts</li><li>Coordinating with Accounting on revenue accuracy, accruals, and reporting</li><li>Acting as a local finance liaison across Tax, Treasury, and CFO functions</li><li>Ensuring compliance with internal policies and external regulations</li></ul><h3>This Role May Be For You If:</h3><ul><li>You enjoy working closely with senior collaborators to support sound decisions</li><li>You like roles that balance strategic perspective with practical execution</li><li>You are comfortable partnering across commercial, medical, and G&A teams</li><li>You value clear country ownership and accountability</li><li>You enjoy collaborating with global and local finance colleagues</li><li>You are motivated by improving processes and strengthening governance</li></ul><h3>To Be Considered:</h3><p>You will have a relevant undergraduate degree, along with a postgraduate qualification (such as an MBA) and/or a recognised professional finance qualification. You will bring at least five years of post‑qualification finance experience, primarily within the biotech or pharmaceutical industry, including experience supporting commercial P&Ls. Fluency in English and the local country language is required. International experience and additional language skills are an advantage.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€95,250.00 - €158,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - TRENTON, NJ]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48012]]></requisitionid>
    <referencenumber><![CDATA[R48012]]></referencenumber>
    <apijobid><![CDATA[r48012]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48012/medical-account-specialist-ii-neurology-trenton-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Trenton]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Trenton (Metro), NJ</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - BALTIMORE, MD]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48015]]></requisitionid>
    <referencenumber><![CDATA[R48015]]></referencenumber>
    <apijobid><![CDATA[r48015]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48015/medical-account-specialist-ii-neurology-baltimore-md/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Baltimore]]></city>
    <state><![CDATA[Maryland]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Baltimore (Metro), MD</li></ul><p><strong> </strong></p><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - FORT WORTH, TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48063]]></requisitionid>
    <referencenumber><![CDATA[R48063]]></referencenumber>
    <apijobid><![CDATA[r48063]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48063/medical-account-specialist-ii-neurology-fort-worth-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Fort Worth]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Fort Worth (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - NEW HAVEN, CT]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48002]]></requisitionid>
    <referencenumber><![CDATA[R48002]]></referencenumber>
    <apijobid><![CDATA[r48002]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48002/medical-account-specialist-ii-neurology-new-haven-ct/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[New Haven]]></city>
    <state><![CDATA[Connecticut]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: New Haven (Metro), CT</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, Immuno-Oncology]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48101]]></requisitionid>
    <referencenumber><![CDATA[R48101]]></referencenumber>
    <apijobid><![CDATA[r48101]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48101/senior-associate-scientist-immuno-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oncology & Immuno-Oncology group is seeking an exceptional Senior Associate Scientist to join a high-performing team dedicated to advancing next-generation bispecific antibodies for solid tumor indications. This role is best suited for a scientifically rigorous, highly driven individual who thrives in a fast-paced, translational research environment where high-quality experimental data directly supports clinical advancement.</p><p>In this role, you will contribute to the development and evaluation of novel bispecific antibody therapeutics, working at the intersection of tumor biology and immune modulation. You will collaborate closely with cross-functional teams and generate robust, reproducible datasets that inform program progression from preclinical development toward clinical studies.</p><p>This position offers the opportunity to work on cutting-edge approaches in cancer immunotherapy with clear line-of-sight to clinical application, while gaining increasing exposure to experimental design, data interpretation, and program-level scientific discussions. The ideal candidate is motivated, organized, detail-oriented, and thrives in a fast-paced, team-driven environment. Experience with tumor models and mammalian cell culture is highly desirable.</p><p><strong>As an Associate Scientist in the immune-oncology group, your typical day might include:</strong></p><ul><li><p>Execute well-designed in vivo studies to evaluate novel bispecific antibodies, including mouse handling, dosing (IP, IV, subcutaneous), and blood/tissue collection</p></li><li><p>Perform ex vivo immune profiling (e.g., flow cytometry, ELISA, MSD) to characterize pharmacodynamic response and mechanism of action</p></li><li><p>Process tissues and tumors for immune cell isolation and downstream analysis</p></li><li><p>Generate high-quality, well-documented datasets suitable for inclusion in internal reports supporting program advancement</p></li><li><p>Collaborate closely with multidisciplinary teams to ensure alignment of experimental design with program needs</p></li><li><p>Present findings in group and cross-functional meetings, contributing to ongoing scientific discussions</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Are energized by working in a science-driven, collaborative environment focused on impactful therapeutic development</p></li><li><p>Bring strong attention to detail, organization, and commitment to experimental rigor and reproducibility</p></li><li><p>Are adaptable and eager to learn new techniques and contribute across multiple workflows</p></li><li><p>Are motivated by the opportunity to contribute to the advancement of novel therapeutics toward the clinic</p></li><li><p>Present findings in group and cross-functional meetings, contributing to ongoing scientific discussions</p></li></ul><p><strong>To be considered, you must meet the following:</strong></p><ul><li><p>B.S./M.S. with 2-3yrs relevant experience in oncology, immunology, or related field</p></li><li><p>Experience with mouse handling and in vivo tumor models strongly preferred</p></li></ul><ul><li><p>Experience with cell culture, flow cytometry, and/or immunoassays (ELISA, MSD) is highly desired</p></li><li><p>Demonstrated ability to generate high-quality data with strong attention to detail</p></li><li><p>Ability to work independently while contributing effectively in a team environment</p></li><li><p>Strong analytical skills and clear communication of scientific findings</p></li></ul><ul><li></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior QA Validation Specialist]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48401]]></requisitionid>
    <referencenumber><![CDATA[R48401]]></referencenumber>
    <apijobid><![CDATA[r48401]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48401/senior-qa-validation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Senior QA Validation Specialist</strong> to join our <strong>Quality Assurance </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Raheen, Limerick</li><li>Some travel may be required.</li></ul><p><strong>What you’ll do:</strong></p><ul><li>Generating, executing and/or reviewing master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria</li><li>Analysing the results of testing and determines the acceptability of results against pre-determined criteria</li><li>Investigating and troubleshooting problems which occur and determines solutions or recommendations for changes and/or improvements</li><li>Reviewing, editing and approval deviation notifications, deviation investigations, and corrective actions</li><li>Reviewing and approval of change controls, SOPs, reports and other documentation</li><li>Coordinating with other departments or outside contractors/vendors to complete validation tasks</li><li>Managing projects and prepares status reports</li><li>Providing oversight to contingent workers may be a requirement</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>Ability to work independently or as part of a team</li><li>Ability to communicate with transparency</li><li>Demonstrate respectful behaviour at all times</li><li>Gathers and organises information</li><li>Meets commitments on scope and on time</li><li>Follows directions, performs well-defined tasks</li><li>Effective time management skills</li><li>Seeks to identify continuous improvement needs</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>To be considered for this opportunity you must have a BS/BA in Engineering, Chemistry or Life Science and requires at least 5 – 8+ years’ proven experience in Commissioning / Qualification experience with Large Scale Process equipment </li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p>#IRELIM #JOBSIEST #LI-Onsite #REGNIEQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Compliance]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44121]]></requisitionid>
    <referencenumber><![CDATA[R44121]]></referencenumber>
    <apijobid><![CDATA[r44121]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44121/manager-compliance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an experienced Manager, Corporate Compliance to join our dynamic team in Japan. Reporting to the Japan Compliance Lead, you will play a pivotal role in supporting Regeneron’s compliance operations, ensuring the highest standards of ethical conduct and regulatory adherence. This is an exciting opportunity to contribute to the development and implementation of compliance programs that support our mission of advancing science and delivering life-changing medicines. If you are passionate about compliance and working in a collaborative, innovative environment, we invite you to explore this opportunity. </p><p><strong>A Typical Day: </strong></p><p>As the Manager, Corporate Compliance, you will: </p><p>- Collaborate with the Japan Compliance Lead and Global Compliance teams on healthcare compliance (HCC) matters. </p><p>- Implement and operationalize Regeneron’s compliance program and policies in Japan in alignment with headquarters. </p><p>- Develop and refine compliance policies, work instructions, and guidance to ensure adherence to local and international regulations, including JPMA and FTC codes. </p><p>- Deliver engaging compliance training programs for employees and third parties to promote understanding of applicable laws and industry codes. </p><p>- Provide compliance oversight and guidance to ensure interactions with healthcare professionals (HCPs) and organizations (HCOs) are conducted ethically and in accordance with established policies. </p><p>- Conduct internal reviews, risk assessments, and monitoring activities to identify and mitigate compliance risks effectively. </p><p>- Partner with cross-functional teams to provide creative solutions to compliance challenges. </p><p>- Support additional compliance projects and strategies as needed to enhance operations in Japan and the broader APAC region. </p><p><strong>This Role May Be For You If: </strong></p><p>- You have a strong knowledge of the pharmaceutical industry and its self-regulatory framework in Japan, including the JPMA and FTC codes. </p><p>- You thrive in collaborative environments and excel at building cross-functional relationships to achieve compliance goals. </p><p>- You are a problem solver with a creative approach to addressing compliance challenges and implementing practical solutions. </p><p>- You are proactive in identifying risks and opportunities to enhance compliance programs. </p><p>- You have exceptional communication skills in both Japanese and English, with the ability to deliver clear, concise, and impactful messages. </p><p>- You are detail-oriented and committed to maintaining the highest ethical standards in all aspects of your work. </p><p>- You are adaptable and willing to travel to meet the needs of the role. </p><p><strong>To Be Considered: </strong></p><p>We are looking for candidates with a minimum of a BA/BS degree (advanced degrees such as MBA or JD are preferred but not required) and at least 5 years of experience in healthcare compliance-related activities within the pharmaceutical industry in Japan. A strong working knowledge of Japan’s healthcare compliance laws, including the JPMA and FTC codes, is essential. Proficiency in both English and Japanese (written and verbal) is required, along with the ability to draft professional documents and guidance materials. </p><p>If you are ready to take the next step in your compliance career and contribute to a culture of integrity and innovation, we encourage you to apply today.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology (f/m/d) - Nürnberg - Erlangen - Weiden - Regensburg - Ingolstadt - Pfaffenhofen]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48501]]></requisitionid>
    <referencenumber><![CDATA[R48501]]></referencenumber>
    <apijobid><![CDATA[r48501]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48501/sales-specialist-immunology-fmd-nuernberg-erlangen-weiden-regensburg-ingolstadt-pfaffenhofen/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Sales Specialist Immunology (f/m/d), you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our ENT (ear - nose - throat) division at key meetings. You will identify the key people in ENT, understand the account context and tailor calls based on individual and account requirements and build KOL support for our portfolio.</p><br><p><strong>Where:</strong></p><br><p><strong>Field based in the territory:</strong> <strong>Nürnberg - Erlangen - Weiden - Regensburg - Ingolstadt - Pfaffenhofen</strong></p><br><br><p><strong>Discover your role:</strong></p><br><ul><li>Competent advice and support for relevant Healthcare Professionals (HCP) and, where applicable, customers in the hospital segment</li><li>Building and maintaining intensive and sustainable customer relationships - in person and using digital channels</li><li>Target-oriented, substantive dialogue focused on the benefits for customers and added value for patients</li><li>Independent regional management including account analyses, route planning and documentation of your activities in the CRM system</li><li>Participation in trade fairs and congresses as well as independent planning, coordination and realization of training events and specialist presentations</li><li>Regular reporting to the sales management</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>Deep understanding of the local healthcare economy, with the ability to identify key players in ENT</li><li>“Patient first” value system</li><li>Bachelor’s degree or equivalent experience and a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</li><li>5+ years of sales experience within the biotech/pharmaceutical sector</li><li>Respiratory experience is preferred</li><li>Proficiency in German as well as conversational English</li><li>Readiness for very frequent travel and a driver's license cl. 3/B.</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>64.125,00 € - 106.875,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Product and  Pipeline Communications Manager]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48082]]></requisitionid>
    <referencenumber><![CDATA[R48082]]></referencenumber>
    <apijobid><![CDATA[r48082]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48082/product-and-pipeline-communications-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Product and Pipeline Communications, Europe and Canada to join our Product and Pipeline Communications International team, supporting Europe and Canada. In this role, you will strengthen and protect Regeneron’s reputation through science-driven, patient-centered communications while collaborating with in-country cross-functional teams, Commercial, Clinical, Medical Affairs, and Global Corporate Affairs. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Munich , Paris , Madrid</p><p>Hybrid model</p><p><strong>Discover your role:</strong></p><ul><li>Lead in-country communications priorities, strategies, and processes.</li><li>Develop country-level strategies for stakeholder communications programs.</li><li>Partner with Commercial, Clinical, and Medical Affairs teams.</li><li>Manage media relations, medical congress support, and milestone communications.</li><li>Identify communications risks and recommend appropriate response strategies.</li><li>Shape Corporate Affairs strategies with regional insights and local updates.</li><li>You advise cross-functional partners with sound judgement and clarity.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree, or equivalent, with 7–9+ years’ relevant experience.</li><li>3+ years’ product and/or pipeline communications experience.</li><li>Global, regional, and in-country communications expertise within Europe.</li><li>Understanding of EU regulatory, commercial, and legal pharmaceutical communications.</li><li>Fluent in English as well as German , French or Spanish</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€79,500.00 - €132,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Immunology - Central CH and Ticino]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48611]]></requisitionid>
    <referencenumber><![CDATA[R48611]]></referencenumber>
    <apijobid><![CDATA[r48611]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48611/key-account-manager-immunology-central-ch-and-ticino/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Switzerland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Sales Specialist Immunology Central Switzerland to join our Immunology Inter. Commercial Team, supporting our Central CH-TI region in a field-based role. In this role, you will achieve territory sales objectives and drive account success while collaborating with alliance partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong><br>Central CH-TI, Switzerland — field-based<br> </p><p><strong>Discover your role:</strong></p><ul><li>Drive territory sales performance against defined business objectives</li><li>Develop annual territory plans using market and data insights</li><li>Manage key accounts and stakeholder engagement across your territory</li><li>Leverage data sources to shape effective territory action plans</li><li>Ensure compliance with regulatory, legal, and reporting requirements</li><li>Collaborate closely with alliance partners to achieve shared goals</li><li>You build strong networks across healthcare stakeholders in your region</li><li>You adapt plans based on evolving market dynamics and insights</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree (or equivalent) and/or pharmaceutical sales certification</li><li>Minimum 5 years’ pharmaceutical sales experience</li><li>Fluency in German and English; Italian or French knowledge is an advantage</li><li>Strong customer engagement and value-based selling capabilities</li><li>Ability to present complex information effectively to varied audiences</li><li>Experience in biologics and immunology is advantageous</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Clinical Data Reporting]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47783]]></requisitionid>
    <referencenumber><![CDATA[R47783]]></referencenumber>
    <apijobid><![CDATA[r47783]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47783/associate-director-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><p>As an Associate Director, Clinical Data Reporting, you will provide leadership and operational oversight for clinical and external data reporting across clinical development programs. You will drive the delivery of high-quality data programming outputs, reconciliation workflows, and reporting solutions that support clinical trial quality, compliance, and informed decision-making.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Leading program-level oversight for clinical data reporting and programming deliverables across development programs</p></li><li><p>Driving development of participant-level listings, exception reports, external data reconciliation outputs, and operational metrics</p></li><li><p>Establishing and maintaining reporting standards, templates, and scalable programming approaches</p></li><li><p>Providing subject matter expertise in data programming, transformation, and visualization to enhance reporting capabilities</p></li><li><p>Collaborating with cross-functional teams to align priorities and ensure timely delivery of reporting outputs</p></li><li><p>Ensuring adherence to regulatory requirements, quality standards, and inspection readiness expectations</p></li><li><p>Driving continuous improvement and automation of reporting workflows</p></li><li><p>Identifying and managing risks related to data quality and delivery timelines</p></li><li><p>Monitoring KPIs to assess reporting performance and enhance processes</p></li><li><p>Leading and mentoring reporting and programming teams to drive operational excellence</p></li></ul><p><strong>This job may be for you if you have:</strong></p><ul><li><p>Strong expertise in clinical data management, reporting, and data visualization</p></li><li><p>Experience working with clinical trial data, including eCRF and external data sources such as PK, biomarker, imaging, and ECG</p></li><li><p>Deep understanding of data transformation, validation, and reconciliation processes</p></li><li><p>Strong knowledge of regulatory standards such as ICH-GCP, CDISC, and 21 CFR Part 11</p></li><li><p>Experience with tools such as SAS, R, Tableau, Power BI, Spotfire, or similar reporting platforms</p></li><li><p>Proven ability to work cross-functionally and manage stakeholder expectations</p></li><li><p>Strong analytical, problem-solving, and communication skills</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Bachelor’s degree with 10+ years of relevant experience</p></li><li><p>10+ years of experience in clinical data management or related areas within pharma/biotech</p></li><li><p>At least 5+ years of leadership experience managing teams and mentoring staff</p></li><li><p>Strong experience in clinical data reporting, programming, and analytics</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, EDC Administration]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48273]]></requisitionid>
    <referencenumber><![CDATA[R48273]]></referencenumber>
    <apijobid><![CDATA[r48273]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48273/specialist-edc-administration/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Specialist, EDC Administration to join our Data Management team in a hybrid role. In this role, you will lead EDC system administration across our clinical trial portfolio — Medidata Rave environment setup, user access management, and platform administration — while collaborating with CRO partners, Clinical Data Management, and cross-functional team members, ensuring these functions meet Regeneron procedures, SOPs, and regulatory requirements. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad, India (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Administer Rave User Management — accounts, roles, and permissions in Medidata Cloud Administration</p></li><li><p>Process access requests, modifications, and deactivations across studies</p></li><li><p>Maintain user access records and respond to queries from internal teams and CRO partners</p></li><li><p>Administer the database access interface across EDC, SharePoint, and other data systems</p></li><li><p>Perform archiving and file legacy study documents into the Trial Master File</p></li><li><p>Coordinate the EDC Administration calendar across environment setup, access provisioning, and release milestones</p></li><li><p>Contribute to platform upgrades, migrations, and integrations, and support inspection readiness for access audit trails and compliance</p></li><li><p>You stay organized and detail-focused while managing multiple concurrent studies</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in mathematics, science, information systems, or a related field</p></li><li><p>2+ years in biotech, pharmaceutical, or healthcare, with 2+ years in EDC or clinical systems administration</p></li><li><p>Medidata Rave platform administration required, including Cloud Administration, User Management, environment configuration, and PDF Generator</p></li><li><p>Strong understanding of access control, audit trails, and system compliance in a regulated environment</p></li><li><p>Knowledge of 21 CFR Part 11, ICH-GCP, and CDISC standards</p></li><li><p>Robust knowledge of Data Management processes and EDC platform administration best practices</p></li><li><p>Proficiency with SharePoint, Microsoft Office Suite, and collaboration tools</p></li><li><p>Communication, cross-functional coordination, and time management in a matrix environment</p></li><li><p>Prior user access management and study environment configuration strongly preferred</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Delivery and Operations Product Lead – Global Patient Safety]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48288]]></requisitionid>
    <referencenumber><![CDATA[R48288]]></referencenumber>
    <apijobid><![CDATA[r48288]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48288/delivery-and-operations-product-lead-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, the Associate Director, Product Lead for Global Patient Safety sits within the Global Development IT organization, and is a key member of the Delivery & Operations function, responsible for coordinating and guiding their team members in delivering, maintaining & enhancing business solutions. This role partners with key business collaborators to intake, design, implement and improve technology products.</p><p><strong>When & where:</strong> </p><p>This role is based at our Armonk, NY or Warren, NJ location with a minimum of four days onsite per week required – this role is not open to fully remote or hybrid work arrangements.</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead implementation, operational support and improvements for Global Patient Safety technology products while guiding Product Analysts and other Delivery & Operations team members.</p></li><li><p>Intake, assess, prioritize, and validate domain specific needs/requirements including partnership with BSPs to ensure alignment between technology roadmaps and product priorities.</p></li><li><p>Act tactically and think strategically, switching leadership styles as needed to influence, guide, and mentor individuals and team.</p></li><li><p>Own end-to-end automating reporting solution, including driving quality and compliance by standardizing report templates, ensuring validated linkages to source data, and automating submission-readiness checks.</p></li><li><p>Harmonize narratives, data structures, and formatting rules to improve report consistency across markets, minimizing regional variability and instilling scientific and regulatory compliance in every output</p></li><li><p>Build relationships with key leaders, partners, and stakeholders to clarify and negotiate (when needed) on demands and solutions.</p></li><li><p>Responsible for identifying resourcing needs and for oversight of internal and vendor delivery, and manage service vendor associates, in support of product.</p></li><li><p>Lead steering committee meetings, working groups, system change requests, issue management, and release management for upgrades to existing product.</p></li><li><p>Accountable for the completion of all necessary project deliverables with responsibility for oversight of Product Analysts, Business Analysts, and other team members as applicable. </p></li><li><p>Responsible for end-to-end product management, including oversight of individual project execution and capability-roadmap planning.</p></li><li><p>Partner with Enterprise IT to help customize service offerings to meet Global Development needs where necessary.</p></li><li><p>Responsible for tracking quantifiable value delivered versus plan and preparing consolidated operational reports summarizing savings.</p></li><li><p>Serves as oversight, quality assurance and escalation point for products within team scope.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelors Degree in a related field.</p></li><li><p>At least 10+ years relevant experience, including product owner experience of Global Patient Safety technology solutions (e.g., Argus)</p></li><li><p>Experience working on end-to-end GxP implementations from requirements gathering to IQ and PQ execution</p></li><li><p>Knowledge of the Information Technology Service Management Framework and ITIL v3x</p></li><li><p>Knowledge of Software Development Life Cycle, and agile methodologies and tools (e.g., Jira, Confluence)</p></li><li><p>Strong record of accomplishment of technology project management, stakeholder management, budget management and collaboration skills</p></li><li><p>Experience motivating and building skills within a team of direct reports, instilling a process improvement culture in junior level colleagues.</p></li><li><p>Experience participating in an end-to-end product launch or shut down across multiple teams.</p></li><li><p>Experience hiring, supervising, managing, and mentoring a team in service of complex issues.</p></li></ul><ul><li><p>Excellent communication skills and the ability to indirectly influence key partners and stakeholders with clear, concise, and well-formed message tailored to the audience</p></li><li><p>Ability to analyze business challenges and present technology solutions</p></li><li><p>Knowledge of pharmaceutical Global Development (e.g., Global Patient Safety, Regulatory Affairs, Clinical Quality) business capabilities, processes, systems, and key trends in the industry</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 08:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Drug Product MSAT Engineer]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48564]]></requisitionid>
    <referencenumber><![CDATA[R48564]]></referencenumber>
    <apijobid><![CDATA[r48564]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48564/senior-drug-product-msat-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is seeking a Senior Drug Product (DP) Manufacturing Sciences and Technology (MSAT) Specialist to join our Process Science Drug Product Engineering department. The Drug Product Manufacturing Science and Technology (MSAT) Engineer supports equipment selection, management of equipment qualification, and process validation activities, and will be responsible for solving issues during technology transfer and cGMP start-up for internal or external manufacturing sites. They also provide on the floor support during operations, as needed, for internal or external manufacturing, reviews process data to ensure operational consistency, and provides support for investigations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>Location: Rensselaer, New York, United States</li><li>Monday-Friday, 8am-4:30pm</li><li>25-50% travel domestic & occasionally internal</li></ul><p>Discover your role:</p><ul><li>Provides drug product manufacturing process knowledge for new product introduction, technology transfer, process validation, process troubleshooting and issue resolution for biopharmaceutical drug products</li><li>With the support of multi-functional teams, acting as the technical lead, for technology transfer of the drug product manufacturing processes to manufacturing facilities</li><li>Tracking and reporting project milestones related to raw material/component procurement, equipment readiness, process transfer, manufacturing document creation, etc.</li><li>Reviewing and approving cGMP batch documentation (master batch records, component specifications, validation protocols, material specifications, etc.) required to support cGMP production at manufacturing facilities</li><li>Assisting with investigation and root cause determination and CAPA identification and implementation for manufacturing deviations</li><li>Trending process performance and collaborates with internal and external teams to establish/improve process performance, process capability to ensure process is operating within intended process control strategy</li><li>Authoring technical reports/protocols in support of cGMP activities</li><li>Supporting development of sampling plans for cGMP batches related to process characterization, process qualification, lot release, stability etc.</li><li>Assisting in equipment selection, qualification, and start up activities and working with manufacturing to ensure robust procedures are used for operation of equipment</li><li>Partnering with strategic sourcing/procurement to specify technical requirements associated with raw materials, components, equipment and services to ensure external vendor on time delivery</li><li>Supporting the drafting of regulatory filings and responding to regulatory information requests</li></ul><p>This role requires:</p><ul><li>BS in Engineering; chemical engineering or biomedical engineering preferred and 5+ years of relevant experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.</p><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><p>For jobs in Canada: this posting is for an existing position.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Diagnostics]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45732]]></requisitionid>
    <referencenumber><![CDATA[R45732]]></referencenumber>
    <apijobid><![CDATA[r45732]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45732/associate-director-clinical-diagnostics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>This role provides an exciting opportunity to lead projects across diverse therapeutic areas. As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy, development, and lifecycle management of companion diagnostic solutions that enable our therapeutics. This role drives cross-functional alignment across biomarker science, clinical development, regulatory, commercial, and external IVD partners to deliver fit-for-purpose assays that meet global regulatory requirements and support clinical decision-making. You will lead the CDx portfolio from early biomarker feasibility through clinical validation, registration, launch, and post-market sustainment, ensuring timely availability of high-quality diagnostics aligned with drug development milestones.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ and Cambridge, MA</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Set the global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines for the therapeutic.</p></li><li><p>Lead selection and oversight of IVD partners; negotiate scopes, timelines, budgets, and quality expectations; manage co-development and governance.</p></li><li><p>Define assay intent and target product profiles (TPP) for CDx platforms (e.g., NGS, PCR, IHC, Immunoassays), ensuring analytical and clinical performance meets intended use.</p></li><li><p>Partner with biomarker and clinical teams to integrate CDx into trial designs (screening, enrichment, stratification), including sample strategy and operational readiness.</p></li><li><p>Drive analytical validation plans (e.g., accuracy, precision, sensitivity/specificity, LoD, reproducibility) and clinical validation strategies linking assay results to drug safety and efficacy.</p></li><li><p>In collaboration with IVD Regulatory, support global regulatory strategy and submissions for CDx (e.g., FDA PMA/supplement, 510(k) where applicable, EU IVDR, PMDA), including pre-submission interactions and labeling alignment.</p></li><li><p>Ensure compliance with applicable standards and regulations (e.g., ISO 13485, ISO 14971, CLSI guidelines, IVDR, GCP alignment for diagnostic use in trials).</p></li><li><p>Coordinate cross-functional working groups, remove program obstacles, and provide transparent status reporting to governance bodies.</p></li><li><p>Oversee design transfer, manufacturing readiness, and supply planning with IVD partners to ensure clinical and commercial availability.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced degree in a relevant field (e.g., MS/PhD in molecular biology, pathology, biomedical engineering, or related) or equivalent experience.</p></li><li><p>8+ years of experience in diagnostics development, with 4+ years leading CDx or IVD programs in pharmaceutical or diagnostics settings</p></li><li><p>Proven track record delivering CDx aligned to drug approvals, including successful analytical/clinical validation and regulatory submissions.</p></li><li><p>Deep understanding of diagnostic platforms (NGS, PCR, IHC, Immunoassays) and associated validation standards and quality systems.</p></li><li><p>Experience managing external IVD partners and complex, cross-functional programs.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Medical Affairs, Neurology]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48596]]></requisitionid>
    <referencenumber><![CDATA[R48596]]></referencenumber>
    <apijobid><![CDATA[r48596]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48596/senior-medical-director-medical-affairs-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Senior Medical Director, Medical Affairs, Neurology</strong></p><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Neurology/Myasthenia Gravis Medical Affairs Team. The Senior Medical Director is responsible for the co-development of medical strategy and planning & execution of medical affairs activities at Regeneron. This hire will provide medical leadership and serve as a key scientific/medical resource.</p><p>The Senior Medical Director will report to Head of Medical Affairs, Neurology and work in a cross-functional, matrix organization. He/she will also collaborate with external stakeholders such as healthcare practitioners, key opinion leaders and payers.</p><p><strong>When & where:</strong></p><p>4 days a week on-site in Sleepy Hollow, New York; Warren, New Jersey; or Cambridge, Massachusetts</p><p><em>*If hired in Warren, NJ or Cambridge, MA, frequent travel to Sleepy Hollow, MA may be required*</em></p><p><strong>Discover your role:</strong></p><ul><li>Maintain deep scientific and medical knowledge of Neurology / Myasthenia Gravis, treatment landscape and clinical decision making</li><li>Function as an integral member of the cross-functional Medical Team</li><li>Responsible for data generation, data analyses and interpretation as it relates to Phase 4 studies, including interventional and observational research</li><li>Responsible for the medical content of post-marketing study reports, analyses of clinical data, safety monitoring, and activities that ensure patient safety</li><li>Provide scientific and medical support for development of strategic medical, publications, communications and integrated evidence generation plans</li></ul><ul><li>Participate in developing and presenting medical content at congresses, symposia and advisory boards</li><li>Proactively bring patients' & physicians' voice on cross-functional teams, to enable effective and impactful decision making</li><li>Provide medical training for internal staff on investigational and/or approved products, disease state and unmet needs</li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li>An M.D. or equivalent with board eligibility or board certification in Neurology is strongly preferred</li><li>A minimum of 8 years Pharmaceutical / Biotech industry experience (launch experience is preferred)</li><li>Direct experience in Myasthenia Gravis or Neurology Rare Disease is strongly preferred</li></ul><ul><li>Experience and ability in working in a dynamic, matrix environment; excellent collaboration and communication skills</li><li>Ability to demonstrate deep understanding of all medical affairs accountabilities</li><li>Thorough understanding of Neurology and Myasthenia Gravis healthcare environment and key stakeholders</li></ul><p> #MDJobs, #MDJobsMA, #GDMAJobs, #Neurology</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Gastro)-Nashville, TN]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48648]]></requisitionid>
    <referencenumber><![CDATA[R48648]]></referencenumber>
    <apijobid><![CDATA[r48648]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48648/medical-specialist-i-gastro-nashville-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Gastroenterology (MS) will report to the District Manager, Gastroenterology, and be responsible for engaging Gastroenterologists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies, and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US. </p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Gastroenterology therapeutic area to generate product utilization. The MS will develop strong working relationships with experts and all Gastroenterologists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, alliance counterparts, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Nashville, TN</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Proven success navigating and demonstrating positive impact with large groups, institutional settings, and Ambulatory Surgery Centers</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Gastroenterology market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Pharmacologist]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47549]]></requisitionid>
    <referencenumber><![CDATA[R47549]]></referencenumber>
    <apijobid><![CDATA[r47549]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47549/clinical-pharmacologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>As a<strong> Clinical Pharmacologist </strong>this individual is expected to plan, design, implement and analyze in-vivo and in-vitro pharmacokinetic & pharmacodynamic studies working with Clinical Pharmacology, Quantitative Pharmacology, Pharmacometrics/Pharmacodynamics (PK/PD), Toxicology, Bioanalytical, Therapeutic Focus areas and Clinical Development / Regulatory Affairs teams.</p><p>This individual contributes to the scientific understanding of PK/PD for assigned projects, based on quantitative evaluation of the pharmacokinetic and pharmacodynamic profile for research programs, through the application of state-of-the-art knowledge in pharmacokinetics and pharmacodynamics.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Plans, designs, implements and analyzes routine Pharmacometrics (PMx) studies to advance scientific knowledge, in collaboration with other team members.</p></li><li><p>Performs analyses such as compartmental modeling, PopPK, translational modelling, disease modelling, Pop PK/PD, E-R analyses (or work closely with Research Specialist or Pharmacometrics Stats Programming team) to deliver Pharmacometrics results, interpretation and discussion.</p></li><li><p>Collaborates with Scientific Writing (and where appropriate with Pharmacometrics Stats Programming team) to ensure TFLs for Pharmacometrics reports are complete. Works in conjunction with Scientific Writing, Quality Control and QAA (as required) to issue study reports in support of IND/CTA submissions and other regulatory documents.</p></li><li><p>With close supervision from senior Pharmacometrics staff, supports preparation of material to be used in regulatory interactions.</p></li><li><p>Contributes to preparation of Pharmacometrics materials for regulatory background packages, e.g. for pre-IND, EOP2, and pre-BLA meetings.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A PhD in Biology, Pharmacology, Engineering or a Pharmacy (Pharm.D.), Medicine (MD) degree and at least 3+ years of relevant Clinical Pharmacology experience.</p></li><li><p>Are able to serve independently as study Clinical Pharmacology/Quantitative Pharmacology/PPKPD lead for moderately complex</p></li><li><p>Is highly skilled in use of relevant software, including MS-Excel, R, R-Studio, Prism, Phoenix WinNonlin, NLME, STAN and NonMem, working in department computing environment to perform advanced PMx analyses.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 11:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - SAN ANTONIO, TX]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48928]]></requisitionid>
    <referencenumber><![CDATA[R48928]]></referencenumber>
    <apijobid><![CDATA[r48928]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48928/medical-account-specialist-ii-hematology-san-antonio-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>San Antonio, TX</strong></p><ul><li><strong>Geography: </strong><strong>San Antonio, Austin, West Texas, Rio Grande Valley</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - CHICAGO SOUTH, IL]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48950]]></requisitionid>
    <referencenumber><![CDATA[R48950]]></referencenumber>
    <apijobid><![CDATA[r48950]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48950/medical-account-specialist-ii-hematology-chicago-south-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- Chicago South</strong></p><ul><li><strong>Geography: Chicago</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - INLAND EMPIRE, CA]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48963]]></requisitionid>
    <referencenumber><![CDATA[R48963]]></referencenumber>
    <apijobid><![CDATA[r48963]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48963/medical-account-specialist-ii-hematology-inland-empire-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialist - Hematology- </strong><strong>Inland Empire</strong></p><ul><li><strong>Geography: </strong><strong>Duarte, Riverside, Loma Linda, Palm Springs </strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Site Office Manager]]></title>
    <date><![CDATA[Fri, 03 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46900]]></requisitionid>
    <referencenumber><![CDATA[R46900]]></referencenumber>
    <apijobid><![CDATA[r46900]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46900/site-office-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Office Manager to coordinate office operations and ensure the business environment, services, and supports are in place for employees to work efficiently and safely. In this role, you will partner with the Site Head, line manager, enabling functions, vendors, service providers, and landlord to keep the office running effectively. This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Mississauga, Ontario</p></li><li><p>Office based</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Coordinate office operations so employees can work efficiently and safely.</p></li><li><p>Partner with HR, Facilities, IT, EHS, Accounting, Communications, and Legal.</p></li><li><p>Manage office vendors, service providers, landlord relationships, and related purchases.</p></li><li><p>Support health, safety, emergency response, security, and visitor tracking processes.</p></li><li><p>Oversee office space, supplies, repairs, inventories, couriers, and workplace needs.</p></li><li><p>You balance requests from multiple stakeholders while keeping site needs clear.</p></li><li><p>You collaborate across locations to share best practice with other Office Managers.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Leaving Cert, A-levels, Abitur, Baccalaureate, or equivalent education.</p></li><li><p>Minimum 2–3 years of experience in a similar role.</p></li><li><p>Technical proficiency in computer and phone systems, including iPhone, Microsoft PowerPoint, Outlook, Excel, Word, SharePoint, and Teams.</p></li><li><p>Ability to handle and prioritise multiple tasks and simultaneous requests while supporting multiple stakeholders.</p></li><li><p>Knowledge of purchase order systems, such as Oracle.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Jul 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[MEDICAL REPRESENTATIVE (MR) - RESPIRATORY *HOKKAIDO AREA]]></title>
    <date><![CDATA[Mon, 06 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48567]]></requisitionid>
    <referencenumber><![CDATA[R48567]]></referencenumber>
    <apijobid><![CDATA[r48567]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48567/medical-representative-mr-respiratory-starhokkaido-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative, Respiratory, Japan to join our ROW Commercial Team, supporting our Japan region in a hybrid work mode. In this role, you will achieve sales objectives in respiratory while collaborating with our alliance partners and internal teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><p>You will be responsible for the Hokkaido area.</p><p>Your place of residence is expected to be either Sapporo or Asahikawa.</p><br><p>Discover your role:<br>Achieve sales objectives in respiratory for the assigned territory<br>Develop and implement annual territory business plans based on market insights<br>Manage territory budgets and expenses to optimize resource allocation<br>Utilize key data sources to strategically develop action plans<br>Perform all required administrative duties, including reporting and compliance<br>Attend local, regional, and national meetings as directed<br>You work collaboratively with alliance partners to deliver objectives<br>You adapt plans in response to changing market dynamics</p><p>This role requires:<br>Bachelor’s degree (or equivalent experience)<br>Minimum five (5) years sales representative experience in the pharmaceutical industry<br>Superior customer engagement skills with a focus on delivering value<br>Excellent technical aptitude and ability to conduct disease/concept selling<br>Superb written, verbal, and presentation skills<br>Excellent planning and organizational skills<br>Ability to work independently and execute strategic plans under tight timelines<br>Computer literacy including word processing, spreadsheets, databases, and email software<br>Valid driver license and MR Certification<br>Therapy area knowledge (respiratory) and sales experience in biologics desirable<br>Up-to-date clinical knowledge of therapy areas and competitor brands desirable<br>Established Key Opinion Leader relationships within respiratory desirable<br>Fluency in English is a plus but not essential for this role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 06 Jul 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Strategic Partnerships & Business Operations]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41651]]></requisitionid>
    <referencenumber><![CDATA[R41651]]></referencenumber>
    <apijobid><![CDATA[r41651]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41651/associate-director-strategic-partnerships-business-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we are committed to developing and maintaining strategic relationships with clinical institutions that support our Clinical Development pipeline such as Academic Medical Centers (AMCs), Site Management Organizations (SMOs), Site Networks and Community Centers. The Global Partnerships team is responsible for establishing and managing relationships at the executive-level that enable operational and scientific engagement throughout the Global Development organization.</p><p>We are seeking an <strong>Associate Director Strategic Partnerships & Business Operations</strong> that will lead and optimize strategic relationships with clinical trial sites and site networks to drive executional and scientific excellence across the clinical development portfolio. This role will be responsible for establishing and managing governance frameworks with priority clinical trial sites including leading governance meetings, partnership metrics and day-to-day issue identification and resolution. You will report to the Director, Global Development Strategic Partnerships and will support across the Global Partnerships team to ensure the success of these strategic relationships.</p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Serve as the primary relationship owner for priority clinical trial sites</li><li>Establish a governance structure to manage relationships with high priority clinical trial sites including but not limited to:</li><li>Planning and facilitation of governance meetings such as joint research committees and portfolio reviews</li><li>Management of partnership metrics</li><li>Management of communication and issue escalation pathways</li><li>Manage the day-to-day activities to achieve the strategic objectives of the relationship</li><li>Act as a key internal and external point of contact for the relationship to proactively identify and resolve any potential issues</li><li>Act as an internal subject matter expert for the clinical institution to provide guidance to other departments within Regeneron</li><li>Manage critical initiatives with high priority clinical trial sites</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Previous experience in and a deep understanding of the drug development process</li><li>Previous experience maintaining relationships with clinical institutions including communication and stakeholder management at the executive level</li><li>Solid organizational and project management skills including strong attention to detail</li><li>A results-oriented, collaborative style</li><li>Experienced in planning and execution; thinks strategically and executes tactically to deliver results for the business</li><li>Demonstrates resiliency; able and willing to explore different paths to achieve an outcome</li><li>Consistently demonstrates good judgment and takes initiative to bring forward new ideas to improve processes</li><li>Previous experience operating across a matrix of teams and influencing without authority</li><li>Advanced skills in Microsoft Office Suite including Excel and PowerPoint</li></ul><p><strong>In order to be considered qualified for this role</strong> a minimum of a Bachelor’s Degree and 10+ years is required. Advanced degrees (MS, MBA) are preferred when accompanied by 8+ years of proven experience in pharma or a related field.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,800.00 - $252,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, ERP Product Management (Cloud Fusion)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45912]]></requisitionid>
    <referencenumber><![CDATA[R45912]]></referencenumber>
    <apijobid><![CDATA[r45912]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45912/senior-director-erp-product-management-cloud-fusion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Director, ERP Product Management, leads the strategy, architecture, and delivery of Regeneron’s enterprise ERP capabilities and the broader Finance, Procurement, Tax, Treasury, Accounting, and Supply Chain ecosystem. Working with BRMs, IT leaders, and functional business executives, this leader shapes a cross‑functional, capabilities‑based roadmap aligned to medium‑ and long‑term business goals. The Sr. Director oversees cross‑functionally aligned product managers and partners with program leadership to ensure seamless delivery during the Oracle EBS → Oracle Fusion transition and beyond.</p><p><em><strong>The role will be based onsite at our office in Sleepy Hollow, NY. This is not open to fully remote-based work arrangements. If eligible, we can offer relocation benefits. </strong></em></p><p><strong>A typical day: </strong></p><ul><li><p>Shape the cross‑functional ERP technology strategy with BRMs, IT leaders, and functional executives, building a cohesive, capabilities‑based framework aligned to 3–5+ year business goals.</p></li><li><p>Lead teams of cross‑functionally aligned product managers overseeing solution design, architecture, and delivery in line with product strategy, standards, and enterprise architecture.</p></li><li><p>Align product delivery and technology plans to strategic goals and multi‑function roadmaps; ensure product managers supporting each function meet their strategic objectives.</p></li><li><p>Manage prioritization and alignment using industry standards, best practices, and ERP/cloud trends; regularly update the ERP roadmap to reflect market and business changes.</p></li><li><p>Advise senior leaders on the optimal mix of ERP capabilities and products that balance functional outcomes and technology strategy over a multi‑year horizon.</p></li><li><p>Own the ERP product organization budget; coordinate with product managers and portfolio management to manage demand, forecasting, and the project portfolio; drive strategic product decisions in line with business objectives and budgets.</p></li><li><p>Serve as executive IT owner for Oracle EBS and adjacent platforms; partner across Finance, Procurement, Tax, Treasury, Accounting, HR, Legal, and Supply Chain to deliver capabilities that support enterprise objectives.</p></li><li><p>Partner closely with the Senior Director, ERP Program Management IT Lead (Oracle Fusion) to stay informed of Fusion program milestones, upcoming go-lives, and wave planning — ensuring the operational ERP team is ready to receive and support each new Fusion capability as it is delivered.</p></li><li><p>Drive execution and optimization: configuration, extensions, integrations, data migration, reporting enablement, identity & access governance (RBAC/ABAC), testing (UAT/SIT), deployment, and hypercare.</p></li><li><p>Own the ERP enhancement backlog: triage requests, determine EBS vs. native Fusion design, and prevent capability gaps during the transition and cutover waves.</p></li><li><p>Manage the EBS-to-Fusion cutover period from an operations perspective: maintain EBS stability during parallel run periods, coordinate data freeze windows with business partners, and ensure hyper care support is in place post-go-live.</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Proven success leading global, multi‑entity ERP implementations, upgrades, or modernization programs (EBS → Fusion experience strongly preferred).</p></li><li><p>Deep knowledge of finance and adjacent business processes (Order to Cash, Procure to Pay, Record to Report, Acquire to Retire), and experience with EPM/reporting.</p></li><li><p>Expertise in ERP architecture, integrations (APIs, middleware), data migration, security, identity/access management, and cloud operations.</p></li><li><p>Demonstrated experience establishing governance, change control, and audit readiness (SOX, ITGC; GxP as applicable).</p></li><li><p>Strong portfolio, budget, and vendor/SI management; able to align investment decisions to multi‑year product and technology strategy.</p></li><li><p>Track record of developing product managers and cross‑functional teams; excellent executive communication and stakeholder influence.</p></li></ul><p><br><strong>To be considered:</strong></p><ul><li><p>15+ years of progressive leadership across ERP and enterprise applications, including significant experience with Oracle Fusion Cloud ERP and Oracle EBS.</p></li><li><p>Experience managing ERP operations during parallel EBS and Fusion waves, including cutover planning and hypercare.</p></li><li><p>Hands‑on familiarity with Oracle Tax (EBTax), Treasury (Cash Management/bank connectivity), and/or EPM (planning/forecasting).</p></li><li><p>Background in global ERP rollouts, M&A integrations, and multi‑entity consolidation on Oracle platforms.</p></li><li><p>Oracle Cloud/EBS certifications; MBA or advanced degree.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Therapeutic Area Genetics (Immunology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46254]]></requisitionid>
    <referencenumber><![CDATA[R46254]]></referencenumber>
    <apijobid><![CDATA[r46254]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46254/associate-director-therapeutic-area-genetics-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an extremely talented Scientist to join our Immunology Therapeutic Area Genetics (TAG) team. Within the RGC, the Immunology TAG team is using large-scale human exome sequencing for discovery and validation of new therapeutic targets in autoimmune and other immune-mediated disease. You will be responsible for designing and executing studies integrating large scale human genetics and multidimensional omics datasets derived from RGC and public resources in the immunology space to identify new targets for inflammatory and auto-immune diseases and accelerate target transition to novel therapeutics. You will collaborate with various RGC teams and with pre-clinical and clinical development teams at Regeneron to catalyze therapeutic development for genetically-validated targets in immunologic diseases.</p><p><em><strong>This role will require 4 days per week onsite at our campus in Tarrytown, NY. This is not available as a fully remote / hybrid work.</strong></em></p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Understand and leverage RGC and Regeneron datasets, external resources, and the scientific/medical literature to generate research questions and then generate relevant phenotypes from longitiudinal clinical data, design and execute genetic association studies, and perform integrative omics analyses to address these research questions</p></li><li><p>Deploy computational methods to integrate genetic data with multiple omics data to more effectively identify/prioritize drug targets illuminated by genetic association data.</p></li><li><p>Work closely with other members of the Immunology and other TAG teams, Analytic Genetics, Sequencing, and GIDE in cross-functional initiatives within the RGC and Regeneron.</p></li><li><p>Collaboratively summarize insights of investigations into a variety of formats (e.g. documents, presentations, patent applications, publications, etc.) for audiences with broad bacgrounds.</p></li><li><p>Partner with Clinical Development to evaluate clinical stage programs and opportunities for human genetics studies to aid in the selection of indications or evaluation of safety considerations.</p></li></ul><p><strong>This job might be for you if you can/have</strong></p><ul><li><p>Bring innovative thinking to human genetics and epidemiological studies</p></li><li><p>Experience leading complex human genetics research incorporating different analytic methods, phenotypes, and study designs.</p></li><li><p>Ability to use medical knowledge to define relevant phenotypes for genetic association studies and to formulate innovative and important research questions.</p></li><li><p>Worked with multidisciplinary teams to characterize the functional consequences of discovered disease gene variants</p></li><li><p>Understanding of drug development and clinical trial design and execution. Experience in the clinical management or medical research relating to autoimmune and immune-mediated disease is a plus.</p></li><li></li></ul><p><strong>To be considered for this opportunity, you must have </strong>a PhD , MD preferred with 8+ years of experience in the use of WES/GWAS datasets, RNA-Seq, proteomics and other large-scale platforms for genomic/proteomics. Demonstrated expertise in immunobiology, genetics, and mechanisms; familiarity with large genetic studies that deliver novel genetic findings and medically relevant gene discoveries; and demonstrated ability to manage and collaborate in a multi-disciplinary team, to discover and evolve immunology-related drug discovery pipelines. Individuals with proficiency in computational immunology research are particularly encouraged to apply.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Utilities Maintenance, Monday-Friday 2nd Shift]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46968]]></requisitionid>
    <referencenumber><![CDATA[R46968]]></referencenumber>
    <apijobid><![CDATA[r46968]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46968/supervisor-utilities-maintenance-monday-friday-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking to add a Supervisor Utilities Maintenance with a Monday- Friday 2pm-10:30pm schedule to our team. Our Supervisor Utilities Maintenance is primarily responsible for the direction, organization and supervision of utilities maintenance operations. This position is responsible for operations and maintenance of High Purity Water/Steam systems and Plant Utility systems that support Process Manufacturing and overall facility buildings. </p><p>As a Supervisor Utilities Maintenance, a typical day might include the following:</p><div><div><ul><li><p>Planning and scheduling of maintenance, repairs and modifications to Plant Boilers, WFI equipment, distribution systems, compressed gas systems, and plant steam</p></li></ul></div><div><ul><li><p>Planning, scheduling and assigning work tasks utilizing the Blue Mountain Work Request System</p></li></ul></div><div><ul><li><p>Directing supervision of Regeneron facilities maintenance technicians to high performance goals in a cGMP - FDA regulated environment</p></li></ul></div><div><ul><li><p>Administration of contract maintenance personnel responsible for repairs and facility modernization to remain compliant with regulatory codes</p></li></ul></div><div><ul><li><p>Maintaining the physical condition and environment of owned areas</p></li></ul></div><div><ul><li><p>Troubleshooting equipment and developing maintenance plans</p></li></ul></div><div><ul><li><p>Leading teams in continuous improvement, 5S, Lean initiatives</p></li></ul></div><div><ul><li><p>Coaching, counselling and managing performance of direct reports</p></li></ul></div><div><ul><li><p>Followig current good manufacturing practices (cGMPs) and good business practices (G)</p></li></ul></div></div><div><div><ul><li><p>Complying with site safety policies and striving to maintain an accident free environment</p></li></ul></div><div><ul><li><p>Reviewing departmental operations and recommending changes to management</p></li></ul></div><div><ul><li><p>Forecasting resource requirements and submitting budget recommendations to management</p></li></ul></div><div><ul><li><p>Preparing reports for management review</p></li></ul></div><div><ul><li><p>Supervising, coordinating and assuring compliance with contractors and Regeneron employees on all applicable codes and standards</p></li></ul></div><div><ul><li><p>Supporting Deviation Management process including NOE, EOE and DNF investigations and reviews</p></li></ul></div><div><ul><li><p>Other duties and responsibilities as assigned</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Develop and implement ideas and suggestions for improving efficiency</p></li><li><p>Possess good demonstrated supervisory skills</p></li><li><p>Have strong interpersonal, oral and written communication skills</p></li><li><p>Proficient understanding of word processing, spreadsheet and database management software</p></li><li><p>Ensure work conduct is completed with a “Safety First” mindset</p></li><li><p>Demonstrate acute organizational skills to direct personnel during a building crisis or emergency</p></li></ul><p>To be considered for this position you must have an AAS in construction or related technologies and 5+ years of experience, including experience in planning, organizing and supervising a diverse workforce involved in the building maintenance of a large multi-building manufacturing complex. You should also have supervisory experience including training, assigning work, setting expectations and performance evaluations. Equivalent combination of education and experience may be considered. You must be willing and able to work a Monday - Friday 2pm-10:30pm schedule.</p><p>#REGENTOSK</p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Critical Utilities]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47222]]></requisitionid>
    <referencenumber><![CDATA[R47222]]></referencenumber>
    <apijobid><![CDATA[r47222]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47222/director-critical-utilities/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director of Critical Utilities and Facility Management safeguards the reliability, safety, and compliance of the campus Central Utility Plant and all Mechanical, Electrical and Plumbing (MEP) systems, ensuring uninterrupted delivery of electricity, chilled water, steam, emergency power, and other crucial services for 24/7 research and operational needs. Reporting to senior facilities leadership, the role blends strategic planning with hands-on oversight, leading a hybrid workforce (internal technicians + outsourced FM provider), partnering with Engineering, EH&S, and Business Resilience teams, and requires occasional travel—up to 25%—to support off-site infrastructure and vendor audits.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Developing and implementing long-term operational strategies for Critical Utilities and Facilities Maintenance programs supporting a complex pharmaceutical/biotech campus environment.</p></li><li><p>Leading organizational development efforts including team structure design, role definition, workforce planning, and operational model optimization across internal staff and outsourced service providers.</p></li><li><p>Establishing and continuously improving maintenance, reliability, and capital planning programs to improve system performance, resiliency, compliance, and operational efficiency.</p></li><li><p>Providing executive oversight of Central Utility Plant and Powerhouse operations while partnering with operational leadership to ensure safe, reliable, and uninterrupted utility delivery.</p></li><li><p>Collaborating cross-functionally with Engineering, R&pD Operations, EH&S, Quality, Procurement, and Capital Projects teams to support site operations, infrastructure initiatives, and future campus growth.</p></li><li><p>Driving governance, performance management, and strategic vendor oversight activities including the development of critical metrics, operational reviews, budget planning, risk mitigation, and continuous improvement initiatives.</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Thrive on keeping utility plants, chillers, boilers, and generators running with zero unplanned downtime.</p></li><li><p>Balance hands-on problem solving with strategic planning, budgeting, and long-range asset management.</p></li><li><p>Motivate and coordinate a mixed team of internal technicians, union trades, and third-party providers.</p></li><li><p>Are comfortable making sure that rigorous safety and regulatory standards in high-risk environments.</p></li><li><p>Turn maintenance data into actionable reliability improvements.</p></li><li><p>Communicate clearly with researchers, engineers, and executives—and don’t mind hitting the road when needed.</p></li></ul><p><strong>In order to be considered for this role, you must have:</strong></p><ul><li><p>A bachelor’s degree in mechanical/electrical/Power/Marine/Energy Engineering—or—15 years of proven experience as an equivalent (Navy Nuclear Power School + 10 years accepted).</p></li><li><p>10+ years leading central utility or power-plant operations (chilled water, steam, emergency power) within a hybrid FM model, plus strong contract-management and vendor-governance skills.</p></li><li><p>Proficiency with BAS platforms (e.g., Metasys, EcoStruxure, Desigo).</p></li><li><p>Proven team-leadership abilities.</p></li><li><p>A valid NYS driver’s license to support up to 25% travel.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs- Allergy (eastern states)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47510]]></requisitionid>
    <referencenumber><![CDATA[R47510]]></referencenumber>
    <apijobid><![CDATA[r47510]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47510/associate-director-field-medical-affairs-allergy-eastern-states/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This is a pre-launch opportunity to join a newly formed field medical team. As an Associate Director, Field Medical Affairs, you will serve as the primary scientific presence in your territory, engaging in meaningful exchange of clinical data and medical information with KOLs, HCPs, clinical research investigators, pharmacists, and other decision makers. You will build investigator relationships, site infrastructure, and medical intelligence that shape our program’s clinical and medical trajectory. We will align field activities with strategic medical plans, gather actionable insights on the evolving treatment landscape, and support research and development that advances both the pipeline and patient outcomes.</p><p>Territory: eastern states</p><p><strong>A Typical Day May Include:</strong><br>• Collaborate with Clinical Development to identify, qualify, and establish clinical research sites in your territory<br>• Cultivating investigator relationships ahead of study activation to build scientific credibility and organizational trust<br>• Mapping the KOL and investigator landscape in allergy/immunology to inform clinical and medical strategy<br>• Gathering early field insights into treatment patterns, unmet needs, and emerging science to shape the medical plan<br>• Supporting development of medical affairs infrastructure, including educational materials and scientific exchange tools, prior to launch<br>• Acting as a primary clinical/scientific resource to HCPs for disease-state and product information to ensure awareness and understanding<br>• Establishing, fostering, and maintaining peer relationships with KOLs in allergy/immunology<br>• Identifying and reporting medical insights<br>• Identifying research gaps and educational needs to inform medical strategy.<br>• Responding to requests for information related to study indications, disease states, and the therapeutic area, and discussing scientific and clinical data with appropriate audiences in a compliant manner.<br>• Ensuring company policies, procedures, principles, and financial controls are upheld with integrity and professionalism.</p><p>T<strong>his may be for you if you:</strong><br>• Thrive working independently making a meaningful impact on the company’s mission.<br>• Are passionate about developing expertise in and sharing clinical and scientific data. <br>• Enjoy building collaborative relationships across academic and clinical practice settings.<br>• Can balance multiple initiatives, prioritize amid ambiguity, and implement independently while keeping partners engaged and informed.<br>• Are energized by pre-launch work and motivated by the opportunity to build investigator networks and scientific infrastructure from the ground up.</p><p>To be considered a Clinical or scientific doctorate: MD, PharmD, PhD, DNP, or DVM is required. 8 years of experience in a relevant scientific, clinical, or pharmaceutical role, including 4+ years as a Medical Science Liaison in the pharmaceutical industry is required. Experience in allergy/immunology is required. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharmaceutical compliance, and OIG guidelines. Ability to travel frequently (approximately 50%), including air travel, overnight stays, and occasional weekend travel. Prior experience in a pre-launch or launch phase MSL role is preferred. Experience supporting clinical trial site identification, feasibility assessment, or investigator engagement would be helpful. <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Cardiovascular/Metabolism]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47613]]></requisitionid>
    <referencenumber><![CDATA[R47613]]></referencenumber>
    <apijobid><![CDATA[r47613]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47613/senior-medical-director-clinical-development-cardiovascularmetabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Medical Director, Clinical Development, will play a key role in clinical development programs within the Cardiovascular/Renal/Metabolism portfolio focused on obesity and related comorbidities. This role serves as Scientific and Medical Lead for Clinical team(s) working closely with Operational Leads to guide and execute clinical development strategies and subsequent regulatory submissions. This role requires a high-performing and highly passionate individual who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research. The Senior Medical Director reports to an Executive Medical Director, Internal Medicine.</p><p>A typical day may include the following:</p><ul><li><p>Acts as medical expert and leader in interactions with external stakeholders</p></li><li><p>Develops unique and innovative clinical strategies to significantly shorten the development cycle in the face of an evolving regulatory landscape. Designs and develops more efficient and innovative, yet robust Phase 2/3 programs.</p></li><li><p>Works closely with discovery teams to provide input on the next generation of targets in the field and leads the development of plans for Phase 1 clinical testing for initial characterization of the molecules PK/PD and safety.</p></li><li><p>Ensures safety of the drug, including the safety aspects of patients in clinical studies and signal detection from post-marketing surveillance, with the support from Global Patient Safety.</p></li><li><p>Plans and executes publication and clinical communication strategy in coordination with Publications team. Provides input to key external presentations.</p></li><li><p>Ensures quality of all clinical documents (e.g., Investigators’ Brochure, protocol, study report, clinical components of regulatory submissions, safety related documents). Develops written responses to regulatory agency questions and regulatory submission documents.</p></li></ul><p><strong>This may be the role for you if:</strong></p><ul><li><p>A minimum of an advanced degree in medicine (i.e., M.D. or D.O. or equivalent).</p></li><li><p>Clinical training in Endocrinology or Cardiology (board certified or eligible or equivalent) is strongly preferred.</p></li><li><p>A minimum of 4 years of relevant clinical development experience in industry leading clinical trials including: protocol design, managing study start-up, directing and guiding study team execution, data cleaning, medical monitoring/review, database locks.</p></li><li><p>Experience with regulatory filings and interactions with health authorities preferred</p></li></ul><p>This role requires 4 days a week / weekly on-site presence in Tarrytown, NY or Warren, NJ.</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Scientific Writing Operations]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47742]]></requisitionid>
    <referencenumber><![CDATA[R47742]]></referencenumber>
    <apijobid><![CDATA[r47742]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47742/associate-manager-scientific-writing-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Assists in managing project timelines and resources and negotiates timelines across various functional areas. Assists with project sequencing, as directed by senior Scientific Writing Operations personnel. Tracks and reports operational metrics for Scientific Writing tools and processes (e.g., cycle times, throughput, adherence) and recommends continuous improvement opportunities. Manages creation and maintenance of document templates for cross-functional use. </p><p>Supports, drives, and tracks implementation of technical solutions that enable Scientific Writing deliverables (e.g., authoring tools, templates, trackers, and workflow improvements). Coordinates implementation activities (testing/UAT, training materials, communications, and rollout plans) to ensure solutions are delivered on time and adopted by end users. </p><p><strong>As an Assoc Manager, A typical day may include: </strong></p><ul><li><p>Assists in managing project timelines and resources and negotiates timelines across various functional areas </p></li></ul><ul><li><p>Assists with project sequencing, as directed by senior Scientific Writing Operations personnel </p></li></ul><ul><li><p>Manages creation and maintenance of document templates for cross-functional use </p></li></ul><ul><li><p>Supports, drives, and tracks implementation of technical solutions that enable Scientific Writing deliverables (e.g., authoring tools, templates, trackers, and workflow improvements) and coordinates implementation activities (testing/UAT, training materials, communications, and rollout plans) to ensure solutions are delivered on time and adopted by end users </p></li></ul><ul><li><p>Tracks and reports operational metrics for Scientific Writing tools and processes (e.g., cycle times, throughput, adherence) and recommends continuous improvement opportunities </p></li></ul><ul><li><p>Provides backup support for nonclinical document processes to maintain continuity of key workflows (e.g., document routing, publishing/readiness checks, QC coordination, and handoffs between authors and reviewers) </p></li></ul><p><strong>You might be a good match for this role if you:</strong></p><ul><li><p>Partners with cross-functional stakeholders to define user requirements, document business needs, and translate Scientific Writing process gaps into actionable technical enhancements </p></li></ul><ul><li><p>Creates and reviews SOPs and Working Practices pertinent to areas of responsibility </p></li></ul><ul><li><p>Participates in relevant cross-functional drug development team meetings </p></li></ul><ul><li><p>Abides by and keeps current with GxP and regulatory guidelines and all pertinent company SOPs or WPs </p></li></ul><p><strong>To be considered for this role you must meet the following: </strong></p><ul><li><p>Bachelor’s degree or MS/PhD/PharmD in a life science </p></li><li><p>Minimum of 3-5 years’ experience in the pharmaceutical industry </p></li><li><p>Must have PPM (Project Portfolio Management Software) experience</p></li><li><p>Experience with operational/project management support for regulatory or technical writing deliverables is a plus </p></li><li><p>1-2 years of experience participating in cross-functional drug development teams is strongly preferred </p></li><li><p>Previous experience in supervising is a plus </p></li><li><p>Ability to manage multiple projects and excellent organizational, interpersonal and communication skills required </p></li><li><p>Computer proficiency (Microsoft Office Suite [Word, Excel], Adobe Acrobat, and related software) and basic experience with job-relevant AI usage are required </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Corporate Compliance Coordinator – Risk Navigation and Advisory Services]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47747]]></requisitionid>
    <referencenumber><![CDATA[R47747]]></referencenumber>
    <apijobid><![CDATA[r47747]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47747/senior-corporate-compliance-coordinator-risk-navigation-and-advisory-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is looking for an outstanding <strong>Senior Corporate Compliance Coordinator. </strong>Reporting to the Senior Director, Corporate Compliance, this role supports the broader Risk Navigation and Advisory Services team within the Corporate Compliance department, by providing day-to-day operational and administrative support, and contributing substantively to project-based compliance initiatives.</p><p><strong>In this role, a typical day might include the following: </strong></p><ul><li>Supporting the maintenance and administration of compliance documentation, records, and tracking systems.</li><li>Assisting with proofreading, quality review and maintenance of guidance documents, standard operating procedures, communications, and other formal documents.</li><li>Crafting high-quality presentations, communications and visual materials using relevant Microsoft applications (i.e., Word, Excel, PowerPoint) and other tools to support compliance training, leadership updates, and client communications.</li><li>Using Microsoft Excel or other internal platforms to perform data analysis and maintain compliance metrics to inform and support communications, training and monitoring.</li><li>Supporting the planning and execution of compliance related events including live training and National Meetings.</li><li>Responding to routine internal inquiries related to compliance policies and raise issues as appropriate.</li><li>Supporting special projects assigned by management in support of Corporate Compliance objectives.</li><li>Assisting in researching and evaluating approved AI and automation tools to improve compliance workflows and efficiencies, documentation, and analytical capabilities.</li></ul><p><strong>This job might be for you if you: </strong></p><ul><li>Possess excellent written and verbal communication skills and are able to prepare clear, professional materials for diverse audiences.</li><li>Have strong organizational skills and attention to detail with the ability to handle multiple tasks simultaneously.</li><li>Are a collaborative teammate who builds effective working relationships across the organization.</li><li>Demonstrate integrity, sound judgment, and a strong ethical compass in all activities.</li><li>Are self-motivated, curious, and adaptable with a proactive approach to problem-solving.</li><li>Are comfortable engaging with colleagues across levels of the organization in an in-person office environment.</li></ul><p><strong>In order to be considered for this role, you must have: </strong></p><ul><li>Bachelor’s degree in business, Law, Life Sciences, or Communications preferred</li><li>0–2 years of relevant professional experience; prior internship or coursework in compliance, legal, regulatory, or related fields is a plus.</li><li>Strong proficiency in Microsoft Office Suite, with particular emphasis on Word (templates, formatting), Excel (data analysis, pivot tables, formulas) and PowerPoint (design, presentation development).</li><li>Proven knowledge of and hands-on experience with AI productivity tools (e.g., Microsoft Copilot, ChatGPT, or comparable platforms) and an eagerness to explore new AI applications in a business setting.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$30.24 - $47.36]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff External Manufacturing Specialist (Clinical Drug Product)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47766]]></requisitionid>
    <referencenumber><![CDATA[R47766]]></referencenumber>
    <apijobid><![CDATA[r47766]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47766/staff-external-manufacturing-specialist-clinical-drug-product/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are currently looking to fill a Staff External Manufacturing Specialist as the technical and operational authority for clinical contract drug product (DP) filling operations at CMO and business partner sites. Owns the tech transfer process end-to-end, drives active batch management from pre-production through lot disposition, and is a key GMP decision-maker. Provides technical mentorship and leadership to mid-level specialists, and collaborates with management on compliance strategy and CMO performance in the clinical operations space.</p><p><strong>When & where:</strong></p><ul><li><p>Rensselaer, NY</p></li><li><p>Monday-Friday</p></li></ul><p><strong>Discover your role:</strong></p><p>Drug Product Filling – Technical Expertise</p><ul><li><p>Apply deep technical knowledge of aseptic filling unit operations: sterile filtration (bioburden reduction and sterilizing-grade filters), filling (time-pressure, peristaltic, rotary piston), stoppering, capping, and lyophilization cycle development and scale-up.</p></li><li><p>Interpret environmental monitoring (EM) data, airborne particulate results, and media fill (APS) outcomes; assess implications for batch disposition and process adequacy.</p></li><li><p>Partner with DP MSAT to evaluate and apply lessons learned across the network as it relates to CCI, APS, filling operations, CMO assessments, etc.</p></li><li><p>Assess cleanroom design and equipment suitability (ISO 5/Grade A filling zones, Grade B/C support areas) relative to product contamination control requirements.</p></li><li><p>Support extractables and leachables (E&L) risk assessments for product-contact materials and container closure system selection.</p></li></ul><p>Technical Transfer:</p><ul><li><p>Own and lead end-to-end operations of tech transfer to CMO filling sites, gap assessments, risk evaluations and assessments, facility/equipment readiness, engineering run execution.</p></li><li><p>Approve Technical requirements document (TRD), Master Batch Records (MBR), validation reports, summary reports, etc</p></li><li><p>Oversee tech transfer, qualification, and validation of filling lines and critical equipment: isolator/RABS, vial/syringe filling systems, lyophilizers, and component prep (depyrogenation tunnels, washers, autoclave).</p></li><li><p>Coordinates/oversees DP manufacturing at CMO as dictated by project tech transfer and clinical operations.</p></li><li><p>Liaises between various departments within Regeneron including, but not limited to Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments, Legal, Regulatory, Strategic Sourcing and contract manufacturers or business partners.</p></li></ul><p>Technical Mentorship & Leadership</p><ul><li><p>Serve as the primary technical resource for mid-level EM Specialists; provide hands-on guidance on aseptic filling operations, batch record review, deviation management, and CMO oversight.</p></li><li><p>Coach Specialists on interpreting in-process data, applying GMP regulations to real-world filling scenarios, and escalating issues appropriately.</p></li><li><p>Lead sub-teams on continuous improvement initiatives, filling technology upgrades, and CMO performance management.</p></li><li><p>Collaborate with management to communicate CMO operational status, proactively, surface risks, and shape external manufacturing strategy.</p></li></ul><p>Active Batch Management:</p><ul><li><p>Serve as Regeneron’s primary technical contact for all active clinical batches at CMO sites — track filling status, in-process results, and lot disposition milestones in real time.</p></li><li><p>Monitor in-process data: fill weight/volume checks, filter integrity test results, visual/automated inspection outcomes, and lyophilization cycle data.</p></li><li><p>Lead deviation investigations and drive CAPA closure for events occurring during or after filling operations; assess impact on batch and filing.</p></li><li><p>Track cycle times, yield trends, and reject rates across batches; analyze data for process drift and drive continuous improvement actions with the CMO.</p></li><li><p>Lead sub-teams in continuous process improvements, system/equipment implementation and/or strategy development.</p></li></ul><ul><li><p>Ensures product integrity and company reputation monitoring of cGMP compliance at external manufacturing contract manufacturers and business partners.</p></li></ul><p>Regulatory & GMP Compliance</p><ul><li><p>Key GMP decision-maker for external DP filling operations; apply FDA 21 CFR, EU GMP Annex 1, and USP/EP/JP compendia requirements.</p></li><li><p>Ensure CMO change controls are appropriately evaluated for regulatory impact; coordinate post-approval change strategies with Regulatory Affairs.</p></li><li><p>Review CMC sections of regulatory submissions (IND, BLA/NDA, MAA) related to DP manufacturing and filling as required.</p></li><li><p>Support GMP audits of CMO sites; identify compliance gaps, assess risk</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor’s degree or advanced degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biochemistry, or related discipline and 10+ years in pharmaceutical/biopharmaceutical DP manufacturing, with significant direct experience in sterile filling and CMO oversight.</p></li><li><p>Hands-on technical experience with sterile drug product filling operations (aseptic filling, lyophilization, CCI, inspection) in a GMP environment.</p></li><li><p>Demonstrated experience leading or executing tech transfer of DP filling processes to CMO sites, including MBR/TRD approval, PPQ, and process validation.</p></li><li><p>Experience leading deviation investigations and CAPA development for sterile filling operations.</p></li><li><p>Demonstrated ability to mentor and develop technical staff; experience providing guidance in a team or lead capacity.</p></li><li><p>Strong analytical, communication, and cross-functional collaboration skills; ability to influence and make decisions in ambiguous situations.</p></li><li><p>Willingness to travel domestically and internationally up to 25%+ as required.</p></li></ul><p>May substitute proven experience for education requirement.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Grand Rapids North]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47818]]></requisitionid>
    <referencenumber><![CDATA[R47818]]></referencenumber>
    <apijobid><![CDATA[r47818]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47818/medical-specialist-i-dermatology-grand-rapids-north/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Grand Rapids]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Grand Rapids, MI</strong></p><p>Our Medical Specialists are at the forefront of engaging Dermatologists and other key customers. We need someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</p></li><li><p>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. Having a minimum of 2 years selling in the Immunology market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role, dermatology experience preferred. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Immunology & Inflammation]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47869]]></requisitionid>
    <referencenumber><![CDATA[R47869]]></referencenumber>
    <apijobid><![CDATA[r47869]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47869/associate-scientist-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an Associate Scientist working in the field of Allergy to join a highly collaborative Immunology & Inflammation team. This individual will have the opportunity to support a broad pipeline by executing in vivo experiments in mice as well as in vitro assays. Candidate should prefer working in a team-driven environment, possess organizational skills and communicate openly and frequently with manager and team members.</p><p><strong>As an Associate Scientist in Inflammation and Immunology, a typical day may include the following:</strong></p><ul><li><p>Working with the mice and demonstrating proper handling and care, general surgical techniques, and the collection of blood and tissue samples</p></li><li><p>Cell culture and conducting in vitro experiments</p></li><li><p>Lab and equipment maintenance, ordering supplies/reagents to help create a safe, effective and efficient working environment</p></li><li><p>Developing new methods or technologies and troubleshooting in order to achieve project advancement</p></li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li><p>Are highly organized, flexible and motivated.</p></li><li><p>Are skilled in interpreting, analyzing and presenting research data</p></li><li><p>Communicate openly and frequently with manager and team members</p></li><li><p>Are capable of working in an innovative, fast-paced and result oriented research environment</p></li></ul><p>T<strong>o be considered for this position, you must have </strong>a BS/MS with at least 1-4 years of experience in allergy, asthma or immunology. Proven experience in tissue culture (maintenance of transformed and primary cells), cell-based assays, flow cytometry, ELISA, and MSD is required. Proven training in the proper handling and care of mice, general surgical techniques, and the collection of blood and tissue samples is highly desired. Basic computer skills and experience collecting and analyzing biological data on the computer is a necessity. Experience with GraphPad Prism, FlowJo, SoftMax Pro and Meso Scale Discovery (MSD) Workbench software is preferred. Additionally, maintenance of state-of-the-art laboratory equipment, and accurate and complete record keeping is an expectation for this role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer I - Synthetic and Bioconjugation Scale-Up Technologies (SBST)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47874]]></requisitionid>
    <referencenumber><![CDATA[R47874]]></referencenumber>
    <apijobid><![CDATA[r47874]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47874/process-development-engineer-i-synthetic-and-bioconjugation-scale-up-technologies-sbst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a <strong>Process Development Engineer I</strong> to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) group as a part of our Preclinical Manufacturing & Process Development (PMPD) department. In this exciting new role, you will develop manufacturing processes for the production of synthetic small-molecules used in Regeneron’s diverse range of therapeutic modalities. You would work in close collaboration with cross-functional teams performing chemical process development and optimization using the principles of Quality by Design (QbD) to deliver processes suitable for GMP production. This role also involves process scale-up and technology transfer of manufacturing related workflows to Contract Development and Manufacturing Organizations (CDMOs) to ensure timely and reliable entrance to the clinic and eventual commercialization.</p><h3>A typical day in the role of a Process Development Engineer I might include:</h3><ul><li>Working at the bench to design and develop scalable, robust and controlled GMP-ready processes for synthetic small molecules.</li><li>Collaborating with analytical groups within or outside the organization to establish supportive analytical characterization of synthetic intermediates and final products.</li><li>Discussing plans and data in multi-functional teams to evaluate processes and determine developmental goals and ensure integrated program success.</li><li>Proactively complying with lab safety and environmental safety expectations of both Regeneron and regulatory bodies such as Food and Drug Administration (FDA), Department of Transportation (DoT), etc.</li><li>Using statistical design of experiments (DOE) to optimize synthetic chemical processes including reaction parameters, purification operations, and analytical characterization.</li><li>Partnering with External Manufacturing group and other key partners at Regeneron’s IOPS organization to provide technical assessment of CDMOs intended for GMP production and successfully transferring processes with immediate, first-time success.</li><li>Researching, identifying, and developing new technologies to improve processes, generate predictive process models, and pioneer novel at-line/in-line process analytical technologies (PAT) to ensure robust and controllable synthetic processes.</li><li>Authoring robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</li><li>Analyzing and presenting data in a clear and cohesive manner to a broad audience facilitating data-driven decision making.</li><li>Authoring, reviewing, or providing domain expertise for publications, reports, tech transfer documents, regulatory support documents and patents.</li><li>Being a responsible lab citizen by ensuring timely maintenance of lab equipment, keeping the lab tidy and organized and proactively planning for lab resources.</li><li>Coaching and mentorship of junior team members of the organization as needed.</li></ul><p><strong> </strong></p><h3>This Role May be for You If You:</h3><ul><li>Enjoy working in the lab to advance exciting new drug modalities to patients</li><li>Have strong initiative and aim to complete challenging tasks and learn new technologies</li><li>Have a strong fundamental understanding of various process chemistry and technology transfer principles</li><li>Are capable of multi-tasking and working both independently and in a collaborative environment involving cross-functional teams.</li><li>Have excellent interpersonal, verbal and written communication skills</li><li>Can think critically and demonstrate problem-solving skills</li></ul><p>This role requires a Bachelor’s + 4 years relevant experience or Master’s +0-3 years relevant experience in active pharmaceutical ingredient (API) process development. Experience with small-molecules in the bioconjugates space will be highly preferable. Hands-on experience with organic molecule synthesis and characterization tools such as mass spectrometry, nuclear magnetic resonance (NMR), infrared (IR) spectroscopy, high-performance liquid chromatography (HPLC) etc. is preferred. Candidate must be well-versed with purification techniques such as crystallization, extraction, chromatography etc. Proven experience in scaling-up synthetic small-molecule reactions and technology transfer to a GMP manufacturing facility is a plus. Experience in handling highly potent compounds using appropriate containment and best‑practice procedures is a plus. Candidate should be well-versed with International Council for Harmonization (ICH)/regulatory guidelines and their impact on process development of synthetic molecules and bioconjugates. Experience in working with cross-functional Chemistry, Manufacturing and Control (CMC) teams and experience in authoring publications, reports, tech transfer documents, regulatory support documents, patents is a plus.</p><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47968]]></requisitionid>
    <referencenumber><![CDATA[R47968]]></referencenumber>
    <apijobid><![CDATA[r47968]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47968/senior-manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our Regulatory Affairs Advertising and Promotion team. This position requires the ability to apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidance to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). They will provide regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with minimal guidance from the Regulatory Affairs, Advertising and Promotion Director. The Senior Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US and Global (if applicable) regulatory activities associated with advertising and promotion of the company’s marketed products, as well as commercial development of pipeline products. Manages commercial activities from a regulatory advertising and promotion perspective with minimal guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with minimal guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with minimal guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Provide input to direct management with respect to process improvement for promotional review activities and establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With minimal guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 3 to 4 years within regulatory affairs, preferably within advertising and promotion</p></li><li><p>At minimum, a Bachelor’s degree (BS) from an accredited College or University in Life Sciences. Advanced degree (Masters, Pharm D, Ph.D., MD or DO) preferred in the field of medicine or science. Regulatory experience can offset education requirements.</p></li><li><p>Advance knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and managing launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Ability to influence cross-functional teams and interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47967]]></requisitionid>
    <referencenumber><![CDATA[R47967]]></referencenumber>
    <apijobid><![CDATA[r47967]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47967/manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager </strong>to join our<strong> Regulatory Affairs Advertising and Promotion</strong> team. In this role, you will apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). This individual will provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; in partnership with management, provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 2 total years relevant experience, preferably within Regulatory Advertising and Promotion</p></li><li><p>At minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences. An Advanced Scientific degree (i.e., Masters, PharmD, Ph.D) is preferred.</p></li><li><p>Knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and support launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison  - Neurology (NY Metro)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48118]]></requisitionid>
    <referencenumber><![CDATA[R48118]]></referencenumber>
    <apijobid><![CDATA[r48118]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48118/associate-director-thought-leader-liaison-neurology-ny-metro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Neurology Marketing team. It will be focused on enhancing and improving interactions with key external US Neurology thought leaders at academic centers and leading community practices for our neurology product.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Neurology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><p><strong>The typical day may include the following:</strong></p><ul><li>The Neurology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You possess a strong science background with deep knowledge of rare neurology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p><strong>To be considered for this opportunity, you will possess the following:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10years of relevant work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in Neurology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry. Launch experience preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li><li>Must have a valid driver’s license</li><li>Must be able to travel 60%-80% of time </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Imaging Scientific Director (Oncology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48148]]></requisitionid>
    <referencenumber><![CDATA[R48148]]></referencenumber>
    <apijobid><![CDATA[r48148]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48148/clinical-imaging-scientific-director-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The <strong>Clinical Imaging Scientific Director for Oncology</strong> will own the strategy and execution of sophisticated early and late phase oncology imaging in clinical trials where imaging plays a key role. Imaging includes all modalities with a special focus on PET and CT. In this role, you will champion the development of imaging endpoints and biomarkers and drive the scientific imaging aspects as well as tumor response assessment of oncology clinical studies.<br><br>The successful candidate will be an independent imaging scientific leader and a member of cross-functional program teams including Regeneron clinical and preclinical colleagues as well as external academic and industry partners. This position provides excellent opportunities to develop innovative imaging endpoints and biomarkers in support of clinical development and contribute to bringing new treatment options to patients.</p><p><strong>When & Where: </strong>Tarrytown, NY </p><p><strong>Discover your role:</strong></p><ul><li><p>Create fit-for-purpose imaging biomarker strategies and work closely with research, clinical imaging and the oncology therapeutic area for the development of imaging endpoints to inform and advance the Regeneron clinical pipeline.</p></li><li><p>Prepare and present clinical imaging strategies to senior management.</p></li><li><p>Manage a complex network of stakeholders across Regeneron.</p></li><li><p>Lead, design and implement multi-modality imaging measures as endpoints for oncology therapeutic clinical studies.</p></li><li><p>Collaborate closely with Regeneron clinical teams as imaging subject matter expert to ensure optimal design and execution of imaging strategy including development of protocols, imaging endpoints, imaging manuals, imaging charters, statistical analysis plans and clinical study reports.</p></li><li><p>Work closely with Clinical Imaging Operations and imaging contract research organizations to ensure the flawless conduct and data integrity of studies’ imaging components and endpoints.</p></li><li><p>Serve as Study Scientific Director for clinical trials focused on qualification and utilization of novel imaging biomarkers.</p></li><li><p>Lead the interaction with regulatory agencies for communications regarding imaging endpoints and procedures.</p></li><li><p>Lead the interaction with regulatory agencies and site ethics committees for approval of clinical imaging biomarker development studies</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD program with a minimum of 10+ years of clinical imaging experience (minimum of 7 years within oncology drug development).</p></li><li><p>Superior written/verbal communication and organization skills.</p></li><li><p>Experience implementing central efficacy assessments using tumor response criteria such as RECIST 1.1, iRECIST, PCWG3, Lugano and IMWG in oncology clinical trials is needed. </p></li><li><p>We also are looking for you to have had successful engagement experience with regulatory agencies and the ability to champion imaging innovations and lead projects effectively.</p></li><li><p>Experience as study scientific director of PET imaging biomarker clinical trials in Oncology.</p></li><li><p>Experience applying PET imaging as a quantitative endpoint in clinical and preclinical studies in Oncology.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Triage]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47759]]></requisitionid>
    <referencenumber><![CDATA[R47759]]></referencenumber>
    <apijobid><![CDATA[r47759]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47759/senior-manager-triage/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><div><p>As a Senior Manager, Triage Team Lead, you will lead the triage of Individual Case Safety Reports (ICSRs) within Argus Safety and oversee a team of healthcare professionals responsible for upfront medical triage activities. This role plays a critical part in ensuring accurate case assessment, regulatory compliance, and inspection-ready documentation while supporting downstream pharmacovigilance operations.</p><p><strong>This position is office-based and will be onsite at Regeneron’s India office.</strong></p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Performing medical triage of incoming ICSRs within defined timelines, including assessment of seriousness, expectedness, and causality</p></li><li><p>Applying expedited vs. non-expedited reporting logic, including 7-day and 15-day reporting requirements</p></li><li><p>Verifying source completeness using standardized intake checklists and identifying follow-up requirements</p></li><li><p>Assigning cases to the appropriate Argus workflow based on reporting criteria and data completeness</p></li><li><p>Escalating complex cases to the Lead Medical Reviewer as needed</p></li><li><p>Authoring structured summaries for serious and high-risk cases, including patient profile, suspect product, adverse events, clinical course, causality assessment, and key review considerations</p></li><li><p>Maintaining compliance with SOPs, data privacy standards, and inspection readiness requirements</p></li><li><p>Developing innovative approaches to enhance operational efficiency through integration of new technologies, including AI</p></li></ul><p><strong>This Role May Be for You If You Have:</strong></p><ul><li><p>Strong knowledge of ICH E2A, E2B, and E2D guidelines and global pharmacovigilance regulations including FDA, EMA, and Health Canada requirements</p></li><li><p>Hands-on experience in ICSR intake, case processing, and expedited reporting workflows</p></li><li><p>Proficiency with Argus Safety or equivalent pharmacovigilance safety databases</p></li><li><p>Ability to interpret Reference Safety Information including IB, USPI, and SmPC documents</p></li><li><p>Strong clinical judgment with the ability to make timely and accurate decisions under pressure</p></li><li><p>Excellent written communication skills with the ability to prepare concise and actionable case summaries</p></li><li><p>Familiarity with MedDRA coding practices</p></li><li><p>Experience or interest in AI and GenAI technologies within pharmacovigilance operations</p></li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li><div><div><div><div><div><div><div><div><div><div><div><div><div><p>You should have one of the following qualifications: MD / MBBS, PharmD (Doctor of Pharmacy), BDS (Bachelor of Dental Surgery), MDS (Master of Dental Surgery), or Nurse Practitioner (NP) with strong pharmacovigilance and hands-on ICSR case processing experience.</p></div></div></div></div></div></div></div></div></div></div></div></div></div></li><li><p>Minimum 8+ years of total industry experience, including at least 5+ years of pharmacovigilance case processing experience</p></li><li><p>Hands-on experience with ICSR intake, Argus Safety, and expedited reporting</p></li><li><p>Experience handling high-volume case processing environments</p></li><li><p>Prior experience in triage or first-line safety review activities preferred</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - ALBANY, NY]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48003]]></requisitionid>
    <referencenumber><![CDATA[R48003]]></referencenumber>
    <apijobid><![CDATA[r48003]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48003/medical-account-specialist-ii-neurology-albany-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Albany]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Albany (Metro), NY</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div></div><div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - BOSTON, MA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48001]]></requisitionid>
    <referencenumber><![CDATA[R48001]]></referencenumber>
    <apijobid><![CDATA[r48001]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48001/medical-account-specialist-ii-neurology-boston-ma/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Boston]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Boston (Metro), MA</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div></div><div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p><p><br> </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Strategy & Operations, Genetic Medicines]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48279]]></requisitionid>
    <referencenumber><![CDATA[R48279]]></referencenumber>
    <apijobid><![CDATA[r48279]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48279/associate-director-strategy-operations-genetic-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Regeneron Genetic Medicines Clinical Development Unit (RGM CDU). The Associate Director Strategy Planning & Operations reports to and works closely with the RGM CDU Leadership Team (LT) in support of the operational management of the department. The scope of this role includes supporting departmental meetings, objective and goal setting, support of cross-functional projects, review and tracking of RGM CDU top deliverables, headcount and resource forecasting, and team communications. The role also supports initiatives to establish a high-performing, strategic, effective, and quality-focused organization that is well-aligned and integrated with other functions, including RGM research, the Regeneron Genetic Center (RGC), and Global Development. A key expectation of this role is the active adoption and promotion of AI-powered productivity tools to elevate quality, speed, and impact of strategic work across the organization.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Tarrytown, NY</p><p>Hybrid: 4 days per week on site</p><p><strong>Discover your role:</strong></p><ul><li><p>Act as a strategic partner across the RGM CDU Leadership Team (LT) and the broader organization, driving alignment in support of portfolio and departmental planning with an emphasis on long-term strategic objectives.</p></li><li><p>Provide comprehensive support to the LT including:</p></li><li><p>Overseeing the collation and tracking of critical program and departmental initiatives, ensuring alignment with organizational goals.</p></li><li><p>Leading cross-functional strategic initiatives, special projects, and organizational planning efforts to foster collaboration and innovation.</p></li><li><p>Developing and delivering high-impact presentations for the Head of the RGM CDU, covering key departmental topics such as pipeline progress, strategic issues, RGM overviews for external collaborators, financial performance updates, and organizational changes</p></li><li><p>Enhancing resource management strategies</p></li><li><p>Strategic mid-range planning for headcount needs, encompassing both permanent and contract staff, while proactively managing the approval process for permanent headcount</p></li><li><p>Guiding RGM line managers in performance and talent management discussions, while partnering with functional leaders to refine succession planning processes</p></li><li><p>Spearhead infrastructure and space planning initiatives, developing strategic recommendations for changes in collaboration with the RGM CDU LT to optimize operational efficiency</p></li><li><p>Lead the preparation and facilitation of monthly departmental meetings, including strategic planning, communications, agenda development, and comprehensive minutes' distribution to ensure accountability and follow-up on key action items</p></li><li><p>Identify and champion opportunities for continuous improvement, proposing innovative solutions to enhance operational efficiencies through regular engagement with RGM CDU & ES LT and their teams</p></li><li><p>Collaborate extensively with other Global Development Strategic Planning & Operations personnel to navigate process changes and address issues impacting RGM CDU and Global Development, ensuring alignment with broader organizational strategies</p></li><li><p>Champion the adoption of AI productivity tools (e.g. Claude, Microsoft Pilot) across RGM CDU to streamline operational workflows, accelerate document and presentation development, synthesize complex information, and enhance strategic output</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and 10+ years experience required; (e.g. MBA, PhD, Pharm D) preferred</p></li><li><p>Demonstrated depth of understanding of the drug development process</p></li><li><p>This role is both strategic and tactical and requires an agile problem solver with strong planning ability, interpersonal and communication skills, along with scientific and business acumen to work across the RGM CDU and with our partners to advance strategic planning and team communication</p></li><li><p>Demonstrated proficiency in AI-powered productivity tools (e.g., Claude, Microsoft Copilot, or equivalent) with a track record of applying them to accelerate knowledge work — including drafting, research synthesis, structured analysis, and presentation development</p></li><li><p>Comfort operating at the frontier of AI tool adoption, with curiosity and initiative to identify new applications, evaluate emerging tools, and guide others in their use</p></li><li><p>Highly organized and detail-oriented, while also demonstrating the ability to synthesize information and think strategically</p></li><li><p>Self-motivated, flexible, proactive, able to follow through in an ambiguous, fast-changing environment</p></li><li><p>Demonstrated ability to prioritize and manage multiple projects simultaneously; Experience in contributing or leading cross-functional strategic change initiatives</p></li><li><p>Expertise in MS applications including (but not limited to) TEAMS, Project, PowerPoint, Word, Excel</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Worldwide Operations Office - Pharmacovigilance]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48196]]></requisitionid>
    <referencenumber><![CDATA[R48196]]></referencenumber>
    <apijobid><![CDATA[r48196]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48196/executive-director-worldwide-operations-office-pharmacovigilance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Regeneron is seeking an Executive Director, Worldwide Operations Office to join our PV Organization!</p></div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><p>The Executive Director, Worldwide Operations Office serves as the single point of accountability for Regeneron’s global-to-local pharmacovigilance model. This role ensures consistency, compliance and operational excellence across all regions and countries by defining the scope and governance of regional PV Hubs, establishes clear boundaries between global, regional, and local responsibilities, and translates regional insights into strategic guidance for GPS leadership. This role drives a unified, patient-centered approach to safety across Regeneron’s global footprint while enabling appropriate local adaptation to meet regional regulatory requirements. </p><p><strong>This role might be for you if can: ​</strong></p><ul><li><p>Partner with cross-functional US and International teams to embed a patient safety mindset across Regeneron’s global operations (e.g., gather feedback from regional leaders, establish knowledge sharing forums) </p></li><li><p>Provide functional oversight of WWOO and regional PV Hubs, ensuring operational performance, quality standards, regulatory compliance, and consistent application of global processes across markets </p></li><li><p>Define execution scope for regional PV Hubs, determining which processes require localization to meet requirements versus which can be executed through centralized global processes, including clear delineation of responsibilities between GPS and affiliate teams </p></li><li><p>Establish governance framework for local process adaptation, defining clear standards for when and how global PV processes may be tailored to meet local regulatory requirements </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li><li><p>Aggregate insights and potential risks from regional and country-level activities to shape, influence, and prioritize objectives for the PV system </p></li><li><p>Coordinate across key GPS functions (e.g., QPPV, Case Management, Quality & Compliance) on matrixed activities, regional priorities, and global to local interdependencies </p></li><li><p>Adapt the international model to fit changing business needs, including assessing future needs for additional PV Hubs based on portfolio expansion, geographic growth, and regulatory landscape changes </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that raise capabilities across the organization </p></li><li><p>Influence cross-functional leaders to align priorities and drive enterprise results </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Advanced degree (PharmD, MD, MS, or MBA) in life sciences, healthcare, or related field preferred; Bachelor's degree required</p></li><li><p>17+ years of experience in pharmacovigilance, international operations within the life sciences industry </p></li><li><p>Minimum 7 years in leadership roles with demonstrated experience managing international or multi-regional operations </p></li><li><p>Proven ability to develop relationships and influence key decision making with GPS and Non-GPS functions (e.g., QPPV, Med Affairs, Regulatory), regions, and senior stakeholders </p></li><li><p>Strong background in PV compliance, inspection readiness, and quality oversight across multiple markets </p></li><li><p>Strategic mindset with the ability to translate regional complexity into clear governance, decisions, and executive-level insights </p></li><li><p>Preferred experience with AI technologies </p></li></ul><p>#GDPSJobs</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€172,500.00 - €288,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Production / Manufacturing Operations]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48341]]></requisitionid>
    <referencenumber><![CDATA[R48341]]></referencenumber>
    <apijobid><![CDATA[r48341]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48341/production-manufacturing-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>Within this role you will be working as part of the Manufacturing Team you will be performing tasks to support the manufacturing operations of both clinical and commercial manufacturing programs at Regeneron Ireland.</div></div><div><div><div><div><div><div><div><div><div><p><strong>Working a shift pattern in a fully gowned, cleanroom environment, a typical shift might include, but is not limited to, the following:</strong></p><ul><li><p>Working as part of the Manufacturing team to carry out tasks in line with the production schedule as advised by Team Leads and Supervisors</p></li><li><p>Ensuring all associated documentation such as manufacturing batch records & logbooks are completed, accurate and verified in accordance with SOPs and cGMP Standards</p></li><li><p>Performing equipment cleaning, preparation and execution as well as completing associated documentation</p></li><li><p>Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks</p></li><li><p>Performing various tests and in-process sampling</p></li><li><p>Maintaining housekeeping in designated area and adhering to the hygiene standards of the facility</p></li><li><p>Ensuring all required training is up to date and completed in a timely manner</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You enjoy working in a team that brings out the best in each other</p></li><li><p>You like tackling problems that need solving, using your verbal and written communication skills to ask questions and adapt quickly</p></li><li><p>You can adhere to the letter and spirit of policies and regulations</p></li><li><p>You can adapt to a changing environment and have the ability to adhere to a schedule</p></li></ul><p>To be considered for this opportunity you must have a Leaving Certificate qualification to include math's and a science or engineering subject as a minimum or equivalent qualification. Experience working shift in a GMP (Good Manufacturing Practice) environment/industry is preferred</p><p>Our site operates on a 24/7 basis, and we offer a number of different shift working patterns that could fit with your lifestyle</p><p><strong>What is on offer?</strong> </p><p>You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. </p><p>Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:</p><ul><li><p>Competitive Salary</p></li><li><p>Shift Premiums</p></li><li><p>Annual Bonus</p></li><li><p>Stock Schemes</p></li><li><p>Employer Pension Contributions </p></li><li><p>Education Assistance</p></li><li><p>Generous Annual & Flexible Leave Programs </p></li><li><p>Competitive Private Medical, Dental & Vision Plans</p></li><li><p>Career & Personal Development</p></li><li><p>Wellness Programs - Onsite Gyms & Fitness Classes </p></li><li><p>Concierge Services – Onsite Beauty Therapist / Barber</p></li><li><p>Community Volunteering</p></li><li><p>Employee Interest Groups / Employee Teams & Clubs</p></li><li><p>Employee & Family Events</p></li></ul><p>#IREADV #JOBSIEST #LI-Onsite #REGNIEEC #REGNIELSM</p></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€12.87 - €22.73]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - Protein Expression Science]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48157]]></requisitionid>
    <referencenumber><![CDATA[R48157]]></referencenumber>
    <apijobid><![CDATA[r48157]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48157/senior-associate-scientist-protein-expression-science/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Senior Associate Scientist to join our Protein Expression Sciences team, assisting with operations of automated liquid handlers to support our VelociMab antibody discovery efforts. The candidate performs high throughput cloning and isolation of potential therapeutic antibodies. In addition to experience with liquid handling platforms, the successful candidate will have experience with general molecular biology and cell biology techniques.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location- Tarrytown, 5 days on-site</p><p><strong>Discover your role:</strong></p><ul><li>Performing high throughput molecular biology techniques including PCR, cloning and DNA isolation. </li><li>Operating and troubleshooting automated protocols on automated systems from but not limited to Hamilton Robotics and HighRes Biosolutions.</li><li>Seeding and transfecting of CHO transient cell lines on automated platform.</li><li>Data recording in ELN (electronic lab notebook) and LIMS</li></ul><p><strong>This Role May Be for You If You Have Experience:</strong></p><ul><li>Enjoy working in a fast-paced environment.</li><li>Exhibit adept technical and problem-solving skills.</li><li>Have excellent communication and organizational skills, exhibit meticulous attention to detail.</li><li>Are comfortable working in a dynamic environment where priorities can change from day to day.</li></ul><p><strong>The role requires: </strong></p><ul><li>B.S with 2+ years of laboratory experience or M.S. in Molecular Biology Cellular Biology, Biology, or related field.</li><li>Strong communication and organizational skills are also required.</li><li>Experience with general molecular biology skills such PCR, DNA sequencing, mutagenesis, plasmid subcloning and mammalian cell transfection is preferred</li><li>Familiarity with automated liquid handlers is desired (preferably Hamilton Stars, Vantages and HighRes RIME)</li><li>Experience in high-throughput assays is a plus</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Facilities Engineer]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47148]]></requisitionid>
    <referencenumber><![CDATA[R47148]]></referencenumber>
    <apijobid><![CDATA[r47148]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47148/senior-facilities-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Facilities Engineer, you will provide engineering support, troubleshooting, & subject matter expertise to the Facilities Operations, Utilities & HVAC teams.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><div><div><ul><li><p>Building and specifies cGMP clean/grey utilities, & HVAC equipment, piping, ducting and/or controls</p></li></ul></div><ul><li><p>Managing small-to-mid sized projects related to utilities & HVAC equipment & services</p></li></ul><div><ul><li><p>Conducting troubleshooting for complex issues with plant equipment issues and associated systems, identifying and recommending corrective actions</p></li></ul></div><div><ul><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li></ul></div><div><ul><li><p>Supporting the QA Validation department by preparation of design documents and assists in protocol execution</p></li></ul></div><div><ul><li><p>Assisting in investigations of utility systems, and control system anomalies as well as safety incidents</p></li></ul></div><div><ul><li><p>Implementing corrective/preventative actions for existing equipment and maintenance processes</p></li></ul></div><div><ul><li><p>Preparing engineering evaluations and test plans for and executes modification change control documentation</p></li></ul></div><div><ul><li><p>Interpreting P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs </p></li></ul></div></div><div><div><ul><li><p>Maintains a clean and safe working environment by enforcing procedures, policies, and regulations</p></li></ul></div></div><p><strong>This role might be for you if:</strong></p><ul><li><p>You have strong analytical and interpersonal skills</p></li><li><p>You are able to prioritise and re-prioritise as needed and adapt to change</p></li><li><p>You are comfortable working in a fast-paced setting</p></li></ul><p>To be considered for this opportunity you should have:</p><ul><li><p>Sr Engineer - Requires BS/BA in Mechanical engineering or equivalent along with 5 years’ experience </p></li></ul><div><ul><li><p>Engineer - Requires BS/BA in Mechanical engineering or equivalent along with 2 years’ experience </p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II NEUROLOGY - - ST. PETERSBURG, FL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48044]]></requisitionid>
    <referencenumber><![CDATA[R48044]]></referencenumber>
    <apijobid><![CDATA[r48044]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48044/medical-account-specialist-ii-neurology-st-petersburg-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[St. Petersburg]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: St. Petersburg, (Metro), FL</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -SAN FRANCISCO, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48076]]></requisitionid>
    <referencenumber><![CDATA[R48076]]></referencenumber>
    <apijobid><![CDATA[r48076]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48076/medical-account-specialist-ii-neurology-san-francisco-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[San Francisco]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: San Francisco (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY- SEATTLE, WA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48074]]></requisitionid>
    <referencenumber><![CDATA[R48074]]></referencenumber>
    <apijobid><![CDATA[r48074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48074/medical-account-specialist-ii-neurology-seattle-wa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Seattle]]></city>
    <state><![CDATA[Washington]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Seattle (Metro), WA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - CLEVELAND, OH]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48006]]></requisitionid>
    <referencenumber><![CDATA[R48006]]></referencenumber>
    <apijobid><![CDATA[r48006]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48006/medical-account-specialist-ii-neurology-cleveland-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cleveland]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Cleveland (Metro), OH</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - SAN ANTONIO, TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48065]]></requisitionid>
    <referencenumber><![CDATA[R48065]]></referencenumber>
    <apijobid><![CDATA[r48065]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48065/medical-account-specialist-ii-neurology-san-antonio-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[San Antonio]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: San Antoinio (Metro), TX</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - NEWARK, NJ]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48011]]></requisitionid>
    <referencenumber><![CDATA[R48011]]></referencenumber>
    <apijobid><![CDATA[r48011]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48011/medical-account-specialist-ii-neurology-newark-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Newark]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Newark (Metro), New Jersey</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 13:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Product Manager - Delivery & Operations Product Lead – Authoring Platform]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47587]]></requisitionid>
    <referencenumber><![CDATA[R47587]]></referencenumber>
    <apijobid><![CDATA[r47587]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47587/senior-product-manager-delivery-operations-product-lead-authoring-platform/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Global Development IT is seeking a strategic, hands-on Senior Product Manager to serve as Product Lead for Regeneron’s enterprise generative-AI document-authoring platform. You will be responsible for a multi-phase implementation that delivers governed, scalable AI capabilities across Clinical, Regulatory, Medical Affairs, Labeling, and other Global Development domains. Partnering with business and technology stakeholders, you will align platform strategy to scientific, regulatory, and operational needs, ensuring secure, compliant, and high-impact outcomes.</p><p>Reporting to the Associate Director, Product Management of Enabling Technologies, you will drive the full product lifecycle—from vision and roadmap through design, build, validation, launch, and optimization. Your blend of clinical-process know-how, agile product leadership, and deep AI expertise will accelerate content creation, improve quality, and reduce cycle times for regulated documents.</p><p><strong>In this role, a typical day might include the following:</strong> <br>- Leading stand-ups, refining backlogs, and approving user stories for AI-powered authoring features <br>- Facilitating workshops with Clinical, Regulatory, and Medical Affairs teams to gather requirements and prioritize enhancements <br>- Reviewing solution architecture to enforce security, privacy, and GxP compliance across RAG, MCP, LLM, Copilot, and Claude integrations <br>- Tracking sprint progress, surfacing risks, and updating program leadership on scope, budget, and return of investment<br>- Defining guardrails for citizen development and coordinating change-control / governance forums <br>- Monitoring platform adoption and performance to identify automation and continuous-improvement opportunities</p><p><strong>This job might be for you if you: </strong> <br>- Translate sophisticated Global Development document workflows into intuitive, AI-enabled products <br>- Excel at influencing cross-functional teams without direct authority and communicating clearly with executive stakeholders <br>- Thrive in agile environments, balancing tactical delivery with long-term platform strategy <br>- Enjoy partnering with data-science teams to embed generative AI into regulated processes <br>- Keep current on industry standard processes and proactively incorporate them into product roadmaps <br>- Maintain a “get-it-done” attitude and balance multiple high-priority initiatives simultaneously</p><p><strong>In order to be considered for this role, you must have: </strong><br>- BS/BA with 8–10 years validated experience (or MS/MBA with 6+ years as an equivalent), including 3 years in enterprise SaaS and 1+ year delivering generative/agentic-AI solutions <br>- Shown success leading end-to-end GxP implementations of AI document-authoring platforms, using agile/DevOps methods <br>- Validated expertise in RAG, MCP, LLMs, Copilot, Claude, and integration across Clinical, Regulatory, and Medical Affairs systems</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead Workplace Services Coordinator]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47635]]></requisitionid>
    <referencenumber><![CDATA[R47635]]></referencenumber>
    <apijobid><![CDATA[r47635]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47635/lead-workplace-services-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As the Lead Workplace Services Coordinator, you will own front-of-house operations for the Executive Suite, ensuring every visitor, caller, and employee receives a seamless, high-touch experience. Reporting to the Associate Director, Workplace Services, you will coordinate reception, switchboard, help-desk, and conferencing functions while providing administrative support to the broader Workplace Services team and executive leadership. Acting as the primary point of contact for complex service requests, you will uphold service standards, drive continuous improvement, and maintain operational readiness—even during staff absences or critical site events.</p><p>Your leadership, customer-centric approach, and proficiency with scheduling and conferencing tools will keep day-to-day operations running efficiently and elevate the overall workplace experience. This role is ideal for a highly organized professional who excels in fast-paced environments and enjoys delivering an outstanding service.</p><p><strong>A typical day includes the following:</strong></p><ul><li><p>Serve as the primary point of contact at the Executive Suite reception, greeting visitors and handling guest interactions</p></li><li><p>Operate the reception desk, handling switchboard calls, front-desk tasks, and help-desk inquiries</p></li><li><p>Act as the primary escalation point for complex service issues, resolving them quickly or routing them to the appropriate parties</p></li><li><p>Implement and supervise processes that improve efficiency, service quality, and front-of-house readiness</p></li><li><p>Provide calendar management, travel coordination, and administrative support to Workplace Services leadership</p></li><li><p>Assist the Associate Director with planning and executing executive meetings, town halls, and corporate events, including room bookings, A/V setups, and on-site support to ensure magnificent conference and meeting experiences</p></li><li><p>Support Board of Directors meetings by coordinating conference-room setup and catering; manage food presentation, post-meeting cleanup, and timely room reset</p></li><li><p>Handle ordering and inventory of kitchen and office supplies to ensure consistent availability</p></li><li><p>Prepare beverages, including coffee, for staff and meetings</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Take pride in delivering outstanding customer service and creating welcoming guest experiences</p></li><li><p>Excel at balancing multiple priorities and remaining calm under pressure in a complex environment</p></li><li><p>Enjoy identifying process gaps and driving continuous improvement in workplace services</p></li><li><p>Communicate clearly and professionally with executives, colleagues, and external partners</p></li><li><p>Are highly organized, meticulous, and proactive in anticipating needs</p></li><li><p>Feel comfortable stepping in as a flexible teammate to cover conferencing services or emergency response situations</p></li></ul><p><strong>In order to be considered for this role, you must have:</strong></p><ul><li><p>Bachelor’s degree and 5+ years of validated experience in reception, administration, or workplace services (executive support or supervisory experience is a plus)</p></li><li><p>Confirmed expertise with Microsoft Office, Outlook/Exchange calendaring, and room-booking/conferencing systems</p></li><li><p>Valid driver’s license recognized by the State of New York, a clear driving record, and willingness to follow company fleet-safety requirements</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$34.47 - $56.20]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Sustaining Engineering]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44518]]></requisitionid>
    <referencenumber><![CDATA[R44518]]></referencenumber>
    <apijobid><![CDATA[r44518]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44518/manager-sustaining-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Join Regeneron’s Combination Products team and lead the engineering charge that keeps our commercial products safe, reliable, and continuously improving in the hands of patients and providers. As a Manager, Sustaining Engineering, you’ll guide a talented team while owning design changes, risk management, and multi-functional problem solving that directly impacts patient experience and product quality. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>East Greenbush, Rensselaer</li><li>Monday-Friday, 8am-4:30pm</li></ul><p>Discover your role:</p><ul><li>Lead and mentor sustaining engineers supporting multiple commercial combination products</li><li>Implement targeted design changes to elevate quality and customer experience</li><li>Conduct design change assessments and technical evaluations for supplier and manufacturing changes</li><li>Drive and document investigations into customer complaints to identify root cause and corrective actions</li><li>Maintain and evolve Risk Management Files leveraging post‑marketing surveillance and manufacturing signals</li><li>Facilitate design transfer of existing products to new manufacturing sites with rigor and speed</li><li>Integrate field‑proven performance enhancements into ongoing and new product development efforts</li><li>Participate in cross‑functional design teams to resolve issues quickly and prevent recurrence</li><li>Build and grow strong relationships with internal stakeholders and key external partners</li><li>Deep understanding of FDA regulations relevant to combination products, including 21 CFR Part 3 and design controls per 21 CFR 820.30</li><li>Hands‑on experience with design history file management and sustaining engineering for medical devices and/or combination products</li><li>Strong analytical problem‑solving skills paired with clear technical writing and crisp oral communication</li><li>Proven project leadership: you balance business objectives with technical constraints and keep cross‑functional teams moving</li><li>A continuous improvement mindset and the interpersonal skills to build trust across functions</li></ul><p>This role requires:</p><p>To be considered for the Manager Sustaining Engineering you must have a B.S in Engineering; Biomedical Engineering, Mechanical Engineering, Industrial Engineering is preferred. For various levels you must have the following:</p><ul><li>Associate Manager Sustaining Engineering: 6+years of relevant experience</li><li>Manager Sustaining Engineering: 7+ years of relevant experience</li></ul><p>Previous experience in manufacturing of medical devices and/or combination products is preferred. Previous supervisory/ people leadership experience is required. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44637]]></requisitionid>
    <referencenumber><![CDATA[R44637]]></referencenumber>
    <apijobid><![CDATA[r44637]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44637/associate-director-clinical-scientist-internal-medicine-cardio-metabolic-renal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director Clinical Sciences, and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3><strong>As an Associate Director, a typical day may include the following: </strong></h3><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies proficient scientific expertise to propose, design, and complete clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Applies proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><h3>This role may be for you if:</h3><ul><li><p>Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>Demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs.</p></li><li><p>Strong cross-functional management, interpersonal and problem-solving skills with a proven track in clinical trial process improvements.</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have ≥ 10 years of pharmaceutical clinical drug development experience. We are seeking experience in managing clinical trials in one or more of the following therapeutic areas – cardiovascular, renal, metabolic disease. Demonstrate proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills. Other levels considered depending on experience. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48188]]></requisitionid>
    <referencenumber><![CDATA[R48188]]></referencenumber>
    <apijobid><![CDATA[r48188]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48188/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br><br>The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.<br><br><strong>When & where:</strong><br><br>Work Location: Uxbridge, UK<br><br>Hybrid; 4 days per week on site<br><br>25% Travel may be required<br><br><br><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective action</p></li><li><p>Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution</p></li><li><p>Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials</p></li><li><p>Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work</p></li><li><p>Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies</p></li><li><p>Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics</p></li><li><p>Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and have at least six years of relevant industry experience</p></li><li><p>Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience</p></li><li><p>Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC</p></li><li><p>Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Imaging Operations]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48452]]></requisitionid>
    <referencenumber><![CDATA[R48452]]></referencenumber>
    <apijobid><![CDATA[r48452]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48452/manager-clinical-imaging-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Manager, Clinical Imaging Operations</strong></p><p><strong> </strong></p><p><em><strong>Summary</strong></em></p><p>As a Clinical Imaging Operations Lead, you will have a leading role in the design and execution of key strategic and operational aspects of complex early and late phase clinical trials across multiple therapeutic areas, where imaging is a primary or key endpoint. You will collaborate with Clinical Imaging Science Leads and be fully integrated within clinical study teams to ensure high-quality image acquisition, data integrity, and compliance with all study specific procedures. You should expect to work closely with our imaging vendor partners, the clinical operations function, the data management function, external clinical research organizations (CROs), and clinical sites to ensure the successful completion of startup activities, ongoing execution, and close-out of clinical studies.</p><p><strong>Building Our Future Together:</strong></p><ul><li><p><strong>Imaging Startup and Project Management Support:</strong> Collaborate with clinical study leads and cross-functional teams to manage the start-up activities of imaging components in clinical trials. Assist with vendor selection, request for proposals, and timeline management.</p></li><li><p><strong>Study Documentation and Compliance:</strong> Author, review, and manage essential study documents such as Imaging Manuals, Independent Review Charters, Communication plans, data transmittal forms, Standard Operating Procedures, and Work Instructions. Ensure all documentation is audit-ready and filed appropriately in the Trial Master File (TMF).</p></li><li><p><strong>Site Management and Training:</strong> Provide technical support and training to clinical site personnel, which may include conducting site initiation visits or Teleconferences. Review and approve training materials for imaging facilities and/or clinical site personnel.</p></li><li><p><strong>Study maintenance:</strong> Track imaging progress during clinical studies and address imaging issues that may come up in close collaboration with clinical study teams, sites, and imaging CROs, including functional oversight through day to day monitoring of key performance indicators related to imaging timeliness, quality, etc., query resolution and troubleshooting</p></li><li><p><strong>Process Improvement:</strong> Participate in process improvement initiatives and ensure strict compliance with all procedures and regulations.</p></li></ul><p><strong>This Role Requires:</strong></p><ul><li>BA/BS with 5+ years of clinical trial imaging experience</li><li>Certification as a Registered Technologist (R.T.) with experience in modalities like CT, MRI, or Nuclear Medicine is highly preferred</li><li>Experience in imaging CRO oversight and implementation of quality control procedures</li><li>Well-developed knowledge of the use of clinical imaging across multiple indications alongside knowledge of imaging vendor operational process. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 23 Jun 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Medical Information]]></title>
    <date><![CDATA[Fri, 26 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46258]]></requisitionid>
    <referencenumber><![CDATA[R46258]]></referencenumber>
    <apijobid><![CDATA[r46258]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46258/associate-director-medical-information/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As Associate Director, Medical Information, you will lead scientific communication and medical information strategy for assigned therapeutic areas, enabling high-quality, compliant scientific exchange with healthcare professionals, patients, and internal team members. You will manage the tactical execution of Global and US Medical Affairs medical information plans, convert insights into strategic recommendations, and serve as a trusted partner. We ensure excellence in delivery while maintaining full adherence to company policies, procedures, and all regulations and industry standards.</p><p><strong>Where & When</strong><br>• On-site 4 days/week in Sleepy Hollow, NY or Warren, NJ<br>• If based in Warren, NJ, occasional travel to Sleepy Hollow, NY is expected<br>• Travel (up to 10% is expected) </p><p><strong>A typical day may include the following: </strong><br>• Develop and deliver high-quality, balanced, and scientifically accurate responses to medical inquiries; resolve complex and brought up inquiries.<br>• Lead the creation and maintenance of deliverables, including literature reviews, Standard Response Documents (SRDs), verbal FAQs, Q&As, AMCP dossiers, and compendium.<br>• Medical reviewer on Promotional and Medical Review Committees, ensuring medical accuracy, clarity, and compliance. <br>• Own department reporting processes and dashboards, including metrics, insights generation, digital analytics, and trend reporting for internal partners.<br>• Evaluate, pilot, and implement AI-enabled tools and technologies to streamline medical information processes and improve efficiency and quality.<br>• Collaborate with global and regional Medical Affairs partners to ensure alignment and share best practices.<br>• Provide scientific support for congress planning, booth activities, and real-time scientific exchange.<br>• Mentor and train new hires and less experienced colleagues; may directly supervise Senior Managers, Specialists, and contractors.</p><p>To be considered a minimum of 5 years of Medical Information experience within the pharmaceutical industry along with a PharmD or PhD is required. Strong scientific knowledge and expertise in a therapeutic area including evaluating and communicating clinical trial and disease state information to a wide range of audiences. Neurology is preferred. Demonstrated experience in conducting scientific literature review, and management of medical inquiries, including the development and review of deliverables (e.g., standard response documents, FAQs, dossier, compendium submissions, etc.). Practical experience and knowledge of FDA guidance’s. <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Baltimore, MD]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48096]]></requisitionid>
    <referencenumber><![CDATA[R48096]]></referencenumber>
    <apijobid><![CDATA[r48096]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48096/medical-specialist-i-pulmonology-baltimore-md/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Baltimore]]></city>
    <state><![CDATA[Maryland]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: <strong>Baltimore, MD - representative must reside within the territory (e.g. Baltimore, Dover, Bel Air).</strong></p></li></ul><p><strong>​</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups.</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p>​<strong>This role requires:</strong></p><ul><li><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oracle IT Applications Analyst]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47008]]></requisitionid>
    <referencenumber><![CDATA[R47008]]></referencenumber>
    <apijobid><![CDATA[r47008]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47008/oracle-it-applications-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oracle IT Applications Analyst is a business facing role with responsibility for the configuration, implementation, maintenance, and ongoing support of various Supply Chain IT applications and systems, primarily Oracle OPM Modules.</p><p>Essential Duties and Responsibilities include, but are not limited to, the following:</p><ul><li>Coordinates across business departments and stakeholders, gathering and implementing enhancement requests across departments.</li><li>Effectively identifies and resolves system issues and appropriately communicates items to management, business process owner and users.</li><li>Responsible for IT Applications documentation, including, converting User Requirement Specifications to a Detail Design Specification, writing Configuration Test Plans and summary reports (tabular, trend and labels).</li><li>Performs daily business administrative tasks related to functional support and general user account administration.</li><li>Provides SME support and works closely with functional departments on projects to develop, implement and enhance the system.</li><li>Provide application assistance prior to, during and post Regulatory/Partner inspections.</li><li>Processes IT Applications change control requests.</li><li>Works with Validation and Quality departments to ensure IT Applications are implemented following development life cycle approach.</li><li>Coordinates with other IT Applications team members to implement the system in an efficient manner.</li><li>Provides end-user support for IT Applications including troubleshooting problems at the application server level.</li><li>Participates or may lead IT Applications systems security access and periodic audit trail reviews.</li></ul><p>This role may be for you if you have:</p><ul><li>Experience in Oracle Applications, Supply Chain and OPM Modules preferably.</li><li>Experience with technical writing & process mapping.</li><li>Good verbal and written communication skills.</li><li>Experience in Project Management and System Administration.</li><li>Experience working with Veeva, Valgenesis, JIRA tools.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field and minimum 2 years relevant experience. May consider equivalent combination of education and experience.</p><ul></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 22 Jun 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temporary Finance Operations Associate Manager]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48492]]></requisitionid>
    <referencenumber><![CDATA[R48492]]></referencenumber>
    <apijobid><![CDATA[r48492]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48492/temporary-finance-operations-associate-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Associate Manager, Finance Operations Accounting to join our Finance Operations Team, supporting our Dublin in a hybrid work mode. In this role, you will ensure accuracy in financial data, optimize accounting workflows, and manage a team of professionals to support key financial goals while collaborating with cross-functional teams, Accounting leadership, and offshore teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. This is a temporary 6 month contract.</p><h3>When & where:</h3><p>Dublin — hybrid</p><h3>Discover your role:</h3><ul><li><p>Lead cross-functional initiatives to improve and automate accounting processes</p></li><li><p>Develop process models and workflow diagrams to support decision-making</p></li><li><p>Manage and support a team delivering accounting analysis and insights</p></li><li><p>Track performance metrics to identify improvements and support financial goals</p></li><li><p>Deliver reports, dashboards, and presentations to Accounting leadership</p></li><li><p>Partner with offshore teams to ensure timely accounting close deliverables</p></li><li><p>You collaborate effectively across teams in a global organisation</p></li><li><p>You manage competing priorities and drive results across multiple projects</p></li></ul><h3>This role requires:</h3><ul><li><p>Bachelor’s degree in Accounting and 6–8+ years’ accounting experience</p></li><li><p>Strong understanding of Sarbanes-Oxley (SOX) controls</p></li><li><p>Expertise in business process design and documentation</p></li><li><p>Experience working in a global multinational accounting environment</p></li><li><p>Knowledge of large-scale Enterprise Resource Planning systems preferred</p></li><li><p>Six Sigma certification preferred</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 23 Jun 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Market Access DACH (f/m/d)]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45066]]></requisitionid>
    <referencenumber><![CDATA[R45066]]></referencenumber>
    <apijobid><![CDATA[r45066]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45066/senior-manager-market-access-dach-fmd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This role has been created to provide end-to-end management of the HTA submissions and price negotiation in Germany, Switzerland & Austria for specific products and their indications, ensuring timely alignment on strategy with affiliate and global teams. As a Senior Manager Market Access, you will manage cross-functional input into the submission and negotiation strategy by working in conjunction with the medical and brand teams at an affiliate level and with market access and pricing at a global level. The role will manage cross-functional input into the submission and negotiation strategy by working in conjunction with the medical and brand teams at an affiliate level and with market access and pricing at a global level. </p><p><strong>A typical day may include the following: </strong></p><ul><li><p>Working with Global and affiliate Market Access leads to ensure robust and timely submissions to HTA bodies in Germany, Switzerland & Austria Leading data analysis in areas of G-BA benefit assessment, access, pricing and contracting, and brand performance </p></li><li><p>Develop and align on a market access and pricing strategy for the medicine with the Affiliate Commercial Teams </p></li><li><p>Identifying and communicating payer needs effectively to local Market Access (for real-world evidence), HEOR and/or Medical Affairs to inform evidence-generation prioritization and content in order to develop Value Dossiers for the effective communication of the value of products, and submit critical Market Access requirements to the Affiliate Head of Market Access/Govt. Affairs </p></li><li><p>Inputting into strategic price-setting at a global level, supporting the local price negotiation process and identifying innovative solutions for market access, including innovative pricing / contracting arrangements with national payers </p></li><li><p>Supporting country to ensure each brand has appropriate market access plans in place to execute global strategy, in the context of local payer environment </p></li><li><p>Supporting and providing input to new indication or new product launches, assessing potential and payer value story, regulatory and label considerations </p></li><li><p>Preparing and developing KPIs and analytics, supporting country-level pricing review </p></li></ul><p><strong>This may be for you if you are: </strong></p><ul><li><p>Experienced in a Market Access role in the Pharma sector in multi-disciplinary, matrix and global context </p></li><li><p>Experienced in delivering HTA submissions </p></li><li><p>Have strong experience designing and implementing market access strategies and achieving exceptional results for product </p></li><li><p>Have a proven track record in developing and delivering compelling value propositions and access strategies </p></li><li><p>Able to demonstrate success in driving price execution to deliver optimal commercial return </p></li><li><p>Experienced in developing KPIs and dashboards, to support sustainable growth and performance </p></li></ul><p><strong>To be considered for this position</strong>, you are required to have: At least 5 years of experience in a Market Access role within the pharmaceutical industry. Strong knowledge of the German, Austrian & Swiss healthcare system and experience negotiating with Health Authorities. Expertise in Oncology is highly desirable, and you have to be comfortable in working in an international environment. A post-graduate qualification such as an MBA, MSc, or equivalent is preferred. Fluency in German & English is required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€92,250.00 - €153,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Market Access Director Oncology]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48536]]></requisitionid>
    <referencenumber><![CDATA[R48536]]></referencenumber>
    <apijobid><![CDATA[r48536]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48536/market-access-director-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director Market Access Oncology International to join our market access team, supporting our international oncology business in a hybrid work model. In this role, you will lead the development and execution of market access, pricing, and reimbursement strategies for an oncology portfolio while collaborating with commercial, health economics and outcomes research, medical affairs, clinical, marketing, and affiliate teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>Madrid - Spain<br>Hybrid</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead market access strategy and execution to enable successful in-country oncology launches, including value propositions, objection handlers, and launch readiness activities</p></li><li><p>Develop and implement pricing and reimbursement strategies across market archetypes to achieve optimal patient access and value</p></li><li><p>Synthesize payer insights and analyse market access environment trends, including competitor dynamics, to inform strategic decisions</p></li><li><p>Guide affiliates in preparing reimbursement dossiers and managing payer negotiations within defined price corridors to ensure timely access</p></li><li><p>Deliver recommendations on payer strategy, evidence generation, data collection, and value demonstration aligned to access objectives</p></li><li><p>Coordinate cross-functional input to address payer requirements throughout reimbursement processes and inform global pricing decisions</p></li><li><p>Develop annual tactical plans, manage project budgets and vendors, and maintain reimbursement tracking tools to monitor execution</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree with a minimum 10 years of in-country market access experience or global commercial strategy experience</p></li><li><p>Minimum 7 years of in-country oncology market access experience preferred</p></li><li><p>Proven experience supporting or leading product launch activities in a market access context</p></li><li><p>Experience developing pricing and reimbursement strategies and supporting payer negotiations and dossiers</p></li><li><p>Ability to integrate payer evidence needs into clinical development programs and identify evidence gaps</p></li><li><p>Strong project and process management skills with the ability to manage multiple priorities</p></li><li><p>Experience leading cross-functional or matrix teams</p></li><li><p>Demonstrated ability to build effective relationships with internal stakeholders</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€96,000.00 - €160,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Quality Control (Microbiology)]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46658]]></requisitionid>
    <referencenumber><![CDATA[R46658]]></referencenumber>
    <apijobid><![CDATA[r46658]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46658/associate-manager-quality-control-microbiology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role you will manage the QC Microbiology team and provide critical microbiology support to manufacturing and facilities.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li>Managing a team of laboratory analysts within the QC microbiology department involved in the analysis of raw materials, intermediates (in process) and bulk drug substance in a cGMP regulatory environment</li><li>Implementing and managing the environmental monitoring programme, including surface, settling and viable and non-viable particulate air monitoring of aseptic operations and controlled areas</li><li>Managing QC microbiological operations to ensure compliance with cGMP standards and accurate sample analysis</li><li>Designing and overseeing microbiological validations as needed for drug substance, in-process controls and buffers</li><li>Managing the design, validation and execution of the clean utilities qualification and re-qualification program</li><li>Supporting manufacturing personnel in the identification of microbiological root cause analysis and provide technical advice on QC related topics as needed</li><li>Participating in the investigation and review of alert and action limit investigations as needed and implements corrective action as appropriate</li><li>Ensuring that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs)</li><li>Reviewing and approving method protocols, reports and SOPs</li><li>Assisting in the preparation for internal/customer/regulatory inspections</li><li>Ensuring a safe working environment within the laboratory</li><li>Overseeing or conducting laboratory investigations and generates reports in response to invalid assays, Deviations, OOS/OOT</li><li>Ensuring that CAPAs and Change Controls are initiated and completed on time and in accordance with site procedures</li><li>Presenting analytical data reports clearly and concisely to senior management, including QC performance metrics and trend</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have the ability to train, develop and mentor direct reports and effectively manage the performance of individuals</li><li>You can proactively identify and implement lab process improvements, lean initiatives</li></ul><p>To be considered for this opportunity you should have a BS/BA in Microbiology or closely related field with 6+ years’ experience in microbiology lab, preferably in the pharmaceutical or biotech industry with 3+ years’ experience in a leadership role in microbiology laboratory management.</p><p>#REGNIRLTO #IREADV #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€63,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Artificial Intelligence Data Engineer]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44147]]></requisitionid>
    <referencenumber><![CDATA[R44147]]></referencenumber>
    <apijobid><![CDATA[r44147]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44147/senior-manager-artificial-intelligence-data-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Global Development is embarking on a Digital Transformation project incorporating AI, machine learning, and automation to help us reduce cycle times, improve quality allowing us to focus on more meaningful work. We focus on developing and improving data pipelines, infrastructure, architecture, and analytic tools to allow resources to fuel our transformation. Working with a team of engineers, analysts, and scientists, you will contribute to modernizing our clinical data infrastructure. This highly visible role will be a technical and strategic liaison between the transformation projects and IT. </p><p>A key responsibility will be developing and optimizing schema and data models for clinical data. We ensure that those products are standard compliant and interoperable with other platforms and data sources. This role will also contribute to data governance strategy and to the development and management of tools improving and monitoring data quality. The data engineer will also develop processes to automate routine workflows. The engineer will also provide technical leadership and mentorship and will stay current with innovations in data engineering so that they may be evaluated for implementation. <br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>This can be a remote position in the US or on-site position at our Armonk, NY or Warren, NJ offices. </p><p><strong>Discover your role:</strong><br>• Work with a cross-functional team to optimize and implement our data strategy with a focus on optimization for digital transformation and the use of AI/ML<br>• Design and document end-to-end data architectures that support diverse analytic, operational, and research needs.<br>• Facilitate the implementation of a modern data platform (e.g. Snowflake, Databricks, etc.)<br>• Identify opportunities and implement solutions to increase data interoperability and standardization among systems and across other business units.<br>• Develop and implement pipelines to monitor and improve both internal and external (i.e., from CRO partners) data quality.<br>• Work with informatics and AI engineers optimizing the utility of data for their respective pipelines.<br>• Monitor and optimize the performance of data architectures and platforms.<br>• Develop or implement critical metrics to measure the impact of the overall data strategy.<br>• Stay up to date with the latest advances in the field and, as appropriate, evaluate them for adoption </p><p><strong>This role requires:</strong><br>An advanced degree in computer science, statistics, biomedical informatics, or a related field is preferred (PhD + 2 years of experience or an MS + 4 years of relevant experience). A minimum of 5 years’ experience developing and leading the implementation of data engineering solutions, including accountability for the success of the implementation, in life sciences or healthcare<br>• Demonstrated expertise in designing and maintaining infrastructure and architecture for clinical or biomedical data in a healthcare or life sciences setting.<br>• Expertise in modern data platforms (e.g., Snowflake, Redshift, BigQuery, Databricks) and programming languages such as Python, SQL, R, etc.<br>• Maintain and manage code repositories (e.g Bitbucket) ensuring clean, well-documented code with proper version control.<br>• Proficiency in cloud architecture (e.g. AWS, Azure, GCP) and DevOps practices. Recognized certifications are a plus.<br>• Experience building, scaling, and maintaining pipelines for structured and unstructured data. Ability to integrate pipelines across the enterprise is essential.<br>• Deep understanding of regulatory frameworks (HIPAA, GDPR, 21 CFR Part 11) and clinical data standards (CDISC, HL7, FHIR).<br>• Knowledge of machine learning pipelines and integration with clinical data platforms.<br>• May require travel up to 20%.<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Biostatistics - Immunology & Inflammation]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46192]]></requisitionid>
    <referencenumber><![CDATA[R46192]]></referencenumber>
    <apijobid><![CDATA[r46192]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46192/senior-director-biostatistics-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Regeneron is seeking a Senior Director, Biostatistics to drive our Immunology and Inflammation therapeutic area.</p></div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><p>The incumbent will have responsibility for strategic and operational activities and for assisting the Head, Biostatistics in the development and implementation of departmental scientific policies, operational guidelines, and administrative structure. The incumbent could also serve as senior research expert, with demonstrated ability to be a leader within Global Development and within the field for specific statistical methodology or application. The successful candidate should have a track record in leading teams and the ability to effectively structure a function to manage the anticipated growth in the product pipeline. They must also possess excellent communication skills to interface with senior leadership on behalf of the department and work closely with medical study directors to provide and receive direction on clinical programs and have the ability to influence the medical and clinical teams.</p><p><strong>This role might be for you if have proven experience:</strong></p><ul><li><p>Determining Department goals and resource allocation in conjunction with the Department Executive Director.</p></li><li><p>Ensure project teams have high quality statistical support for creation of clinical development plans, study design, and operational aspects.</p></li><li><p>Work with senior management to ensure statistical representation in key project decisions and regulatory meetings. Serve as departmental representative on corporate‐wise teams.</p></li><li><p>Oversee process for statistical reporting. Review critical documents, such as SAP, analysis results presentations, CSR, and integrated summaries. Ensure compliance with data submission guidelines.</p></li><li><p>Plan and track project activities, timelines, and resource use. Provide justification for planned resource needs. Seek to optimize resource utilization across projects or areas. Effect long‐range planning.</p></li><li><p>Ensure technical direction and mentoring for staff. Encourage personal development in the context of project work. Learn and apply techniques to promote teamwork, quality, and motivation. Recruit, develop, and retain high quality staff.</p></li><li><p>Maintain awareness of industry standards and regulatory requirements. Alert staff to new or changing standards. Within area of control, harmonize policies with departmental guidelines SOPs and with industry standards. Develop polices promoting application of corporate values in work practices.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Ph.D. in statistics or related discipline with 10+ years of experience (or MS in statistics or related discipline with 15+ years) in the biotechnology, pharmaceutical or health related industry, including significant interaction with both FDA and EMEA, history of successful project and people management (6+ years), and expertise in multiple therapeutic areas.</p></li><li><p>Active research interests in area related to clinical trial.</p></li><li><p>Demonstrated ability to work in a changing and busy environment and to exercise judgment in interpreting, modifying, and adapting procedures, practices, methods, etc. in accordance with existing policies and standards for application to specific problems or tasks.</p></li><li><p>Ability to work independently – self‐directed, high energy and strong work ethic. High degree of creativity, latitude and attention to detail required.</p></li><li><p>Demonstrated strong leadership, project management, teamwork and interpersonal skills.</p></li><li><p>Excellent presentation skills.</p></li><li><p>Experience and proven ability leading and managing major process and technology initiatives with utilization and impact across multiple functional groups.</p></li><li><p>Broad knowledge and superior understanding of advanced statistical concepts and techniques.</p></li><li><p>Outstanding ability and skills to effectively represent Biostatistics and Data Management in interactions with senior management or cross‐functional committees.</p></li><li><p>Thorough knowledge of pharmaceutical clinical development and life cycle management; ability to innovatively apply technical principles, theories and concepts to clinical drug development leading to regulatory approvals.</p></li><li><p>Thorough working knowledge of regulatory guidelines on drug development, regulatory submissions, and statistical practice.</p></li><li><p>Understanding of the drug discovery and development process, regionally and globally.</p></li><li><p>Strong administrative skills.</p></li><li><p>Ability to influence others to achieve results.</p></li></ul><p>#GDBDMJobs</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - Bioinformatics]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47854]]></requisitionid>
    <referencenumber><![CDATA[R47854]]></referencenumber>
    <apijobid><![CDATA[r47854]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47854/senior-scientist-bioinformatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking Senior Scientist (AI/ML) to join our tech-dev research team at the Regeneron Tarrytown location. The Scientist will be dedicated to incorporating cutting-edge generative AI for biomolecule design and optimization and collaborating with a cross-functional team in a closed-loop cycle to bridge artificial intelligence technology and therapeutic development in multiple diseases.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown – Onsite 4 days and 1 day Remote</p><p><strong>This role might be a fit for you if: </strong></p><ul><li>Apply and tailor state-of-the-art generative foundation models for biomolecule (protein, antibody, small molecules and nucleic acid) design and optimization</li><li>Work with different types of experimental datasets (curation, distillation, encoding) for model training, fine-tuning and optimization, and specifically in model learning and adaptation incorporating feedback data from downstream experimental validation assays</li><li>Work closely with web lab teams and clinicians for closed-loop AI model development and inference</li></ul><p><strong>The role Requires: </strong></p><ul><li>PhD in one of the following fields: Computational Biology, Bioengineering, Bioinformatics, Systems Biology, Computer Sciences, Mathematics, Engineering, or other related fields</li><li>2+ years of experience of utilizing AI for biomolecule (proteins, antibodies or other molecules) research;</li><li>Previous experience, background or knowledge in structural biology and/or biochemistry is a plus</li><li>Familiar with cutting-edge generative AI foundation models (with applications in biomolecules)</li><li>Proficiency in one of the commonly used programming languages, such as R, Python, Perl, Java, or Linux</li></ul><ul><li>Self-motivated, passionate about computational data, and conduct research collaboratively in a team setting</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Specialist – Data Lake Operations]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48284]]></requisitionid>
    <referencenumber><![CDATA[R48284]]></referencenumber>
    <apijobid><![CDATA[r48284]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48284/senior-specialist-data-lake-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist, Clinical Data Lake Operations to join our Data Management team, supporting our clinical data operations in a hybrid work model. In this role, you will execute, maintain, and ensure quality oversight of GxP clinical data lake operations while collaborating with Safety, Clinical Sciences, Biostatistics, Precision Medicine, external partners, and Data Management teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad, India(Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Complete daily clinical data lake operations and pipeline monitoring</p></li><li><p>Perform onboarding and validation of non-EDC clinical data sources</p></li><li><p>Build reusable clinical data structures aligned with data standards</p></li><li><p>Develop data marts supporting clinical and safety applications</p></li><li><p>Maintain governance documentation, metadata, and audit-ready traceability</p></li><li><p>Write Python automation frameworks for validation and data delivery</p></li><li><p>You collaborate effectively across cross-functional clinical data stakeholders</p></li><li><p>You apply analytical thinking to strengthen data quality and governance</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s or Master’s degree in Computer Science, Data Science, Bioinformatics, or a related field</p></li><li><p>4+ years of experience in clinical data engineering and data lake management</p></li><li><p>Strong expertise in Python, ETL frameworks, SQL, and automation development</p></li><li><p>Experience with clinical trial data systems and clinical data standards including Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation Model (SDTM), and Analysis Data Model (ADaM)</p></li><li><p>Familiarity with Electronic Data Capture (EDC) systems such as Medidata Rave</p></li><li><p>Experience with cloud platforms including AWS, Snowflake, Dremio, or similar query engines</p></li><li><p>Knowledge of GxP, ICH-GCP, and 21 CFR Part 11 regulatory requirements</p></li><li><p>Advanced degree such as MBA or MS preferred</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager - Statistical Programming, Central Services]]></title>
    <date><![CDATA[Wed, 27 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47788]]></requisitionid>
    <referencenumber><![CDATA[R47788]]></referencenumber>
    <apijobid><![CDATA[r47788]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47788/senior-manager-statistical-programming-central-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. As we continue to expand our global footprint, our Global Capability Centers play a critical role in enabling scalable, high-quality operations and delivering impactful business services.</p><p>As a Senior Manager – Statistical Programming, you will serve as a technical leader within Global Development, providing oversight and guidance for statistical programming activities across multiple clinical programs. You will play a key role in delivering high-quality, compliant data outputs for regulatory submissions, integrated analyses, and clinical trial transparency. This role will also focus on driving operational excellence, enabling innovation, and collaborating with cross-functional global teams to ensure timely and accurate reporting aligned with industry and regulatory standards.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong></p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li>Act as a technical lead and primary point of contact for statistical programming activities across assigned projects and regions.</li><li>Lead and oversee the development of integrated datasets (e.g., pooled ADaM) and analysis outputs for clinical studies and submissions.</li><li>Ensure timely, high-quality delivery of programming outputs, adhering to internal standards and regulatory requirements.</li><li>Collaborate with biostatisticians, data management, and cross-functional stakeholders to support clinical reporting and analysis needs</li><li>Lead the preparation and review of electronic submission packages (eCTD) in compliance with global regulatory standards (FDA, EMA, PMDA).</li><li>Support clinical trial transparency and disclosure activities, ensuring accurate and timely delivery of required datasets and outputs.</li><li>Provide subject matter expertise in statistical programming, including development of tools, standards, and best practices.</li><li>Drive process improvements and innovation initiatives to enhance efficiency, quality, and compliance across programming functions.</li><li>Support inspection readiness activities and address regulatory queries related to programming deliverables.</li><li>Mentor and guide team members, fostering capability building and promoting a culture of continuous learning.</li><li>Collaborate across global teams to ensure alignment with enterprise standards and successful delivery of project milestones.</li></ul><p><strong>This Role May Be for You If You Have:</strong></p><ul><li>Strong experience in statistical programming within clinical trials, including integrated analyses and regulatory submissions</li><li>Deep understanding of CDISC standards (SDTM, ADaM, Define-XML) and regulatory requirements</li><li>Proficiency in SAS programming, with additional exposure to R or Python considered beneficial.</li><li>Experience with tools such as Pinnacle 21 (P21) for validation and compliance checks.</li><li>Demonstrated ability to lead teams, manage multiple projects, and deliver results in a fast-paced environment.</li><li>Strong analytical, problem-solving, and troubleshooting skills.</li><li>Excellent communication and stakeholder management capabilities.</li><li>Ability to work effectively in a matrixed, global organization and collaborate cross-functionally.</li><li>High attention to detail with a focus on quality and compliance.</li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li>8+ years of relevant experience in statistical programming within pharmaceutical, biotech, or clinical research settings, including leadership experience.</li><li>Bachelor’s degree required; Master’s degree or higher in Statistics, Computer Science, Mathematics, Life Sciences, or related field preferred.</li><li>Proven experience supporting regulatory submissions and global compliance standards (FDA, EMA, PMDA).</li><li>Strong experience working with clinical trial data and regulatory reporting processes.</li><li>Prior experience in global or GCC environments is preferred.</li><li><p>Fluency in English and ability to collaborate effectively with global stakeholders.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Internal Auditor]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45138]]></requisitionid>
    <referencenumber><![CDATA[R45138]]></referencenumber>
    <apijobid><![CDATA[r45138]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45138/senior-internal-auditor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Under the direction of the Internal Audit management, the Senior Internal Auditor is responsible for the execution the annual risk-based audit plan that identify value-added recommendations to enhance Company processes and controls. The Senior Auditor will audit the Company’s operations, strategic initiatives, critical business processes and key third-party outsourcing arrangements, as well as participate in the annual Sarbanes-Oxley (SOX) audit of internal controls over financial reporting. This individual will need to have the ability to manage relationships with middle management and work in a highly autonomous manner.</p><p><strong>In this role, a typical day might include the following:</strong> </p><ul><li><p>Under the direction of Internal Audit management, independently review processes and functions as authorized in the approved annual audit plan.</p></li><li><p>Participate in the development of risk-based audit programs and related planning documents for audits.</p></li><li><p>Responsible for the execution of assigned audit sections with little supervision.</p></li><li><p>Conduct audits consistent with IIA practices and in accordance with internal policies and procedures. Additionally, ensure timely completion of assigned testing areas.</p></li><li><p>Identify weaknesses in compliance-related exposures, operational processes and internal controls.</p></li></ul><p><strong>This role might be for you if have experience with :</strong></p><ul><li><p>Promoting internal control practices within the Company by providing internal control expertise as needed to any functions or departments requesting guidance.</p></li><li><p>Identify opportunities to enhance operational efficiencies.</p></li><li><p>Interact autonomously with middle management.</p></li><li><p>Take a lead role in closing meeting with auditees by presenting the findings and related recommendations identified by him/her.</p></li><li><p>Assist Internal Audit management in preparing draft recommendations and audit reports for Senior Management and Audit Committee.</p></li><li><p>Contribute to the Company’s SOX 404 compliance program by completing process review and test of controls as assigned by Internal Audit management.</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><div><ul><li><p>A Bachelor's degree in a relevant field, CPA/CIA certifications preferred </p></li></ul></div><div><ul><li><p>At least 3 years of relevant experience</p></li><li><p>Background in Big 4 Audit is ideal</p></li><li><p>Industry exposure to pharmaceutical/biotech, manufacturing, CPG or a similar field preferred</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 11:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Nurse Educator - Hematology - Northeast]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48935]]></requisitionid>
    <referencenumber><![CDATA[R48935]]></referencenumber>
    <apijobid><![CDATA[r48935]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48935/associate-director-nurse-educator-hematology-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>The Nurse Educator (NE) provides education to health care providers (HCPs) in support of relevant disease states that align with Regeneron’s hematology business unit for our bispecific antibody for Multiple Myeloma (MM). This role will focus on education regarding product dosing and administration and potential adverse event and adverse event management to support proper usage of our Multiple Myeloma bispecifc antibody. This position will report to the Director of Nurse Educators who reports into the Executive Director of Strategic Customer Engagement for Oncology.</p><p>The NE is a field-based position that collaborates with other field teams and cross-functional partners to identify educational needs within accounts and delivers on-label education to targeted customers to support their usage of our Multiple Myeloma bispecific antibody. The NE role includes delivering on-label presentations to APPs and Nurses and supporting other external groups as appropriate with approved educational initiatives. The NE will deliver education in a compliant manner with a high degree of integrity, strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. The nurse educator is a support role that provides education to prescribers and relevant staff once a prescriber or office has decided to use Regeneron products. It is not a sales or marketing role, is not compensated on sales performance and does not promote Regeneron products.</p><h3>When & where:</h3><p>Northeast- ME, VT, NH, MA, RI, CT, NY and need to have the ability to travel and must live within the geographic area of the assigned territory and hold a valid driver's license.</p><h3>Discover your role:</h3><ul><li>Provides educational support to HCPs, nurses, and APPs regarding dosing/administration, adverse event and adverse event management regarding our approved Multiple Myeloma bispecific antibody when a clear educational need has been identified.</li><li>Appropriately collaborates with internal cross-functional partners, including field sales, training, marketing, thought leader liaisons, oncology key account leaders, and medical affairs</li><li>Coordinates and implements strategic plans to support educational responsibilities</li><li>Interacts with HCPs, such as APPs (i.e., NP, PA), nurses, pharmacists, and other key stakeholders in the assigned geography to ensure they are informed on current, key information about Regeneron’s Multiple Myeloma bispecifc antibody</li><li>Conducts educational and in-service programs through 1:1 HCP and group presentations</li><li>Consistently works to improve disease state/product clinical knowledge/account management via ongoing approved NE training curriculum and appropriate cross-functional collaboration at POA meetings.</li><li>Completes all training requirements and proactively seeks to strengthen ongoing scientific knowledge regarding disease-state, competitive products, and healthcare trends</li><li>Maintains the highest level of integrity and acts per company compliance/legal guidelines at all times</li></ul><h3>This role requires:</h3><ul><li>A minimum of BSN is required; a graduate-level degree (i.e., MSN, NP, DNP) is preferred</li><li>Oncology Certified Nurse (e.g., OCN, AOCN, CBNC, etc.) is preferred</li><li>Minimum 5+ years of clinical experience in oncology with expertise in hematology-oncology and bone marrow transplant, a strong plus</li><li>Demonstrated ability to access and understand challenges and educational needs of key HCPs and accounts within the assigned geography</li><li>Excellent oral and written communication skills</li><li>Demonstration of strong Presentation/Platform skills</li><li>Superior clinical skills and business acumen with the proven ability to excel in a technically complex and ambiguous environment</li><li>Exceptional collaborator who can effectively develop and work with internal functional partners and external customers</li><li>Experience in the pharmaceutical/biotechnology industry is preferred</li><li>Working knowledge of pharmaceutical regulatory and compliance required</li><li>Ability to travel and cover large geographic territories</li></ul><p>Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - SAN FRANCISCO, CA]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48961]]></requisitionid>
    <referencenumber><![CDATA[R48961]]></referencenumber>
    <apijobid><![CDATA[r48961]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48961/medical-account-specialist-ii-hematology-san-francisco-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialist - Hematology- </strong><strong>San Francisco</strong></p><ul><li><strong>Geography: San Francisco, East Bay, Northern California</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Warehouse Associate]]></title>
    <date><![CDATA[Fri, 03 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45739]]></requisitionid>
    <referencenumber><![CDATA[R45739]]></referencenumber>
    <apijobid><![CDATA[r45739]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45739/temp-warehouse-associate/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role you will be responsible for the receipt, documentation, and movement of inventory and non-inventory items within the plant and from outside sources. This position also performs labeling and shipping functions as needed. The successful candidate will be required to work shift.<br> </p><p>Please note this is a 12-month contract position</p><p><strong>As a Temp Warehouse Associate, a typical day might include, but is not limited to, the following:</strong> </p><ul><li><p>Scheduling receipt and transfer of all inbound/outbound raw materials and product</p></li><li><p>Documenting all inbound/outbound raw material and product with documentation filed manually or electronically</p></li><li><p>Interacting with multiple electronic systems including an inventory management system & electronic training system</p></li><li><p>Distributing materials to end user through electronic requisition process</p></li><li><p>Managing inventory including cycle counting of inventory items</p></li><li><p>Maintaining a high standard in housekeeping throughout the facility</p></li><li><p>Following established safety practices and SOPs in a cGMP environment</p></li></ul><p><strong>This role might be for you if:​ </strong></p><ul><li><p>You demonstrate an ability to follow detailed instructions and procedures, you apply your strong attention to detail to complete tasks and required documentation</p></li><li><p>You are a strong multi-tasker; you are able to work on your own initiative using your proven interpersonal and communication skills</p></li><li><p>You enjoy working in a dynamic environment with cross functional teams</p></li></ul><p>To be considered for this opportunity you should have Leaving Certificate and 0-2 years of relevant work experience. Experience directly related to materials operations in the pharmaceutical/biotechnology industry, or other regulated industry is a distinct advantage. Good knowledge of Microsoft applications is required.</p><p>#LI-Onsite #JOBSIEST #IRELIM #REGNIEEC </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Jul 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, QA Microbiology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46191]]></requisitionid>
    <referencenumber><![CDATA[R46191]]></referencenumber>
    <apijobid><![CDATA[r46191]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46191/executive-director-qa-microbiology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is hiring! The Executive Director, QA Microbiology is responsible for the development and execution of the strategy and plan for the Regeneron GMP Microbiology program. The individual in this position is also responsible for providing direction to the function areas to ensure high-quality, safe, and effective products that are compliant with global regulatory expectations with respect to microbiological topics. This position will direct the efforts of the applicable functional areas in support of compliance and business objectives and will ensure that the Microbiology program remains current with industry expectations and help liaison with subject matter experts within the lines of businesses. </p><p>In this role, a typical day might include the following:</p><ul><li><p>Implement a value-added microbiology program based on sound science and the application of the appropriate quality, regulatory and legal requirements.</p></li><li><p>Monitor the performance of the microbiology program using the appropriate metrics and demonstrate a commitment to continuous improvement.</p></li><li><p>Embed quality tools and risk management processes within the microbiology program.</p></li><li><p>Stay abreast of changing requirements/expectations and proactively address within the microbiology program.</p></li><li><p>Use quality and risk management tools to make timely, science-based decisions to protect patient safety.</p></li><li><p>Implement appropriate solutions that address complex technical, legal and global regulatory standards.</p></li><li><p>Partners with QA Operations functions within the lines of business to translate strategy to implementation, and ensure compliant and robust aseptic practices.</p></li><li><p>Demonstrate confidence during difficult decision-making and influence internal and external business partners to ensure acceptable outcomes.</p></li><li><p>Lead as microbiology decision maker to ensure the safety and effectiveness of the products.</p></li><li><p>Represent as the face of Regeneron to internal and external stakeholders, including regulatory agencies and corporate partners regarding microbiological topics.</p></li><li><p>Translate the vision and business strategies of the microbiological program into executable action plans.</p></li><li><p>Ensure the Microbiological Control Strategy is transparent and the organization is engaged in its execution.</p></li><li><p>Allocate resources based on microbiology program priorities and corresponding business needs.</p></li><li><p>Establish high standards for performance management and accountability to achieve microbiological and organizational objectives.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Comprehensive knowledge of microbiological expectations throughout drug development process, pharmaceutical technology, drug manufacturing processes and related issues, drug laws, global regulations, and guidelines, particularly CMC and GMP.</p></li><li><p>Experience building up a quality culture and quality management capabilities.</p></li><li><p>Comprehensive knowledge and experience in CMC section content for investigational and marketed product submissions (IND, BLA, CBE, PAS) for FDA and equivalent submissions for Europe.</p></li><li><p>A sense of passion and commitment for delivering things as quickly and efficiently as possible.</p></li><li><p>The ability to think and operate in a rapidly evolving and ambiguous environment.</p></li><li><p>Ability to articulate and execute concepts for developing and ensuring the highest quality throughout the network (internal and external).</p></li><li><p>Intellect for quality risk identification, mitigation, and management.</p></li><li><p>Strong communication skills —written and oral.</p></li><li><p>Experience with businesses in different phases of the business lifecycle and the quality and validation issues associated with these phases.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Engineering, Chemistry, Biology or related science/technical field and the following amount of experience in a regulated industry (ie., Biotech, Pharma, Medical Device) for each level:</p><ul><li><p>Sr Director – 15+ years</p></li><li><p>Executive Director – 18+ years</p></li></ul><p>Level to be determined based on qualifications relevant to the role. Equivalent combination of education and experience will be considered.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$239,600.00 - $399,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Statistical Genetics (Oncology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46218]]></requisitionid>
    <referencenumber><![CDATA[R46218]]></referencenumber>
    <apijobid><![CDATA[r46218]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46218/director-statistical-genetics-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an exceptional senior leader with deep expertise in cancer genetics and genomics to join our team at the Regeneron Genetics Center. This Director-level role carries full accountability for the strategy and execution of cancer genetic product development — from aligning the vision with senior leadership and translating it into an actionable operational plan, through overseeing product development and setting the strategy for commercialization. The ideal candidate will bring a demonstrated track record of independence and impact, and will serve as the driving force for bringing cancer risk genomics into clinical and commercial reality.</p><p><strong>In this role, a typical day might include the following:</strong></p><p>• Develop and deliver on cancer genetics testing opportunities, including germline testing partnerships, serving as the senior leader accountable for clinical cancer test development.</p><p>• Define and own the end-to-end strategy for germline genetic cancer risk product development, translating organizational vision — aligned with senior leadership — into a clear, actionable operational roadmap with measurable milestones.</p><p>• Develop and execute a comprehensive somatic genetics strategy for Regeneron’s oncology portfolio, identifying new opportunities for somatic profiling studies across tumor types and leveraging existing cancer genomics databases.</p><p>• Lead and execute large-scale somatic cancer sequencing analyses, including whole-exome and whole-genome sequencing of tumor samples, RNA-seq, and integrative multi-OMICS studies to identify driver mutations, therapeutic vulnerabilities, and mechanisms of resistance.</p><p>• Design and contribute to cancer molecular profiling and clinical correlation analyses that integrate germline and somatic mutational profiles with multi-modal transcriptomic, epigenetic, and proteomic data to support target discovery, indication selection, and patient stratification strategies.</p><p>• Oversee all phases of product development for cancer risk genomics programs, ensuring scientific rigor, cross-functional alignment, and on-time delivery against strategic objectives.</p><p>• Develop and execute the commercialization strategy for RGC cancer products, identifying market opportunities, go-to-market pathways, and partnerships that maximize clinical and commercial impact.</p><p>• Collaborate with and lead a multidisciplinary genetics team consisting of human genetics scientists, bioinformaticians, and statistical geneticists to design, execute, and interpret genetics studies related to cancer risk, somatic evolution, mechanisms, and therapeutic outcomes.</p><p><strong>This job might be for you if you:</strong></p><p>• Have a demonstrated ability to independently own and drive strategic programs in cancer risk genomics or oncology product development from conception through commercialization.</p><p>• Bring innovative thinking and hands-on leadership to large-scale somatic cancer sequencing studies and integrative genomic analyses.</p><p>• Have deep expertise in analyzing tumor sequencing data, including variant calling, mutational signature analysis, clonal evolution, copy number alterations, and structural variant detection.</p><p>• Have experience in developing or contributing to germline diagnostic tests for cancer predisposition, risk assessment, or clinical decision-making.</p><p>• Are a motivated senior leader with a desire to pursue genetic discovery in a fast-paced multidisciplinary environment and can effectively guide teams and align stakeholders toward strategic goals.</p><p>• Have demonstrated experience in quantitative problem solving, statistical analyses, and translating somatic and germline genetic findings into clinical applications.</p><p><strong>To be considered for this role</strong>, you must have an MD or MD/PhD with a strong background in quantitative biology applied to cancer genetics and genomics, and a proven ability to design and lead large-scale human cancer genomic programs delivering medically- and commercially-relevant outcomes.</p><p>A minimum of 12 years of research experience in cancer genetics, genomics, or oncology product development is required, with a commensurate level of independence, seniority, and demonstrated responsibility for program strategy and execution.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist - Quantitative Translational Scientist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46821]]></requisitionid>
    <referencenumber><![CDATA[R46821]]></referencenumber>
    <apijobid><![CDATA[r46821]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46821/principal-scientist-quantitative-translational-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Precision Medicine Quantitative Biomarker team (PMQBS) is seeking a Principal Scientist with a blend of deep biomarker and translational-science expertise coupled with advanced computational and analytical skills. This role will focus primarily on the Oncology portfolio, and will encompass exploratory analyses and visualization of omics, EHR, wearable sensor, imaging, and other biomarker data. This position is also involved in the development of tools and dashboards for querying, visualizing, and cleaning data. The individual will work collaboratively with internal and external groups to assure data integrity, best practices for analytics and data visualization, and offering strategic insights to drive Precision Medicine objectives. </p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li><p>Set and refine quantitative biomarker strategies across multiple programs, aligning with Precision Medicine Strategy Leads and senior stakeholders.</p></li><li><p>Translate program objectives into testable hypotheses, analytical roadmaps, and decision criteria that inform clinical development and asset strategy.</p></li><li><p>Architect exploratory analyses of multi-modal datasets (genomic, transcriptomic, proteomic, metabolomic, clinical, and other biomarkers) to generate actionable insights.</p></li><li><p>Define and review statistical frameworks, including hypothesis testing, modeling approaches, and power/sample-size analyses, ensuring appropriate interpretation.</p></li><li><p>Oversee the correct application of statistical models on integrated datasets and drive clear, decision-oriented interpretation for translational and clinical teams.</p></li><li><p>Contribute to the vision for scalable, reproducible pipelines and automated workflows that support enterprise-wide biomarker discovery and clinical development.</p></li><li><p>Direct the design and enhancement of computational workflows for novel biomarkers; evaluate, integrate, or build tools as needed.</p></li><li><p>Provide guidance on data cleaning, integration, and visualization standards to enable robust, interpretable analyses.</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Proficient in statistical modeling/regression, machine learning, and related data integration/blending techniques.</p></li><li><p>Experienced in implementing scalable workflows on cloud platforms (AWS, GCP, or Azure)</p></li><li><p>Experienced in Linux and/or cloud environments, shell scripting, and notebook-based workflows.</p></li><li><p>Knowledgeable of structured data and data mapping for systems integration, data provisioning, and consumption.</p></li><li><p>Experience with version control and AI coding assistants such as Claude Code is strongly preferred.</p></li><li><p>Knowledgeable of structured data and data mapping for systems integration, data provisioning, and consumption.</p></li></ul><p><strong>To be considered for this role,</strong> you must have at minimum a PhD with 2 years, or Masters with 5 years of relevant industry experience in one of the following or otherwise related quantitative fields: Computer Science, Computational Biology, Systems Biology, Quantitative Biology, Bioinformatics, Data Analytics, Biostatistics. A working understanding of Clinical trials is a strong plus.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician, Saturday-Wednesday 3rd shift]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46909]]></requisitionid>
    <referencenumber><![CDATA[R46909]]></referencenumber>
    <apijobid><![CDATA[r46909]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46909/hvac-technician-saturday-wednesday-3rd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a HVAC Technician to our growing team, working a Saturday-Wednesday 10:00pm – 8:30am shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment; troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><p><strong>Please note training will take place Monday-Friday 7:00am-3:30pm for approximately 6 months. Working hours thereafter will be Saturday-Wednesday 10:00pm-8:30am. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a HVAC Technician, a typical day might include the following:</p><ul><li><p>Maintaining coolers and freezers including Ultra Low temperature Freezer</p></li><li><p>Maintaining Centrifugal and Reciprocating refrigeration chillers</p></li><li><p>Maintaining Chilled water systems including distribution and condenser pumps</p></li><li><p>Maintaining Air Compressors</p></li><li><p>Electrical power systems and stand-by power generation equipment</p></li><li><p>Following current good manufacturing practices (cGMPs) and good business practices (G)</p></li><li><p>Participating in rotational on-call for site emergency work</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOP's, cGMP's, GDP’s and quality standards</p></li><li><p>Becoming fully gown qualified to work within Production areas</p></li><li><p>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</p></li><li><p>May plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Demonstrate basic problem-solving skills</p></li><li><p>Are able to learn and follow routine procedures independently as well as part of a team</p></li><li><p>Are comfortable and have the flexibility to work in a changing environment</p></li><li><p>Can lift, push, and pull at least 50lbs</p></li><li><p>Seek to build and maintain positive working relationships with the business</p></li><li><p>Possess strong written and verbal communication skills</p></li><li><p>Maintain effective time management skills to allow deadlines to be met in a timely manner</p></li><li><p>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</p></li></ul><p>To be considered for the HVAC Technician position you must be willing and able to work a Saturday-Wednesday 10:00pm – 8:30am schedule. Applicants ideally should have technical school training with field experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance and the following minimum amounts of experience for each level:</p><ul><li><p>HVAC Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li><li><p>HVAC III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p></li><li><p>HVAC IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</p></li></ul><p>Level will be determined based on qualifications relevant to the role. Will substitute relevant work experience in lieu of education. Electronic, PLC, mechanical and building automation systems experience in Pharmaceutical Industry preferred. EPA certified for refrigeration gases.</p><p>#REGENTOSK </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Medical Affairs-Classical Hematology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47118]]></requisitionid>
    <referencenumber><![CDATA[R47118]]></referencenumber>
    <apijobid><![CDATA[r47118]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47118/senior-manager-medical-affairs-classical-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Senior Manager, Medical Affairs -Classic Hematology you will serve as a scientific and strategic resource leading the execution of our medical plans across bleeding and clotting disorders. Take an active participation in an integral role to drug launch readiness and early access programs. </p><p>This position is at our Sleepy Hollow, NY offices and will require you to be onsite 4 days/week. If eligible, we can offer relocation benefits. We cannot offer a remote work option. </p><p><strong>A typical day may include the following: </strong><br>• Translating scientific and clinical insights into medical strategies supporting evidence generation and product positioning.<br>• Ensuring our medical activities are conducted in strict compliance with applicable regulations, company policies, and industry codes of practice.<br>• Establishing, developing, and sustaining peer-level relationships with KOLs and academic institutions. <br>• Support the development and oversight of company-sponsored clinical trials, including identification and selection of investigators and trial sites.<br>• Manage investigator-initiated studies with our Field Medical team. <br>• Gather and report relevant scientific, clinical, and competitive intelligence. <br>• Drive launch readiness activities, contributing medical expertise to cross-functional planning and execution.<br>• Support early access programs, including data collection, management, and reporting in alignment with regulatory requirements.<br>• Coordinate and facilitate advisory boards and scientific meetings, ensuring robust insight capture and actionable outputs.</p><p><strong>This may be for you if you:</strong><br>• Want to be a part of the early-stage buildout of a new team<br>• Have an exceptional ability to communicate clinical and medical data to clinical and non-clinical audiences.<br>• Demonstrated ability to work independently and effectively within a matrix organizational structure.<br>• Want to have an impact of patient health</p><p>To be consider it is required to have a doctorate level education in life sciences (MD, PharmD, PhD) and a clinical background in hematology. Your experience must 3+ years of experience in a Medical Manager or Medical Affairs role within the biotech or pharmaceutical industry. Solid understanding of anticoagulation or thrombosis along with their treatment guidelines, and clinical research processes is preferred. Willingness to travel including overnight and occasional weekend travel.<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Regulatory Intelligence]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47246]]></requisitionid>
    <referencenumber><![CDATA[R47246]]></referencenumber>
    <apijobid><![CDATA[r47246]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47246/senior-manager-regulatory-intelligence/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Senior Manager, Regulatory Intelligence to play a key role in monitoring, interpreting, and communicating changes in the global regulatory landscape, with a strong focus on EU regulatory strategy and pharmacovigilance.</p><p>In this role, we partner closely with cross‑functional teams to translate regulatory developments into clear, actionable insight that supports drug development, regulatory strategy, and GxP compliance across the organization.</p><h3>A Typical Day May Include</h3><ul><li>Monitoring and assessing new and emerging regulatory guidance, legislation, and policy from global health authorities and industry bodies.</li><li>Evaluating regulatory developments to determine relevance and impact on development programs, regulatory strategy, and internal processes.</li><li>Preparing concise regulatory intelligence summaries, reports, and presentations tailored to different stakeholder groups.</li><li>Acting as a point of contact for regulatory intelligence questions and ad‑hoc requests.</li><li>Identifying business‑critical regulatory changes and proactively communicating implications to cross‑functional stakeholders.</li><li>Supporting regulatory commenting activities, including review and drafting of submissions to health authorities and industry organizations.</li><li>Facilitating regulatory intelligence briefings, meetings, and knowledge‑sharing sessions.</li><li>Maintaining regulatory intelligence content and contributing to improvements in how intelligence is captured and shared.</li><li>Mentoring junior team members, as needed.</li></ul><h3>This Role May Be For You If You</h3><ul><li>Enjoy staying ahead of regulatory change and applying it in a practical, business‑focused way.</li><li>Have strong experience in regulatory affairs and/or pharmacovigilance within pharma or biotech.</li><li>Are confident interpreting regulatory guidance and understanding its impact across the drug development lifecycle.</li><li>Are comfortable working cross‑functionally and engaging with a range of stakeholders.</li><li>Can work independently, manage competing priorities, and deliver to deadlines.</li><li>Value clarity, accuracy, and quality in your work.</li><li>Are motivated to improve processes and contribute to how regulatory intelligence is delivered across the organization.</li></ul><h3>What You’ll Bring</h3><ul><li>8+ years’ experience in the pharmaceutical or biotech industry, or within a health authority, with a focus on Regulatory Affairs and/or Pharmacovigilance.</li><li>Strong understanding of EU and US regulatory and pharmacovigilance requirements across the drug development lifecycle.</li><li>Experience sourcing, monitoring, and interpreting regulatory information from health authority platforms and other intelligence sources.</li><li>Strong analytical skills, with the ability to identify key regulatory risks and implications.</li><li>Clear, concise written and verbal communication skills.</li><li>Strong organizational skills and attention to detail.</li><li>A collaborative, practical approach to working across teams and functions.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Southeast]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47574]]></requisitionid>
    <referencenumber><![CDATA[R47574]]></referencenumber>
    <apijobid><![CDATA[r47574]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47574/regional-director-neurology-southeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Georgia]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the [INSERT] Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Southeast (Georgia, Florida & Alabama)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Precision Medicine Strategy Lead (Clinical Biomarkers)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47645]]></requisitionid>
    <referencenumber><![CDATA[R47645]]></referencenumber>
    <apijobid><![CDATA[r47645]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47645/principal-scientist-precision-medicine-strategy-lead-clinical-biomarkers/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Precision Medicine Strategy Lead (PMSL) at the Principal Scientist level responsible for the clinical biomarker strategy for multiple clinical stage assets in Regeneron's Immunology & Inflammation (I&I), Ophthalmology and Infectious Diseases portfolios.</p><p>The successful candidate will be motivated and innovative in their proposals for clinical biomarker strategies that drive the success of both early and late-stage clinical programs. They will be knowledgeable regarding key literature and relevant technologies. They will thrive in a collaborative environment and regularly partner with research teams, clinical development, laboratory operations, companion diagnostics, clinical operations, tech centers, alliance partners, external academic collaborators, and others. They will be exceptional communicators as they routinely present their strategy, rationale and data to senior leaders.</p><p>This is a high-impact, highly visible role at the intersection of science and strategy in Regeneron’s Translational Medicine organization. The work done as a Principal Scientist will enable endpoint selection, choice of clinical indication, and demonstration of target engagement, early signs of activity, mechanism of action and patient stratification/selection.</p><p><strong>As a Lead, a typical day may include:</strong></p><ul><li><p>Define and champion the strategic vision and scientific rationale for clinical biomarker plans supporting one or more programs in I&I, Ophthalmology, and/or Infectious Disease</p></li><li><p>Serve as a Precision Medicine representative on clinical development teams, driving biomarker strategy from initial concept through execution, data delivery, and interpretation.</p></li><li><p>Partner with clinical and laboratory operations to implement biomarker and exploratory sample collection and analyses</p></li><li><p>Ensure clinical biomarker assays are fit-for-purpose — whether developed internally or through external collaborators/CROs</p></li><li><p>Present translational project plans, biomarker data, and results to internal and external stakeholders, including senior leadership</p></li><li><p>Contribute to the highest-quality Precision Medicine content in clinical protocols, study reports, data reviews, biomarker reports and manuscripts/publications</p></li></ul><p><strong>This role might be for you if can:</strong> ​</p><ul><li><p>Translate complex immunology and disease biology into clear, testable clinical biomarker hypotheses and decision criteria.</p></li><li><p>Lead cross-functional teams to design, operationalize, and troubleshoot end-to-end biomarker plans across global studies.</p></li><li><p>Drive fit-for-purpose assay development and validation with internal labs and CROs, balancing scientific rigor, cost, and timelines.</p></li><li><p>Synthesize and communicate biomarker insights into compelling narratives for diverse stakeholders, including senior leadership, to inform key decisions.</p></li><li><p>Navigate ambiguity, prioritize across multiple programs, and foster a collaborative, innovative culture in a matrixed environment.</p></li></ul><p><strong>To be considered for this role, you must have: </strong></p><ul><li><p>Ph.D. with post-doctoral experience in Immunology or closely related field is highly desirable</p></li><li><p>5+ years of relevant experience in pharmaceutical/biotech industry research and/or translational clinical development</p></li><li><p>Exceptional communicator with strong emotional intelligence and enthusiasm for presenting to senior leaders</p></li><li><p>Collaborative, innovative, and energized by working in a matrixed environment</p></li><li><p>Understanding of biomarker strategy in clinical development, including assay development, validation, and implementation with a track record of high-impact contributions to drug development programs is a huge plus</p></li><li><p>Experience authoring industry documents (protocols, CSRs, biomarker reports) is a plus</p></li><li><p>Alternative levels will be considered commensurate with experience</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Business Analyst]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47668]]></requisitionid>
    <referencenumber><![CDATA[R47668]]></referencenumber>
    <apijobid><![CDATA[r47668]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47668/principal-business-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is looking for an outstanding Principal Business Analyst to drive consistency across the Global Development (GD) IT team, and be a member of the GD Digital Transformation Program. This individual will work closely with GD IT leadership, and GD partners such as Business Process Owners, Subject Matter Experts, Training and Process & Procedures teams members in support of the overall Program and specific use cases.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Collaborate with GD IT Leadership to support the GD Digital Transformation Program, including overall program management.</p></li><li><p>Support the delivery of a GD Digital Transformation Program “use case” (new digital solution to improved efficiency and ways of working across GD)</p></li><li><p>Develop frameworks to gather accurate, measurable requirements that dictate project outcomes</p></li><li><p>Build flexible processes and frameworks in support of traditional (e.g., waterfall) and hybrid (e.g., agile) delivery methods</p></li><li><p>Collect GD IT operational metrics, analyze, identify & develop action plans for areas of improvement</p></li><li><p>Introducing new insights, approaches, solutions and technologies for GD IT</p></li><li><p>Collaborating with GD IT agile Delivery & Operations and Data Enablement leads to ensure that solutions are appropriately planned, accomplished, and improved upon</p></li><li><p>Provide direction on projects and technology products to optimally manage user expectations, timelines, budget and overall efforts for value realization</p></li><li><p>Work collaboratively with GD functions, Corporate IT, and other relevant functions in the management of enterprise systems, including development and adherence to standards and governance</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Knowledge of pharmaceutical Global Development business capabilities, processes, applications, and key trends in the industry</p></li><li><p>Experience in one or more of the following Clinical Development functions in support of IT: Medical Affairs, Regulatory Affairs, Global Patient Safety, Clinical Operations, Biostatistics & Data Management, Clinical Quality, etc.</p></li><li><p>Robust business acumen and analytical expertise, to consistently drive operational enhancements and work practices' optimization</p></li><li><p>Self-drive & ability to work in ambiguity, with minimal oversight</p></li><li><p>Basic to intermediate proficiency in AI tools (e.g. CoPilot), and building AI agents</p></li><li><p>Excellent communication skills and the ability to indirectly influence key partners and stakeholders</p></li><li><p>Experience with Waterfall/Hybrid/Agile project methodologies and associated tools (e.g., Jira, Confluence)</p></li><li><p>Strong track record of technology project, stakeholder, and budget management </p></li><li><p>Ability to coordinate, influence and empower diverse teams to achieve goals</p></li><li><p>Experience working within and knowledge of GXP/GCP and regulatory ICH 6 guidelines</p></li><li><p>Expertise with MS Office Suite</p></li></ul><p><strong>This job might be for you if: </strong></p><ul><li><p>You are a self-starter, and are a proactive independent contributor who excels in evolving environments </p></li><li><p>You thrive in a fast-paced environment working across multiple scientific and business domains</p></li></ul><p><strong>Level commensurate on experience and qualifications:</strong></p><ul><li><p>Bachelor's degree in a related field BS/BA Degree with 7-9+ years of relevant work experience</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Product Management - Delivery & Operations Product Lead]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47750]]></requisitionid>
    <referencenumber><![CDATA[R47750]]></referencenumber>
    <apijobid><![CDATA[r47750]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47750/senior-manager-product-management-delivery-operations-product-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Delivery & Operations Product Lead (Senior Manager) drives end-to-end delivery, support, and optimization of a Global Development technology product focused on standards-led protocol digitization, biospecimen lifecycle management, and AI-enabled orchestration. Partnering with process owners, IT teams, and vendors, the role turns ICH M11/USDM and CDISC standards into reusable digital assets that power Digital Data Flow (DDF) and improve study build speed, data quality, and regulatory compliance. </p><p>You will own product vision, roadmap, and operations—balancing strategic planning with hands-on execution—while ensuring secure integrations, validated AI capabilities, and high levels of customer satisfaction.</p><p><strong>In this role, a typical day might include the following: </strong></p><p>- Leading agile ceremonies, refining backlogs, and approving user stories for protocol-to-data and sample-workflow features </p><p>- Facilitating workshops with clinical, biometrics, and lab SMEs to gather requirements and prioritize improvements </p><p>- Reviewing architecture and validation plans to ensure security, privacy, and GxP compliance for API and AI components </p><p>- Supervising platform usage, data-quality dashboards, and AI guardrail metrics to drive continuous improvement </p><p>- Managing vendor results, budgets, and risks while preparing executive-ready status updates </p><p>- Coordinating change, release, and incident processes to maintain audit-ready, high-performing operations </p><p><strong>This job might be for you if you: </strong></p><p>- Translate complex protocol, biospecimen, and standards concepts into intuitive digital products </p><p>- Enjoy orchestrating multi-system integrations (EDC, LIMS, IRT, CTMS) and ensuring traceable data lineage </p><p>- Thrive in fast-paced, agile environments and can balance strategic goals with day-to-day execution </p><p>- Communicate clearly with executives and engineers alike, influencing without direct authority </p><p>- Stay current on AI/agentic and CDISC 360 trends and apply them pragmatically in regulated settings </p><p>- Possess a “get-it-done” attitude, solving issues quickly while keeping long-term value in focus </p><p><strong>In order to be considered for this role, you must have: </strong></p><p>- BS/BA with 8–10 years (or MS with 6+ years) in Global Development IT, including protocol digitization, biospecimen workflows, and standards (ICH M11/USDM, CDISC SDTM/ADaM) </p><p>- Consistent track record delivering GxP-validated, AI-enabled products with integrations across EDC, LIMS, and analytics platforms </p><p>- Deep experience in agile product management, vendor oversight, and regulated change/validation processes</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Thought Leader Liaison Oncology (NMSC) -Northeast & Great Lakes Region]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47762]]></requisitionid>
    <referencenumber><![CDATA[R47762]]></referencenumber>
    <apijobid><![CDATA[r47762]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47762/associate-director-thought-leader-liaison-oncology-nmsc-northeast-great-lakes-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oncology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Oncology Marketing team reporting into the Senior Director, Scientific Marketing. The role is focused on enhancing and improving interactions with key external US Oncology thought leaders at academic centers and leading community practices for our Oncology Non-Melanoma Skin Cancer portfolio, particularly in the area of high risk Cutaneous Squamous-Cell Carcinoma (CSCC), advanced CSCC, and advanced basal cell carcinoma (BCC).</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Oncology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><h3>The typical day may include the following:</h3><ul><li>Engaging in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Sharing with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Supporting congress planning efforts, including sponsorship recommendations and identification of speakers for product theaters</li><li>Coordinating thought leader engagements for senior executives at local/regional/national conferences and/or during day-to-day business</li><li>Conducting substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embracing a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Developing/maintaining list of key thought leaders in the assigned geography</li><li>Assisting with thought leader development</li><li>Supporting speaker bureau efforts, including identification of potential speakers, contracting, managing logistics related to speaker training, and providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Supporting regional/national advisory board and advisory council planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Supporting monthly field team calls, gathering feedback on speaker programs & p2p content</li><li>Ensuring all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><h3>This role may be for you if:</h3><ul><li>You possess a strong science background with deep knowledge of Oncology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p>To be considered for this opportunity, we expect you to have a bachelor’s degree required; Master’s degree or other advanced education/certification is a plus. Along with specialty pharmaceutical/biopharmaceutical experience, with a minimum of 8 years of work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in hematology/oncology markets strongly preferred. You also have expertise in marketing strategies within the pharmaceutical industry. Ideally, you would have launch experience. You must be able to travel 60%-80% of time</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Material Supplier Specialist (Change Notification)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47914]]></requisitionid>
    <referencenumber><![CDATA[R47914]]></referencenumber>
    <apijobid><![CDATA[r47914]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47914/principal-qa-material-supplier-specialist-change-notification/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Our Material & Supplier Quality Assurance team is hiring a Principal QA Material Supplier Specialist to lead end-to-end management of supplier-initiated changes to GMP materials and components, safeguarding product quality, compliance, and supply. This role provides global coordination for supplier change notifications.</p><p><strong>When & where:</strong></p><ul><li><p>Rensselaer, NY</p></li><li><p>Monday-Friday</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Reviews and coordinates Supplier Change Notifications across global suppliers, including intake, triage, risk assessment, cross functional impact evaluation, communication, and closure.</p></li><li><p>Supports the resolution of internal and external deviations, and Supplier Corrective Action Requests (SCARs) related to materials and supplier changes.</p></li><li><p>Maintain and update controlled documents related to supplier change notification.</p></li><li><p>May execute Corrective/Preventative Actions (CAPAs) arising from supplier changes, audits, or process gaps.</p></li><li><p>Gathers, evaluates and provides information/documentation to support regulatory inspections and inquiries, as well as partner and internal audits.</p></li><li><p>Performs continuous improvement of the Material & Supplier Quality program with a focus on SCN workflow efficiency, cycle time reduction, and right first time.</p></li><li><p>Manages and tracks projects to ensure milestones are achieved while complying with established timelines.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor’s degree in scientific subject area or related field and the following years of experience for each level: </p><ul><li><p>Sr. Specialist: 5+ years</p></li><li><p>Principal Specialist: 8+ years</p></li></ul></li><li><p>Experience partnering with suppliers of GMP materials/components preferred.</p></li><li><p>Previous quality experience in a GMP environment.</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, AI and Data Science]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47991]]></requisitionid>
    <referencenumber><![CDATA[R47991]]></referencenumber>
    <apijobid><![CDATA[r47991]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47991/process-development-engineer-iii-ai-and-data-science/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Data Enablement and Analytics (DEA) team within the PAPD (Product, Analytics and Process Development) organization drives PAPD’s digital transformation by making data usable, useful, and impactful in support of our mission of Transforming Therapeutic Molecules into Products for a Diversified Pipeline.</p><p>We are seeking a Process Development Engineer III, AI and Data Science to join our Artificial Intelligence (AI) and Advanced Analytics (AA) team in DEA, who pairs deep bioprocess‐engineering expertise with sophisticated AI/ML and Data Science (DS) capabilities to accelerate biologics development and manufacturing.</p><p>You will design, implement, and operationalize AI and DS models for upstream (cell-culture/bioreactor), downstream (purification) operations, Formulation Development and multiple Analytics teams while partnering closely with process-development, manufacturing-sciences, and digital teams. You will turn data into prescriptive guidance, deploy production-grade models, and build innovative AI solutions that enhance process understanding, optimization, and automation.</p><p><br><strong>A Typical Day in the Role of Process Development Engineer III Might Look Like:</strong></p><ul><li>Build and deploy AI/ML-powered solutions to accelerate our digitalization journey.</li><li>Advance PAPD’s broader AI, DS and related digital-maturity initiatives.</li><li>Collaborate with process engineers, citizen data scientists, IT, and manufacturing colleagues to coordinate AI and Advanced modeling efforts enterprise wide.</li><li>Explore, prototype and implement GenAI approaches and solutions (e.g., Retrieval-Augmented Generation) to enhance knowledge management, and decision support.</li><li>Develop, validate, and maintain mechanistic, hybrid, and data-driven models for cell culture, purification, formulation and other processes. These include digital twins, advanced predictive modelling, and process control techniques.</li><li>Translate complex bioprocess questions into quantitative modeling strategies that inform scale-up, tech transfer, and continuous improvement.</li><li>Mentor citizen data scientists and champion best practices in model development, method selection, and code quality.</li></ul><p><strong>This Role Might Be For You If You Have:</strong></p><ul><li>Analytical rigor and creative problem solving</li><li>Ability to drive projects autonomously while thriving in cross-functional teams</li><li>Excellent written and verbal communication</li><li>Passion for innovation and continuous learning</li></ul><p><strong>Required Qualifications</strong></p><ul><li>This role requires a Ph.D. in Chemical/Biochemical Engineering, Biotechnology, Applied Mathematics, Computer Science or related field with 0-2+ years of industrial experience OR- Master’s with 7+ years.</li><li>Expert programming proficiency in Python and experience with statistical/computational tools such as JMP, SIMCA or MATLAB is required.</li><li>Proven ability to communicate technical concepts to multidisciplinary stakeholders. </li></ul><p><br><strong>Preferred Qualifications</strong></p><ul><li>Hands-on experience with cloud analytics platforms (e.g., Dataiku, Databricks).</li><li>Strong working knowledge of Quality-by-Design (QbD) principles and statistically rigorous Design-of-Experiments (DoE) for defining design space, optimizing critical process parameters, and informing robust control strategies.</li><li>Familiarity with PAT and chemometric modeling (e.g., Raman spectroscopy) for bioprocess monitoring and control.</li><li>Understanding of operation research techniques such as combinatorial optimization, linear programming, mixed integer programming is a plus.</li><li>Ability to deal with data from both SQL and NoSQL systems to support analytics, real-time processing, and application performance is a plus.</li><li>Publication record in bioprocess modeling or AI for biomanufacturing is a plus.</li><li>Mechanistic understanding of upstream and/or downstream bioprocess unit operations, scale-up/down principles, and critical quality attributes is strongly preferred.</li><li>A demonstrated success modeling bioprocesses via first-principles, hybrid, or data-driven (ML) methods is preferred.</li><li>A strong foundation in AI/ML algorithms (regression, classification, Bayesian methods, deep learning, time-series, probabilistic modeling) is a plus, along with expertise in multivariate statistics for process modeling, real-time monitoring, and control.</li><li>Some experience with GenAI stacks (LLMs, vector databases, RAG pipelines) and multimodal techniques is necessary/required/strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison  - Neurology (Mountain West)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48122]]></requisitionid>
    <referencenumber><![CDATA[R48122]]></referencenumber>
    <apijobid><![CDATA[r48122]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48122/associate-director-thought-leader-liaison-neurology-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Minnesota]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Neurology Marketing team. It will be focused on enhancing and improving interactions with key external US Neurology thought leaders at academic centers and leading community practices for our neurology product.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Neurology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><p><strong>The typical day may include the following:</strong></p><ul><li>The Neurology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You possess a strong science background with deep knowledge of hematology/oncology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p><strong>To be considered for this opportunity, you will possess the following:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10years of relevant work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in Neurology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry. Launch experience preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li><li>Must have a valid driver’s license</li><li>Must be able to travel 60%-80% of time </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Summer 2026 MD Intern, Internal Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43354]]></requisitionid>
    <referencenumber><![CDATA[R43354]]></referencenumber>
    <apijobid><![CDATA[r43354]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43354/summer-2026-md-intern-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>If you’re currently a medical school student interested in drug discovery and development, you may be a fit for an internship in our Internal Medicine Clinical Development Unit.</p><p><strong>In this role, a typical internship will include:</strong></p><ul><li><p>Achieving a general understanding of what happens in our global development organization</p></li><li><p>Completing a hands-on project that has an impact on the business</p></li><li><p>Engaging with Regeneron leadership</p></li><li><p>Collaborating with a specific hiring manager and other interns</p></li><li><p>Establishing connections with Regeneron’s diverse employee resource groups</p></li><li><p>Participating in professional development sessions</p></li><li><p>Showcasing the knowledge you gained through end of program presentation sessions</p></li><li><p>Getting paid for your hard work!</p></li></ul><p><strong>Internship Project Specifics:</strong></p><p>The summer intern will be placed on a project team in the Internal Medicine Clinical Development Unit at Regeneron. During this project the summer intern may visually and/or descriptively analyze clinical trial data from recent studies or databases. Disease areas that comprise the focus of the summer interns project may include: cardiovascular, pulmonary and/or immunological & inflammatory diseases.</p><p>The student will be trained on basic statistical modeling techniques using SAS JMP. The summer project may involve reviewing pharmacokinetic (PK) and pharmacodynamic (PD) data from clinical trials. Students will be trained on techniques for data cleaning, statistical analysis, and linear regression (univariate and multivariate). The student will work closely with the global program head, medical director and clinical pharmacology director during the project.</p><p>Additionally, students will be trained in Good Clinical Practice (GCP) standards for human clinical trials including relevant International Conference on Harmonization (ICH) and FDA Guidelines. The student will also attend relevant team meetings including: Strategic Project Team, Global Clinical Sub Team, Global Regulatory Sub Team and others as needed.</p><p>At the end of the summer internship period, the student will be expected to give a presentation/summary of their research experiences to an internal audience at Regeneron.</p><p>To be considered for this opportunity, you must be currently enrolled in medical school and returning to school the semester following the internship). A cumulative GPA of 3.0 is preferred. We want someone who is able to commit to 40 hours per week for a minimum of 6-8 weeks during a time-period from the end of May/ early June through August. The specific weeks of the internship are flexible and intended to accommodate the intern’s time out of school. Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community is also preferred.</p><p>Requirements:</p><ul><li><p>Medical student currently enrolled in an accredited US medical school (MD)</p></li><li><p>Must have completed at least the first-year basic science curriculum. Students who have completed the second year and beyond will also be considered but must have adequate time available during an elective or research rotation to be on site at Regeneron.</p></li><li><p>Familiarity with Microsoft Office tools (Word, Outlook, Powerpoint).</p></li><li><p>Prior research experience is preferred but not required. Understanding of biostatistics, experimental design and the scientific method is preferred. Experience with R studio, Python, SPSS, SAS or SAS JMP is a plus.</p></li><li><p>On site attendance at Regeneron offices in Tarrytown NY is expected 5 days per week</p></li></ul><p><strong><em>Please note our intern pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for Tarrytown, NY: $32.00-$40.70 per hour. </em></strong></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Biotech Production Specialist]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48340]]></requisitionid>
    <referencenumber><![CDATA[R48340]]></referencenumber>
    <apijobid><![CDATA[r48340]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48340/associate-biotech-production-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>Within this role you will be working as part of the Manufacturing Team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors.<br> </div></div><div><div><div><div><div><div><div><div><div><p><strong>As an Associate Biotech Production Specialist, a typical shift might include, but is not limited to, the following:</strong></p><ul><li><p>Working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors</p></li><li><p>Monitoring production processes</p></li><li><p>Participating in equipment start-up, commissioning, and validation activities</p></li><li><p>Assisting with troubleshooting in case of equipment failure</p></li><li><p>Performing manufacturing level maintenance on equipment</p></li><li><p>Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks</p></li><li><p>Performing equipment cleaning, preparation and execution as well as completing associated documentation</p></li><li><p>Performing various tests and in-process sampling</p></li><li><p>Reviewing, editing and revising completed batch records, logbooks, and SOPs in accordance with cGMP standards</p></li><li><p>Maintaining housekeeping in designated area and adhering to the clean standards of the facility</p></li></ul><p><br><strong>This role might be for you if:</strong></p><ul><li><p>You possess excellent verbal and written communication skills</p></li><li><p>You enjoy problem solving</p></li><li><p>You demonstrate a can-do attitude</p></li><li><p>You are proficient in Microsoft Word, Excel, PowerPoint, and Outlook</p></li><li><p>You demonstrate an ability to work within a successful team</p></li><li><p>You can adapt to a changing environment and have the ability to adhere to a schedule</p></li></ul><p><br>To be considered for this opportunity you should have a BS/BA in Life Sciences or a related field. Relevant experience may be substituted in lieu of the educational requirement.</p><p>Our site operates on a 24/7 basis, and we offer a number of different shift working patterns that could fit with your lifestyle</p><p><strong>What is on offer?</strong> </p><p>You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. </p><p>Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:</p><ul><li><p>Competitive Salary</p></li><li><p>Shift Premiums</p></li><li><p>Annual Bonus</p></li><li><p>Stock Schemes</p></li><li><p>Employer Pension Contributions </p></li><li><p>Education Assistance</p></li><li><p>Generous Annual & Flexible Leave Programs </p></li><li><p>Competitive Private Medical, Dental & Vision Plans</p></li><li><p>Career & Personal Development</p></li><li><p>Wellness Programs - Onsite Gyms & Fitness Classes </p></li><li><p>Concierge Services – Onsite Beauty Therapist / Barber</p></li><li><p>Community Volunteering</p></li><li><p>Employee Interest Groups / Employee Teams & Clubs</p></li><li><p>Employee & Family Events</p></li></ul><p>#LI-Onsite #JOBSIEST #REGNIELSM #IRELIM</p></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€16.42 - €25.59]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Commercial Finance]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48094]]></requisitionid>
    <referencenumber><![CDATA[R48094]]></referencenumber>
    <apijobid><![CDATA[r48094]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48094/manager-commercial-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. As we continue to scale globally, strong financial planning, data integrity, and data-driven decision-making are critical to supporting our commercial strategy.</p><p>As a Senior Associate / Manager – Commercial Finance (FP&A), you will play a key role in supporting the US/Global Commercial Finance teams by delivering standardized reporting, enhancing data quality, and driving automation initiatives. You will partner with cross-functional collaborators to provide meaningful insights, improve planning cycles, and strengthen financial governance.</p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li><p>Partner with US/Global Commercial Finance teams to provide reporting and analysis across Commercial Business Units, Operations, Market Access, and Commercial IT</p></li><li><p>Prepare daily, weekly, and monthly performance reports, including sales dashboards, P&L views, and OpEx tracking</p></li><li><p>Support budgeting, forecasting, and scenario planning, including maintaining driver-based models and assumptions</p></li><li><p>Own and manage headcount planning, including tracking actuals vs plan, cost allocations, and organization alignment</p></li><li><p>Perform variance analysis against plan, forecast, and prior periods, with clear commentary for collaborators</p></li><li><p>Collaborate with Commercial IT and business teams on project approvals, business cases, and cost tracking</p></li><li><p>Prepare and submit accurate accruals in line with accounting timelines and requirements</p></li><li><p>Design, standardize, and enhance recurring reporting processes to improve efficiency and consistency</p></li><li><p>Build and maintain important metric dashboards using BI tools to support business decision-making</p></li><li><p>Drive automation in reporting, data preparation, and reconciliations to reduce manual effort</p></li><li><p>Improve data governance, quality, and documentation across financial processes</p></li><li><p>Partner with global collaborators across time zones to ensure alignment and delivery.</p></li></ul><p><strong>This Job May Be for You If You Have:</strong></p><ul><li><p>Experience in Commercial Finance or FP&A with strong reporting and analytical capabilities</p></li><li><p>Strong understanding of financial planning, forecasting, and variance analysis</p></li><li><p>Ability to standardize processes and drive automation initiatives</p></li><li><p>Strong data handling and analytical approach with attention to detail</p></li><li><p>Experience working with global collaborators across multiple time zones</p></li><li><p>Strong communication and collaborator management skills</p></li><li><p>Ability to manage multiple priorities in a fast-paced environment.</p></li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li><p>7–9+ years of experience in FP&A, Commercial Finance, or related field (pharma/biotech/healthcare preferred)</p></li><li><p>Experience in Global Capability Center / Shared Services environment preferred</p></li><li><p>Strong knowledge of US GAAP, accrual accounting, and SOX compliance</p></li><li><p>Advanced Excel skills with experience in data tools (Power Query, Alteryx, SQL)</p></li><li><p>Hands-on experience with ERP/Planning tools (Oracle/Hyperion preferred)</p></li><li><p>Experience with BI tools such as Power BI or Tableau</p></li><li><p>Proven experience in reporting standardization, automation, and data governance</p></li><li><p>Strong verbal and written communication skills</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Category Management]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48239]]></requisitionid>
    <referencenumber><![CDATA[R48239]]></referencenumber>
    <apijobid><![CDATA[r48239]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48239/associate-director-category-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking an Associate Director, Global Procurement Category Management to join our Global Procurement team, supporting our global categories in a hybrid work model. In this role, you will lead category management across global procurement categories while collaborating with team members, suppliers, Law, procurement colleagues and direct reports. This position offers the opportunity to help shape a procurement capability that acts as a competitive advantage to Regeneron.</p><p><strong>When & where:</strong></p><p>Hyderabad - (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead category management across a range of global categories.</p></li><li><p>Align category priorities with leaders, team members and suppliers.</p></li><li><p>Manage negotiations, supplier relationships and stakeholder engagement.</p></li><li><p>Drive cost savings, cash flow and efficiency improvements.</p></li><li><p>Negotiate contract terms with Law and business partners.</p></li><li><p>Use data and market insight to guide category decisions.</p></li><li><p>Coach procurement skills and career development across the team.</p></li><li><p>You bring clarity and integrity when driving change.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in a relevant field of study.</p></li><li><p>Progressive procurement experience, including Pharma or BioPharma experience.</p></li><li><p>Experience managing global category processes and suppliers.</p></li><li><p>S-u+ccess leading cross-functional teams across sourcing, negotiations and contracting.</p></li><li><p>Experience managing supply market evaluation using market intelligence, risk, compliance and financial assessment tools.</p></li><li><p>Working knowledge of sourcing, contracting, ERP and eRFx systems preferred, including Oracle, Zycus or Ariba.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Compliance - Canada]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47219]]></requisitionid>
    <referencenumber><![CDATA[R47219]]></referencenumber>
    <apijobid><![CDATA[r47219]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47219/director-compliance-canada/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization.</p><p>We are looking for a <strong>Canada Compliance Director</strong> to join our International Compliance team, playing a central role in supporting business operations and strengthening our compliance program across Canada and selected international markets. Working closely with global teams, you will develop policies, guide business practices, and support ethical decision-making across the organization. This is a meaningful opportunity to influence compliance culture, partner with senior leadership, and help ensure our activities are aligned with industry standards and regulations.</p><p><strong>Compliance Director – Canada</strong></p><p><strong>(Office based – Toronto)</strong></p><p><strong>A Typical Day:</strong></p><ul><li>Leading compliance activities across Canada and selected international markets</li><li>Driving implementation of compliance programs with global and legal teams</li><li>Developing and refining policies, procedures, and compliance guidance</li><li>Delivering and improving training for employees and external partners</li><li>Advising on compliance risks related to business initiatives and HCP interactions</li><li>Supporting internal investigations and monitoring activities when required</li><li>Collaborating on audits, risk assessments, and remediation actions</li><li>Identifying emerging risks and proactively shaping mitigation strategies</li></ul><p><strong>This Role May Be For You:</strong></p><ul><li>You enjoy partnering with senior leaders to guide compliant business decisions</li><li>You are comfortable navigating sophisticated regulatory environments in pharma</li><li>You take a proactive approach to identifying and mitigating compliance risks</li><li>You value collaboration across cross-functional and international teams</li><li>You like translating regulatory requirements into practical business guidance</li><li>You are motivated by shaping training, policies, and compliance frameworks</li><li>You are confident providing oversight on activities involving HCPs and HCOs</li><li>You appreciate balancing critical thinking with hands-on execution</li></ul><p><strong>To Be Considered</strong></p><p>You bring a minimum of 7 years of experience working in or with pharmaceutical companies on healthcare compliance activities, along with deep knowledge of Canadian healthcare compliance laws, regulations, and industry codes of practice. You have experience drafting and implementing policies, as well as supporting monitoring, auditing, and training programs. A strong understanding of compliance across commercial, medical affairs, market access, and clinical development is required. Fluency in English is essential, and French is considered an asset. This role is based in Toronto with a hybrid working model and may require travel.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regulatory Affairs Strategy - Oncology]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44633]]></requisitionid>
    <referencenumber><![CDATA[R44633]]></referencenumber>
    <apijobid><![CDATA[r44633]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44633/director-regulatory-affairs-strategy-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture so responsibilities will include support to some clinical study activities. The candidate will also supply, lead and/or supervise IND/CTA and BLA submissions activities.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Provide interpretation of regulatory authorities’ feedback, policies and guidelines.</p></li><li><p>Lead the development of regulatory strategic plans either directly in conjunction with project teams or through your reports. Own the preparation of major clinical submissions required for regulatory approval.</p></li><li><p>Work with project teams to resolve complex project issues. Utilize regulatory expertise and knowledge of regulatory requirements and regulations to strategically interpret, plan, and communicate requirements to ensure attainment of governmental approvals.</p></li><li><p>Responsible for quality and timeliness of IND/CTA and BLA submissions. Interact with other functions and partners, in the preparation, review, and completion of documents for regulatory submissions.</p></li><li><p>Successfully plan, prioritize, supervise and/or conduct activities in close collaboration with leads from other areas. Assure compliance with regulations and with project team timelines.</p></li><li><p>Provide interpersonal support and lead personnel.</p></li><li><p>Critical thinking, leadership skills, assertiveness, excellent negotiation and project management skills as evidenced by past performance on drug development project teams</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>If you bring strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices.</p></li><li><p>If you are interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred</p></li><li><p>If you have a high attention to detail; ability to coordinate and prioritize assigned projects according to company goals</p></li><li><p>You bring strong interpersonal skills both written and verbally</p></li></ul><p><strong>To be considered,</strong> you must possess excellent written and verbal communication skills along with a MD, Ph.D. or Pharm D. degree. We expect a minimum of 10 years of pharmaceutical industry experience, at least 7 of which should include regulatory experience.</p><p><em>This role requires you to work onsite 4 days per week in either Warren, NJ, Tarrytown, NY or Cambridge, MA. If you are not local and qualify we can offer relocation support. </em></p><p>#MDJOBSRA #GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44660]]></requisitionid>
    <referencenumber><![CDATA[R44660]]></referencenumber>
    <apijobid><![CDATA[r44660]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44660/senior-manager-internal-medicine-clinical-scientist-immuneinflammatory/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>The Senior Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Associate Director/Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p></div><div><div><div><div><p><strong>As a Senior Manager in Clinical Sciences, a typical day may include the following:</strong></p><ul><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Develops/maintains understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Collaborates with internal functions and external vendors to promote clinical study integrity</p></li><li><p>Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis; supports identification and/or identifies critical risks and mitigations</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies; Reviews clinical data review plan and medical monitoring plan for assigned studies</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>Demonstrated ability to influence within team and may influence cross functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related field. Additionally, ≥ 8 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in one or more of the following therapeutic areas – Immune/Inflammatory related clinical trials.</p></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II-NEUROLOGY- FORT LAUDERDALE, FL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48031]]></requisitionid>
    <referencenumber><![CDATA[R48031]]></referencenumber>
    <apijobid><![CDATA[r48031]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48031/medical-account-specialist-ii-neurology-fort-lauderdale-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Fort Lauderdale]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Fort Lauderdale (Metro), FL</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Laboratory Assistant, Bioanalysis]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45695]]></requisitionid>
    <referencenumber><![CDATA[R45695]]></referencenumber>
    <apijobid><![CDATA[r45695]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45695/senior-laboratory-assistant-bioanalysis/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The LabOps team is primarily responsible for managing and optimizing all aspects of the Lab Environment. This may include but not limited to ensuring labs are equipped, maintained and run efficiently in the areas of Lab Management, Process Optimization, Compliance and Safety, Resource Allocation & Coordination and Communication.</p><p>This role requires knowledge of laboratory procedures, ability to perform moderate complex tasks, make recommendations to enhance processes to do the job effectively, work cross-functionally with others in department.</p><p> <strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li><p>Performs daily routine tasks, which can include monitoring and re-stocking inventory in labs and storage areas, equipment managment, and recording appropriately in electronic lab notebooks</p></li><li><p>May have modified working schedule to include weekend days with purpose of providing general support to group.</p></li><li><p>Be adaptable to learning and supporting additional activities that may arise to continuously support the team through future growth and expansion</p></li><li><p>Anticipates and recognizes potential problems, presents them to supervisor, and works to identify key operational improvements and devise strategies to increase the speed and efficiency</p></li><li><p>Provide guidance to and/or assists others on non-routine or escalated issues</p></li><li><p>Participates effectively as a member of the team within functional area, may provide guidance to others within group</p></li><li><p>Communicate effectively with all functions and levels within the organization, exemplify strong interpersonal and customer service skills while leveraging prior technical experience/knowledge </p></li></ul><p><strong>This Role Might Be For You If You:</strong></p><ul><li><p>Possess good organization, communication, and collaboration skills; can work well within a team and individually</p></li><li><p>Have a service-oriented mindset and desire to provide quality customer service</p></li></ul><ul><li><p>Actively seeks opportunities for skill enhancement and knowledge enrichment</p></li></ul><ul><li><p>Possess strong operational skills to drive and execute core responsibilities with limited supervisory guidance</p></li></ul><p><strong> To Be Considered, You Must Have</strong>: High School Diploma and 2 - 4 years of experience, or combination of training and experience. A 2-year college degree may be preferred. Experience in inventory management is a plus. </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$30.24 - $47.36]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -MOBILE, AL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48046]]></requisitionid>
    <referencenumber><![CDATA[R48046]]></referencenumber>
    <apijobid><![CDATA[r48046]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48046/medical-account-specialist-ii-neurology-mobile-al/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mobile]]></city>
    <state><![CDATA[Alabama]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Mobile (Metro), AL</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - DETROIT North, MI]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48047]]></requisitionid>
    <referencenumber><![CDATA[R48047]]></referencenumber>
    <apijobid><![CDATA[r48047]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48047/medical-account-specialist-ii-neurology-detroit-north-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Detroit]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Detroit North (Metro), Michigan </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PHOENIX S, AZ]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48072]]></requisitionid>
    <referencenumber><![CDATA[R48072]]></referencenumber>
    <apijobid><![CDATA[r48072]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48072/medical-account-specialist-ii-neurology-phoenix-s-az/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Phoenix]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Pheonix (South Metro), AZ</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Global Site Start-Up Lead]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48462]]></requisitionid>
    <referencenumber><![CDATA[R48462]]></referencenumber>
    <apijobid><![CDATA[r48462]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48462/manager-global-site-start-up-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The <strong>Manager, Global Site Start-Up Lead</strong> (SSU Lead) is responsible for driving the global execution of site activation for clinical trials, performing the role with moderate oversight to ensure efficient and compliant processes aligned with Regeneron SOPs, ICH-GCP guidelines, and industry standards. Partnering closely with cross-functional teams and Clinical Research Organizations (CROs), this role balances strategic oversight with hands-on leadership to address challenges and deliver study objectives. The SSU Lead develops site activation projections, mitigates risks impacting site activation, and monitors CRO performance by analyzing metrics. Additionally, they lead all aspects of site start-up activities, including fast-track initiation, milestone tracking, and document collection, while ensuring timely submissions and leveraging country intelligence for informed decision-making.</p><br><h3>When & where:</h3><p>This role is an in office role in either Warren, NJ or Armonk, NY</p><br><h3>Discover your role:</h3><h3>Site Start-up Strategy</h3><ul><li>Develop the site start up strategy for each study, outlining all dependencies impacting site activation and actively mitigating and escalating risks. Oversee the tracking and analysis of study metrics, including risks and mitigation strategies and to evaluate CRO performance and implement corrective actions.</li><li>Advocate for optimized site selection strategies, leveraging data-driven insights to guide cross-functional teams toward effective decision-making.</li><li>Lead the development, assessment, and alignment of site activation projections, ensuring cross-functional and CRO collaboration to meet strategic objectives.</li><li>Ensure comprehensive and compliant documentation of site start-up materials in the Trial Master File (TMF) to maintain inspection readiness.</li></ul><h3>Country Start-up</h3><ul><li>Partner with cross functional and CRO partners (where applicable) to develop a comprehensive global country start up strategy, outlining all dependencies impacting country start up and actively mitigating and escalating risks cross functionally.</li><li>Monitor and maintain country intelligence data to support informed decision-making and develop accurate startup projections and strategic plans.</li><li>Support regulatory submissions as needed, including activities such as: providing required site documentation, coordinating submissions to Central Institutional Review Boards (CIRBs), supporting sites with Local Institutional Review Board (LIRB) submissions, and handling or supervising Clinical Research Organization (CRO) insurance requests, etc.</li><li>Ensure timely country submission deliverables (ensure task completion; all roles clarity, identification of critical path items, effective communication pathway).</li></ul><h3>Site Start up Management</h3><ul><li>Lead and oversee all aspects of site start-up activities, including fast-track site initiation, site calls, document collection, and milestone tracking, ensuring timely and efficient completion of processes.</li><li>Serve as the subject matter expert for essential site documents, providing training, guidance, and support to teams and sites on regulatory requirements, document management, and TMF filing.</li><li>Oversee CRO site start up management or in house site facing regional SSU team, where applicable</li><li>Lead the collection and analysis of site intelligence to support strategic site selection and site start-up.</li><li>Oversee the preparation and approval of site regulatory package, ensuring compliance with country-specific requirements, TMF standards, and ICH-GCP guidelines, while supporting inspection readiness and maintaining high-quality site documentation.</li></ul><h3>Team Interactions</h3><ul><li>Represent SSU on cross-functional teams, providing updates, escalating challenges, and proposing mitigation strategies for site start-up issues.</li><li>Act as the escalation point for CRO and internal team to ensure timely SSU issue resolution</li></ul><h3>Process Improvement</h3><ul><li>Recommends and participates in cross functional and department process improvements.</li></ul><br><h3>This role requires:</h3><ul><li>A Bachelor's degree and 6+ years relevant work experience</li><li>Demonstrated interpersonal & leadership skills</li><li>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</li><li>A data driven approach to planning, executing, and problem solving</li><li>Effective communication skills via verbal, written and presentation abilities</li><li>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</li><li>Ability to influence and negotiate across key stakeholders</li><li>Ability to build productive study teams collaborations</li><li>Experience in the clinical drug development process, with expertise in study start-up</li><li>Demonstrated vendor management experience</li><li>Technical proficiency in trial management systems (CTMS, TMF) and MS applications including (but not limited to) Project, PowerPoint, Word, Excel</li><li>Knowledge of ICH/GCP and regulatory guidelines/directives</li><li>Effective project management skills, cross-functional team interaction and organizational skills</li><li>May require up to 25% travel</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - LONG ISLAND, NY]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48008]]></requisitionid>
    <referencenumber><![CDATA[R48008]]></referencenumber>
    <apijobid><![CDATA[r48008]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48008/medical-account-specialist-ii-neurology-long-island-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Garden City]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Long Island (Metro), NY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 13:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Product Manager - Delivery & Operations Product Lead - Business Process Management]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47515]]></requisitionid>
    <referencenumber><![CDATA[R47515]]></referencenumber>
    <apijobid><![CDATA[r47515]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47515/senior-product-manager-delivery-operations-product-lead-business-process-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Global Development Information Technology (GD IT) is seeking an outstanding Senior Product Manager to lead product delivery for innovative Business Process Management (BPM) applications that transform the way clinical studies are developed, planned, and assessed. As the Product Lead on the Enabling Technologies team, you will drive low-code BPM (Appian) and generative/agentic AI solutions that streamline study design, feasibility, and downstream planning.</p><p>You will be responsible for the full product lifecycle—roadmap, design, build, testing, launch, and operations, while ensuring alignment with business goals, regulatory standards, and data-privacy requirements. Your blend of clinical process expertise, agile leadership, and technical savviness will be critical to delivering measurable value across Global Development.</p><p><strong>In this role, a typical day might include the following:</strong> <br>- Leading stand-ups, grooming backlogs, and approving Appian user stories for study-design workflows <br>- Facilitating workshops with clinical stakeholders to map current vs. future processes and prioritize AI-enabled improvements <br>- Reviewing solution architecture to ensure secure, scalable integrations with data, analytics, and LLM-based services <br>- Supervise sprint progress, mitigating risks, and updating program leadership on timelines, budget, and return of investment.<br>- Monitoring platform performance and adoption, then identifying automation or reporting improvements <br>- Preparing and presenting demos or governance materials for steering committees and change-control boards </p><p><strong>This job might be for you if you: </strong><br>- Combine deep knowledge of clinical development processes with hands-on product and low-code platform expertise <br>- Enjoy partnering with clinical, data, and architecture leaders, to translate complex operational problems into clear, innovative digital solutions and roadmaps <br>- Excel at stakeholder management, influencing cross-functional teams without direct authority <br>- Thrive in agile environments, balancing short-term results with long-term strategy <br>- Enjoy working with data science teams to embed RAG, MCP, or LLM capabilities into business workflows <br>- Keep a “get-it-done” mentality, balancing multiple high-impact initiatives while maintaining quality </p><p><strong>In order to be considered for this role, you must have: </strong><br>- BS/BA with 8–10 years proven experience (or MS/MBA with 6+ years as an equivalent), including 3 years in enterprise SaaS and 1+ year delivering generative/agentic AI solutions <br>- Shown success implementing Appian or similar BPM platforms for clinical or regulated environments <br>- Proven track record driving process optimization, agile delivery, and cross-system integrations in Global Development</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -  CINCINNATI, OH]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48024]]></requisitionid>
    <referencenumber><![CDATA[R48024]]></referencenumber>
    <apijobid><![CDATA[r48024]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48024/medical-account-specialist-ii-neurology-cincinnati-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cincinnati]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Cincinnati (Metro), OH</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 08:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - COLUMBIA, SC]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48019]]></requisitionid>
    <referencenumber><![CDATA[R48019]]></referencenumber>
    <apijobid><![CDATA[r48019]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48019/medical-account-specialist-ii-neurology-columbia-sc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbia]]></city>
    <state><![CDATA[South Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Columbia (Metro), SC</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 08:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Patient Advocacy]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48174]]></requisitionid>
    <referencenumber><![CDATA[R48174]]></referencenumber>
    <apijobid><![CDATA[r48174]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48174/senior-director-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Senior Director, Patient Advocacy</strong></p><p><strong>Role Summary:</strong><br>The Senior Director, Patient Advocacy leads Regeneron’s disease area enterprise-wide advocacy strategy and operating model, integrating the patient voice across the continuum of discovery, development, and commercialization. This leader exercises independent judgment in ambiguous environments, influences executive decision-making, and builds scalable processes that elevate patient impact, operational efficiency, and company reputation. The role serves as a trusted advisor to senior leadership and a visible ambassador to advocacy and professional organizations.</p><p><strong>Location and Work Model:</strong><br>This role is based in Sleep Hollow, NY, 4 days/week.</p><p><strong>Impact and Scope:</strong></p><ul><li>Develops the overarching patient advocacy strategy across multiple therapeutic areas, with enterprise visibility and executive engagement</li><li>Establishes standard methodologies and governance for engagement with advocacy and professional societies</li><li>Advises cross-functional contributors in Medical, Commercial, Market Access, Policy, and Clinical Development with view to multi-year roadmap on advocacy strategy</li><li>Accountable for measurable improvements in disease awareness, time to diagnosis, clinical trial awareness, access, and patient experience</li><li>Operates at both strategic and operational level; drives outcomes through cross-functional leadership</li></ul><p><strong>Roles and Responsibilities</strong></p><p><strong>Strategy and Leadership</strong></p><ul><li>Define and evolve the disease area patient advocacy strategy, translating corporate objectives into a prioritized, outcome-based portfolio</li><li>Standardize engagement frameworks, decision rights, and operating mechanisms that scale across therapeutic areas and regions</li><li>Anticipate external trends and policy shifts as well as shifting company priorities to frame and be comfortable and strategic about recommending tactical choices and trade-offs with clear implications for patients and the business</li><li>Help establish governance and operating mechanisms that support alignment, speed and accountability across department</li></ul><p><strong>Advocacy Strategy and Execution</strong></p><ul><li>Create and maintain therapeutic area strategies and operating plans, including educational programs, disease awareness, advisory boards, patient speaker engagement, clinical trial awareness, and coordination on relevant policy initiatives</li><li>Support development and deployment of advocacy campaigns; ensure external partner plans align to Regeneron’s goals and compliance standards</li><li>Define and report outcome-based KPIs; implement dashboards to monitor reach, quality, and ROI of advocacy efforts</li></ul><p><strong>Executive Engagement and Influence</strong></p><ul><li>Serve as a trusted advisor to senior executives; deliver board-ready materials that articulate patient impact, risks, and investment options</li><li>Lead executive forums and steering committees to drive aligned decisions across competing priorities</li></ul><p><strong>Relationship Management</strong></p><ul><li>Lead relationship development with key patient advocacy and professional societies to build durable, mission-aligned partnerships</li><li>Ensure Regeneron’s leadership position is evident through presence at priority events; synthesize and disseminate insights to internal stakeholders</li></ul><p><strong>Cross-Functional Collaboration and Alignment</strong></p><ul><li>Build strong, collaborative relationships with Medical, Commercial/Brand, Market Access, Government Affairs, Health Policy, Clinical Development, and Legal/Compliance</li><li>Drive cross-functional alignment (including at top senior leadership levels, e.g. VP level) and execution of advocacy initiatives; co-create plans with Alliance partners where applicable</li><li>Contribute to departmental strategy, annual planning, budgeting, and digital portal development</li></ul><p><strong>Patient Voice and Insights</strong></p><ul><li>Systematically capture and translate patient insights to inform clinical trial design, evidence generation, disease education, patient services, and access strategies</li><li>Champion a patient-centric mindset and embed patient perspectives in enterprise decisions and roadmaps</li></ul><p><strong>Financial and Business Acumen</strong></p><ul><li>Own budgeting and optimize for impact</li></ul><p><strong>Grants and Governance</strong></p><ul><li>Strategically fund programs that advance patient engagement and disease education aligned to therapeutic priorities </li><li>Oversee transparent, compliant grant review processes; manage budgets and financial stewardship effectively and in a timely manner</li></ul><p><strong>Operational Excellence and Metrics</strong></p><p><strong>QualificationsRequired</strong></p><ul><li>Bachelor’s degree and 12+ years of industry experience, including 10-15+ years in Patient Advocacy leading multi-stakeholder programs </li><li>Demonstrated enterprise thinking with a track record of cross-functional visibility, influence and company-wide impact </li><li>Executive presence with superior communication skills; able to craft concise, data-driven narratives and board-ready materials</li><li>Proven operational rigor: building repeatable processes, governance, and metrics with measurable outcomes Experience collaborating with Medical, Commercial, Market Access, and Policy partners; strong familiarity with compliance in advocacy contexts</li></ul><p><strong>Preferred</strong></p><ul><li>Experience in rare diseases, oncology, hematology, ophthalmology, immunology, and/or cardio-metabolic </li><li>Background operating in complex, matrixed, or global environments; alliance management experience</li></ul><p><strong>Reporting and Collaboration</strong></p><p><strong>Reporting Line:</strong></p><ul><li>Reports to Executive Director, Patient Advocacy May manage direct report(s)</li></ul><p><strong>Key Internal Partnerships:</strong></p><ul><li>Up to SVPs across Medical, Commercial, Market Access, Government Affairs, and Health Policy imbedded in the business </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 19 Jun 2026 07:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Analytical Scientist (Automation)]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48399]]></requisitionid>
    <referencenumber><![CDATA[R48399]]></referencenumber>
    <apijobid><![CDATA[r48399]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48399/principal-analytical-scientist-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Analytical Scientist to join our Quality Control team in Rensselaer, NY, supporting our IOPS organization on-site. In this role, you will shape the future of QC analytical testing by designing, developing, and scaling automated assay workflows across advanced laboratory platforms, while mentoring scientists and fostering a culture of technical growth and innovation. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><div></div><p><strong>When & where</strong></p><p><strong>Location: </strong>Rensselaer, NY (Tempel Lane)</p><p><strong>Work Model: </strong>On-site</p><p><strong>Travel: </strong>Minimal</p><div></div><p><strong>Discover your role</strong></p><p>As a Principal Analytical Scientist, you will:</p><ul><li>Lead the design, implementation, and optimization of automated assay workflows across modern laboratory platforms, applying deep expertise in mass spectrometry, chromatography, bioassay, electrophoresis, and ELISA.</li><li>Mentor and develop junior and mid-level scientists, building team capability in analytical science and laboratory automation.</li><li>Set priorities, coordinate work, and track progress on analytical and automation initiatives against key milestones.</li><li>Independently design and execute studies to evaluate emerging automation technologies and troubleshoot existing systems with limited supervision.</li><li>Lead complex investigations into automated method performance, supporting verification activities and driving continuous improvement.</li><li>Transfer automated workflows to QC and partner functions by developing training materials, transfer plans, and acceptance criteria.</li><li>Engage cross-functional collaborators and equipment vendors to evaluate new technologies and assess their fit for QC applications.</li><li>Prepare clear scientific reports, automation procedures, and SOPs; communicate findings, risks, and mitigation strategies to management and cross-functional teams.</li></ul><div></div><p><strong>This role might be for you if you...</strong></p><ul><li>Bring hands-on experience programming and optimizing automated liquid handling systems (e.g., Hamilton/Venus, Andrew+/OneLab, or Cellario) and scripting in Python, R, or VBA.</li><li>Apply strong troubleshooting skills across both analytical methods and automated instrumentation to resolve complex technical challenges.</li><li>Make sound, independent decisions and proactively recommend experiments or solutions based on deep expertise in analytical science and automation.</li><li>Lead by example in technical discussions, elevating the team's capabilities in automation strategy, method development, and process optimization.</li><li>Thrive in a collaborative, fast-paced environment and can prioritize effectively across multiple responsibilities while adapting to evolving business needs.</li><li>Communicate complex automation concepts clearly to diverse audiences—both in written reports and in cross-functional settings.</li><li>Proactively share knowledge and take pride in developing others through structured training and mentorship.</li><li>Deliver on commitments safely, with high quality, and in compliance with regulatory expectations.</li></ul><p><strong>Shift Requirements: </strong>Standard 1st shift, Monday–Friday, 8:00a–4:30p.</p><div></div><p><strong>This role requires</strong></p><p><strong>Must-haves:</strong></p><ul><li>8+ years of industry experience in analytical development, laboratory automation, and QC method lifecycle management (or equivalent combination of education and experience).</li><li>Demonstrated hands-on expertise in automated liquid handling platforms and associated software programming.</li><li>Proficiency in scripting languages (Python, R, or VBA) for data analysis, workflow automation, or system integration.</li><li>Deep knowledge of QC analytical techniques including mass spectrometry, chromatography, electrophoresis, bioassay, or ELISA.</li><li>Proven ability to work independently, design scientifically sound studies from broad objectives, and drive projects to completion.</li><li><em>Level will be determined based on qualifications at the time of offer.</em></li></ul><p><strong>Preferred / nice to haves:</strong></p><ul><li>PhD in Chemistry, Biochemistry, Biology, or a related field.</li><li>Previous experience working in a cGMP or cGLP regulated environment.</li><li>Familiarity with Cellario, Venus (Hamilton), or OneLab (Andrew+) automation platforms.</li><li>Experience developing and executing technology transfer plans across QC or partner functions.</li></ul><p><strong>Physical Requirements: </strong>Ability to work in a laboratory environment, including standing for extended periods and handling laboratory equipment.</p><p><strong>Gowning & Environment: </strong>This role operates in a GMP analytical laboratory. Appropriate gowning and PPE are required in designated areas.</p><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oncology Account Specialist-Oncology - Central Illinois, IL]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48354]]></requisitionid>
    <referencenumber><![CDATA[R48354]]></referencenumber>
    <apijobid><![CDATA[r48354]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48354/oncology-account-specialist-oncology-central-illinois-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Peoria]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Peoria, IL</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p>​<strong>This role requires:</strong></p><ul><li><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred). Buy and bill experience with biologics required. </p></li><li><p>A Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions. </p></li><li><p>Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. </p></li><li><p>You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. </p></li><li><p>You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. </p></li><li><p>We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. </p></li><li><p>Must have ability to travel and cover large geography territories.</p></li></ul><p><strong>Salary range (annually)</strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Drug Production, Associate Manufacturing Specialist]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46369]]></requisitionid>
    <referencenumber><![CDATA[R46369]]></referencenumber>
    <apijobid><![CDATA[r46369]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46369/drug-production-associate-manufacturing-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Biotech Production Specialist to join our Global Manufacturing team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment.</p><p>When & where:</p><ul><li><p>We offer multiple shifts that are 4 working days (10 hours) to support 24/7 production</p></li><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Occasional flexibility may be requested for on-call schedule/weekend work</p></li></ul><p>What you'll do:</p><ul><li><p>Covering all facets of drug production in a clean room including cell culture and purification of monoclonal antibodies</p></li><li><p>Completing and reviewing batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)</p></li><li><p>Performing in-process sampling and analysis of buffer solutions, cell culture, and drug substance</p></li><li><p>Operating automated equipment such as bioreactors, chromatography columns, and filtration skids</p></li><li><p>Supporting equipment start-up, troubleshooting, and validation</p></li><li><p>Partnering with R&D teams to implement new drug manufacturing processes and technologies</p></li><li><p>Enjoy working in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients</p></li><li><p>Are highly organized, detail oriented and perform work accurately the first time</p></li><li><p>Work well in both small and large teams to accomplish tasks adhering to a schedule</p></li><li><p>Can operate in a highly regulated environment strive to continuously improve processes and maintain compliance to manufacture safe and effective medicines for patients</p></li><li><p>Are able to learn and use computerized systems for daily performance of tasks</p></li><li><p>Are a good communicator and can give and receive feedback constructively</p></li></ul><br><p>The environment and physical rhythms of the role:</p><ul><li><p>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><br><p>Let's find out if we're a fit:</p><ul><li><p>HS diploma + 4 years of relevant work experience is required</p></li><li><p>Or AS, BS or BA in Life Sciences or related field</p></li><li><p>Level will be determined based on experience</p></li></ul><p>Thrive today. Grow Tomorrow.</p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family care benefits</p></li><li><p>Relocation assistance</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.78 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 18 Jun 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, CMC Regulatory Affairs (Hematology/Oncology)]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48184]]></requisitionid>
    <referencenumber><![CDATA[R48184]]></referencenumber>
    <apijobid><![CDATA[r48184]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48184/associate-director-cmc-regulatory-affairs-hematologyoncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross-functional and external partners, and serving as a key liaison in regulatory authority interactions.<br><br><strong>Where and when:</strong></p><p>This is a Dublin, Ireland based position and would you to be on-site 3 days per week and 2 days from home. A fully remote role is not possible for this position. If eligible, we can offer relocation benefits.</p><h3>Discover your role:</h3><p>• Lead product development activities from a CMC regulatory standpoint with input from senior management.</p><p>• Represent CMC RA at program meetings and independently provide regulatory interpretation, position, and covering clinical development, initial market applications, and approval/post-approval activities.</p><p>• Identify program issues and develop appropriate regulatory strategies to mitigate risks to filings, independently find alternative solutions/work-arounds, and obtain consensus.</p><p>• Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.</p><p>• Lead and facilitate interactions with global regulatory authorities (e.g., meetings, IR responses, inspections).</p><p>• Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country-specific regulatory guidance documents;</p><p>• Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks.</p><p>• Develop and create working instructions, SOPs, and/or templates to facilitate consistent and efficient practice across the CMC RA groups.</p><p>• Identify gaps in the IOPS and global RA processes, bring up to higher management, and help to improve business efficiency.</p><p>• Support establishing, managing, and maintaining a knowledge base of current and emerging regulatory requirements and guidelines in the CMC field.</p><p>• Find opportunities to initiate operational changes and policy modifications.• Manage and coach team member(s).<br><br><br><strong>This role requires: </strong><br> </p><ul><li><p>To be considered a bachelor’s degree with a minimum of 10 years of pharmaceutical/biotech industry experience, including 5+ years of relevant CMC experience. An advanced degree is preferred.</p></li><li><p>Proven track record supporting biological products through development and approval is a distinct advantage.</p></li><li><p>It is required to have a good understanding of current CMC worldwide regulations and guidelines.</p></li><li><p>Experience in interacting with the US FDA and other regulatory authorities. Experience with device regulatory requirements and development processes for combination products is a plus.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€101,500.00 - €165,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 16:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialty Representative, Immunology - Southwestern Ontario]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48513]]></requisitionid>
    <referencenumber><![CDATA[R48513]]></referencenumber>
    <apijobid><![CDATA[r48513]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48513/specialty-representative-immunology-southwestern-ontario/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together:</strong> </p></div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Specialty Representative, Immunology in Southwestern Ontario </strong>to join our International Immunology team, supporting our Canada in a hybrid work mode. In this role, you will drive sales growth and deliver impactful customer engagement while collaborating with regional teams, business partners, and management. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p></div><div><p><strong>When & where:</strong> </p></div><div><ul><li><p>Ontario, Canada </p></li></ul></div><div><ul><li><p>Field based </p></li></ul></div><div><p><strong>Discover your role:</strong> </p></div><div><ul><li><p>Establish and lead high quality HCP interactions by continuously keeping scientific knowledge around the product, indication and brand sales messaging up to date and optimally implementing sales & marketing plan. </p></li></ul></div><div><ul><li><p>Consistently deliver on the value proposition for the brand through key message communication to HCPs. </p></li></ul></div><div><ul><li><p>Work in alignment with the Brand Plan, develop and implement a local account plan based on key data sources and local market insights. </p></li></ul></div><div><ul><li><p>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs. </p></li></ul></div><div><ul><li><p>Leverage all communication channels including digital channels, in collaboration with other functions, to achieve the best possible share of voice in the market. </p></li></ul></div><div><ul><li><p>Report results and developments proactively and clearly to the Immunology leadership team </p></li></ul></div><div><p><strong>This role requires:</strong> </p></div><div><ul><li><p>Bachelor’s degree </p></li></ul></div><div><ul><li><p>Minimum 5 years’ experience as a Specialty Pharmaceutical Representative </p></li></ul></div><div><ul><li><p>Experience working within a commercial alliance environment is desirable </p></li></ul></div><div><ul><li><p>Proven track record to run accounts and meet performance objectives </p></li></ul></div><div><ul><li><p>Experience engaging healthcare professionals using multiple communication channel </p></li></ul></div><div><ul><li><p>Ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice. </p></li></ul></div><div><ul><li><p>Working in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful. </p></li></ul></div></div><div><div><ul><li><p>Balancing multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.). </p></li></ul></div><div><ul><li><p>You can operate optimally in a “start-up” model as this is a completely new team. </p></li></ul></div><div><ul><li><p>Regular travel and have a valid driver's license. Proficiency in English is required. </p></li></ul></div><div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 19 Jun 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Product and  Pipeline Communications Manager]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48509]]></requisitionid>
    <referencenumber><![CDATA[R48509]]></referencenumber>
    <apijobid><![CDATA[r48509]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48509/product-and-pipeline-communications-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Product and Pipeline Communications, Europe and Canada to join our Product and Pipeline Communications International team, supporting Europe and Canada. In this role, you will strengthen and protect Regeneron’s reputation through science-driven, patient-centered communications while collaborating with in-country cross-functional teams, Commercial, Clinical, Medical Affairs, and Global Corporate Affairs. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Munich , Paris , Madrid</p><p>Hybrid model</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead in-country communications priorities, strategies, and processes.</p></li><li><p>Develop country-level strategies for stakeholder communications programs.</p></li><li><p>Partner with Commercial, Clinical, and Medical Affairs teams.</p></li><li><p>Manage media relations, medical congress support, and milestone communications.</p></li><li><p>Identify communications risks and recommend appropriate response strategies.</p></li><li><p>Shape Corporate Affairs strategies with regional insights and local updates.</p></li><li><p>You advise cross-functional partners with sound judgement and clarity.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree, or equivalent, with 7–9+ years’ relevant experience.</p></li><li><p>3+ years’ product and/or pipeline communications experience.</p></li><li><p>Global, regional, and in-country communications expertise within Europe.</p></li><li><p>Understanding of EU regulatory, commercial, and legal pharmaceutical communications.</p></li><li><p>Fluent in English as well as German , French or Spanish</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€60,750.00 - €101,250.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 07:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Sciences]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47082]]></requisitionid>
    <referencenumber><![CDATA[R47082]]></referencenumber>
    <apijobid><![CDATA[r47082]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47082/medical-director-clinical-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Are you ready to make a meaningful impact on clinical development programs in Japan? At Regeneron, we are seeking a dedicated Medical Director, Clinical Sciences, to join our dynamic team. In this pivotal role, you will collaborate closely with the Japan Clinical Development Lead (J-CDL) to advance scientific and clinical aspects of our programs. From contributing to global clinical teams to supporting regulatory filings, your expertise will drive innovation and deliver results that matter.</p><p>Join us in shaping the future of clinical development, where your skills and insights will play a vital role in transforming lives.</p><p><strong>A Typical Day:</strong></p><p>As the Medical Director, Clinical Sciences, your day will be filled with impactful activities, such as:</p><ul><li><p>Supporting the clinical components of assigned clinical development programs (CDPs) in Japan.</p></li><li><p>Providing clinical and scientific input for regulatory documents, including J-NDA/J-CTD submissions.</p></li><li><p>Contributing to the development and adaptation of clinical trial protocols and related documentation for Japan-specific needs.</p></li><li><p>Collaborating with cross-functional teams to ensure clinical feasibility and address local medical needs in global studies.</p></li><li><p>Participating in investigator meetings, site initiation visits, and vendor kick-off meetings to drive study execution.</p></li><li><p>Offering medical/scientific input to resolve issues during study conduct and execution.</p></li><li><p>Staying current on scientific advancements in therapeutic areas and representing the company at national and international conferences.</p></li><li><p>Building and maintaining relationships with key opinion leaders (KOLs) and investigator sites.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You have a strong understanding of the drug development process, clinical trial design, and good clinical practice (GCP).</p></li><li><p>You excel in both Japanese and English, with business-level proficiency in English communication.</p></li><li><p>You enjoy collaborating across cross-functional teams, bringing diplomacy and influence to your interactions.</p></li><li><p>You are detail-oriented and possess exceptional analytical and problem-solving skills.</p></li><li><p>You thrive in dynamic environments and are adept at managing regulatory interactions effectively.</p></li><li><p>You value diversity, different perspectives, and are committed to fostering inclusive teamwork.</p></li></ul><p><strong>To Be Considered:</strong></p><p>We are looking for candidates with the following qualifications:</p><ul><li><p><strong>Required:</strong> MD or MD/PhD with at least 5 years of pharmaceutical industry experience, including 3 years of clinical development experience.</p></li><li><p>Expertise in regulatory filings and clinical document preparation, particularly CTN and J-NDA/J-CTD submissions.</p></li><li><p>Proven ability in protocol design, clinical data review, and familiarity with medical monitoring activities.</p></li><li><p>Strong knowledge of Phase I–III clinical trial design and objectives.</p></li><li><p><strong>Preferred:</strong> Experience with clinical feasibility assessments and Japan-specific enrollment considerations.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development IT & Digital]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45997]]></requisitionid>
    <referencenumber><![CDATA[R45997]]></referencenumber>
    <apijobid><![CDATA[r45997]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45997/senior-manager-global-development-it-digital/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong> Tokyo, Japan</p><p>We are seeking a dedicated and innovative <strong>Global Development IT & Digital Manager</strong> to join our team in Tokyo. This pivotal role supports our Global Clinical Development, Patient Safety, Regulatory Affairs, and Medical Affairs organizations by leveraging IT solutions to drive high business value. As a trusted partner, you will collaborate across diverse teams, blending technical expertise with a deep understanding of pharmaceutical industry processes to deliver impactful results.</p><p>If you are passionate about IT, thrive on solving complex challenges, and are eager to make a meaningful difference in the pharmaceutical space, this role offers an exciting opportunity to grow and lead in a globally connected environment.</p><p><strong>A Typical Day:</strong><br>In this role, you will:</p><ul><li>Develop and implement IT action plans aligned with global and local business strategies.</li><li>Collaborate with local business units to understand and address goals, challenges, and regulatory requirements.</li><li>Manage IT projects and products, ensuring compliance with GxP regulations.</li><li>Promote IT-based business improvements using automation, data utilization, and cloud technologies.</li><li>Drive digital transformation initiatives leveraging AI, cloud, and data analytics.</li><li>Facilitate meetings and presentations in business-level English while coordinating with international teams.</li><li>Build and maintain a stable IT infrastructure, ensuring operational excellence.</li><li>Utilize development methodologies (agile, waterfall, hybrid) tailored to business needs.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You enjoy connecting IT with business needs and bridging different viewpoints through structured thinking and effective communication.</li><li>You have a curious and open mindset toward understanding multiple business domains and perspectives.</li><li>You thrive in collaborative environments and build trusted relationships with stakeholders.</li><li>You excel at problem-solving and are motivated by continuous improvement.</li><li>You are detail-oriented and capable of translating complex ideas into clear, actionable plans.</li><li>You are proficient in business-level English and skilled in facilitating conferences and delivering impactful presentations.</li></ul><p><strong>To Be Considered:</strong><br>You must have:</p><ul><li>Over five years of experience in the pharmaceutical industry, specifically in IT for development and medical departments.</li><li>A solid understanding of operational processes in drug development, clinical trials, and medical affairs.</li><li>Proven experience as an IT business analyst, IT project manager, or IT product manager.</li><li>Knowledge of GxP, regulatory compliance, and Computer System Validation (CSV).</li><li>Basic programming knowledge and familiarity with IT infrastructure (hardware, software, databases, networks, cloud).</li><li>Experience with agile and waterfall development methodologies.</li></ul><p>Preferred qualifications include:</p><ul><li>Execution and stakeholder management skills demonstrated through collaboration and accountability.</li><li>A constructive, positive approach to challenges and problem-solving.</li></ul><p>Join us to shape the future of IT-driven innovation in the pharmaceutical industry. Apply today to become part of a team that values curiosity, collaboration, and excellence.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Field Medical Affairs Oncology - France]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46686]]></requisitionid>
    <referencenumber><![CDATA[R46686]]></referencenumber>
    <apijobid><![CDATA[r46686]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46686/director-field-medical-affairs-oncology-france/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Director, Head of Field Medical Oncology to lead Regeneron’s field medical oncology organization in France and serve as a key medical leader within Global Medical Affairs.</p><p>In this role, you will guide in-country medical and clinical activities, align local execution with global strategy, and strengthen Regeneron’s scientific presence across Oncology. It is a meaningful opportunity to shape team performance, support innovation access, and influence how medical insights inform patient care and business decisions.</p><p><strong>Director, Head of Field Medical Oncology – Paris </strong></p><p><strong>(hybrid)</strong></p><p><strong>A Typical Day:</strong></p><ul><li>Leading the field medical oncology team across France.</li><li>Coaching direct reports through field visits and 1:1 discussions.</li><li>Recruiting, training, and developing team members for strong execution.</li><li>Guiding compliant medical initiatives, field activities, and performance metrics.</li><li>Supporting clinical development through site identification and investigator engagement.</li><li>Coordinating support for IIS proposals, AOIs, and potential EAP activities.</li><li>Partnering with Medical Directors on congresses, symposia, and advisory boards.</li><li>Contributing field medical insight to launch readiness, market access, and lifecycle plans</li></ul><p><strong>This Role May Be For You:</strong></p><ul><li>You enjoy leading and developing a field medical team.</li><li>You like balancing scientific depth with practical in-country execution.</li><li>You work comfortably across medical affairs, clinical, operations, regulatory, and commercial interfaces.</li><li>You are motivated by building trusted relationships with investigators and external experts.</li><li>You naturally keep compliance at the center of how work gets done.</li><li>You are energized by shaping strategy while staying close to field realities.</li><li>You can move between team leadership, scientific exchange, and operational support.</li><li>You value bringing clear, actionable medical insights into decision-making.</li></ul><p>To be considered, you will bring a PhD, PharmD, MD, DVM, or equivalent, along with 7+ years of relevant Medical Affairs Oncology experience, including experience as a Field Medical Manager in the biotech or pharmaceutical industry within oncology, especially lung and skin cancer. You will also need strong knowledge of in-country Medical Affairs and Clinical Development, a thorough understanding of the local healthcare environment, experience across product lifecycle development, and fluency in English.</p><p>The role requires willingness to travel 30–50%. Preferred experience includes immuno-oncology, new product launches in country, and an established external network with key opinion leaders in lung and skin cancer.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€100,275.00 - €167,125.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager HR Business Partner]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48083]]></requisitionid>
    <referencenumber><![CDATA[R48083]]></referencenumber>
    <apijobid><![CDATA[r48083]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48083/senior-manager-hr-business-partner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, HR Business Partner to join our Human Resources function, supporting our France, Canada, and Belgium operations in a hybrid work mode. In this role, you will deliver the full spectrum of HR activities supporting the international Commercial business while collaborating with HR Centers of Excellence, business leaders, and the Legal team. This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><br><br><h3><strong>When & where:</strong></h3><br><p>Paris, France; Hybrid</p><br><h3><strong>Discover your role:</strong></h3><br><ul><li>Deliver full spectrum HR activities across employee lifecycle</li><li>Manage employee relations cases and regulatory compliance requirements</li><li>Partner with business leaders to align HR priorities and solutions</li><li>Lead labour relations engagement with works council representatives</li><li>Support talent acquisition, onboarding, and talent review processes</li><li>Drive organisational development initiatives with leadership teams</li><li>Navigate complexity and balance operational and strategic priorities</li><li>Build constructive relationships with employee representatives and stakeholders</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree in HR or related discipline, or equivalent experience</li><li>Minimum 8 years’ HR experience including international commercial support</li><li>Fluency in French and English languages</li><li>Demonstrated expertise in labour relations and works council engagement</li><li>Experience across full HR lifecycle from administration to strategic partnering</li><li>Strong data literacy and experience with HR systems and Microsoft tools</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€71,925.00 - €119,875.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs - Neurology (Mountain West)]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46426]]></requisitionid>
    <referencenumber><![CDATA[R46426]]></referencenumber>
    <apijobid><![CDATA[r46426]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46426/associate-director-field-medical-affairs-neurology-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. As a scientific expert in your territory, you will demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities to shape our medical strategy. You will be considered a scientific and clinical expert on our current and future Neurology assets. </p><p><strong>Territory: </strong>UT, ID, OK, CO, Kansas City MO</p><p><strong>A typical day may include the following</strong>: </p><ul><li><p>Establish, foster, cultivate and maintain peer relationships with KOLs in Neurology </p></li><li><p>Act as a primary clinical/scientific resource to HCPs for information pertaining to disease state and our products to ensure awareness and understanding. </p></li><li><p>Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans. </p></li><li><p>Support evidence generation (company sponsored trials and investigator-initiated studies) research initiatives. </p></li><li><p>Identify and report medical insights. </p></li><li><p>Identifies gaps in research and educational needs to inform medical strategy. </p></li><li><p>Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific and clinical data to appropriate audience in a compliant manner. </p></li><li><p>Performs disease management and therapeutic area education with identified practitioners, payers and researchers. </p></li><li><p>Attends conferences to collect and report relevant, scientific, clinical, & competitive intelligence. </p></li><li><p>Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally. </p></li></ul><p>To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) with a minimum 8 years of experience, including 4+ years working as a Medical Science Liaison in the pharmaceutical industry. Experience as a Neurology MSL or in Neurology is preferred. Demonstrated experience communicating complex data sets and the ability to be seen as a scientific peer while educating top KOLs is required. Established relationships with KOLs in neuromuscular centers is preferred, as is product launch experience. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. Capable of frequent business travel (approximately 70% of time), including air travel, ability to travel overnight and occasionally on weekends.</p><p>#msl #medicalscienceliaison</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 22 Jun 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lab Equipment Maintenance Technician III (2nd Shift: 3:00PM-11:30PM)]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41868]]></requisitionid>
    <referencenumber><![CDATA[R41868]]></referencenumber>
    <apijobid><![CDATA[r41868]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41868/lab-equipment-maintenance-technician-iii-2nd-shift-300pm-1130pm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Laboratory Equipment Maintenance Technician III to join our Equipment Services team supporting scientific operations across laboratory and vivarium environments. In this role, you will install, maintain, calibrate, and repair laboratory and vivarium equipment to ensure safe, reliable, and compliant operations that directly support research innovation and high-quality animal care.</p><p><strong>A Typical Day Might Include:</strong></p><ul><li>Conducting preventive and corrective maintenance on key laboratory and vivarium equipment, including:<ul><li>CO₂ incubators and biosafety cabinets</li><li>Cryogenic liquid nitrogen freezers</li><li>Autoclaves & sterilizers</li><li>Vivarium industrial tunnel and cage washers</li><li>Clean steam generation systems</li><li>RO/DI laboratory water purification system</li></ul></li><li>Troubleshooting electromechanical, control-system, and monitoring device issues to minimize equipment downtime</li><li>Responding to equipment and site emergencies, including 24/7 support</li><li>Responding to environmental and equipment alarms from Rees, Dickson, Watchdog EX, and related monitoring systems</li><li>Maintaining accurate electronic work order documentation, calibration records, and asset compliance data</li><li>Supporting audit and inspection readiness for AAALAC, IACUC, and internal compliance activities</li><li>Partnering closely with researchers, veterinarians, and animal care specialists to ensure equipment performance meets scientific study requirements</li></ul><p><strong>This Role Might Be for You If You:</strong></p><ul><li>Possess strong mechanical, electrical, and controls troubleshooting abilities</li><li>Communicate clearly and professionally with cross-functional partners</li><li>Demonstrate excellent attention to detail in regulated documentation</li><li>Stay calm and organized when prioritizing urgent research-impacting needs</li><li>Enjoy working in specialized laboratory areas with strict safety and cleanliness standards</li></ul><p><strong>In Order To Be Considered, You Must Have:</strong></p><ul><li>High school diploma or equivalent and 4+ years relevant technical experience in laboratory, or industrial equipment maintenance<ul><li>Trade school in a related field (Engineering Technology, Biomedical Technology, etc.) is a plus</li></ul></li><li>Hands-on experience with:<ul><li>Motors, pumps, valves, and sensors</li><li>VFDs and PLC-controlled systems</li><li>24 VDC, 3-Phase 208V, and 480V</li><li>Technical schematics and electrical diagrams</li></ul></li><li>Ability to lift and/or move equipment up to 100 lbs.</li><li>Willingness to work in vivarium research facilities as required (around animals)</li><li>Valid driver’s license recognized by the State of New York</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$29.81 - $46.63]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 23 Jun 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Aggregate Reporting Management]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48819]]></requisitionid>
    <referencenumber><![CDATA[R48819]]></referencenumber>
    <apijobid><![CDATA[r48819]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48819/senior-manager-aggregate-reporting-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Patient Safety organization is seeking a Senior Manager, Aggregate Reporting Management to join our team!</p><p><strong>In this role, a typical day might include:</strong></p><p>This position in the Global Patient Safety (GPS) Operations is responsible for management of aggregate safety reporting activities across all phases of the product lifecycle. This role supports the consistent, compliant, and scientifically robust preparation, distribution and submission of periodic and ad-hoc safety reports to health authorities, collaborators and contract research organizations worldwide.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Drives preparation, development and maintenance of Aggregate Reporting (i.e., PSURs/PBRER, PAER, DSURs, Local Periodic Reports, SUSARs) Deliverables</p></li><li><p>Leads Aggregate Report planning, production and distribution activities across GPS and other functions across US, EU, Japan and other ICH regions, as well as non-ICH regions</p></li><li><p>Provides expertise and guidance to authors and contributors of aggregate reports</p></li><li><p>Maintains compliance metrics and contributes to implementation of Quality Events and Corrective Action and Preventive Action (CAPA) for non-compliance</p></li><li><p>Implements effective structure, procedures and tools to ensure aggregate reports and other functional deliverables are completed timely and with high quality</p></li><li><p>Develops and oversees functional specifications of data requirements for aggregate deliverables from the safety and clinical databases</p></li><li><p>Collaborates with Global Patient Safety (GPS) and with other functional areas (Epidemiology, Clinical Development, Regulatory Affairs, Statistics, etc.) contributing to aggregate safety reports</p></li><li><p>Acts as subject matter expert during audits and inspection.</p></li><li><p>Provides oversight, and training as needed of CRO respective activities in support of high quality and timely aggregate reports</p></li><li><p>Acts as a functional vendor management overseeing and driving high quality outputs from our vendors</p></li><li><p>Develops and maintains aggregate report procedural package (SOPs, Work Instructions), reports’ templates, KPIs</p></li><li><p>Drives process improvement through automation and other tech initiatives.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor’s degree required (advanced degree or HCP‑focused background preferred) and 5+ years of Pharmacovigilance experience, with a demonstrated focus on Aggregate Safety Reporting.</p></li><li><p>Project management experience strongly preferred, PMP preferred</p></li><li><p>Experience with health authority inspections (PV and GCP)</p></li><li><p>Medical writing experience with regulatory documentation</p></li><li><p>Strong project management skills</p></li><li><p>Excellent strategic decision-making and analytical skills</p></li><li><p>Strong communication and writing skills</p></li><li><p>Strong understanding of Scientific content</p></li><li><p>Proven experience with technology implementations allowing for streamlined process execution.</p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Direct and FC&L Procurement]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48234]]></requisitionid>
    <referencenumber><![CDATA[R48234]]></referencenumber>
    <apijobid><![CDATA[r48234]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48234/manager-direct-and-fcl-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Direct Materials Procurement to join our Global Procurement team, supporting our India operations in a hybrid work model. In this role, you will drive category strategy, sourcing, and supplier performance for direct materials while collaborating with cross-functional partners and global procurement colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Drive the definition and implementation of global direct material category strategies aligned to regional and global business needs</p></li><li><p>Partner with collaborators to manage category priorities, sourcing decisions, and procurement activities across direct materials</p></li><li><p>Lead negotiations, contracting, and supplier management to deliver cost savings, cash flow improvements, and operational efficiencies</p></li><li><p>Ensure category activities align with GxP and applicable regulatory standards</p></li><li><p>Collaborate with Legal to negotiate contract terms and conditions aligned to business requirements</p></li><li><p>Use market intelligence, supplier insights, and data analytics to inform decision-making and improve category performance</p></li><li><p>Contribute to organizational decisions and initiatives that shape global procurement capabilities and category outcomes</p></li><li><p>You operate effectively in a matrixed, global environment and build strong, trusted relationships with internal and external partners.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field with progressive experience in procurement, including Pharma/Biopharma.</p></li><li><p>Proven experience managing category strategies, sourcing, contracting, and supplier relationships across direct materials or related categories.</p></li><li><p>Strong negotiation capability with understanding of cost structures, rates, and supply market dynamics.</p></li><li><p>Demonstrated success working with cross-functional teams to deliver results across procurement activities.</p></li><li><p>Experience supporting supplier evaluation processes using market intelligence, risk, compliance, and financial assessment tools.</p></li><li><p>Knowledge of global procurement processes and operating models within the biopharmaceutical industry.</p></li><li><p>Ability to demonstrate data and analytics to drive category decisions and project outcomes</p></li><li><p>Experience managing or coaching professional-level employees preferred.</p></li><li><p>Working knowledge of sourcing and contracting tools, ERP systems, and eRFx platforms (e.g., Oracle, Zycus, Ariba) preferred.</p></li><li><p>Proficiency in standard business applications (Word, Excel, PowerPoint)</p></li><li><p>Strong communication, collaboration, and collaborator management skills with the ability to work effectively in ambiguous environments.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Federal Government Affairs]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48475]]></requisitionid>
    <referencenumber><![CDATA[R48475]]></referencenumber>
    <apijobid><![CDATA[r48475]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48475/senior-director-federal-government-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Washington]]></city>
    <state><![CDATA[District of Columbia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Senior Director, Federal Government Affairs at Regeneron is responsible for advancing the company’s public policy priorities through strategic engagement with U.S. federal policymakers. In close partnership with internal stakeholders, this role cultivates relationships and engages with federal legislators, congressional staff, administration officials, and regulators to advance Regeneron’s patient-centered, science-driven mission.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Washington, D.C,</p></li><li><p>Hybrid: 4 days per week on site</p></li><li></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Develop and execute strategic federal advocacy plans to advance Regeneron’s public policy priorities and initiatives, with a focus on patient access and innovation issues.</p></li><li><p>Lead engagement with federal legislators, administration officials, and regulators to proactively shape policy outcomes, serving as a key advocate to House Democratic members and staff, including the Energy & Commerce Committee.</p></li><li><p>Monitor and analyze relevant policy developments to provide strategic guidance and updates to internal stakeholders, leveraging strong knowledge of issues affecting the biopharmaceutical industry and policymaking processes.</p></li><li><p>Partner with Regeneron Policy and Alliance leads to help internal stakeholders incorporate federal policy implications into business and corporate objectives.</p></li><li><p>Engage with trade associations, various organizations, and policy influencers to shape the external environment and elevate Regeneron’s policy perspectives in collective advocacy efforts.</p></li><li><p>Support development of advocacy materials, including policy content and talking points, in partnership with cross-functional teams, as well as memoranda for senior leaders and internal stakeholders.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Must have a bachelor’s degree or higher in public policy, law, political science, or a related field, or equivalent relevant experience.</p></li><li><p>Minimum of 15 years relevant experience in Congress, a regulatory or policy advocacy organization, or government relations.</p></li><li><p>A strong understanding of government affairs, public policy, and the patient, provider, and health care organization landscape is essential, as is knowledge of the health care system and key policies affecting the biopharmaceutical sector.</p></li><li><p>Excellent communication and presentation skills, with the ability to convey complex and changing policy and business issues to internal and external stakeholders.</p></li><li><p>Strong strategy and execution skills with a proven track record of working collaboratively to advance policy objectives.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 19 Jun 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Quality Assurance Compliance]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48370]]></requisitionid>
    <referencenumber><![CDATA[R48370]]></referencenumber>
    <apijobid><![CDATA[r48370]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48370/manager-quality-assurance-compliance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>Regeneron is currently seeking a Manager Quality compliance to join our Quality Assurance team. This position is responsible for managing the compliance, audit, training and operations team for the internal fill finish site. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Monday-Friday, 8am-4:30pm</p></li></ul><p>Discover your role:</p><div><ul><li><p>Lead and develop the QA compliance team: set work plans and objectives, prioritize and assign tasks, coach performance, and manage hiring and separations while aligning deliverables with company goals</p></li><li><p>Partner with Managers and Directors to communicate compliance status, audit readiness, and training initiatives, and provide concise, actionable project reporting</p></li><li><p>Oversee the lifecycle of quality records (Notices of Event, Change Controls, CAPAs): track, report, and drive timely closure</p></li><li><p>Drive audit readiness and execution: align QA practices with requirements, run the audit-ready-365 program, plan and track coaching, and support internal and regulatory audits, including coordinating requests for the internal fill-finish team</p></li><li><p>Promote cross-site continuous improvement by collaboratively identifying gaps and sharing best practices</p></li><li><p>Shape governance by influencing local and global policies, procedures, and business processes to align with industry standards and best practices</p></li><li><p>Stay current on industry trends and regulatory updates and translate insights into changes and improvements</p></li></ul></div><p>This role requires:</p><ul><li><p>BS/BA in Life Sciences or related field; or equivalent combination of education and experience</p><ul><li><p>Associate Manager Quality Compliance: 6+ years of relevant experience</p></li><li><p>Manager Quality Compliance: 7+ years of relevant experience</p></li></ul></li><li><p>Experience with drug product manufacturing and/or fill finish is preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 15:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Assay Development]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48710]]></requisitionid>
    <referencenumber><![CDATA[R48710]]></referencenumber>
    <apijobid><![CDATA[r48710]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48710/associate-scientist-assay-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Assay Development Group (ADG), located in Tarrytown, NY, is seeking a highly motivated <strong>Associate Scientist</strong> to join the team. The ADG in Bioanalytical sciences develops preclinical and clinical assays to support program pipeline. In this role, you will support ongoing work, sample preparation, assay runs, data processing ensuring compliance with current GxP guidance documentation.</p><p><strong>Responsibilities during a typical day might include the following:</strong></p><ul><li><p>Designs and executes immunoassays (e.g., ELISA) with limited supervision, based on protocols provided by literature, seminars and other scientists. Troubleshoots assay-related problems with minimal guidance of his/her supervisor and performs follow-up experiments. Suggest modifications to protocols or alternative protocols.</p></li><li><p>Develops immunoassay methods and writes assay validation protocols for review with minimal supervision by supervisor and/or Study Director.</p></li><li><p>Routinely multi-tasks and can work on multiple projects simultaneously.</p></li><li><p>Summarizes and presents results to supervisors in a logical manner, verbally and in written reports or presentations.</p></li><li><p>Performs validation experiments, summarizes results in a tabular manner. Writes/reviews validation reports and procedure documents for review by the Study Director.</p></li><li><p>Communicate effectively with supervisor and other members of the Assay Development Group.</p></li><li><p>Oversee the preparation of reagents and buffers for use within the Assay Development Group and may coordinate the re-ordering of laboratory supplies and reagents when needed.</p></li><li><p>Effectively operates a range of laboratory instrumentation and may oversee instrument verifications and/or maintenance, if required.</p></li><li><p>May evaluate new technologies for the development of immunoassays using new formats or techniques.</p></li><li><p>Maintains GLP compliance for all laboratory work and documentation related to assay validations in accordance with FDA regulations and company SOPs. Assists in maintaining GLP compliance in the laboratory.</p></li><li><p>Maintains cleanliness of individual and communal work areas.</p></li><li><p>Learns and complies with safety requirements of his/her laboratory. Recognizes potential safety problems and takes action to correct them.</p></li></ul><p><strong>This role may be for you, if you: </strong></p><ul><li><p>Must have Bachelor or Master (0-3+) degree in biology or a related field with proven experience.</p></li><li><p>Hands-on knowledge in immunoassays using a variety of detection systems</p></li><li><p>Proven understanding of additional methodologies to measure proteins and immunogenicity is needed.</p></li><li><p>Prior experience in bioanalytical assay development is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager LCoE Training Operations]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47647]]></requisitionid>
    <referencenumber><![CDATA[R47647]]></referencenumber>
    <apijobid><![CDATA[r47647]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47647/manager-lcoe-training-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Manager, Training Operations </strong>leads development and deployment of LCoE (Learning Center of Excellence) supported Learning projects from in-take, tracking and reporting to close-out. They use in-depth learning technology and GxP training skills and knowledge to define efficient processes and solutions. This person partners with LCoE Business Partners, designers, and the C3 team to deliver LCoE projects.</p><p><strong>A typical day in this role looks like: </strong></p><ul><li>Lead Training Business Partners and designers to develop and maintain project scope, timelines & deliverables on moderately complex projects</li><li>Partner and advise on the requirements and specifications of a project using knowledge of learning techniques and learning technologies</li><li>Responsible to track, analyze and optimize project timeline and status from kickoff to completion, provide status updates via email and Operations meetings</li><li>Lead Project meetings to call out risks to timelines and delivery dates and to drive decision making for resource needs</li><li>Use strong stakeholder and relationship skills to resolve issues as they arise</li><li>Design and implement a robust content maintenance plan for LCoE assets including training materials, Academy pages and Onboarding guides</li><li>Partner with C3 team to refine collaboration with Ops team, identify opportunities for streamlining current deployment processes</li><li>Drive process improvements for the Operations team and have skillset required to document and implement</li><li>Identify opportunities for automation of routine tasks. Use strong technology background to design the solution in O365 and manage development of the solution.</li><li>Identify opportunities for AI in Learning Operations and use pragmatic approach to application.</li><li>Ensure that all process and productivity improvements are scalable to an Enterprise level</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Strong hands-on Learning Technology knowledge and experience</li><li>O365, Power Apps, Sharepoint design and development</li><li>Excellent communication and interpersonal skills</li><li>Strong time management skills</li><li>Strong Copilot and Claude skills</li><li>Strong LMS technical knowledge and experience</li></ul><p><strong>In order to be considered qualified for this rol</strong>e, a minimum of a Bachelor's Degree in Business, Human Resources or related work experience + 7+ years of relevant work experience</p><ul><li>5 years plus in development and management of Learning solutions</li><li>3 years of experience in Pharma preferred</li><li>Advanced degree can be considered in lieu of years of experience (e.g., Masters degree and 5 years of relevant experience can be considered)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager EDC Administration]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47770]]></requisitionid>
    <referencenumber><![CDATA[R47770]]></referencenumber>
    <apijobid><![CDATA[r47770]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47770/manager-edc-administration/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>About Regeneron</strong> </p></div><div><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p></div><div><br><p>This role is responsible for leading EDC system administration activities across Regeneron’s global clinical trial portfolio. You will ensure efficient, compliant, and scalable administration of the Medidata Rave platform, while driving operational excellence, governance, and team leadership within the EDC function.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><h3><strong>A typical day may include the following:</strong></h3><ul><li><p>Leading and developing a team of EDC Administration professionals, providing coaching, feedback, and performance management</p></li><li><p>Driving resource planning and workload allocation to ensure timely delivery of EDC administration activities</p></li><li><p>Managing EDC environments, including user access provisioning, role assignment, and deactivation within Medidata platforms</p></li><li><p>Ensuring compliance with governance frameworks, access controls, and regulatory standards</p></li><li><p>Partnering with cross-functional teams (Database Developers, Study Data Managers) for study setup, build, UAT, and go-live activities</p></li><li><p>Supporting clinical database development activities including Rave setup, user administration, alert configuration, and system integrations</p></li><li><p>Monitoring KPIs and operational metrics to improve team performance and delivery outcomes</p></li><li><p>Contributing to SOPs, work instructions, and continuous improvement initiatives</p></li><li><p>Driving inspection readiness and ensuring alignment with quality and regulatory requirements</p></li></ul><h3><strong>This job may be for you if you have:</strong></h3><ul><li><p>Strong expertise in EDC administration, including Medidata Rave (Cloud Administration, user management, environment configuration)</p></li><li><p>Proven experience leading and developing teams in a matrix environment</p></li><li><p>Deep understanding of clinical data management processes and cross-functional workflows</p></li><li><p>Knowledge of regulatory frameworks including 21 CFR Part 11 and ICH-GCP guidelines</p></li><li><p>Ability to drive process improvements, governance, and operational excellence</p></li><li><p>Strong problem-solving, project management, and stakeholder management skills</p></li><li><p>Excellent communication skills with the ability to influence and collaborate across teams</p></li></ul><h3><strong>To be considered for this role, you must have:</strong></h3><ul><li><p>Bachelor’s degree in mathematics, science, information systems, or a related field</p></li><li><p>Minimum of 7+ years of experience in biotechnology, pharmaceutical, or healthcare industry</p></li><li><p>At least 4+ years of direct experience in EDC or clinical systems administration</p></li><li><p>Prior people management or team lead experience preferred</p></li><li><p>Experience in establishing governance frameworks, SOPs, and processes in a regulated environment</p></li></ul></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Statistical Programming]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44717]]></requisitionid>
    <referencenumber><![CDATA[R44717]]></referencenumber>
    <apijobid><![CDATA[r44717]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44717/manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>***Please note this is an onsite role and NOT eligible remote.</em></p><p>A Manager provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study team, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan, programming specification or user requirements document using internal standards and guidelines. The incumbent provides guidance in implementing and executing the programming and project standards. The incumbent will be responsible for leading the programming aspect of a project, both internally or CROs, for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards and annual reports. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. Meets statistical ad hoc requests of senior management.<br> </p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Develop an expertise within a therapeutic area or standard tool. Work with minimal supervision to perform, coordinate and oversee the preparation, execution, reporting and documentation of a project</li><li>Function as a lead programmer in the development and QC of tables, listings, graphs, or systems in support of analysis requirements utilizing Regeneron tools and methodologies and current industry standards (i.e. CDISC SDTM / ADaM)</li><li>Manage the effort, including esubmssion deliverables, using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Provide programming support for complex presentations and more complex statistical ad-hoc requests. </li><li>Act as programming representative in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports.</li><li>If applicable, lead an application development and act as the programming representative to the user audience.</li><li>Work with management to determine resource requirements for therapeutic area or department function <br>responsibilities. </li><li>Review and select resumes, screen and interview candidates for contractor and permanent positions.</li><li>Provide feedback to management regarding team member’s contributions to the work effort for evaluating individual's performance and recommend yearly goals.</li><li>Advises all direct reports about the procedures surrounding retention of data, records, and information for <br>employees in their group.<br> </li></ul><p><strong>In order to be considered qualified for this role</strong></p><ul><li>Master’s Degree</li><li>8-10 years of relevant work experience</li><li>SAS Certification desirable.</li><li>Also acceptable - 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience with a Master’s Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.</li></ul><p>#statprogramming</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate  Director Global Patient Safety]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48802]]></requisitionid>
    <referencenumber><![CDATA[R48802]]></referencenumber>
    <apijobid><![CDATA[r48802]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48802/associate-director-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, PV Case Operations to join our Global Patient Safety team, supporting case processing across global development and commercial programmes in a hybrid work mode. In this role, you will lead vendor oversight, Individual Case Safety Report (ICSR) quality governance, and inspection readiness while collaborating with vendor teams, internal partners, license partners, auditors, and Health Authority inspectors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Uxbridge, UK (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Own accurate, timely case processing across global development and marketed products, per applicable regulations and Regeneron SOPs.</p></li><li><p>Lead vendor oversight for end-to-end ICSR receipt, processing, distribution, and submission.</p></li><li><p>Own ICSR quality standards covering narrative, case validity, and source document reconciliation.</p></li><li><p>Establish tiered quality review frameworks aligned to case complexity, risk, and product lifecycle stage.</p></li><li><p>Monitor submission timelines and vendor SLAs, maintain inspection readiness, and respond to audit findings.</p></li><li><p>Lead root cause analysis and own CAPAs through closure and effectiveness checks.</p></li><li><p>Evaluate AI-enabled tools for data ingestion, workflow automation, and metrics.</p></li><li><p>You mentor staff and communicate clearly with senior management and partners.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Pharmacy, nursing, or equivalent degree required; advanced degree preferred.</p></li><li><p>Typically 10 years of Pharmacovigilance, Drug Safety, or PV Quality experience in pharma or biotech.</p></li><li><p>Well-informed on FDA, EU, and ICH guidelines governing pharmacovigilance for clinical trial and post-marketing environments.</p></li><li><p>Experience managing teams on complex, cross-functional projects.</p></li><li><p>Proven ability to deliver organisational projects through individual contributors or other managers.</p></li><li><p>Strong communication and partner management skills, with ability to resolve and escalate complex issues.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 04:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48306]]></requisitionid>
    <referencenumber><![CDATA[R48306]]></referencenumber>
    <apijobid><![CDATA[r48306]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48306/specialist-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a Specialist, External Data Acquisition and Delivery to join our Clinical Data Management team. In this role, you will manage non-Case Report Form data across assigned studies or Clinical Development Units while collaborating with external data vendors, CRO partners, Clinical Data Management and cross-functional stakeholders. This position offers the opportunity to support data integrity, improve external data delivery and strengthen compliant study execution.</p><p><strong>When & where:</strong></p><p>Hyderabad (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Manage end-to-end non-Case Report Form data delivery.</li><li>Develop low-complexity Data Transfer Specifications for assigned studies.</li><li>Reconcile external vendor data with clinical database outputs.</li><li>Track specification status across data types and programmes.</li><li>Support data structure issue resolution and change requests.</li><li>Maintain documentation, audit trails and inspection readiness standards.</li><li>You collaborate across teams to resolve data discrepancies.</li><li>You support continuous improvement in external data processes.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in Science, Health, Mathematics, Engineering, Computational or related field.</li><li>2+ years in external clinical data acquisition or management.</li><li>Experience managing clinical data types such as biomarker, eCOA, imaging, ECG, PK, genomics and laboratory data.</li><li>Knowledge of 21 CFR Part 11, ICH-GCP and CDISC standards.</li><li>Experience extracting data into SAS, CSV and XML formats.</li><li>Knowledge of EDC platforms and external data reconciliation processes.</li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 05:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Southeast)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48131]]></requisitionid>
    <referencenumber><![CDATA[R48131]]></referencenumber>
    <apijobid><![CDATA[r48131]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48131/field-reimbursement-manager-neurology-southeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Atlanta]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Atlanta (Metro), GA Jacksonville (Metro), AL Fort Lauderdale, (Metro) FL, Miami (Metro), FL, Tampa (Metro), FL, Saint Petersburg (Metro), FL, Birmingham (Metro), AL, Mobile (Metro), AL</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  MILWAUKEE, MADISON, WI]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48951]]></requisitionid>
    <referencenumber><![CDATA[R48951]]></referencenumber>
    <apijobid><![CDATA[r48951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48951/medical-account-specialist-ii-hematology-milwaukee-madison-wi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- Milwaukee, WI</strong></p><ul><li><strong>Geography: Milwaukee, Madison</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) *Tokyo Area]]></title>
    <date><![CDATA[Mon, 06 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48850]]></requisitionid>
    <referencenumber><![CDATA[R48850]]></referencenumber>
    <apijobid><![CDATA[r48850]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48850/medical-representative-mr-startokyo-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology Commercial Team, supporting our operations in Japan in a hybrid work model. In this role, you will achieve sales objectives while delivering on Regeneron’s promise to put patients first, collaborating with our alliance partners and healthcare professionals. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Tokyo, Japan</p><br><p><strong>Discover your role:</strong></p><ul><li>Achieve brand sales objectives through effective management of territory budget and expenses.</li><li>Develop and implement annual territory business plans based on market insights.</li><li>Incorporate marketing brand plans to ensure consistency in strategy execution.</li><li>Utilize key data sources to strategically develop territory action plans.</li><li>Perform administrative duties, including expense reports, marketing and field insight reporting.</li><li>Work within Regeneron’s regulatory and legal compliance guidelines.</li><li>Attend local, regional, and national meetings as directed.</li><li>You think strategically and manage your time effectively to maximize customer engagement.</li><li>You work collaboratively with key stakeholders to deliver impactful solutions.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree (or equivalent).</li><li>Minimum five (5) years of sales representative experience in the pharmaceutical industry.</li><li>Driver’s license.</li><li>MR Certification.</li><li>Superior customer engagement skills, with a focus on delivering value.</li><li>Excellent technical aptitude and ability to conduct disease/concept selling.</li><li>Superb written, verbal, and presentation skills.</li><li>Strong planning and organizational skills.</li><li>Ability to work independently and execute strategic and tactical plans under tight timelines.</li><li>Familiarity with word processing, spreadsheets, databases, and email software.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 06 Jul 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - General Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45803]]></requisitionid>
    <referencenumber><![CDATA[R45803]]></referencenumber>
    <apijobid><![CDATA[r45803]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45803/director-global-patient-safety-sciences-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director </strong>to join our <strong>Patient Safety</strong> team.</p><p>The Global Patient Safety (GPS) Lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s)/asset(s) assigned within a given therapeutic area (TA), and is the GPS representative on the cross functional strategic program team (SPT) for the compound. The GPS Lead leads the safety strategy and ensures the optimal support from within GPS and works collaboratively with stakeholders to deliver the safety strategy. This position requires the ability to work with and influence colleagues in a matrix environment within and external to GPS including senior management. The GPS Director joins Regeneron’s industry leading scientific organization, and has a direct impact on drug development, operations, and commercialization in all relevant global territories.</p></div><div><div><div><div><div><div><div><div><div><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.)</p></li><li><p>Leads cross-functional Safety Monitoring Team (SMT) activities</p></li><li><p>Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs)</p></li><li><p>Proactively identify and develop safety strategies and planning for non-compound specific Global Patient Safety activities (mechanism of action etc.)</p></li><li><p>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds</p></li><li><p>Actively participate in the development and maintenance of relevant SOPs, working practices and guides </p></li><li><p>Actively participates in continuous improvement activities within both the TA and the GPS organization, including cultivating cross functional relationships and mentoring junior safety scientists</p></li><li><p>Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.</p></li><li><p>Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest.</p></li><li><p>A proven ability to lead and develop a diverse team of Safety Professionals in a constructive, goal-oriented environment.</p></li><li><p>An ability to work across organizational levels, effectively communicating safety viewpoints and findings as required, and recommended risk management and minimization activities.</p></li><li><p>Ability to utilize GPS safety database for purposes of medical case review and simple queries. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum 10+ years of total relevant experience in PV and/or relevant medical field or equivalent of industry experience in drug safety including significant experience with PSURs/ DSURs/(d) RMPS; or in clinical development with demonstrated achievements in safety (ex. supporting an ISS; responsible for CSR content). </p></li><li><p>5+ years of total relevant experience in PV and/or relevant medical field with PharmD / PhD / MD degree required.</p></li><li><p>Clinical experience and/or industry experience in Oncology is a plus</p></li></ul><p>#MDJOBSPS #GDPSJobs</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Endocrinology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46850]]></requisitionid>
    <referencenumber><![CDATA[R46850]]></referencenumber>
    <apijobid><![CDATA[r46850]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46850/medical-director-clinical-development-endocrinology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Director, Clinical Development, Endocrinology </strong></p><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Endocrinology team supporting our Clinical Development Unit. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>4 days a week on-site in Tarrytown, NY, Washington, D.C., or Cambridge, Massachusetts</p><p><strong>Discover your role:</strong></p><ul><li>You guide the Global Clinical Study Team to deliver high-quality trials on time.</li></ul><ul><li>You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance</li><li>You lead clinical study and protocol development and present to internal and external stakeholders.</li><li>You provide clinical and scientific leadership for data review, study reports, and publications.</li><li>You work closely with cross-functional partners to advance program goals and key deliverables.</li><li>You collaborate with discovery teams to help shape future targets and development opportunities in the field.</li></ul><p><strong>This role requires:</strong></p><ul><li>An M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable.</li><li>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</li><li>Experience in rare disease drug development strongly preferred</li><li>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</li></ul><p>#MDJobsCD, #MDJobs, #GDTherapeuticJobs, #Obesity</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Contracts & Trade Controls]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47099]]></requisitionid>
    <referencenumber><![CDATA[R47099]]></referencenumber>
    <apijobid><![CDATA[r47099]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47099/associate-director-contracts-trade-controls/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Corporate Counsel serves as legal counsel and business partner for Regeneron's manufacturing division (IOPS – Industrial Operations and Product Supply), providing legal support across a broad range of business operations within this complex, global organization. As a member of the IOPS Law Group, this attorney will draft, review, and negotiate a wide array of contracts — including complex, international supply, material transfer, equipment purchase, consulting, confidentiality, and license agreements. We are looking for a business-savvy attorney who can effectively partner with Law Department colleagues and cross-functional teams across Regeneron, providing practical legal advice on contracts, trade laws and regulations, and other operational matters.</p><p><strong>As Associate Director, Corporate Counsel, a typical day might include the following:</strong></p><ul><li><p>Providing advice and counseling to IOPS business operations on legal issues related to manufacturing, supply, distribution, and other related areas</p></li><li><p>Guiding internal clients through the entire contract life cycle, including determination of internal form vs. vendor paper, coordination with procurement and business clients, negotiating with vendors, etc.</p></li><li><p>Identifying legal and business issues in contracts for resolution through negotiating, drafting, and internal client discussions</p></li><li><p>Working as an on-site corporate contract specialist for the Rensselaer sites, handling legal matters as they arise</p></li><li><p>Collaborating regularly with colleagues in the Regeneron Law Dept, IOPS Law group (including Rensselaer and Raheen, Ireland), business partners, and procurement professionals</p></li><li><p>Assisting the Export Trade Controls (ETC) function with policy and procedure drafting, training, assessments, and counsel on U.S. and international import and export regulatory matters — including Office of Foreign Assets Control (OFAC) sanctions programs; anti-boycott compliance; export control classification and export licensing under the Export Administration Regulations (EAR) and other applicable laws and regulations; tariff classification, customs valuation, country of origin determination, and preference programs/FTAs under Customs and Border Protection (CBP) regulations and other applicable laws and regulations; and Partner Government Agency (PGA) requirements impacting import and export compliance for biotech products, including those administered by the FDA, USDA, and CDC/APHIS</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven contract drafting skills and the ability to work in a fast-paced, dynamic environment requiring agility and emotional intelligence; some experience in real estate and regulatory law is helpful but not required</p></li><li><p>You have experience with, or a strong willingness to learn, U.S. and international import and export trade compliance laws, regulations, and agency requirements relevant to a global biotech company</p></li><li><p>You have exceptionally strong interpersonal and communication (written and spoken) skills</p></li><li><p>You can work efficiently with others cross-functionally, within the Law Department, and across business units</p></li><li><p>You demonstrate sound judgment in novel or evolving regulatory areas and are comfortable navigating ambiguity</p></li></ul><p><strong>To be considered for this role, you must have</strong> a BA/BS and JD with excellent law school credentials, and a license to practice law in New York or eligibility for licensure as registered in-house counsel. We need someone with at least 3 years of legal experience, including some pharmaceutical and/or biotech work, or an equivalent combination of education and experience. Law firm experience is strongly preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$147,800.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Translational Pharmacokinetics and Pharmacokinetic/Pharmacodynamic]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47268]]></requisitionid>
    <referencenumber><![CDATA[R47268]]></referencenumber>
    <apijobid><![CDATA[r47268]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47268/associate-director-translational-pharmacokinetics-and-pharmacokineticpharmacodynamic/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director role involves supporting PK and PK/PD requirements for early-stage drug discovery and IND projects. Responsibilities include providing input and oversight for preclinical in vivo studies, coordinating with and influencing scientific teams conducting these studies, managing nonclinical PK studies, analyzing and presenting PK/PD data to project teams and senior management, and preparing summary reports for regulatory submissions</p><p><strong>The daily responsibilities of this role include:</strong></p><ul><li><p>Serving as a subject matter expert on Preclinical PK/PD within Discovery-stage project teams and guiding the design of preclinical PK/pharmacology studies.</p></li><li><p>Collaborating with various internal groups such as Therapeutic Proteins, Therapeutic Function Areas, Assay Development, Precision Medicine, Preclinical Operations, and PPK/PD management to develop and execute PK strategies for projects.</p></li><li><p>Effectively communicating project team queries, expectations, and timelines to management.</p></li><li><p>Conducting and reporting PK/PD analyses based on data from preclinical studies.</p></li><li><p>Working closely with Toxicology, Pathology, Clinical Pharmacology, and Quantitative Pharmacology teams within the Drug Safety and Pharmacometrics department to deliver data and regulatory documents supporting project progression.</p></li><li><p>Maintaining current knowledge of scientific literature, regulatory guidance, and best practices related to PK/PD.</p></li></ul><p><strong>This Role Might Be for You If You :</strong></p><ul><li><p>Thrive in a fast-paced, collaborative environment.</p></li><li><p>Are passionate about science and motivated to contribute to bringing new drugs to patients.</p></li><li><p>Desire exposure to multiple therapeutic areas and emerging modalities.</p></li><li><p>Excellent written and verbal communication, presentation, influencing, and leadership skills.</p></li></ul><p><strong>To be considered for this opportunity, you must have:</strong></p><ul><li><p>PhD in Pharmacology, Pharmacokinetics, Biology/Molecular Biology, or Biochemistry with more than 8 to 10 years of relevant experience in biotech or pharma.</p></li><li><p>Deep theoretical and applied understanding of PK and PD to interpret the pharmacology and biology of therapeutic proteins. Experience with other modalities such as siRNA, CRISPR-based therapeutics, and cell therapies is highly beneficial.</p></li><li><p>Proven ability to plan, coordinate, lead PK and/or PK/PD studies, and analyze related data.</p></li><li><p>Familiarity with PK/PD (e.g., WinNonLin), data visualization and AI software and experience writing scientific reports and regulatory summaries.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Compliance Counsel]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47379]]></requisitionid>
    <referencenumber><![CDATA[R47379]]></referencenumber>
    <apijobid><![CDATA[r47379]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47379/director-compliance-counsel/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is looking for a Director, Compliance Counsel to investigate compliance matters across a global organization to ensure compliance with all laws, regulations, and company policies. This is a high-impact role at the intersection of law, ethics, and business - one for a seasoned attorney who is comfortable building relationships across the enterprise and identifying and addressing cross-border issues. This role will provide guidance to internal stakeholders and perform other compliance-related tasks, as needed, to support the company’s compliance program. A successful attorney for this role will be able to work across the organization, assess risk, and provide a neutral and informed perspective.</p><p><strong> </strong></p><p><strong>This role is based at Regeneron's office in Sleepy Hollow, NY (4 days a week onsite) - we offer a comprehensive relocation package.</strong></p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Lead end-to-end compliance investigations from evaluating initial allegations to recommending remedial action to ensure compliance with all laws, regulations, and company policies, across the U.S. and internationally.</p></li><li><p>Respond to alleged violations of policies, procedures, and standards of Regeneron’s Code of Business Conduct and Ethics by evaluating or recommending the initiation of investigative procedures.</p></li><li><p>Liaise with other Compliance or Law Department functions both in the US and globally to ensure integrated support and timely updates.</p></li><li><p>Provide guidance to internal stakeholders on risks emanating from international laws, codes and regulations.</p></li><li><p>Provide input into policies, procedures and guidance documents.</p></li><li><p>Monitor and assess legislative and regulatory developments impacting Regeneron’s global operations.</p></li></ul><p><strong> </strong></p><p><strong>This role might be for you if you:</strong></p><ul><li><p>Have experience conducting internal, compliance, and/or government investigations.</p></li><li><p>Possess high level of influencing skills and ability to inspire change as it relates to implementing remedial actions.</p></li><li><p>Have the ability to effectively deliver sound and clear Compliance advice in a business setting.</p></li><li><p>Have in-depth knowledge of anti-kickback and anti-bribery prohibitions as they apply to pharmaceutical sales, off-label/inappropriate promotion issues, Open Payments Act reporting obligations, and other primary laws governing key pharmaceutical compliance areas.</p></li></ul><p><strong>To be considered for this opportunity,</strong> you must have a JD with 8+ years of validated experience, with at least two years working in or with pharmaceutical companies on healthcare compliance related activities. Licensed to practice law in New York or eligible for licensure as a registered in-house counsel.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II-Oncology-Seattle, WA]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47378]]></requisitionid>
    <referencenumber><![CDATA[R47378]]></referencenumber>
    <apijobid><![CDATA[r47378]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47378/medical-account-specialist-ii-oncology-seattle-wa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Seattle]]></city>
    <state><![CDATA[Washington]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Seattle, WA</strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><h3><strong>A typical day may include the following:</strong></h3><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><h3><strong>This role might be for you if:</strong></h3><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred). Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Ophthalmology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47444]]></requisitionid>
    <referencenumber><![CDATA[R47444]]></referencenumber>
    <apijobid><![CDATA[r47444]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47444/senior-medical-director-clinical-development-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Medical Director will play a key role in clinical development programs within the Ophthalmology portfolio, including being accountable for deliverables of the assigned program(s), supporting resourcing, budget, and timelines of these programs. This role serves as scientific and medical lead for clinical team(s) working closely with operational leads. This role requires a high-performing and highly passionate individual who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.</p><p>The incumbent will collaborate with multi-disciplinary clinical teams, assisting in guiding and executing clinical development strategies and subsequent regulatory submissions. This role is responsible for the design and execution of first-in-human through registration-enabling studies. This role will serve as a representative to a range of audiences, including Internal Medicine leadership, executive leadership, development partners, and US and global regulatory agencies. The Senior Medical Director, Ophthalmology reports to the Vice President, Ophthalmology Therapeutic Area Lead.</p><p><strong>A typical day in the life of a Senior Medical Director, Clinical Development may include the following: </strong></p><ul><li>Acts as medical expert and leader in interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards), internal stakeholders (e.g., Research, Global Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards.</li><li>Develops unique and innovative clinical strategies to significantly shorten the development cycle in the face of an evolving regulatory landscape. Designs and develops more efficient and innovative, yet robust Phase 1, 2, and 3 programs.</li><li>Works closely with the research and discovery teams to provide input on the next generation of targets in the field.</li><li>Ensures safety of the drug, including the safety aspects of patients in clinical studies and signal detection from post-marketing surveillance, with the support from Global Patient Safety.</li><li>Ensures quality of all clinical documents (e.g., investigators’ brochure, protocol, study report, clinical components of regulatory submissions, safety related documents).</li><li>Develops written responses to regulatory agency questions and prepares regulatory submission documents.</li><li>Has strong consensus-building skills and the ability to collaborate with multi-disciplinary teams towards sound decision-making. Key member of dynamic and matrixed clinical teams in a fast-paced and hands-on environment. </li></ul><p><strong>This role may be for you if you have the following:</strong></p><ul><li>A M.D. or D.O. or equivalent medical degree and relevant training</li><li>A trained Ophthalmologist (board certified or eligible or equivalent) is essential.</li><li>A minimum of 4 years of industry experience (early or late clinical development); however, a candidate with a strong academic background and less experience may be considered.</li><li>Experience in leading proof of concept and/or registrational clinical trials, including protocol design, managing study start-up, directing, and guiding study team execution, data cleaning, medical monitoring/review, database locks.</li><li>Solid knowledge of compliance and global regulatory requirements (ICH) for development of pharmaceutical candidate products is required.</li><li>A strong commitment to clinical research and the ability to work well within a team setting are essential.</li><li>This role requires 4 days a week on-site in Tarrytown, NY, Cambridge, MA, or Warren, NJ</li></ul><p>#MDJobs, #MDJOBSCD, #GDTherapeuticJobs, SKC</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Associate, Synthetic and Bioconjugation Scale-Up Technologies (SBST) (1 of 2)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47542]]></requisitionid>
    <referencenumber><![CDATA[R47542]]></referencenumber>
    <apijobid><![CDATA[r47542]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47542/process-development-associate-synthetic-and-bioconjugation-scale-up-technologies-sbst-1-of-2/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking a hardworking and dynamic <strong>Process Development Associate </strong>for its new Synthetic and Bioconjugation Scale-up Technologies (SBST) group. In this exciting new role, you will develop conjugation and purification processes for bioconjugation of proteins to a diverse range of small-molecules. You would work in close collaboration with cross-functional teams for process development and optimization using the principles of Quality by Design (QbD) to make the processes suitable for GMP production. This role also involves process scale-up and technology transfer of manufacturing related workflows to Contract Development and Manufacturing Organizations (CDMOs) or Regeneron based manufacturing suites to ensure timely and reliable entrance to the clinic through product commercialization.</p><h3><strong>A typical day in the role of Process Development Associate II might include:</strong></h3><ul><li><p>Working at the bench to design and develop scalable, robust and controlled GMP-ready bioconjugation and purification processes.</p></li><li><p>Collaborating with analytical groups within or outside the organization to establish supportive analytical characterization techniques.</p></li><li><p>Discussing plans and data in cross functional teams to evaluate processes and determine developmental goals and ensure integrated program success.</p></li><li><p>Proactively complying to lab safety and environmental safety expectations of both Regeneron and regulatory bodies such as Food and Drug Administration (FDA), Department of Transportation (DoT), etc.</p></li><li><p>Using statistical design of experiments (DOE) to optimize bioconjugation processes including conjugation reactions, purification operations, and analytical characterization.</p></li><li><p>Partnering with External Manufacturing group and other key partners at Regeneron’s IOPS organization to provide technical assessment of CDMO’s intended for GMP production and successfully transferring processes with immediate, first-time success.</p></li><li><p>Researching, identifying, and developing new technologies to improve processes, generate predictive process models, and pioneer novel at-line/in-line process analytical technologies (PAT) to ensure robust and controllable bioconjugation and purification processes.</p></li><li><p>Authoring robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</p></li><li><p>Analyzing and presenting data in a clear and cohesive manner to a broad audience facilitating data-driven decision making.</p></li><li><p>Authoring, reviewing, or providing domain expertise for publications, reports, tech transfer documents, regulatory support documents and patents.</p></li><li><p>Being a responsible lab citizen by ensuring timely maintenance of lab equipment, keeping the lab tidy and organized and proactively planning for lab resources.</p></li><li>Coaching and mentorship of junior team members of the organization as needed.</li></ul><h3><strong>This Role May be for You if You:</strong></h3><ul><li><p>Enjoy working in the lab to advance exciting new drug modalities to patients.</p></li><li><p>Have strong initiative and aim to complete challenging tasks and learn new technologies.</p></li><li>Have a strong fundamental understanding of various protein purification and technology transfer principles</li><li><p>Are capable of multi-tasking and working both independently and in a collaborative environment involving cross-functional teams.</p></li><li><p>Have excellent interpersonal, verbal and written communication skills.</p></li><li><p>Can think critically and demonstrate problem-solving skills.</p></li></ul><p>This role requires a Bachelor’s + 0-3 years relevant experience in chemical/biochemical engineering or a related field. Experience with antibodies in the bioconjugates space is highly preferable. Hands on experience with bioconjugation processes (lysine-based, cysteine-based, site-specific etc.) with practical knowledge of downstream purification techniques such as chromatography, ultrafiltration/diafiltration, membrane technologies etc. is preferred. Experience with a variety of analytical characterization tools such as electrophoresis, mass spectrometry, high-performance liquid chromatography (HPLC), UV spectroscopy, etc. is preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, CBU Operational Effectiveness - Pulmonology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47559]]></requisitionid>
    <referencenumber><![CDATA[R47559]]></referencenumber>
    <apijobid><![CDATA[r47559]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47559/director-cbu-operational-effectiveness-pulmonology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>The Director, Marketing Operations supports strategic and operational activities of the Pulmonology Therapeutic Business Unit. Partners with sales leadership, marketing and market access to find opportunities, gaps and solutions to drive commercial success. Serves as the point person to connect activities across CBU functions as well as functions not reporting into CBU. Enables Therapeutic Business Unit Head to focus on critical strategic and operational issues.</div><div><div><div><div><div><div><div><div><div><h3>A typical day might include the following:</h3><ul><li><p>Supports strategic and operational analysis as well as takes a lead role in driving large projects within the business, allowing for deep insight and access to the organizational strategy and direction.</p></li><li><p>Analyzes existing business strategy and derives recommendations</p></li><li><p>Partners with senior leadership to set operational strategy</p></li><li><p>Tracks key deliverables for Pulmonology CBU and follows up with responsible individuals</p></li><li><p>Identifies solutions that support operational efficiencies/effectiveness of Pulmonology CBU</p></li><li><p>Provide Marketing Operations Support for the Marketing and CBU field teams.</p></li></ul><h3>This role might be for you if:</h3><ul><li><p>You are a strong program manager and able to track multiple projects</p></li><li><p>You can create presentation materials and design projects</p></li><li><p>You can collaborate and engage effectively with a global group</p></li><li><p>You communicate clearly and concisely across various groups</p></li><li><p>You are detail oriented and a self-starter </p></li></ul><p>To be considered for this opportunity, we are requiring 10+ years of pharmaceutical/biotech or related experience or an equivalent combination of education and experience. We would like to see Pulmonology experience. We are looking for someone who also has experience in field management (DM/RD) and home office experience (marketing and other relevant experiences). We need you to possess the business sense necessary to interpret and draw business insights from data analysis to formulate recommendations and complete action plans. Lastly, we require you to be in the Sleepy Hallow office a few times a week.</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development Quality Lead Japan]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45173]]></requisitionid>
    <referencenumber><![CDATA[R45173]]></referencenumber>
    <apijobid><![CDATA[r45173]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45173/senior-manager-global-development-quality-lead-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a passionate and experienced Senior Manager to join our Global Development Quality & Regulatory Compliance team as the Global Development Quality Lead for Japan (GDQL-J). In this key role, you will lead quality and compliance initiatives within our local affiliate operations, supporting GCP, GVP, Medical, and Regulatory Affairs. This position offers an exciting opportunity to create strategic partnerships, drive proactive, risk-based quality activities, and foster a culture of continuous improvement. If you are ready to make a meaningful impact and grow with us, we encourage you to apply.</p><p><strong>A Typical Day:</strong><br>In this dynamic role, you will:</p><ul><li>Lead GVP-compliant quality activities in collaboration with the business and GDQM team.</li><li>Provide expert guidance on inspection readiness, preparation, and management at the local affiliate level.</li><li>Partner with cross-functional teams to implement and sustain quality processes.</li><li>Conduct audits and support issue management related to GVP, GCP, Regulatory, and Medical Affairs.</li><li>Mentor, coach, and manage junior team members, fostering their professional growth.</li><li>Collaborate with local and global stakeholders to align quality strategies and operations.</li><li>Act as a subject matter expert in GCP and GVP, providing training and consultations.</li><li>Drive process improvement initiatives to enhance efficiency and compliance.</li></ul><p><strong>This Role May Be For You If:</strong><br>You are someone who:</p><ul><li>Thrives in a collaborative environment and builds strong stakeholder relationships.</li><li>Has a proactive approach to quality management and risk assessment.</li><li>Excels in managing complex quality issues and compliance activities.</li><li>Enjoys mentoring and developing team members to achieve their full potential.</li><li>Is detail-oriented and committed to maintaining the highest standards of quality.</li><li>Values innovation and continuous learning to stay ahead in the pharmaceutical industry.</li><li>Communicates effectively and influences peers and senior leaders alike.</li><li>Is adept at managing multiple priorities and delivering results under tight deadlines.</li></ul><p><strong>To Be Considered:</strong><br>Candidates must have a Bachelor’s degree and at least 8 years of relevant experience in the healthcare or pharmaceutical industry, with a strong background in quality management or clinical development. Advanced knowledge of GCP and GVP guidelines, along with experience in regulatory inspection management, is essential. Preferred qualifications include expertise in risk-based quality management and proficiency in Microsoft Office tools. Native level Japanese proficiency and business level English proficiency is required.</p><p>This is your chance to be part of a team that values integrity, innovation, and excellence. Join us in shaping the future of quality and compliance in the pharmaceutical industry. Apply today!</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Head of Regeneron Cell Medicines]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47871]]></requisitionid>
    <referencenumber><![CDATA[R47871]]></referencenumber>
    <apijobid><![CDATA[r47871]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47871/head-of-regeneron-cell-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Head of Regeneron Cell Medicines</strong></p><p>Location: Cambridge, MA (primary site)</p><p>The Head of Regeneron Cell Medicines (RCM) sets the vision, strategy, and execution for Regeneron’s cell medicines portfolio and technology platform. Scope includes ex vivo and in vivo CAR T programs and enabling technologies for delivery, including chemo-free conditioning. This leader oversees cross-functional initiatives from discovery through early clinical development, builds and mentors high-performing teams, and partners across the enterprise and with external collaborators to deliver transformative cell-based therapies. Based in Cambridge, MA, this role serves as the site’s senior scientific executive and advances the RCM portfolio in alignment with Regeneron’s broader scientific vision.</p><p><strong>In This Role, You Will:</strong></p><p><strong>Strategy and Portfolio Leadership</strong></p><ul><li>Define and drive the long-term scientific vision and portfolio strategy for ex vivo and in vivo cell medicines, aligned to enterprise priorities.</li><li>Prioritize programs and platform investments using data-driven governance, scenario planning, and risk/benefit frameworks.</li><li>Champion innovation in cell engineering, in vivo delivery (e.g., LNPs, viral vectors), and manufacturing to create differentiated therapies.</li><li>Establish and evolve the CAR T strategy, including target selection, tissue/cell targeting, potency enhancement, and combinations with antibody-based approaches.</li></ul><p><strong>Scientific Program Oversight</strong></p><ul><li>Lead matrixed teams to deliver milestones from target validation to IND, Phase I manufacturing, and early clinical readouts.</li><li>Guide technical problem solving across modalities, including CAR T design, delivery optimization, biodistribution/PK, on/off-target assessment, and safety risk mitigation.</li><li>Integrate enabling platforms where justified (e.g., CAR Ts, antibody-based approaches such as CPIs and bispecifics, encoded potency enhancements, ARMoR’ing strategies).</li><li>Drive benign conditioning initiatives that enable chemo-free delivery of cell-based medicines (including T cells and hematopoietic stem cells).</li></ul><p><strong>People Leadership and Organizational Development</strong></p><ul><li>Build, mentor, and retain a diverse, high-performing organization of senior scientific leaders and functional experts.</li><li>Foster a culture of scientific excellence, accountability, collaboration, and inclusion across sites and functions.</li><li>Implement succession planning, talent development, and performance management.</li></ul><p><strong>Cross-Functional and Cross-Site Collaboration</strong></p><ul><li>Partner closely with Research, Preclinical Development, Clinical, Regulatory, Quality, CMC, Manufacturing, BD, and Finance.</li><li>Serve as the senior scientific leader for the Cambridge site; maintain strong operating rhythms with Seattle and Tarrytown leadership.</li><li>Coordinate with vector/delivery, immunology, and translational biomarker teams to accelerate RCM programs to clinical evaluation.</li></ul><p><strong>External Innovation and Partnerships</strong></p><ul><li>Identify and evaluate external opportunities (academia, biotech, consortia, platforms) to accelerate the pipeline and capabilities.</li><li>Negotiate and govern collaborations to clear, value-creating outcomes.</li></ul><p><strong>Operational Excellence and Compliance</strong></p><ul><li>Own budgets, headcount planning, and resource allocation across programs and platform functions.</li><li>Ensure adherence to biosafety, ethical guidelines, and regulatory standards (e.g., IND enabling, GxP interfaces), including nonclinical programs specific to ex vivo and in vivo cell therapy (biodistribution, preclinical safety).</li><li>Drive reproducibility, data integrity, and robust decision records.</li></ul><p><strong>Executive Communication and Governance</strong></p><ul><li>Provide clear, concise updates to executive leadership and governance bodies on strategy, progress, risks, and mitigation plans.</li><li>Represent Regeneron Cell Medicines at internal and external forums, scientific conferences, and with partners.</li></ul><p><strong>What You Need to Succeed:</strong></p><p><strong>Required Qualifications</strong></p><ul><li>Advanced degree (PhD, MD, or MD/PhD) in cell biology, immunology, bioengineering, or related discipline.</li><li>20+ years of biopharmaceutical R&D experience with a substantial focus on cell-based therapies; track record advancing programs from discovery to IND and early clinical.</li><li>Demonstrated leadership of multidisciplinary, multisite teams and senior people leaders in a fast-paced environment.</li><li>Deep expertise across key domains:<ul><li>Cell engineering (e.g., CAR design, viral vectors), potency/identity assays, process and analytical development, and translational biology.</li><li>In vivo gene delivery for in vivo CAR T, including viral and non-viral modalities (e.g., LVV, LNPs), tissue/cell targeting strategies, biodistribution/PK, on/off-target risk assessment, and immunogenicity management.</li><li>CMC considerations for in vivo modalities (vector design, release testing, stability) versus ex vivo products.</li></ul></li><li>Familiarity with regulatory pathways for cell and gene therapies (e.g., FDA/EMA guidance, IND preparation, RMAT considerations), including in vivo gene therapy nonclinical packages (biodistribution, toxicology, shedding).</li><li>Strong portfolio management, resource planning, and financial acumen.</li><li>Exceptional communication, influence, and stakeholder management; effective in executive forums and cross-functional decision making.</li><li>Commitment to building an inclusive culture and developing talent.</li></ul><p><strong>Leadership Competencies</strong></p><ul><li>Strategic vision and critical thinking that drive high-quality decisions.</li><li>Scientific rigor and an innovation mindset, balanced by a patient-centric bias for action.</li><li>Talent development and coaching.</li><li>Cross-functional collaboration and influence beyond direct reporting lines.</li><li>Results orientation and accountability.</li><li>Change leadership and resilience.</li></ul><p><strong>Work Model</strong></p><ul><li>On-site presence 4+ days per week in Cambridge, MA; regular travel to Tarrytown, NY and Seattle, WA.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - Great Lakes]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48151]]></requisitionid>
    <referencenumber><![CDATA[R48151]]></referencenumber>
    <apijobid><![CDATA[r48151]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48151/neurology-account-director-great-lakes/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Michigan]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: Great Lakes (Michigan, Indiana, Illinois and Wisconsin)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Process Engineer 2nd Shift]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45996]]></requisitionid>
    <referencenumber><![CDATA[R45996]]></referencenumber>
    <apijobid><![CDATA[r45996]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45996/associate-process-engineer-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill an Associate Process Characterization & Technology Engineer position on our Process Sciences CORE (Cross-Operational Research Extension) team with a 2nd shift, Saturday-Thursday, 6pm-2:30am schedule. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Process Characterization & Technology Engineers are on the front line, running small scale studies in support of manufacturing operations. The cross-functional premium shift team operates in support of both upstream and downstream lab teams, generating data used to determine proven acceptable ranges for manufacturing, characterizing cell banks, executing raw material screening studies and supporting technical evaluations at small scale.<br><br>As an Associate Process Characterization & Technology Engineer, a typical day might include the following:</p><ul><li>Performs laboratory-scale scientific investigations related to upstream biologics manufacturing process unit operations.</li><li>Conducts scaled-down production procedures to improve the efficiency and yield of candidate or existing bioprocesses.</li><li>Performs and completes small-scale development and characterization studies used to develop IPC programs for upstream and purification processes.</li><li>Performs cGLP cell banking and characterization.</li><li>Assists in the analysis of samples generated from lab scale studies.</li><li>Produces and maintains accurate records.</li><li>Maintains lab supplies and equipment.</li><li>Develops and writes protocols for small-scale studies.</li><li>Tabulates experimental results; writes process evaluation summary reports.</li><li>Presents findings at group, and possibly, at interdepartmental meetings.</li></ul><p>This role might be for you if you have:</p><ul><li>Experience with mammalian cell culture expansion using aseptic technique.</li><li>Knowledge of small-scale, fed-batch bioreactors (2L).</li><li>Lab skills in protein separation, filtration and purification.</li><li>Strong attention to detail.</li><li>Strong interpersonal, oral, and written communication skills.</li><li>Ability to operate efficiently in a fast-paced lab environment.</li><li>Ability to adapt quickly to change and be flexible.</li><li>Strong organizational skills and ability to multi-task.</li><li>Good record-keeping skills and understanding of GDP.</li></ul><p>To be considered for this position, you must be willing and able to work 2nd shift, Saturday-Thursday, 4pm-12:30am. You must have a BS in Engineering, preferably Chemical or Biomedical Engineering.</p><p>Level is determined based on qualifications relevant to the role. <br><br>Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</p><p><br>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications, etc.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $92,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Marketing]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47355]]></requisitionid>
    <referencenumber><![CDATA[R47355]]></referencenumber>
    <apijobid><![CDATA[r47355]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47355/senior-manager-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>We are looking for a Senior Manager, Oncology Marketing to help shape and deliver brand strategy across our international markets, with a focus on Austria, Switzerland, and Portugal. In this role, we work closely across teams to bring marketing plans to life for key oncology indications, supporting both current brands and future launches. You’ll play an important part in connecting global strategy with local market needs, ensuring our approach is relevant, practical, and grounded in real insight.</p><h3>A Typical Day:</h3><ul><li>Leading development and execution of local brand marketing plans</li><li>Analysing market dynamics to identify opportunities and risks</li><li>Shaping local brand strategy with input from global teams</li><li>Partnering with Medical Affairs to align on market approach</li><li>Driving execution of promotional activities across channels</li><li>Adapting global materials for local use and consistency</li><li>Planning and supporting congresses, HCP engagement, and events</li><li>Managing budgets and tracking spend against priorities</li></ul><h3>This Role May Be For You If You:</h3><ul><li>Enjoy working across markets to tailor strategy to local needs</li><li>Like balancing planning with hands-on execution</li><li>Are comfortable working with cross-functional teams</li><li>Stay close to the market and value customer insight</li><li>Can prioritise effectively across multiple brands or indications</li><li>Build strong working relationships with internal and external partners</li><li>Take a thoughtful approach to budgets and resource decisions</li><li>Pay attention to compliance and high standards of conduct</li></ul><p>To be considered, you should bring 8–10+ years of experience in pharmaceutical or biotech brand marketing, along with a bachelor’s degree (business or science preferred). Strong knowledge of the Austrian and Swiss markets is required, along with experience managing agencies and external partners. You should have a solid understanding of healthcare compliance and promotional regulations, as well as proficiency in English. Willingness to travel (approximately 30–40%) is expected. Experience in oncology marketing, including immuno-oncology, and launch experience are preferred, along with additional European language skills.</p><p><em>In Austria, the minimum annual gross salary is based on Trade CBA with a willingness to overpay depending on qualification and relevant experience. </em></p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€87,525.00 - €145,875.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 03:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II- Ophthalmology- Columbus/Cincinnati, OH]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47059]]></requisitionid>
    <referencenumber><![CDATA[R47059]]></referencenumber>
    <apijobid><![CDATA[r47059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47059/medical-specialist-ii-ophthalmology-columbuscincinnati-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Columbus</strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.</p><p><strong>A typical day might include the following: </strong></p><p>The Ophthalmology Medical Specialist will report to the Regional Director and will be responsible for developing and managing relationships with retina specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The Medical Specialist will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you have:</strong></p><p>· Experience in biologics and buy and bill products</p><p>· Demonstrated history of high sales performance</p><p>· Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Buy and Bill experience. Ophthalmology with relevant retina experience is preferred. Must be based in or located in close proximity to the assigned territory (relocation will not be provided). Ability to travel (40-60%).</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 09:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oncology Account Specialist -Oncology- Rochester, MN]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47524]]></requisitionid>
    <referencenumber><![CDATA[R47524]]></referencenumber>
    <apijobid><![CDATA[r47524]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47524/oncology-account-specialist-oncology-rochester-mn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Minnesota]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Rochester, MN</strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred). Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42034]]></requisitionid>
    <referencenumber><![CDATA[R42034]]></referencenumber>
    <apijobid><![CDATA[r42034]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42034/hvac-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add an experienced HVAC Technician to our growing team at our SUNY campus with a Monday-Friday 8:00am-4:30pm shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. We perform all tasks necessary for troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><div><p>As an HVAC Technician, a typical day might include the following:</p><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC and facilities related equipment</li></ul><p>This role might be for you if you:</p><ul><li>Follow current good manufacturing practices (cGMPs) and good business practices (G)</li><li>Ensure safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, GDPs and quality standards</li><li>Can communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Are able to coordinate with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Have a solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>Are EPA certified for refrigeration gases</li><li>Have the ability to become fully gown qualified to work in production areas</li></ul><p>To be considered for the HVAC Technician you ideally should have an AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level. Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred.</p><ul><li>HVAC Technician II: AAS with 2+ years of relevant experience or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years of relevant experience or equivalent combination of education and experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Solid Tumor Oncology]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45090]]></requisitionid>
    <referencenumber><![CDATA[R45090]]></referencenumber>
    <apijobid><![CDATA[r45090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45090/medical-director-clinical-development-solid-tumor-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials. This role may work on studies in ovarian cancer.</p></div><div><p><strong>As a Medical Director, a typical day may include the following:</strong></p><ul><li><p>Defines clinical trial-related goals and objectives.</p></li><li><p>Conducts literature and database research on clinical trials as needed</p></li><li><p>Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and with the Therapeutic Area Program Manager</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings.</p></li><li><p>Leads and supervises the Clinical Team to produce high quality program deliverables on schedule</p></li><li><p>Maintains and develops relationship with key study investigators</p></li></ul><p><br><strong>This role may be for you if:</strong></p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p><br><strong>To be considered for this role</strong>, you must have a MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience. Oncology clinical fellowship training with translational and/or clinical research experience is strongly preferred.</p><div><p><em>This role has a 4-day onsite minimum requirement in Tarrytown, NY.</em></p></div><div><div><div><div></div></div></div></div><p>#MDJOBSCD, #MDJOBS, #GDTher, #Oncology</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Mgr Global Procurement- Lab Consumables]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44951]]></requisitionid>
    <referencenumber><![CDATA[R44951]]></referencenumber>
    <apijobid><![CDATA[r44951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44951/sr-mgr-global-procurement-lab-consumables/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Senior Manager for the Research and Pre-Clinical Development (R&pD) Lab Consumables team. In this role you will develop and manage strategies for our subcategories, as well as planning and executing strategic sourcing initiatives. The Senior Manager will be responsible for developing sourcing specifications, requirements, and scopes of work for RFIs, RFQs, and RFPs. They will gather and assess data through benchmarking, market intelligence reports, and Voice of the Customer (VoC) interviews, and perform analytics on spend, inventory levels, utilization, and KPI measurements. We are looking for a proactive and collaborative individual who can effectively manage supplier relationships, mitigate risks, and contribute to the success and development of our team.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Being accountable for supporting the definition and implementation of the global Lab Consumables Category strategy to serve global and regional business needs as assigned.</p></li><li><p>Work closely with stakeholders to manage discussions related to the Lab Consumables Categories and aligns category priorities with Procurement management and stakeholders.</p></li><li><p>Manage negotiations, supplier management activities, and stakeholder engagement activities for the Lab Consumables Category as assigned.</p></li><li><p>Take direction to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</p></li><li><p>Represent Global Procurement by participating in organizational decisions in the Lab Consumables categories with critical short and long-term impact on the success, efficiency, growth, and results of Global Procurement.</p></li><li><p>Demonstrate knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities.</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.</p></li></ul><p>This role may be a fit for you if you:</p><ul><li><p>Have experience successfully managing category processes, and suppliers across a breadth of categories</p></li><li><p>Can demonstrate success working effectively with cross-functional teams to drive results in the Lab Consumables category or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Use external data sources, market information, and supplier engagement to constantly improve Regeneron’s knowledge of supply market dynamics.</p></li><li><p>Can support the primary relationship manager with key supplier relationship management activities.</p></li><li><p>Have knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Can leverage standard business applications for communicating, presenting and analyzing (Word, Excel, Powerpoint)</p></li><li><p>Have working knowledge and hands on experience supporting sourcing platform technologies preferred (LabViva, Zageno, ScienceExhange, Scientist.com, others)</p></li><li><p>Ability to use data analytics, automation and visualization tools to drive insights and communicate to stakeholders and senior leadership (PowerBI, Tableau, Power Automate)</p></li><li><p>Management and implementation of inventory management programs including technology solutions (RFID, QR codes, others), consignment programs, VMI solutions, single use materials, bioreagents and media etc.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma.</p><p>Sr Manager Level: 8+ years of experience in relevant experience, functions or industries. The ideal candidate will have in-depth knowledge of managing global category processes, and suppliers.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - RALEIGH , NC]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48018]]></requisitionid>
    <referencenumber><![CDATA[R48018]]></referencenumber>
    <apijobid><![CDATA[r48018]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48018/medical-account-specialist-ii-neurology-raleigh-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Raleigh]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Raleigh (Metro), NC</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - NASHVILLE, TN]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48025]]></requisitionid>
    <referencenumber><![CDATA[R48025]]></referencenumber>
    <apijobid><![CDATA[r48025]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48025/medical-account-specialist-ii-neurology-nashville-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Nashville-Davidson6]]></city>
    <state><![CDATA[Tennessee]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Nashville (Metro), TN</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - KANSAS CITY, MO - Mountain West]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48067]]></requisitionid>
    <referencenumber><![CDATA[R48067]]></referencenumber>
    <apijobid><![CDATA[r48067]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48067/medical-account-specialist-ii-neurology-kansas-city-mo-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Kansas City]]></city>
    <state><![CDATA[Kansas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Kansas City (Metro), MO</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -JACKSONVILLE South, FL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48029]]></requisitionid>
    <referencenumber><![CDATA[R48029]]></referencenumber>
    <apijobid><![CDATA[r48029]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48029/medical-account-specialist-ii-neurology-jacksonville-south-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Jacksonville]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Jacksonville South (Metro), FL</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 18:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - DENVER, CO]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48070]]></requisitionid>
    <referencenumber><![CDATA[R48070]]></referencenumber>
    <apijobid><![CDATA[r48070]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48070/medical-account-specialist-ii-neurology-denver-co/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Denver]]></city>
    <state><![CDATA[Colorado]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Denver (Metro), Co</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, R&D Thought Leadership and Reputation]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45847]]></requisitionid>
    <referencenumber><![CDATA[R45847]]></referencenumber>
    <apijobid><![CDATA[r45847]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45847/manager-rd-thought-leadership-and-reputation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As Manager, R&D Thought Leadership & Reputation Communications, you will play a key role in shaping and executing integrated external communications that strengthen Regeneron’s reputation, advance our scientific narrative, and position our Research & Development (R&D) senior leaders as industry authorities. You’ll translate complex science into compelling stories and orchestrate programs that engage key audiences across channels.</p><p><strong><em>This role is based at our Sleepy Hollow, NY or Tarrytown, NY location with a minimum of four days onsite per week required – this role is not open to fully remote or hybrid work arrangements.</em></strong></p><p><strong>Why it matters:</strong></p><p>You will bridge corporate reputation and stakeholder engagement through public-facing, above-brand R&D storytelling, reputation campaigns, and executive communications across owned, earned and social channels—elevating visibility, trust and impact among key audiences.</p><p>Reporting to the Director, Research Communications—with a dotted line to the Director, Global Development Communications—this role sits within the Corporate Communications team in Corporate Affairs. You will partner closely with the Product & Pipeline Communications, Patient Advocacy and R&D teams.</p><p><strong>A typical day might include:</strong></p><ul><li><p>Supporting development of a comprehensive external communications strategy aligned to R&D and enterprise objectives, clarifying goals and audiences, key messages, and the owned, earned, social and paid channel mix.</p></li><li><p>Collaborating with scientists, physician-scientists, medical affairs, regulatory, and operational teams to translate complex scientific topics into compelling stories for use on our corporate website, social media channels, and communications campaigns.</p></li><li><p>Identifying and securing speaking engagements, media opportunities, and events for R&D functional leaders; preparing spokespeople with briefing documents and message maps; and building and maintaining relationships with trade media by proactively pitching stories and responding to inquires, as appropriate. </p></li><li><p>Leading project management and execution of reputation-building campaigns including content planning and creation, managing reviews and approvals, and ensuring on-time delivery.</p></li><li><p>Overseeing external PR agencies/vendors and external partners to drive quality, timelines, budgets, and integration across workstreams. </p></li><li><p>Defining measurement plans and dashboards using data and feedback to optimize content and demonstrate impact.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You think strategically and execute tactically to deliver measurable business outcomes.</p></li><li><p>You have exceptional writing, storytelling, and editing skills, and can translate complex scientific concepts into engaging multimedia content.</p></li><li><p>You excel at project management and can lead multiple initiatives simultaneously within a matrixed organization.</p></li><li><p>You bring strong business acumen and a creative, innovative mindset to problem-solving.</p></li><li><p>You have experience shaping executive presence and social media campaigns (LinkedIn).</p></li><li><p>You thrive in a dynamic, fast-paced and collaborative team environment. </p></li><li><p>You are proactive and agile, adaptable, and comfortable navigating ambiguity.</p></li></ul><ul><li><p>You have experience managing agencies and/or multiple vendors with strong integration skills. </p></li><li><p>You take a data-driven approach to communications planning, optimization and measurement.</p></li><li><p>You are passionate about science and relentlessly curious.</p></li></ul><p><br><strong>To be consider for this role you have:</strong></p><p>A Bachelor’s degree in a related field is required. You bring 7+ years of professional experience in strategic corporate healthcare communications, with a focus on pharmaceutical or biotech communications preferred. Agency experience preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Worldwide Operations Office - Pharmacovigilance]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47622]]></requisitionid>
    <referencenumber><![CDATA[R47622]]></referencenumber>
    <apijobid><![CDATA[r47622]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47622/executive-director-worldwide-operations-office-pharmacovigilance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an Executive Director, Worldwide Operations Office to join our PV Organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Executive Director, Worldwide Operations Office serves as the single point of accountability for Regeneron’s global-to-local pharmacovigilance model. This role ensures consistency, compliance and operational excellence across all regions and countries by defining the scope and governance of regional PV Hubs, establishes clear boundaries between global, regional, and local responsibilities, and translates regional insights into strategic guidance for GPS leadership. This role drives a unified, patient-centered approach to safety across Regeneron’s global footprint while enabling appropriate local adaptation to meet regional regulatory requirements. </p><p><strong>This role might be for you if can: ​</strong></p><ul><li><p>Partner with cross-functional US and International teams to embed a patient safety mindset across Regeneron’s global operations (e.g., gather feedback from regional leaders, establish knowledge sharing forums) </p></li><li><p>Provide functional oversight of WWOO and regional PV Hubs, ensuring operational performance, quality standards, regulatory compliance, and consistent application of global processes across markets </p></li><li><p>Define execution scope for regional PV Hubs, determining which processes require localization to meet requirements versus which can be executed through centralized global processes, including clear delineation of responsibilities between GPS and affiliate teams </p></li><li><p>Establish governance framework for local process adaptation, defining clear standards for when and how global PV processes may be tailored to meet local regulatory requirements </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li><li><p>Aggregate insights and potential risks from regional and country-level activities to shape, influence, and prioritize objectives for the PV system </p></li><li><p>Coordinate across key GPS functions (e.g., QPPV, Case Management, Quality & Compliance) on matrixed activities, regional priorities, and global to local interdependencies </p></li><li><p>Adapt the international model to fit changing business needs, including assessing future needs for additional PV Hubs based on portfolio expansion, geographic growth, and regulatory landscape changes </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that raise capabilities across the organization </p></li><li><p>Influence cross-functional leaders to align priorities and drive enterprise results </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Advanced degree (PharmD, MD, MS, or MBA) in life sciences, healthcare, or related field preferred; Bachelor's degree required</p></li><li><p>17+ years of experience in pharmacovigilance, international operations within the life sciences industry </p></li><li><p>Minimum 7 years in leadership roles with demonstrated experience managing international or multi-regional operations </p></li><li><p>Proven ability to develop relationships and influence key decision making with GPS and Non-GPS functions (e.g., QPPV, Med Affairs, Regulatory), regions, and senior stakeholders </p></li><li><p>Strong background in PV compliance, inspection readiness, and quality oversight across multiple markets </p></li><li><p>Strategic mindset with the ability to translate regional complexity into clear governance, decisions, and executive-level insights </p></li><li><p>Preferred experience with AI technologies </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists  - Hematology - Alabama/Louisiana]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48144]]></requisitionid>
    <referencenumber><![CDATA[R48144]]></referencenumber>
    <apijobid><![CDATA[r48144]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48144/medical-account-specialists-hematology-alabamalouisiana/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Alabama]]></city>
    <state><![CDATA[Alabama]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually)</strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Developer - Research and Development]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48042]]></requisitionid>
    <referencenumber><![CDATA[R48042]]></referencenumber>
    <apijobid><![CDATA[r48042]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48042/senior-developer-research-and-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an outstanding Senior Developer to design, develop, and deliver informatics solutions that enable our research and preclinical development pipeline. This role focuses on LIMS/ELN platform development, scientific data integrations, and building AI-powered capabilities that accelerate scientific workflows. The ideal candidate brings a data-first perspective — approaching every problem by understanding the underlying data, its structure, and how it flows across systems before writing code. You will serve as a technical lead — driving architecture decisions, mentoring team members, and delivering high-quality solutions on COTS platforms including Sapio, Benchling, and Dotmatics.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Own the design and development of server-side plugins, integrations, and workflows on LIMS/ELN platforms (Sapio preferred) using Java and Python</p></li><li><p>Architect and build AI/GenAI-enabled solutions (LLM agents, RAG pipelines, prompt-engineered workflows) to streamline R&pD informatics processes</p></li><li><p>Develop data pipelines and integrations between scientific instruments, LIMS/ELN systems, and enterprise data platforms — owning data modeling, transformation logic, and data quality validation end-to-end</p></li><li><p>Serve as technical lead on projects — defining technical approach, conducting code reviews, and mentoring developers</p></li><li><p>Partner with scientists, lab operations, and product owners to translate scientific requirements into scalable technical solutions</p></li><li><p>Evaluate and implement COTS platform capabilities (Sapio, Benchling, Dotmatics) to enhance out-of-the-box functionality before custom development</p></li><li><p>Design and develop REST APIs, webhooks, and middleware to enable interoperability across R&PD systems</p></li><li><p>Apply a data-first approach to problem-solving — analyze scientific datasets, identify data quality issues, build dashboards and reporting solutions, and translate data insights into actionable recommendations for scientific collaborators</p></li><li><p>Contribute to platform modernization initiatives, including cloud migration and containerized deployments</p></li><li><p>Ensure solutions meet GxP compliance requirements where applicable</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Have a data-first mentality with strong analytical skills — SQL, Python (pandas/NumPy), data visualization, statistical analysis, and experience deriving insights from complex scientific datasets</p></li><li><p>Possess the ability to lead technical initiatives as an individual contributor: architecture decisions, code quality standards, and peer mentorship</p></li><li><p>Exhibit excellent communication skills, being able to bridge the gap between scientists and engineering teams</p></li><li><p>Have knowledge of pharma/biotech R&D workflows: screening, sample management, assay tracking, and the data models that support them</p></li><li><p>Are proeficient with AI-powered development tools such as Claude Code and GitHub Copilot for accelerating software delivery</p></li></ul><p><strong>In order to be considered for this role, you must have:</strong></p><ul><li><p>Bachelor's degree in Computer Science, Bioinformatics, Life Sciences, or related field</p></li><li><p>3+ years of work experience in software development supporting life sciences R&D or laboratory informatics</p></li><li><p>Proficiency in Java (server-side development, plugin architectures)</p></li><li><p>Proficiency in Python (scripting, data pipelines, webhooks, automation)</p></li><li><p>Experience with at least one LIMS or ELN platform: Sapio, Benchling, or Dotmatics. Experience with Sapio LIMS/ELN (server-side plugins, workflows, data model configuration) is preferred.</p></li><li><p>Proven experience with AI/GenAI technologies: building LLM-powered agents, prompt engineering, retrieval-augmented generation (RAG), or AI-assisted workflow automation. Experience with AI agent frameworks (LangChain, LlamaIndex, Claude/Anthropic APIs, OpenAI APIs) is preferred.</p></li><li><p>Familiarity with containerization (Docker, Kubernetes) and CI/CD pipelines (Jenkins, GitHub Actions) is a plus</p></li><li><p>Experience with instrument integrations (TetraScience or direct instrument interfaces) is preferred</p></li><li><p>Experience with data analytics and visualization tools (Spotfire, Tableau, Power BI, or Jupyter notebooks) to support data-driven decision-making is a plus</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 16:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Auditor]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47018]]></requisitionid>
    <referencenumber><![CDATA[R47018]]></referencenumber>
    <apijobid><![CDATA[r47018]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47018/senior-it-auditor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior IT Auditor is responsible for contributing towards planning, executing, and reporting on operational IT audits, evaluating risks and controls, including application, infrastructure, cloud, data management, SDLC, change management, and IT operations, in accordance with IIA standards and department methodologies. Perform IT SOX control walkthroughs and testing, along with preparing the related documentation. Assess the effectiveness of cybersecurity controls, including identity and access management, vulnerability management, logging and monitoring, incident response, and security governance. <br> </p><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include the following:</strong> </p><div><ul><li><p>Review controls related to cloud computing (e.g., AWS, Azure), SaaS platforms, data lakes, and analytics environments, including shared responsibility models. </p></li></ul></div><div><ul><li><p>Design and execute data analytics‑driven audit procedures using tools such as Dataiku or equivalent, to identify anomalies, trends, and control gaps. </p></li></ul></div><div><ul><li><p>Apply automation, continuous auditing techniques, and responsible use of AI, where appropriate, to improve audit efficiency, coverage, and insight, including assessing AI‑enabled business processes and controls. </p></li></ul></div><div><ul><li><p>Manage timely completion of audit tasks, including communication of status to the auditee and the Manager/Director. </p></li></ul></div><div><ul><li><p>Identify, document, and communicate control deficiencies, root causes, technology risks, and opportunities for improvement, providing practical, actionable recommendations aligned with business objectives. </p></li></ul></div><div><ul><li><p>Present the results of audit work to Internal Audit Management and auditees, including practical recommendations to address identified risks and/or weaknesses in internal controls as well as opportunities to enhance operational efficiencies. </p></li></ul></div><div><ul><li><p>Prepare clear, concise, and professional audit reports and executive‑level presentations for Internal Audit leadership, management, and key stakeholders. </p></li></ul></div><p><strong>This role might be for you if have experience with :</strong></p><div><ul><li><p>Advanced knowledge of IT infrastructure, applications, cybersecurity, and automated controls </p></li></ul></div><div><ul><li><p>Strong understanding of SOX, COSO, COBIT, NIST, GxP, GDPR, and other relevant regulatory and governance frameworks. </p></li></ul></div><div><ul><li><p>Strong analytical, critical‑thinking, and problem‑solving skills, with the ability to independently assess risk and propose solutions. </p></li></ul></div><div><ul><li><p>Comfortable working and learning independently and as part of a team </p></li></ul></div><div><ul><li><p>Excellent interpersonal, communication and writing skills, strong organizational abilities, and attention to detail are required </p></li></ul></div><div><ul><li><p>Experience with data analytical tools (e.g. Dataiku, Alteryx, etc.) </p></li></ul></div><div><ul><li><p>Understanding of AI concepts, associated risks (e.g., model governance, data quality, access, ethical use), and internal controls relevant to AI‑enabled processes. </p></li></ul></div><p><strong>To be considered for this role</strong>, you must have a Bachelor's degree with a<strong> </strong>minimum of 3 - 4 years of progressive experience in IT audit, information security, or technology risk. CISA, CISM and/or CISSP certifications/license preferred. Experience auditing and evaluating infrastructure, cybersecurity risks/controls and auditing operating systems. Pharmaceutical, life sciences, or other regulated industry experience strongly preferred. Big 4 or public accounting experience preferred but not required. </p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 03:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QA Specialist, Drug Product]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48374]]></requisitionid>
    <referencenumber><![CDATA[R48374]]></referencenumber>
    <apijobid><![CDATA[r48374]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48374/qa-specialist-drug-product/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Quality Assurance (QA) Specialist to join our QA Drug Product team. This position will support QA initiatives for a broad range of topics relative to the start-up and operations of a drug product facility. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>1st shift, Monday-Friday, 8am-4:30pm</li><li>Location: Rensselaer, New York, United States</li></ul><p>What you’ll do:</p><ul><li>Work on and potentially lead efforts to establish new programs including start-up of formulation, filling, inspection, assembly, and pack and label team</li><li>Perform assessments of existing procedures/documents to gauge appropriateness for the inclusion of drug product operations; where current documents are not adequate, identify path forward for establishment of procedures</li><li>Develop, write, review, and approve SOPs, specifications, and other documents. This includes documents for operation and facility SOPs, quality training, batch documentation, etc.</li><li>Maintain project timelines to support the evolving business</li><li>Perform on-the-floor quality review of documents, such as: equipment logs, training records, testing results, batch records and supporting documents</li><li>Review and approval of documents (electronic and paper-based)</li><li>Provide mentorship during on-the-floor manufacturing</li><li>Support audits, inspections and investigations</li><li>Perform quarantine, segregation of material and line clearances</li><li>Contribute to the continuous improvement initiatives</li><li>Adjust schedule based on facility start up, filling, and manufacturing needs</li><li>Collaborate with cross-functional internal teams</li></ul><p>The environment and physical rhythms of this role:</p><ul><li>Gowning: full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p>Let’s find out if we’re a fit:</p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>Assoc QA Specialist : 2+ years of experience</li><li>QA Specialist : 4 + years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p>Thrive today. Grow tomorrow.</p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family Care Benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 18 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer I, Purification Development]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48722]]></requisitionid>
    <referencenumber><![CDATA[R48722]]></referencenumber>
    <apijobid><![CDATA[r48722]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48722/process-development-engineer-i-purification-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Preclinical Manufacturing & Process Development Group (PMPD), located in Tarrytown, NY, is seeking a Process Development Engineer as a full-time position to work in the Purification Development group. In this role, you will be responsible for purification process development and support purification of various pre-clinical biological molecules to provide reagents for Regeneron’s research and discovery groups and assist in technology transfers to internal manufacturing sites.</p><p>A Typical Day in the Role Might Look Like:</p><ul><li>Perform process development for pre-clinical and clinical processes</li><li>Document experiments, results, and findings in electronic laboratory notebook</li><li>Reads and understands scientific literature and technical documentation. Executes experimental plans to verify literature findings with direction and prepares comparison of internal data to literature for review with manager.</li><li>Maintain instruments and tackle instrumental/experimental problems</li><li>Development of technology and automation to increase process throughput and efficiency of preclinical manufacturing; support of improvement initiatives</li><li>Presents work at group and department meetings</li><li>Builds relationships within subgroup to support shared goals and may train peers and indirectly lead, guide, and assist co-op students/interns. Proactively assists others in execution of experiments and knows when to ask for help from peers.</li></ul><h3>This Role Might Be For You If You :</h3><ul><li>Enjoy working in a fast-paced, team environment.</li><li>Have initiative and drive to complete ambitious tasks and learn new technologies.</li><li>Contribute to lab equipment maintenance and safety to help create a safe, effective and efficient working environment.</li><li>Anticipate and recognize potential problems with laboratory supplies / equipment and act to prevent and tackle problems.</li><li>Keep up with SOP training and/or compliance responsibilities.</li></ul><p>The role requires a Bachelor’s and/or Master’s degree in either Chemical Engineering, Biochemical Engineering, or Biochemistry, and 0 - 3 years’ experience in the biotech or pharmaceutical industry. A strong fundamental understanding of various protein purification and technology transfer principles a plus. Experience with Downstream Development and with equipment like: Akta Avant, Akta Pilot, Akta Process Skid, Disc Stack Centrifuge, Depth filtration, Tangential flow filters, Normal flow filters, Chromatographic columns, HPLC, UPLC, Ultrafiltration/Diafiltration skid, Laminar Flow Hood, Chemical Fume hood, Empower, Unicorn, JMP, LIMS, PI Historian a plus. Experience with robotic liquid handlers, Raman spectroscopy and/or software programming a plus.</p><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - Immunization]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47878]]></requisitionid>
    <referencenumber><![CDATA[R47878]]></referencenumber>
    <apijobid><![CDATA[r47878]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47878/senior-associate-scientist-immunization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Associate Scientist to join our group in Technology and Discovery Centers investigating B Cell biology. We study methods to elicit robust B cell responses as well as develop approaches to characterize and isolate B cells of interest.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location- Tarrytown, NY- 5 days on-site</p><p><strong>Discover your role:</strong></p><ul><li>Optimizing strategies to elicit robust B cell responses in vivo </li><li>Characterizing B cell development in genetically engineered mice </li><li>Developing approaches to characterize plasma cell responses </li><li>Planning and executing in vivo mouse immunization studies </li><li>ELISA-based assays to measure antibody responses </li><li>Multi-color flow cytometry staining and analysis </li><li>Primary B cell culture </li><li>Presenting data in small and large group settings </li></ul><p><strong>This Role May Be for You If You Have Experience:</strong></p><ul><li>You can drive a project under the supervision of a Senior Principal Scientist by designing and executing experiments, interpreting data and making figures </li><li>You are highly organized and have experience managing a project, including maintaining an up-to-date lab notebook and detailed records </li><li>You have exceptional critical thinking skills with appreciation for rigorous optimization and controls </li><li>You can work collaboratively and are adaptable based on the evolving needs of the group </li></ul><p><strong>The role requires: </strong></p><ul><li>Senior Associate Scientist: you must possess a bachelor's degree with at least 4 years of experience or a master's degree with at least 2 years of experience working in a cellular immunology research laboratory, in either academia or industry</li><li>Associate Scientist: you must possess a bachelor’s degree with at least 2 years of experience working in a cellular immunology research laboratory, in either academia or industry </li><li>Experience with vaccination, tissue isolation, blood sampling, multi-parameter flow cytometry, and ELISA is required </li><li>Some knowledge of B cell and plasma cell biology, as well as experience in primary culture of B cells and plasma cells, is a plus </li><li>Outstanding candidates with relevant technical experience but in an adjacent field of immunology will be considered </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regulatory Affairs Strategy - Genetics Medicine]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48560]]></requisitionid>
    <referencenumber><![CDATA[R48560]]></referencenumber>
    <apijobid><![CDATA[r48560]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48560/director-regulatory-affairs-strategy-genetics-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Regulatory Affairs Strategy </strong>team.<strong> </strong></p><p>The Director, Regulatory Affairs Strategy will provide leadership on global regulatory activities for assigned products within the Genetic Medicine portfolio. This role is focused on regulatory strategy and filings, with responsibility for providing regulatory leadership across project teams. Consistent with our hands-on culture, the Director will be actively involved in clinical study support and will lead IND/CTA and BLA submission activities.</p><p>The Director will develop and maintain regulatory strategy at the study, indication, and program level, lead interactions with global health authorities, and serve as a key cross-functional partner and subject matter expert. This role also carries people management responsibility, including mentoring and developing regulatory staff.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Providing interpretation of regulatory authority feedback, policies, and guidelines, and communicating strategic implications to project teams and senior management.</p></li><li><p>Leading the development and maintenance of regulatory strategic plans, either directly in conjunction with project teams or through direct reports. Owning the preparation of major clinical submissions required for regulatory approvals.</p></li><li><p>Working with cross-functional project teams to resolve complex regulatory issues, utilizing deep expertise in global regulations and guidances to strategically plan and communicate requirements.</p></li><li><p>Ensuring the quality and timeliness of regulatory submissions for IND/CTA/BLA; collaborating with other functions and partners in the preparation, review, and completion of submission documents.</p></li><li><p>Leading health authority interactions, including preparation of briefing books and meeting slides, and advising relevant stakeholders on agency feedback.</p></li><li><p>Representing regulatory affairs at senior program team meetings, providing strategic input and direction as a subject matter expert.</p></li><li><p>Planning, prioritizing, and overseeing regulatory activities in close collaboration with leads from other functions to ensure compliance and alignment with project timelines.</p></li><li><p>Mentoring and developing regulatory staff, providing direction and supporting career growth.</p></li><li><p>You bring a strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development processes, and industry standard practices.</p></li><li><p>You have demonstrated success leading regulatory strategy and health authority interactions across global programs, with the ability to influence cross-functional teams and senior leadership.</p></li><li><p>You are comfortable operating in ambiguous, fast-paced environments and can manage multiple programs and priorities simultaneously.</p></li><li><p>You have experience managing or interacting with CROs in the management of ex-US/ex-EU CTAs toward clinical trial activations.</p></li><li><p>You bring strong interpersonal and communication skills, both written and verbal, with the ability to produce persuasive and high-quality regulatory documents.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>An MD, Ph.D., Pharm.D., or equivalent advanced degree; a relevant scientific discipline is strongly preferred.</p></li><li><p>A minimum of 10 years of pharmaceutical or biotechnology industry experience, with at least 7 years in regulatory affairs, including direct experience as a regulatory liaison.</p></li><li><p>This role requires onsite presence 4 days per week in Tarrytown, NY or Warren, NJ. Relocation support is available for qualified candidates.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Commercial Operations - Oncology]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44699]]></requisitionid>
    <referencenumber><![CDATA[R44699]]></referencenumber>
    <apijobid><![CDATA[r44699]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44699/senior-manager-commercial-operations-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Join Us in Driving Innovation and Excellence in Oncology Commercial Operations </p><p>We are seeking a dynamic and results-oriented Senior Manager, Commercial Operations (Oncology Japan) to join our team. In this pivotal role, you will empower our Sales & Marketing team by facilitating the local implementation effectively of Commercial strategies</p><p>and driving continuous improvements. Reporting directly to the Associate Director, Commercial Operations (Oncology Japan), you will play a key role in ensuring business optimization in a fast-paced and evolving environment. If you are eager to drive business impact while collaborating with stakeholders in Japan and overseas and to lead future pipeline launches, we invite you to be part of our journey.</p><br><p>---</p><br><p>A Typical Day: </p><p>- Lead continuous improvement of local Commercial processes and support the design of organizational growth associated with future pipeline launches and ensure continuous improvement in operational quality and scalability.</p><p>- Oversee governance and content management for promotional materials and product websites, ensuring compliance with Medical, Legal, and Regulatory review processes (MLR). </p><p>- Facilitate and ensure governance of local Healthcare Professional (HCP) contracting requests for engagements, such as advisory boards and consulting agreements in collaboration with internal and external stakeholders. </p><p>- Execute local field sizing, alignments, targeting, and segmentation in partnership with analytics teams, both locally and above-market and deploy the outputs to the sales team with follow-up.</p><br><p>---</p><br><p>This Role May Be For You If: </p><p>- You thrive in a collaborative environment and excel in partnering with cross-functional teams, including vendors and field-based employees.</p><p>- You have a strategic perspective and want to lead building an operational system that spans multiple brands and across all areas.</p><p>- You have strong organizational and project management skills, with the ability to deliver results while balancing multiple projects. </p><p>- You are skilled in data visualization and storytelling, with a knack for turning insights into actionable strategies. </p><p>- You are proficient in tools such as Microsoft PowerPoint, Excel, Word, and Veeva, and have advanced English communication skills. </p><p>- You are passionate about the oncology field and have experience navigating Japan’s biopharmaceutical Commercial market dynamics. </p><p>- You enjoy working in a fast-paced, evolving environment and are committed to driving continuous improvements. </p><br><p>---</p><br><p>To Be Considered: </p><p>Candidates must have at least 8 years of relevant pharmaceutical or biotech industry experience in Commercial roles with increasing responsibilities, including 5 years of global Commercial Operations experience. A Bachelor’s degree is required, with equivalent experience considered. Preferred qualifications include prior experience in the pharmaceutical industry or consulting, alongside expertise in change management, data storytelling, and cross-functional collaboration.</p><br><p>---</p><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology (f/m/d) - Oberösterreich Ost, Wein-, Wald-, Mostviertel, Wien Nord]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48537]]></requisitionid>
    <referencenumber><![CDATA[R48537]]></referencenumber>
    <apijobid><![CDATA[r48537]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48537/sales-specialist-immunology-fmd-oberoesterreich-ost-wein-wald-mostviertel-wien-nord/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Sales Specialist Immunology (f/m/d), you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our Respiratory division at key meetings. You will identify the key people in Pneumology, understand the account context and tailor calls based on individual and account requirements and build KOL support for our portfolio.</p><br><br><p><strong>Where:</strong></p><br><p>Field based in the territory: <strong>Oberösterreich Ost, Wein-, Wald-, Mostviertel, Wien Nord</strong></p><br><br><p><strong>Discover your role:</strong></p><br><br><ul><li>Competent advice and support for relevant Healthcare Professionals (HCP) and, where applicable, customers in the hospital segment</li><li>Building and maintaining intensive and sustainable customer relationships - in person and using digital channels</li><li>Target-oriented, substantive dialogue focused on the benefits for customers and added value for patients</li><li>Independent regional management including account analyses, route planning and documentation of your activities in the CRM system</li><li>Participation in trade fairs and congresses as well as independent planning, coordination and realization of training events and specialist presentations</li><li>Regular reporting to the sales management</li></ul><br><br><p><strong>This role requires:</strong></p><br><br><ul><li>Deep understanding of the local healthcare economy, with the ability to identify key players in Pneumology</li><li>“Patient first” value system</li><li>Bachelor’s degree or equivalent experience and a "Pharmareferent:in" qualification</li><li>5+ years of sales experience within the biotech/pharmaceutical sector</li><li>Respiratory experience is preferred</li><li>Proficiency in German as well as conversational English</li><li>Readiness for very frequent travel and a driver's license</li></ul><br><br><br><p>For this position, the Collective Bargaining Agreement for Trade (Kollektivvertrag Handel) applies; depending on qualifications and professional experience, we offer a salary above the collectively agreed minimum.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>62.475,00 € - 104.125,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager - Business Intelligence Architect]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47727]]></requisitionid>
    <referencenumber><![CDATA[R47727]]></referencenumber>
    <apijobid><![CDATA[r47727]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47727/senior-manager-business-intelligence-architect/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. As we continue to expand our global footprint, our Global Capability Centers play a critical role in enabling scalable, high-quality operations and delivering impactful business services.</p><p><strong>Role Overview</strong></p><p>As a Senior Manager – Business Intelligence Architect, you will serve as a key liaison between global collaborators and the GCC, driving the design, development, and implementation of scalable data architecture and analytics solutions. You will play a critical leadership role in enabling high-quality, reusable data products and supporting enterprise analytics, reporting, and AI use cases. This role combines technical expertise, critical thinking, and people leadership to ensure robust data modeling practices, architecture standards, and seamless collaboration across cross-functional teams.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong></p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li><p>Act as a primary point of contact for data architecture and BI initiatives across global and regional teams.</p></li><li><p>Lead the design and development of analytical datasets, data models, and data products using platforms such as Databricks and Snowflake.</p></li><li><p>Provide technical leadership and mentorship to the BI architecture team, including performance management and capability development.</p></li><li><p>Define and implement data modeling standards, architecture principles, and protocols across the organization.</p></li><li><p>Collaborate with reporting, analytics, and business teams to ensure alignment between data models and downstream consumption.</p></li><li><p>Oversee data pipeline design, transformation workflows, and ensure scalability and maintainability of solutions.</p></li><li><p>Ensure data accuracy, consistency, and integrity through strong validation frameworks and quality checks.</p></li><li><p>Support roadmap planning and execution in partnership with leadership.</p></li><li><p>Serve as a critical issue point for architectural decisions, trade-offs, and complex data challenges.</p></li><li><p>Identify opportunities to enable advanced analytics, including AI/ML-driven use cases.</p></li></ul><p><strong>This Role May Be for You If You Have:</strong></p><ul><li><p>Strong experience in data architecture, data engineering, or business intelligence within a global or shared services environment.</p></li><li><p>Deep understanding of data modeling, data pipelines, and modern data stack (cloud-based platforms).</p></li><li><p>Proven ability to design scalable, reusable data solutions that support reporting and analytics.</p></li><li><p>Strong collaborator management skills with the ability to translate business needs into technical solutions.</p></li><li><p>Excellent communication, presentation, and collaboration capabilities.</p></li><li><p>Strong leadership and team development experience.</p></li><li><p>A structured and meticulous approach with the ability to manage multiple priorities.</p></li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li><p>8+ years of relevant experience in data engineering, BI architecture, or analytics roles within a multinational or GCC environment.</p></li><li><p>Bachelor’s degree required; advanced degree (Master’s or equivalent) preferred (e.g., Data Science, Analytics, Computer Science).</p></li><li><p>Strong hands-on experience with Databricks, Snowflake, and modern data platforms.</p></li><li><p>Proficiency in SQL and programming languages such as Python or R.</p></li><li><p>Experience designing data pipelines, transformation workflows, and data products</p></li><li><p>Familiarity with BI/reporting tools such as Tableau and integration with downstream analytics layers.</p></li><li><p>Experience in pharmaceutical, biotech, or regulated industries is preferred.</p></li><li><p>Understanding of AI/ML data enablement and advanced analytics is a plus.</p></li><li><p>Fluency in English and ability to collaborate effectively with global teams.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[R42183 Associate Director, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44601]]></requisitionid>
    <referencenumber><![CDATA[R44601]]></referencenumber>
    <apijobid><![CDATA[r44601]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44601/r42183-associate-director-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div><div><div><div><div><div><div><div><div><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><p>As an Associate Director, External Data Acquisition and Delivery (EDAD), you will provide strategic oversight and operational leadership for External Data Acquisition and Delivery activities across Regeneron’s clinical trial portfolio and initiatives. You will ensure readiness of external data collection platforms, data conformance tools, reconciliation processes, and the delivery of high-quality, compliant external data from third-party vendors including laboratory, biomarker, Digital Health Technologies, imaging, ECG, PK, genomics, and specialty data. You will partner closely with Clinical Data Management, CROs, external vendors, and cross-functional partners to drive external data strategy, operational excellence, vendor oversight, digital transformation initiatives, and process improvements.</p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Leading External Data Acquisition, integration, quality oversight, and delivery strategy across the clinical trial portfolio</p></li><li><p>Serving as a portfolio-level lead for external data quality and clinical-data operational strategy</p></li><li><p>Reviewing protocol requirements, vendor specifications, and operational data flows</p></li><li><p>Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents to ensure compliance with Regeneron standards and timelines</p></li><li><p>Providing expert mentorship on external data services including biomarker, eSource, eCOA, imaging, ECG, PK, genomics, and laboratory data</p></li><li><p>Driving external vendor oversight, onboarding, qualification, governance, and ongoing performance monitoring</p></li><li><p>Establishing and handling vendor KPIs, SLAs, and quality metrics</p></li><li><p>Governing reconciliation activities between EDC systems and vendor data platforms to ensure data integrity and consistency</p></li><li><p>Monitoring reconciliation metrics, discrepancy trends, and resolution timelines across studies</p></li><li><p>Collaborating with Database Development, Biostatistics, Study Data Managers, and external vendors to resolve complex data discrepancies</p></li><li><p>Leading process improvement initiatives, automation opportunities, and implementation of innovative external data solutions</p></li><li><p>Managing and developing a team of EDAD Managers, Specialists, and associates through coaching, mentoring, and performance management</p></li><li><p>Supporting SOP development, inspection readiness, audit activities, and regulatory compliance</p></li><li><p>Representing EDAD in leadership forums, governance committees, and technology discussions</p></li></ul><p><strong>This Role May Be For You If You Have:</strong></p><ul><li><p>Strong expertise managing multiple clinical external data types including biomarker, imaging, eCOA, ECG, PK, genomics, laboratory, and Digital Health Technology data</p></li><li><p>Advanced knowledge of external data reconciliation processes and EDC platforms such as Medidata Rave, Veeva, or Oracle Inform</p></li><li><p>Experience working with SAS, CSV, and XML data formats</p></li><li><p>Strong understanding of industry regulations including 21 CFR Part 11, ICH-GCP, and CDISC standards</p></li><li><p>Proven experience handling external vendor relationships and driving accountability for quality deliverables</p></li><li><p>Strong leadership, people management, coaching, and mentoring capabilities</p></li><li><p>Strategic thinking, creativity, problem-solving, and analytical skills</p></li><li><p>Strong project management and stakeholder management capabilities</p></li><li><p>Excellent verbal and written communication skills</p></li><li><p>Ability to work effectively in a fast-paced, matrixed, and global environment</p></li></ul><p><strong>To Be Considered For This Role, You Must Have:</strong></p><ul><li><p>Minimum 10+ years of experience in Clinical Data Acquisition/Management within biotechnology, pharmaceutical, or healthcare industries</p></li><li><p>Minimum 4+ years of people management experience</p></li><li><p>Demonstrated experience overseeing external data reconciliation activities between EDC systems and vendor platforms</p></li><li><p>Experience driving process improvements and vendor oversight in supervised environments</p></li><li><p>Bachelor’s degree in Science, Health, Mathematics, Computing, Information Systems, or a related field</p></li><li><p>Advanced degree preferred</p></li></ul></div></div></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director - Hematology (Great Plains)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48918]]></requisitionid>
    <referencenumber><![CDATA[R48918]]></referencenumber>
    <apijobid><![CDATA[r48918]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48918/regional-director-hematology-great-plains/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong><br> <br>The Regional Director (RD), Hematology will report to the National Business Director, Hematology and be responsible for hiring, leading, developing and retaining the Hematology Medical Specialist team in the Great Plains region to support our Multiple Myeloma Bispecific Antibody.</p><p>The RD is responsible for ensuring strong and consistent sales performance that meet or exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Hematology market. The RD will work closely with their cross functional partners to ensure full cooperation and transparency within the region. The RD will work closely with Training and Development to ensure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field Role</p></li><li><p><strong>Location: </strong><strong>Great Plains Region- UT, CO. WY, ND, SD, MN, IA, MO, IL, WI</strong></p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Build and develop a high integrity, high quality sales team and provide overall leadership to the team.</p></li></ul><ul><li><p>Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p></li><li><p>Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p></li><li><p>Ensure each employee is trained on, and effectively implements, customer education.</p></li><li><p>Communicate most current knowledge of the industry and competitor products to regional teams.</p></li><li><p>Ensure participation in industry related trade shows, meetings, conferences, etc.</p></li><li><p>Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p></li><li><p>Allocate and manage the region's budget and utilization of promotional resources</p></li></ul><ul><li><p>Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p></li><li><p>Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Oncology, preferably Hematology.</p></li><li><p>Experience in Biologics and buy and bill products or strong relevant experience in the Oncology field required. Experience in hematology oncology a strong plus</p></li><li><p>Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p></li><li><p>Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p></li><li><p>Strong ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel extensively with local and regional influence.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Corporate Counsel - Collaborations & Contracts]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48229]]></requisitionid>
    <referencenumber><![CDATA[R48229]]></referencenumber>
    <apijobid><![CDATA[r48229]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48229/director-corporate-counsel-collaborations-contracts/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Director, Corporate Counsel, will serve as legal counsel for Regeneron’s manufacturing division (IOPS - Industrial Operations and Product Supply), providing legal support in connection with business development and strategic transactions, including: procurement, license and M&A agreements, collaborations, and various business development transactions. This position works in close partnership with the Law Department’s Mergers and Acquisitions (M&A) and Transactions group, with a particular focus on supporting IOPS’ manufacturing and supply chain roles in corporate transactions, including technology transfers, manufacturing agreements, and supply-related due diligence arising in connection with M&A and other strategic transactions. </p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Rensselaer, NY</p></li><li><p>Hybrid: 4.5 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Drafting, reviewing and negotiating agreements and providing advice to management regarding proposed transactions and compliance with existing contractual obligations, regulations, company policy and general corporate and commercial law. </p></li><li><p>Working closely with internal clients (including scientific and business leaders) in connection with collaborations, licensing arrangements and other strategic transactions. </p></li><li><p>Drafting, reviewing and negotiating intellectual property and technology license agreements, collaboration agreements, material transfer agreements, sponsored research agreements, confidentiality agreements, and consulting agreements. </p></li><li><p>Partnering with the Law Department’s M&A/Transactions group to support IOPS’ involvement in corporate transactions, including advising on manufacturing, supply chain, regulatory and technology transfer aspects of mergers, acquisitions, licensing deals, and other strategic arrangements.</p></li><li><p>Working closely with the intellectual property group to ensure accurate protection of intellectual property assets.</p></li><li><p>Partnering with the regulatory, quality, and compliance groups to advise on relevant regulatory and legal matters impacting existing or proposed arrangements, including GMP requirements, FDA and international regulatory frameworks, privacy, antitrust, as well as general corporate and commercial law.</p></li><li><p>Oversight and coordination of relevant legal matters handled by outside counsel.</p></li><li><p>Serving as an embedded member of the IOPS Law Group, developing deep familiarity with IOPS’ manufacturing operations, supply chain structure, and third-party relationships to provide proactive and informed legal counsel.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A BA/BS and JD with excellent law school credentials and a minimum of 8–12 years of relevant experience.</p></li><li><p>Active bar membership in New York or eligibility for licensure as registered in-house counsel.</p></li><li><p>Technology and intellectual property licensing experience (biotech, pharmaceutical and/or life sciences experience preferred)</p></li><li><p>Demonstrated experience in drafting agreements and transactional documents, advising on intellectual property matters and technology licensing arrangements.</p></li><li><p>Experience with general corporate, privacy and regulatory matters specific to the biotechnology and pharmaceuticals industries, specifically within a GMP-related environment, as well as experience supporting or collaborating with M&A and transactions teams on manufacturing or supply chain matters.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 11:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - MANCHESTER, NH]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48913]]></requisitionid>
    <referencenumber><![CDATA[R48913]]></referencenumber>
    <apijobid><![CDATA[r48913]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48913/medical-account-specialist-ii-hematology-manchester-nh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New Hampshire]]></city>
    <state><![CDATA[New Hampshire]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>MANCHESTER, NH</strong></p><p><strong>Geography: </strong><strong>ME, VT, NH</strong></p><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - ALABAMA]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48922]]></requisitionid>
    <referencenumber><![CDATA[R48922]]></referencenumber>
    <apijobid><![CDATA[r48922]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48922/medical-account-specialist-ii-hematology-alabama/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Alabama</strong></p><ul><li><strong>Geography: </strong><strong>Pensacola, Mobile, Montgomery, Huntsville, Decater</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - COLUMBIA, SC]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48924]]></requisitionid>
    <referencenumber><![CDATA[R48924]]></referencenumber>
    <apijobid><![CDATA[r48924]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48924/medical-account-specialist-ii-hematology-columbia-sc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Columbia, SC</strong></p><ul><li><strong>Geography: </strong><strong>Columbia, Charleston, Myrtle Beach, Anderson</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - GRAND RAPIDS, MI]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48900]]></requisitionid>
    <referencenumber><![CDATA[R48900]]></referencenumber>
    <apijobid><![CDATA[r48900]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48900/medical-account-specialist-ii-hematology-grand-rapids-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- Grand Rapids</strong></p><ul><li><strong>Geography: Grand Rapids, Kalamazoo, Fort Wayne</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  INDIANAPOLIS, IN]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48899]]></requisitionid>
    <referencenumber><![CDATA[R48899]]></referencenumber>
    <apijobid><![CDATA[r48899]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48899/medical-account-specialist-ii-hematology-indianapolis-in/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- Indianapolis, IN</strong></p><ul><li><strong>Geography: Indianapoils</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Physician Scientist – Obesity and Liver Disease Human Genetics]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R39319]]></requisitionid>
    <referencenumber><![CDATA[R39319]]></referencenumber>
    <apijobid><![CDATA[r39319]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r39319/physician-scientist-obesity-and-liver-disease-human-genetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an exceptional Physician Scientist to join our Cardiometabolic Therapeutic Area Genetics (TAG) team at the Regeneron Genetics Center (RGC). Within the RGC, the Cardiometabolic TAG team is using massive scale human exome sequencing for discovery and validation of new therapeutic targets in obesity and obesity associated metabolic disease. The position holder will collaborate with various RGC teams and with pre-clinical and clinical development teams at Regeneron to accelerate therapeutic development for genetically-validated targets in obesity and metabolic disease via the generation of new human genetics and epidemiological insights.<br> </p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Accelerate therapeutic development for genetically-validated targets via the generation of new human genetics and epidemiological insights.</p></li><li><p>Generate key research questions and then design and execute studies and analyses to help address these questions, interpret the results of these studies and summarize ensuing insights in a variety of formats for different audiences (e.g. documents, presentations, patent applications, publications, etc.).</p></li><li><p>Understand and leverage RGC and Regeneron datasets, external resources and the scientific/medical literature to address key research questions at hand and summarize results giving appropriate weight to quantitative and qualitative strength of evidence.</p></li><li><p>Support target nominations and validation utilizing the RGC’s human genetics capabilities and leveraging Regeneron’s extensive internal therapeutics platforms and development modalities.</p></li><li><p>Partner with Clinical Development to evaluate clinical stage programs and opportunities for human genetics studies to aid in the selection of indications or evaluation of safety considerations.</p></li><li><p>Participate in the intellectual life of the Cardiometabolic TAG, the RGC and Regeneron at large and help build an inclusive work culture where everyone can perform at their best and fully develop their talent and potential.</p></li><li><p>Represent the Therapeutic Area Genetics team in cross-functional initiatives within RGC and Regeneron.</p></li></ul><p><strong>This job might be for you if you have:</strong></p><ul><li><p>Demonstrated ability to design and lead human genetics and epidemiological studies delivering medically-relevant findings in a team-based environment.</p></li><li><p>Ability to use medical knowledge to define relevant phenotypes for genetic association studies and to formulate innovative and important research questions. Familiarity with clinical genetics concepts and various genetic models of disease.</p></li><li><p>Strong computational and quantitative skills including ability to design and execute complex analyses using large scale datasets both with individual-level as well as result-level data (e.g. UK Biobank, All of US, MVP, Biobank Japan, meta-analysis of genome-wide summary statistics, etc). This includes proficiency with R or similar software and familiarity with high performance computing environments.</p></li><li><p>Experience leading complex human genetics research endeavors. Knowledge of different study designs and analyses including GWAS, exome or genome sequencing in cohort, case-control or family-based studies. Ability to integrate different data resources to translate initial findings.</p></li><li><p>Familiarity with the applications of genetics to gain medically-actionable insights including polygenic risk scores, quantitative traits analyses and Mendelian randomization.</p></li><li><p>Understanding of drug development and clinical trial design and execution. Experience as investigator in Randomized Controlled Trials is a plus. Experience in the clinical management or medical research relating to cardio-metabolic disease is not strictly required but is a plus.</p></li></ul><p>.</p><p><strong>To be considered for this role,</strong> you must have a MD with strong background in and knowledge of human genetics and genetic epidemiology. An outstanding candidate will be an MD/PhD with training and experience in translational human genetics, genetic epidemiology, epidemiology (or related disciplines) and strong quantitative skills.</p><p>#MDJOBSGG #MDJobs</p><ul></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$173,500.00 - $283,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, CMC Regulatory Affairs (Hematology/Oncology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45185]]></requisitionid>
    <referencenumber><![CDATA[R45185]]></referencenumber>
    <apijobid><![CDATA[r45185]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45185/associate-director-cmc-regulatory-affairs-hematologyoncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross-functional and external partners, and serving as a key liaison in regulatory authority interactions.</p><p>For US locations, this role is on-site 4 days in the office and 1 day from home. For Uxbridge, UK or Dublin, Ireland this role would be on-site 3 days per week and 2 days from home. A fully remote role is not possible for this position . If eligible, we can offer relocation benefits.</p><p><strong>A typical day may include the following: </strong><br>• Lead product development activities from a CMC regulatory standpoint with input from senior management.<br>• Represent CMC RA at program meetings and independently provide regulatory interpretation, position, and covering clinical development, initial market applications, and approval/post-approval activities.<br>• Identify program issues and develop appropriate regulatory strategies to mitigate risks to filings, independently find alternative solutions/work-arounds, and obtain consensus. <br>• Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.<br>• Lead and facilitate interactions with global regulatory authorities (e.g., meetings, IR responses, inspections).<br>• Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country-specific regulatory guidance documents; <br>• Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks.<br>• Develop and create working instructions, SOPs, and/or templates to facilitate consistent and efficient practice across the CMC RA groups.<br>• Identify gaps in the IOPS and global RA processes, bring up to higher management, and help to improve business efficiency.<br>• Support establishing, managing, and maintaining a knowledge base of current and emerging regulatory requirements and guidelines in the CMC field.<br>• Find opportunities to initiate operational changes and policy modifications.<br>• Manage and coach team member(s). </p><p><strong>This may be for you if you: </strong><br>• Have a strong grasp of CMC worldwide regulations and guidelines.<br>• Have been successful in building collaboration and teamwork across cross-functional teams.<br>• Can demonstrate a proven track record managing and mentoring people.<br>• Demonstrated skill in managing multiple priorities.</p><p><br>To be considered a bachelor’s degree with a minimum of 10 years of pharmaceutical/biotech industry experience, including 5+ years of relevant CMC experience. An advanced degree is preferred. Proven track record supporting biological products through development and approval is a distinct advantage. It is required to have a good understanding of current CMC worldwide regulations and guidelines. Experience in interacting with the US FDA and other regulatory authorities. Experience with device regulatory requirements and development processes for combination products is a plus.<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Scientist, Biologics Characterization]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45916]]></requisitionid>
    <referencenumber><![CDATA[R45916]]></referencenumber>
    <apijobid><![CDATA[r45916]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45916/sr-scientist-biologics-characterization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><br>Regeneron’s Product Biochemistry in Tarrytown, NY is seeking a motivated and innovative Senior Scientist to drive late-stage development (Phase II through commercialization) of biologics. You will develop and deploy analytical methods and purification strategies, enrich and characterize product variants, and help onboard new technologies that deepen product understanding and improve processes across the pipeline. This role is for you if you are scientifically creative, hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment.<br><br> </p><h3>Key Responsibilities:</h3><ul><li>Develop analytical methods and purification protocols to support extended characterization of therapeutic proteins and gene therapy vectors.</li><li>Conduct biochemical/biophysical characterization to support development, regulatory submissions, and commercialization.</li><li>Apply DOE, advanced statistics, and risk assessments to evaluate and optimize methods and processes.</li><li>Author high-quality technical documents (protocols, reports, memos) and contribute to regulatory sections and publications. Ensure timely documentation of experiments following established SOPs and guidelines.</li><li>Maintain instruments, troubleshoot issues, and improve lab/data workflows within your area of expertise. Adhere to procedures, guidance, and best practices to ensure lab safety.</li></ul><ul><li>Proactively identify process improvement opportunities across Product Biochemistry and Regeneron and help drive implementation.</li></ul><br><h3>A Typical Day in the Role Might Look Like:</h3><ul><li>Design and execute experiments to enrich, purify, and characterize size/charge variants, complexes, and high-concentration formulations.</li><li>Integrate learnings from internal data and external literature to make science-based study design recommendations.</li><li>Documents experiments, results and findings in electronic laboratory notebook; presents work at group and department meetings; contributes to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed articles for publication.</li><li>Lead or participate in technology initiatives and continuous improvement projects; may also mentor and guide junior analysts in a matrix-based environment.</li><li>Maintain instruments, troubleshoot instrumental/experimental problems, and order/maintain supplies.</li></ul><h3>This Role Might Be For You If:</h3><ul><li>Possess strong lab skills in protein separation, purification, and tangential flow filtration (TFF). Possess skills in protein/product identification using mass spectrometry.</li><li>Thrive in a fast-paced, team environment and can also work independently across multiple projects.</li><li>Demonstrate initiative, calculated risk-taking, and a passion for innovation and continuous improvement.</li><li>Communicate clearly, manage projects effectively, and solve complex problems with data-driven rigor.</li><li>Mentor others and contribute to a safe, efficient, and inclusive lab environment.</li></ul><p>This role requires a BS/MS/Ph.D. in Biochemistry/Biophysics, or related field plus 8-10 yrs+ (BS/MS) or 0-2 yrs+ of proven experience (Ph.D.). Technical proficiency in automated FPLC and/or HPLC (SEC, IEX, affinity), electrophoresis (capillary or microchip, SDS-PAGE, western blots), spectroscopy and light scattering is recommended. A fundamental understanding of protein structure/function, mass spectrometry, and immunology/immunogenicity preferred. Preference will be given to candidates who have experience working in the biopharmaceutical industry. Excellent oral and written communication skills and evidence of teamwork are required. This role is fully onsite.</p><p>The ideal candidate must have strong initiative to complete tasks, learn new technologies, and demonstrate a commitment to continuous learning. This role requires the ability to manage multiple priorities in a fast‑moving R&D environment, operate effectively both independently and within a collaborative team environment, and communicate clearly, transparently, and in a timely manner with key stakeholders.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Data Science]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46197]]></requisitionid>
    <referencenumber><![CDATA[R46197]]></referencenumber>
    <apijobid><![CDATA[r46197]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46197/process-development-engineer-iii-data-science/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Data Enablement and Analytics (DEA) team within Preclinical Manufacturing and Process Development (PMPD) is seeking a Machine Learning Engineer to develop, build and deploy analyses and machine learning models that support bioprocess development. This role is ideal for a data scientist with a strong foundation in chemical or biomedical engineering and a passion for building impactful solutions in close collaboration with scientists and process engineers.</p><p>You will work at the intersection of software engineering, data science, and bioprocess domain expertise—developing models that will be put into action within PMPD’s laboratory and manufacturing operations. You will mentor and coordinate citizen data scientists. Your work will streamline workflows, enable automation, and accelerate decision-making across PMPD.</p><h3>A Typical Day in the Role Might Look Like:</h3><ul><li><p>Partner closely with scientists, engineers, and analysts to understand bioprocess workflows and identify high‑impact data science opportunities.</p></li><li><p>Acquire, clean, and structure complex datasets to enable scalable, repeatable analyses.</p></li><li><p>Design, develop, and apply advanced analytics and machine learning models to drive data‑informed decision‑making.</p></li><li><p>Deploy models into production environments, enabling automated and autonomous operations where appropriate.</p></li><li><p>Lead, mentor, and coordinate citizen data scientists on critical initiatives across PMPD</p></li><li><p>Enhance, maintain, and extend existing analytics tools and platforms to support new use cases and evolving business needs.</p></li><li><p>Contribute as an active member of Agile teams within a Scaled Agile Framework, supporting planning, delivery, and continuous improvement.</p></li><li><p>Continuously evaluate emerging technologies and methodologies to strengthen data science capabilities within the organization</p></li></ul><h3>What You Bring</h3><ul><li><p>Bachelor’s or Master’s degree in Chemical Engineering, Biomedical Engineering, or a related discipline. 5-7 years of experience in bioprocess development, pharmaceutical manufacturing, or a closely related domain.</p></li><li><p>Demonstrated ability to apply machine learning and predictive analytics to complex, real‑world problems.</p></li><li><p>Strong programming skills in Python and SQL, with a solid understanding of data modeling and database design.</p></li><li><p>Experience working in Linux/Unix environments and using Git for version control and collaboration.</p></li><li><p>Excellent communication skills and a collaborative mindset, with the ability to partner effectively with scientists, engineers and analysts, while mentoring citizen data scientists.</p></li><li><p>Familiarity with DevOps and deployment technologies such as Kubernetes, NixOS, and Jenkins.</p></li><li><p>Experience with Operational Technology and analytics platforms (e.g., PI Historian, OPC, MQTT, Dataiku, Seeq) is a plus.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Commercial Martech & Field Enablement Lead]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46228]]></requisitionid>
    <referencenumber><![CDATA[R46228]]></referencenumber>
    <apijobid><![CDATA[r46228]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46228/executive-director-commercial-martech-field-enablement-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a transformative and strategic senior leader with a wealth of diverse experience to work in close collaboration with BU SVPs and VPs and their leadership teams to develop and lead the vision, strategy, and execution for field-facing colleague engagement and operations to enable exceptional colleague and customer experiences.</p><p>This individual will be responsible for significantly elevating the enablement of customer-facing teams and a critical focus of this role is modernizing systems, capabilities and effectiveness through MarTech (Marketing Technology) solutions, including CRM systems, AI-driven tools, and digital engagement platforms.</p><p>This leader will ensure that technology investments are aligned with business priorities, enhance field enablement, and deliver measurable outcomes. The role requires close collaboration with not only Business Unit leaders but also with enablement leaders such as IT, SI&A, and Market Access. Responsibilities will also be to design and oversee institution of new programs and offerings as well as the development and implication of required behavior change solutions to ensure transformations are adopted, effectively integrated into work flow, and optimized to deliver continuous improvement in service of the business.</p><br><h3><strong>A Typical Day Might Look Like This:</strong></h3><br><p>MarTech Strategy & Enablement:</p><ul><li>Develop and implement a comprehensive <strong>MarTech strategy</strong> to optimize CRM systems, AI-driven initiatives, and digital engagement platforms for field enablement.</li><li>Lead the implementation and integration of CRM technology to support pre-call planning, next-best-action recommendations, and first-call resolution (FCR). Role will also require designing well-rounded engagement solutions to harness entire x functional customer facing team</li><li>Prioritize technology investments based on business needs, ensuring alignment with BU priorities and organizational goals.</li><li>Oversee enablement for AI-driven solutions that enhance customer engagement, improve field productivity, and deliver actionable insights.</li><li>Collaborate with IT, SI&A, and commercial operations teams to ensure seamless integration of tools and technologies into field workflows.</li><li>Drive adoption and utilization of MarTech solutions across field teams, ensuring measurable improvements in engagement effectiveness and operational efficiency.</li><li>Partner with training teams to ensure field colleagues are equipped to harness MarTech tools effectively in their daily activities.</li></ul><p>Strategy & Vision:</p><ul><li>Define and communicate the long-term vision for field enablement and engagement strategy across businesses, ensuring alignment with each BU</li><li>Develop a well-rounded strategy for how field-facing colleagues engage customers (HCPs, institutions, payers, and how the organization supports them through tools, training, CRM, and processes.)</li><li>Translate vision into a prioritized roadmap, outlining capabilities, tools, processes, and metrics to optimize over the next 1-3 years.</li><li>Collaborate with BU and enablement leaders to identify business priorities and ensure enablement initiatives address specific needs while maintaining appropriate consistency.</li><li>Design, implement and optimize system for ongoing behavior change to ensure effective adoption and utilization of solutions</li></ul><p>Field Enablement & Excellence:</p><ul><li>Lead enablement initiatives for customer-facing colleagues, ensuring they have the tools, processes, and support to deliver differentiated engagements.</li><li>Partner closely with training teams to design and implement programs that address role-specific needs and capabilities, ensuring effective adoption and readiness.</li><li>Define metrics and success criteria and oversee and monitor performance of new solutions</li><li>Drive continuous improvement by identifying gaps in performance or engagement quality and leading interventions such as training (in partnership with training team), process redesign, or technology upgrades.</li><li>Develop operational standards and make recommendations to optimize customer engagements</li></ul><p>Engagement Strategy:</p><ul><li>Codify role scope, remits and ways of working across functions and business units (xRole and xBU), ensuring alignment and consistency in engagement approaches where appropriate.</li><li>Support the voice of the customer in the organization, ensuring that we understand the needs of HCPs, institutions, payers, and other pharma customers so they can receive meaningful, consistent, high-quality engagements.</li><li>Partner with commercial, medical, marketing, and enablement teams to ensure a seamless, supportive, and compliant engagement journey that differentiates the company from competitors.</li><li>Lead initiatives to design or optimize engagement models, feedback loops, and metrics.</li><li>Ensure governance and compliance appropriate to the pharmaceutical industry, including adherence to promotional regulations, data privacy standards, and HCP engagement codes.</li><li>Oversee the end-to-end healthcare provider (HCP) experience, ensuring interactions are seamless, supportive, and impactful.</li></ul><p>Cross-Functional Leadership & Execution:</p><ul><li>Act as a senior partner across the business, collaborating with leaders in Marketing, Sales, Medical Affairs, Access, Commercial Operations, Compliance, IT/Analytics, and others to ensure alignment of enablement and engagement strategy with business plans.</li><li>Lead and develop a small and high-performing team, fostering a culture of excellence, accountability, and continuous learning.</li><li>Oversee budgeting, resource allocation, vendor/agency relationships, and execution of major projects and initiatives.</li></ul><h3><strong>This role may be for you if</strong><strong>:</strong></h3><ul><li>You have expertise in CRM technologies, digital engagement solutions, and data/analytics to drive enablement effectiveness.</li><li>You are an exceptional cross-functional collaboration skills, influencing at senior levels, and strong communication and executive presence.</li><li>You demonstrated ability to lead teams, manage change, optimize processes, scale operations, and thrive in a dynamic, regulated environment.</li></ul><p>To be considered you have a Bachelor’s degree required; MBA or advanced degree preferred. You bring at least 15 years of dynamic experience in the pharmaceutical or biotech industry, with significant leadership experience in commercial, field, enablement, or engagement roles. IT experience, either in role or as part of cross functional team, preferred. You bring a proven track record of developing and implementing enablement, field excellence, and MarTech strategies, particularly CRM and AI-driven solutions, in pharma or life sciences (or analogous regulated industries).</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Program Management Process and Standards]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46277]]></requisitionid>
    <referencenumber><![CDATA[R46277]]></referencenumber>
    <apijobid><![CDATA[r46277]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46277/director-program-management-process-and-standards/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Director, Development Program Operations</strong> will have a leadership role in the building and optimization of the Strategic Program Team’s (SPTs) operating model and Development capabilities (processes, tools, services) that contribute to the company’s performance and operational excellence. Under this role’s leadership, the team is accountable for generating actionable insights and recommendations to senior leadership to drive how we scale our operating model, for example our team membership composition, roles/responsibilities, deliverables.</p><p>Additionally, this role is responsible for designing, building and managing cross-functional business-critical initiatives that drive the acceleration of portfolio delivery. These initiatives require strong matrix leaders with drug development and business acumen and are passionate about applying robust strategic change execution methods and best practices. The role will need to anticipate business needs through strategic planning and trend analysis and with alignment of key stakeholders across Development with interfaces in Research, Manufacturing and Commercial. Operates with a continuous improvement mindset to enable cross functional operational efficiencies.</p><p>This role is a hands-on contributor and people manager responsible to build relationships at all levels of the organization in order to solicit and action stakeholder input regarding the SPT operating model. This role will navigate the fast-paced and agile environment of Regeneron in a collaborative and innovative manner.</p><p><em>***Note: this role requires 4-days onsite in either Tarrytown, NY or Warren, NJ and is not eligible fully remote. </em></p><p><strong>A typical day in this role looks like: </strong></p><ul><li>Identify, create and drive strategic initiatives related to the DPM and SPT operating model with direct impact to drive Development portfolio and pipeline </li><li>Partner with Program and Portfolio Management (PPM) Leadership Team and Development functional areas to monitor and measure implementation impacts and take action when needed </li><li>Develop, maintain and implement project/program management methodology, including processes, tools, metrics and policies to ensure efficiency, quality and business success </li><li>Drive consistency and standardization across program strategy execution and ensures compliance to the application of these execution methodologies and standards </li><li>Design and implement the operating cadence, including running coordination meetings, project updates and overall oversight of projects </li><li>Work with Development and PPM Leadership to define innovative operational Key Performance Indicators (KPIs) for the projects and services delivered, tracking these KPIs across the department and projects to ensure goals are consistently achieved </li><li>Build strong, interdependent partnerships and manages the communication effectively with functional area heads in Development, key stakeholders in Research, Commercial and Manufacturing </li><li>Responsible for the coaching and development of department members as well as ensuring that the organizational strategy delivers the skills, capabilities and processes that enable portfolio delivery are present in his/her team </li></ul><p><strong>This role may be for you if you have: </strong></p><ul><li>Significant experience in the biotechnology or pharmaceutical industry with a strong understanding of drug development activities in context of line functions and project teams </li><li>Consulting experience and experience with developing a Project Management Office (PMO) is desirable </li><li>Proven experience in a similar role; understanding of Operational Excellence, Six Sigma/LEAN and business process management preferred </li><li>Proven leadership skills with the ability to innovate and drive framework and change in a matrixed environment, amidst ambiguity </li><li>Lead the department with a customer-first demeanor </li><li>Strong analytical, problem-solving and strategic thinking abilities </li><li>Strong organizational and multitasking abilities, overseeing multiple projects simultaneously </li><li>Excellent interpersonal skills with a proven ability to negotiate, influence and work effectively with individuals at all levels of the organization, including senior leadership </li><li>Excellent communication skills (written/verbal), including presenting complex information and insights effectively </li><li>Experience in building and leading high performing teams and driving cross-functional initiatives </li><li>IT proficiency with MS software and project management tools, analytics and visual reporting applications (e.g. SharePoint, MS Project, PowerPoint, Word, Excel, PowerBI, etc) </li><li>Ability to travel (<10%) </li></ul><p><strong>In order to be considered qualified</strong>, a minimum of a Bachelor’s degree (Bachelor of Science) and 12+ years industry experience with a minimum of 5+ years in project management experience required. MBA preferred. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Aggregate Reporting Management]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46482]]></requisitionid>
    <referencenumber><![CDATA[R46482]]></referencenumber>
    <apijobid><![CDATA[r46482]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46482/senior-manager-aggregate-reporting-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Regeneron's Patient Safety organization is seeking a Senior Manager, Aggregate Reporting Management to join our team!</p></div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><p>This position in the Global Patient Safety (GPS) Operations is responsible for management of aggregate safety reporting activities across all phases of the product lifecycle. This role supports the consistent, compliant, and scientifically robust preparation, distribution and submission of periodic and ad-hoc safety reports to health authorities, collaborators and contract research organizations worldwide.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Drives preparation, development and maintenance of Aggregate Reporting (i.e., PSURs/PBRER, PAER, DSURs, Local Periodic Reports, SUSARs) Deliverables</p></li><li><p>Leads Aggregate Report planning, production and distribution activities across GPS and other functions across US, EU, Japan and other ICH regions, as well as non-ICH regions</p></li><li><p>Provides expertise and guidance to authors and contributors of aggregate reports</p></li><li><p>Maintains compliance metrics and contributes to implementation of Quality Events and Corrective Action and Preventive Action (CAPA) for non-compliance</p></li><li><p>Implements effective structure, procedures and tools to ensure aggregate reports and other functional deliverables are completed timely and with high quality</p></li><li><p>Develops and oversees functional specifications of data requirements for aggregate deliverables from the safety and clinical databases</p></li><li><p>Collaborates with Global Patient Safety (GPS) and with other functional areas (Epidemiology, Clinical Development, Regulatory Affairs, Statistics, etc.) contributing to aggregate safety reports</p></li><li><p>Acts as subject matter expert during audits and inspection.</p></li><li><p>Provides oversight, and training as needed of CRO respective activities in support of high quality and timely aggregate reports</p></li><li><p>Acts as a functional vendor management overseeing and driving high quality outputs from our vendors</p></li><li><p>Develops and maintains aggregate report procedural package (SOPs, Work Instructions), reports’ templates, KPIs</p></li><li><p>Drives process improvement through automation and other tech initiatives.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor’s degree required (advanced degree or HCP‑focused background preferred) and 5+ years of Pharmacovigilance experience, with a demonstrated focus on Aggregate Safety Reporting.</p></li><li><p>Project management experience strongly preferred, PMP preferred</p></li><li><p>Experience with health authority inspections (PV and GCP)</p></li><li><p>Medical writing experience with regulatory documentation</p></li><li><p>Strong project management skills</p></li><li><p>Excellent strategic decision-making and analytical skills</p></li><li><p>Strong communication and writing skills</p></li><li><p>Strong understanding of Scientific content</p></li><li><p>Proven experience with technology implementations allowing for streamlined process execution.</p></li></ul><p>#GDPSJobs</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Manager, Medical Device Quality Assurance]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47283]]></requisitionid>
    <referencenumber><![CDATA[R47283]]></referencenumber>
    <apijobid><![CDATA[r47283]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47283/sr-manager-medical-device-quality-assurance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>Regeneron is currently seeking a Senior Manager, Medical Device Quality Assurance (QA) to join our Medical Device QA team. This expanded leadership role will provide QA oversight across two critical functions: Combination Products Sustaining Engineering and Compliance. The position will lead a team engineer and quality specialists.</p><p>When & where:</p><ul><li>Monday-Friday, 8am-4:30pm</li><li>Location: East Greenbush, New York, United States</li></ul><p>What you'll do:</p><ul><li>Manage, mentor, and develop quality engineering and compliance teams</li><li>Standardize, streamline, and improve processes across sustaining and compliance</li><li>Implement digital, data-driven tools for accurate, consistent, and timely reporting</li><li>Lead teams through complex, ambiguous challenges in a pharmaceutical/medical device environment</li><li>Sustaining Engineering Support:<ul><li>Support sustaining engineering programs through risk assessment, design change management, and maintenance of the Design History File and Risk Management File</li><li>Advice and actively participate in Design Reviews associated with combination products</li><li>Provide QA and technical support to quality engineers and project teams during ongoing maintenance of the combination product</li><li>Interact with partners and contract organizations to ensure accurate completion of project milestones, including post-commercialization activities</li></ul></li></ul><ul><li>Combination Product Support:<ul><li>Act as Management Representative for the combination products QMS; own policies and procedures</li><li>Support regulatory inspections and partner audits for combination products</li><li>Keep the QMS current and inspection-ready via monitoring, gap assessments, and updates</li></ul></li></ul><p>This role requires:</p><ul><li>B.S in Engineering and 8+ years of experience; including combination product or medical device experience; or equivalent combination of education & experience</li><li>Previous supervisory/ people leadership experience</li><li>Knowledge of the combination device development and lifecycle process</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Part_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Accountant, Corporate Accounting]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47371]]></requisitionid>
    <referencenumber><![CDATA[R47371]]></referencenumber>
    <apijobid><![CDATA[r47371]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47371/staff-accountant-corporate-accounting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Staff Accountant who is a collaborative team member, communicates effectively with colleagues, thrives in a dynamic environment, and is eager to take on challenges and contribute to Regeneron's growth.</p><p>This position will perform accounting duties primarily within the Product Revenue and SG&A expense areas. Responsibilities include timely completion of activities within the monthly and quarterly close process, such as recording journal entries and preparing revenue, expense, and balance sheet account analyses. This is a highly visible role that works closely with Accounting, Finance, Commercial, Trade, and other departments to gather information, prepare schedules, and ensure accurate accounting for assigned areas.</p><p><strong>A Typical Day in the Role Might Look Like</strong><strong>:</strong></p><p><strong> </strong></p><ul><li><p>Perform Product Revenue accounting activities, including journal entries for sales, gross‑to‑net deductions, and receivables; balance sheet reconciliations; and detailed trend analysis of product sales‑related deductions</p></li><li><p>Prepare SG&A expense schedules and balance sheet account reconciliations for assigned areas</p></li><li><p>Partner with Finance to ensure completeness and accuracy of accruals and reclasses</p></li><li><p>Ensure compliance with the Company’s Prepaid Expense Accounting Policy and other relevant accounting policies</p></li><li><p>Perform fluctuation analyses and prepare variance explanations for Management</p></li><li><p>Maintain knowledge of and compliance with Company accounting policies and internal controls</p></li><li><p>Support compliance with Sarbanes‑Oxley (SOX) requirements, including maintaining documentation and supporting control execution</p></li><li><p>Assist with internal and external audit requests, as needed</p></li><li><p>Support cross‑functional requests and initiatives related to areas of responsibility</p></li><li><p>Participate in the Oracle Fusion Cloud Financials ERP implementation, including user acceptance testing (UAT) and updates to process documentation and workpapers</p></li><li><p>Assist with special projects, analyses, and process improvement initiatives, as needed</p></li></ul><p><strong>This Role May Be for You If You:</strong></p><ul><li><p>Are a team player who collaborates effectively, thinks independently, and proactively proposes solutions with a continuous improvement mindset</p></li><li><p>Have a solid understanding of accounting principles and can apply them to real‑world operational processes</p></li><li><p>Are analytical and able to organize and interpret large data sets to support sound accounting conclusions</p></li><li><p>Have strong organizational skills and a high level of attention to detail and accuracy</p></li><li><p>Can operate in a fast‑paced environment and comfortably manage multiple priorities</p></li><li><p>Have strong written and verbal communication skills</p></li></ul><p>To be considered for this role, you must have a Bachelors degree in Accounting or Finance and 2+ years of relevant accounting experience. Prior product revenue (gross to net) accounting experience preferred. Big 4 Accounting experience and CPA or CPA track are preferred. High proficiency with Microsoft applications is required, specifically Microsoft Excel. Experience with Oracle GL, SmartView, and Hubble are a plus.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Immunology & Inflammation]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47486]]></requisitionid>
    <referencenumber><![CDATA[R47486]]></referencenumber>
    <apijobid><![CDATA[r47486]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47486/associate-scientist-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Immunology and Inflammation group is seeking an Associate Scientist to support the development of therapeutics for autoimmune disease. This role involves joining a highly collaborative team working in autoimmunity, immune cell biology, and tissue immunity. You will have the opportunity to engage in cutting edge immunological research as part of our discovery efforts and to contribute to human health. </p><p><strong>As an Associate cientist in the Immunology and Inflammation group, your typical day might include: </strong></p><ul><li><p>Handling and caring for mice, including performing procedures such as blood and/or tissue sample collection or injections (IP, IV and subcutaneous) </p></li><li><p>Processing of organs for immune cell isolation and analysis </p></li><li><p>Maintaining, expanding, and/or modulating cells in vitro </p></li><li><p>Evaluating cell phenotypes and function using ex vivo or in vitro assays such as flow cytometry and immunoassays. </p></li><li><p>Analysis of data using biological and statistical software such as Flowjo, OMIQ, Excel, Prism </p></li><li><p>Close collaborative interactions with teams across the organization </p></li><li><p>Documentation of experimental procedures and results </p></li></ul><p><strong>This role may be for you if you: </strong></p><ul><li><p>Enjoy working in an innovative and team-driven environment </p></li><li><p>Are highly organized, detail-oriented, and motivated, with a creative approach to problem-solving. </p></li><li><p>re adaptable, flexible, and enjoy learning new techniques or switching tasks as needed. </p></li><li><p>Are excited to contribute to the development of novel therapeutics </p></li><li><p>Communicate openly and frequently with manager and team members </p></li></ul><p><strong>To be considered for this role, you should have </strong></p><ul><li><p>B.S. or M.S. degree in a relevant field with 0-2 years of experience in immunology or a related discipline. </p></li><li><p>Experience in tissue culture, cell-based assays, flow cytometry, or immunoassays (e.g. ELISA, MSD, Luminex), as well as proficiency in basic computer applications and experience with biological data collection and analysis highly preferred </p></li><li><p>Experience in mouse handling is highly preferred. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists - Hematology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47538]]></requisitionid>
    <referencenumber><![CDATA[R47538]]></referencenumber>
    <apijobid><![CDATA[r47538]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47538/medical-account-specialists-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Washington]]></city>
    <state><![CDATA[Washington]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if: </strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Great Lakes]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47579]]></requisitionid>
    <referencenumber><![CDATA[R47579]]></referencenumber>
    <apijobid><![CDATA[r47579]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47579/regional-director-neurology-great-lakes/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Michigan]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the Great Lakes Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Great Lakes (Michigan, Indiana, Illinois and Wisconsin)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Dir GPO & Account Management - South Central]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47596]]></requisitionid>
    <referencenumber><![CDATA[R47596]]></referencenumber>
    <apijobid><![CDATA[r47596]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47596/dir-gpo-account-management-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Ophthalmology Account Director (OAD) - South Central (AL, AR, FL, GA, LA, MS, TX, TN & VA)</strong></p><p>The Ophthalmology Account Director (OAD) will represent the entire Regeneron ophthalmology product portfolio. The OAD connects to the key business decision-makers and all other relevant Key Opinion Leaders (KOLs) within their assigned accounts and will be a critical liaison between their customers and Regeneron. Leveraging their account and contract management capabilities, the OAD will be required to lead and appropriately educate and influence customers including large provider practices and private equity groups, as well as internal audiences including senior Regeneron Market Access, Brand and Executive leadership teams.</p><p>Working in the context of an integrated account business plan, the OAD will play an important account management role working both independently and closely with the ED Ophthalmology Accounts to educate on, administer, and pull-through provider contracts as well as other partnership opportunities targeted at financial, operational, and other relevant business decision-makers and their teams. The OAD will be an expert in customer engagement and contract management and will work closely with other Regeneron internal team members within Market Access and the Brand sales force.</p><p>Additionally, OADs will have a strong understanding of the customer healthcare environment and will play a pivotal role not only in effective customer and contract education and management, but also in navigating both the external complexity and the internal dynamics of product and customer priorities. The OAD will represent current and potentially future contracted ophthalmology products within their customer base and provide relevant customer feedback to internal stakeholders and leadership in a timely manner.</p><p><strong>In this role, a typical day includes:</strong></p><ul><li>MBO Driven, customer facing role</li><li>Focused on maximizing customer executive engagement, reach and frequency, and contract education and pull-through efforts within assigned customers and geography to help customers and patients understand the GPO contracts</li><li>Works collaboratively as a partner with Sales, Marketing, Reimbursement, and other internal colleagues to appropriately and efficiently develop and execute account plans for assigned customers within their assigned geography</li><li>Seeks to maximize depth of customer engagements by identifying, engaging, and educating all relevant audiences at the customer about the GPO program including as appropriate C-suite, KOLs, and business and reimbursement staff</li><li>Thoroughly explains quarterly GPO program changes, if any, to customers</li><li>Delivers regular contract performance updates to customers</li><li>Performs quarterly business reviews with customers</li><li>Seeks customer feedback on the Regeneron GPO program and shares with Market Access and Brand leadership</li><li>Looks for opportunities to engage customers at regional and national retinal meetings</li><li>Fully understands other elements of customer considerations such as payer mix, ensure customer awareness of existing inventory levels, operational challenges, and reimbursement dynamics</li><li>Spends 75% of time in customer facing activities, prioritizing in-person meetings when possible</li></ul><p><strong>To be considered for this role you must have</strong></p><ul><li><p>10-12 years of "progressive" industry/relevant professional experience</p></li><li><p>10+ years of pharmaceutical/biotech or related experience</p></li><li><p>Additional broad-based experience valued: sales operations, corporate partnerships, marketing, and/or sales management, and/or supply chain.</p></li><li><p>Previous experience in launching new Specialty Pharmaceutical/Biologics products or indications. Proven knowledge and relationships with key Executive level decision makers from retina and other market GPOs and institutional trade partners. Prior retina account or brand experience. Demonstrated ability to work collaboratively with and influence peers and management. Demonstrated communication skills, including presentation, negotiation and content development. Demonstrated results orientation. Demonstrated strategic planning capabilities, including event planning and meeting facilitation. Understanding of financial concepts and contracting issues and demonstrated ability to measure contract performance. Demonstrated outsourced vendor management skills.</p></li><li><p>Ability to travel 50-75%, including weekends as necessary.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II, Analytical Sciences: Synthetic and Bioconjugation Scale-Up Technologies (SBST)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47643]]></requisitionid>
    <referencenumber><![CDATA[R47643]]></referencenumber>
    <apijobid><![CDATA[r47643]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47643/process-development-engineer-ii-analytical-sciences-synthetic-and-bioconjugation-scale-up-technologies-sbst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Preclinical Manufacturing & Process Development (PMPD) organization in Tarrytown, NY is seeking a highly motivated <strong>Process Development Engineer II</strong> to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics group. In this role, you will serve as the analytical lead to develop fit-for-purpose analytical methods to characterize critical intermediates (small molecules, siRNA, and/or peptides) to support our growing and diverse bioconjugate pipeline. You will lead and implement analytical deliverables working closely with cross-functional teams and external collaborators (CDMOs) to advance bioconjugate programs from development to commercialization.</p><p><em><strong>A Typical Day in the Role of Process Development Engineer II Might Look Like:</strong></em></p><ul><li><p>Design and execute analytical testing, method development and characterization of critical intermediates to enable bioconjugate development.</p></li><li><p>Compile, analyze, and interpret complex datasets; connect key findings across experiments and propose clear, actionable next steps.</p></li><li><p>Communicate results and recommendations clearly to technical and non-technical audiences to enable timely, data-driven decisions.</p></li><li><p>Serve as the analytical lead for critical intermediates and bioconjugates; coordinate internal and external analytical deliverables (development, transfer, and troubleshooting) to support program milestones.</p></li><li><p>Provide technical support and troubleshooting to receiving labs to keep analytical activities off the critical path.</p></li><li><p>Author high-quality documentation (e.g., procedures, method development reports, characterization reports, ELN entries) to support program timelines.</p></li><li><p>Build and improve business workflows for documentation standardization, data digitization, and sample management.</p></li><li><p>Maintain compliance with lab and environmental safety and promote a safe lab culture.</p></li><li><p>Support equipment upkeep, troubleshooting, maintain an organized workspace, and proactively plan for lab resources.</p></li><li><p>Train and mentor peers and junior team members as needed (directly and/or indirectly).</p></li></ul><p><em><strong>This Role May Be For You If You:</strong></em></p><ul><li><p>Enjoy hands-on lab work and consistently generate high-quality, reproducible data.</p></li><li><p>Take initiative, deliver on challenging work, and learn new technologies quickly.</p></li><li><p>Have hands-on experience with analytical techniques for synthetic molecules (i.e., peptide, siRNA, and small-molecule) characterization and relevant software’s.</p></li><li><p>Possess a customer-centric mindset to analytical development and understand how analytical deliverables enable program decisions across drug development in different phases of the program</p></li><li><p>Thrive in a fast-paced, highly collaborative environment working on complex problems.</p></li><li><p>Communicate clearly (written and verbal), simplify messages for impact, and build strong working relationships.</p></li><li><p>Think critically and apply strong problem-solving skills, and comfortable navigating ambiguity.</p></li></ul><p>This role requires B.S. with 6+ years of relevant experience, or M.S. with 4+ years of relevant experience, in analytical chemistry, biochemistry, biology, chemical engineering, or a related field. Hands-on experience with analytical method development for synthetic molecules (e.g., small molecules, PEG, peptides, and/or oligos), i.e. electrophoresis, HPLC, MS, UV spectroscopy and associated software (e.g., Empower). Experience transferring methods to internal/external development labs, and troubleshooting. Demonstrated experience serving as an analytical lead, working with internal teams and external CDMOs. Strong written and verbal communication skills, including the ability to present data clearly to diverse audiences. Ability to work with minimal guidance and collaboratively across cross-functional teams, with strong attention to detail and documentation practices. Demonstrated initiative, learning agility, and a growth mindset in a fast-paced environment. Experience with antibodies and/or bioconjugates is strongly preferred.</p><p><strong> #pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Quality Control Scientist (Chemistry)]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46048]]></requisitionid>
    <referencenumber><![CDATA[R46048]]></referencenumber>
    <apijobid><![CDATA[r46048]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46048/principal-quality-control-scientist-chemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Sr Quality Control Scientist in the Technical Resources Department. This position performs assay development, characterization, optimization, transfer, validation, and investigations for QC. You would provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.</p><p>As a Sr QC Scientist for Chemistry in the Technical Resources Department, a typical day might include the following:</p><ul><li><p>Performs assay development/validation for QC.</p></li><li><p>Reviews new test procedures and assays.</p></li><li><p>Evaluates and bring in new methodologies/techniques when needed.</p></li><li><p>Facilitate assay transfer from R&D and to business partners</p></li><li><p>Organize analytical assay transfer internally and externally.</p></li><li><p>Set product specification.</p></li><li><p>Participates in technical troubleshooting and problem investigation.</p></li><li><p>Review analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance.</p></li><li><p>Participates in training programs for analysts.</p></li></ul><p>This job might be for you if:</p><ul><li><p>You have in-depth knowledge with HPLC based assays.</p></li><li><p>You like dealing with technical issues, troubleshooting, and constant change</p></li><li><p>You are a team player who can work with a variety of different people on different tasks</p></li><li><p>You have strong written and verbal communication skills</p></li><li><p>You enjoy mentoring and training others on systems, processes and problem solving</p></li><li><p>You enjoy working in a fast-paced environment and are flexible to changing requirements</p></li><li><p>You can take on new and sometimes ambiguous challenges and learn quickly</p></li></ul><p>To be considered for a Sr QC Scientist (Chemistry) Technical Resources role you must have a BS in Chemistry, Biochemistry, Biology, or a related field, and 6+ years of relevant experience. Higher level degree preferred.</p><p>Experience with cell or gene therapy in a Biopharmaceutical environment is strongly preferred.</p><p>Level is determined based on experience relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Dermatology-New Jersey / Queens / Brooklyn]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47898]]></requisitionid>
    <referencenumber><![CDATA[R47898]]></referencenumber>
    <apijobid><![CDATA[r47898]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47898/associate-director-field-medical-affairs-dermatology-new-jersey-queens-brooklyn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs, you will play a pivotal role as a field-based professional within Dermatology. Use your expertise that will provision the business objectives across the product life cycle. We deliver strategic and operational support by establishing, developing, maintaining scientific exchange with medical specialists, health care professionals, and payers, aligned with our strategic objectives. We provide clinical and health economic information that enhances the value and appropriate use of Regeneron products. You will work on clinical research sites and investigators, and support of research activities as directed by the Global Medical Functional head.<br> <br>Responsibilities of this role are to ensure accurate exchange and distribution of clinical and scientific information relevant to in-line and pipeline products in a timely, ethical and customer-focused manner</p><p>Territory: New Jersey, Brooklyn, Queens<br><br>A typical day may include<br>•Engaging in scientific discussions with medical and scientific specialists, including Healthcare Professionals and population health decision makers (“payers”) consistent with Medical Affairs objectives.<br>•Demonstrates deep scientific expertise about assigned molecules/products and the associated therapeutic area to exchange relevant information and insights with specialists within a region<br>•Builds and develop relationships with key external scientific and medical specialists and organizations in a region to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape<br>•Shapes and executes local medical strategy based on Global Medical Affairs strategy within planned timelines<br>This may be for you if:<br>•Enjoy working independently in the field, while having an impact on the company’s mission.<br>•You are passionate about developing knowledge of and sharing clinical scientific data<br>•You like working corroboratively and developing relationships in academic and clinical practice settings<br>•You have the innate ability to balance multiple initiatives, prioritize them and execute them independently, while excelling at keeping all partners advised and engaged </p><p>To be considered for this position, you must have a Clinical/Science Degree required (e.g., MD, PharmD, PhD) with a minimum of 5 years related work experience (clinical, managed care, or industry experience). Experience in Immunology, Respiratory, or Dermatology is preferred as is experience as a field medical representative. It is required to have the ability to communicate and disseminate scientific and clinical data. Residency in the territory is required.</p><p>#msl #medicalscienceliaison</p><p>#i&I<br><br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager - Pulm/Gastro (Knoxville,TN)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48092]]></requisitionid>
    <referencenumber><![CDATA[R48092]]></referencenumber>
    <apijobid><![CDATA[r48092]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48092/field-reimbursement-manager-pulmgastro-knoxville-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Knoxville]]></city>
    <state><![CDATA[Tennessee]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p><strong> </strong></p><p>The Field Access & Reimbursement environment for specialty biologics has proven to be highly challenging for HCPs and Patients. Payer Formularies and restrictive Utilization Management Criteria including: Prior Authorization Processes, Step Edits, Appeals, detailed Clinical Documentation, Peer to Peer reviews etc., requires dedicated and focused customer facing support through the Reimbursement Management Team.</p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. The primary purpose of this role is to support Health Care Practitioner offices in obtaining appropriate access to Regeneron products for patients. Ensuring optimal access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron product portfolio. Support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate across multiple internal stakeholders, sales teams, Payer teams, Alliance partners, HUBs, etc. The Field Reimbursement Management reports to the District Manager of Field Market Access. </p><p>Regeneron has an Alliance partner for commercializing Dupixent. As a result, members of the Regeneron Field Reimbursement Team must demonstrate the ability to in a proactive and highly collaborative environment across an Alliance team. </p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: <strong>Knoxville, TN, Chattanooga, TN, and Johnson City, TN) </strong></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</p></li><li><p>Execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</p></li><li><p>Execute against established performance parameters and monitor personal performance against these agreed parameters:</p></li><li><p>Work closely with REGN and Sanofi partners as assigned; REGN and Sanofi District Sales Managers, Medical Specialists, other FRM, Reimbursement, Marketing and Access team members in assigned geographical areas to ensure optimal coverage and customer knowledge of this process and all REGN patient services within defined accounts</p></li><li><p>Provide appropriate process, payer, and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products, in efforts to streamline the coverage and specialty pharmacy processes to obtain alliance products</p></li><li><p>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</p></li><li><p>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that complies with Regeneron policies, processes, and standard operating procedures</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s Degree. Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience.</p></li><li><p>Experience working with products delivered through a Specialty Pharmacy network is critical.</p></li><li><p>Knowledge of CMS policies and processes with expertise in Part D (Pharmacy Benefit design and coverage policy).</p></li><li><p>Assist in providing appropriate field insights throughout the development of Market Access marketing support materials as needed</p></li></ul><ul><li>Ensure individual training and knowledge is maintained to the level required to guarantee that personnel are seen as the most knowledgeable team in the industry as it pertains to access and reimbursement across Alliance therapeutic areas as well as future product markets</li><li>This is a field-based position. Candidates must live within the geographical territory that includes Knoxville, TN, Chattanooga, TN, and Johnson City, TN.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison  - Neurology (South Central)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48121]]></requisitionid>
    <referencenumber><![CDATA[R48121]]></referencenumber>
    <apijobid><![CDATA[r48121]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48121/associate-director-thought-leader-liaison-neurology-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Neurology Marketing team. It will be focused on enhancing and improving interactions with key external US Neurology thought leaders at academic centers and leading community practices for our neurology product.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Neurology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><p><strong>The typical day may include the following:</strong></p><ul><li>The Neurology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You possess a strong science background with deep knowledge of rare neurology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p><strong>To be considered for this opportunity, you will possess the following:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10 years of relevant work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in Neurology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry. Launch experience preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li><li>Must have a valid driver’s license</li><li>Must be able to travel 60%-80% of time </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Applications Analyst - Oracle]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46999]]></requisitionid>
    <referencenumber><![CDATA[R46999]]></referencenumber>
    <apijobid><![CDATA[r46999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46999/principal-it-applications-analyst-oracle/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal IT Applications Analyst is a technical expert responsible for the configuration, implementation, maintenance, and ongoing support of Oracle Supply Chain IT applications and systems, including the Oracle ERP. The position requires expertise in Oracle ERP systems, including system architecture, integration, and performance monitoring, as well as the ability to lead strategic initiatives and deliver solutions that improve user experience and operational efficiency.</p><p>As a Principal IT Applications Analyst, a typical day might include the following:</p><ul><li>Lead the technical configuration and deployment of Oracle Supply Chain modules within Oracle ERP, ensuring alignment with business requirements and compliance with regulatory standards.</li><li>Support and manage system integrations with other enterprise applications, including middleware tools, APIs, and EDI configurations and are in compliance with applicable regulatory guidelines and all Regeneron procedures and policies.</li><li>Develop and implement customizations, extensions, and workflows using Oracle Application Development Framework (ADF), Business Process Management (BPM), and other Oracle tools.</li><li>Collaborate with IT and business teams to design and implement scalable solutions, including the creation of technical documentation, test plans, and deployment strategies.</li><li>Coordinate ongoing maintenance of Oracle EBS or Fusion ERP systems, including monitoring system performance, solving issues, and ensuring high availability and reliability of applications.</li><li>Manage application upgrades, patches, and security configurations while adhering to change management protocols.</li><li>Provide technical support and guidance to users, including root cause analysis and resolution of complex system issues.</li><li>Monitor system metrics and performance indicators to proactively identify areas for optimization and improvement.</li><li>Follows the methodologies and standards for IT project documentation and implementation, which includes guidelines, procedures, standards, and monitoring for organizational compliance.</li><li>Works with IOPS IT team and applicable vendors to develop and drive a strategic roadmap related to the application.</li><li>Works with business partners to develop and deploy system functionality to applicable user communities.</li><li>May manage and oversees a small staff of specialists on department projects and initiatives.</li><li>Recommends, negotiates and manages vendor contracts and ensures relationships are managed in an effective manner.</li><li>May serve as an SME or spokesperson for IOPS IT during a regulatory inspection.</li><li>Provides leadership in continuous improvement of GMP training programs including the methodologies for delivery, maintenance, and tracking of all GMP training, such as Standard Operating Procedure (SOP) training assessment and on-the-job training (OJT), through Kaizen and other continuous improvement approaches.</li><li>Maintains strong relationships with key business leaders to ensure acceptance and operational applicability of key processes and programs.</li></ul><p>This role may be for you if you have:</p><ul><li>Advanced knowledge of Oracle EBS or Fusion ERP, including Supply Chain modules such as Procurement, Inventory, Order Management, and Manufacturing.</li><li>Expertise in Oracle SQL, PL/SQL, and reporting tools like Oracle BI Publisher and OTBI.</li><li>Experience with integration platforms such as Oracle Integration Cloud (OIC), middleware, and APIs.</li><li>Strong understanding of regulatory guidelines, including GMP compliance, and experience supporting audits and inspections.</li><li>Proven track record of supporting complex ERP, upgrades, and customizations.</li><li>Excellent leadership, communication, and problem-solving skills.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field and</p><ul><li>Senior IT Applications Analyst: 5 years of progressive industry/relevant experience.</li><li>Principal IT Applications Analyst: 8 years of progressive industry/relevant experience.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Pharmaceuticals, life sciences or medical device manufacturing industry experience highly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Medical Director, Clinical Development, Hematology Cell Therapy]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47077]]></requisitionid>
    <referencenumber><![CDATA[R47077]]></referencenumber>
    <apijobid><![CDATA[r47077]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47077/executive-medical-director-clinical-development-hematology-cell-therapy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Executive Medical Director, Hematology, will provide overall clinical scientific leadership for the cell therapy program and have responsibility for our clinical development strategy and execution of clinical trials in this area. This role will be a key partner with the Global Program Head to design the optimal development strategy for this portfolio. This role requires an impactful and highly hard-working individual who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to hematology clinical research. The Executive Medical Director, Hematology reports directly to the VP, Therapeutic Area Lead, Hematology.</p><p><strong>A typical day in the life may include the following:</strong></p><ul><li><p>Acts as medical expert and leader in interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards.</p></li><li><p>Uses excellent scientific standing among peers and the ability to address issues with scientific rigor and creative solutions. Uses that creativity and knowledge to easily build and defend data driven plans and decisions, both with internal scientific management and the Company’s partners / collaborators.</p></li><li><p>Develops unique and innovative clinical strategies to significantly shorten the development cycle in the face of an evolving regulatory landscape. Designs and develops smaller, yet robust and innovative FIH as well as Phase 2/3 programs.</p></li><li><p>Drives for strong consensus-building skills and the ability to lead multi-disciplinary teams towards sound decision-making. Leads dynamic and matrixed clinical teams in a fast-paced and hands-on environment. </p></li><li><p>Leads and develops a team of MDs and clinical scientists to meet personal and business needs</p></li></ul><p><strong>This job may be for you if you have the following:</strong></p><ul><li><p>Demonstrated consistent track record in a range of leadership roles that include working with senior clinical development staff, establishing credibility with external collaborators such as opinion leaders and regulators, and demonstrating substantial experience in drug development (including experience with both IND and BLA/NDA submission).</p></li><li><p>Experience in leading study start-up, directing and guiding study team execution, data cleaning, medical review, database locks, handling health authority responses are also required.</p></li><li><p>A strong commitment to impacting patients through drug development and the ability to work well within a team setting are critical</p></li></ul><p>In order to be considered for this position, you must have an advanced degree in medicine (MD or equivalent), with a MD/PhD strongly preferred. Specialized fellowship training Hematology or Oncology is preferred. The incumbent will have a minimum of 6-8 years of industry experience in related therapeutic area clinical development. Cell therapy drug development experience is preferred. People management experience is a plus. This role requires a minimum of 4 days on-site weekly in Tarrytown, NY or Warren, NJ.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$390,000.00 - $527,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Director Medical Communications - Switzerland]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47245]]></requisitionid>
    <referencenumber><![CDATA[R47245]]></referencenumber>
    <apijobid><![CDATA[r47245]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47245/assoc-director-medical-communications-switzerland/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Basel]]></city>
    <state><![CDATA[Basel-City]]></state>
    <country><![CDATA[Switzerland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. </p><p>We are looking for an <strong>Associate Director, Medical Communications</strong> to bring high-quality medical information and scientific communications to healthcare professionals, patients, and internal partners across Switzerland & the Nordic hub. </p><p>In this role, you’ll shape and maintain audience-appropriate medical response documents and scientific Q&As, provide medical/scientific review of materials, and deliver communication strategies aligned with global medical direction. If you enjoy connecting science to real-world decisions—while keeping quality, compliance, and clarity at the center—this is a meaningful place to grow your impact. </p><p><strong>Associate Director, Medical Communications - Basel, Switzerland </strong></p><p><strong>A Typical Day may include:</strong> </p><ul><li>Developing and updating standard medical response documents / Q&As and custom response documents </li></ul><ul><li>Guiding MedicaI Information call center colleagues on inquiries and response quality </li></ul><ul><li>Reviewing promotional and medical materials for scientific accuracy and compliance </li></ul><ul><li>Preparing country-specific analytics from case trends and call volumes </li></ul><ul><li>Partnering with Medical Director, Field Medical, and Global Comms teams </li></ul><ul><li>Driving congress communication opportunities, scientific communications strategy at local level and contributing to the above countries strategy, supporting booth medical information </li></ul><ul><li>Keeping inspection-ready records to support audits and health authority reviews </li></ul><p><strong>This role may be for you if:</strong> </p><ul><li>You enjoy translating complex science for diverse audiences </li></ul><ul><li>You like owning content end-to-end, from creation through maintenance to delivery </li></ul><ul><li>You feel confident advising others on medical information inquiry management </li></ul><ul><li>You are comfortable balancing several communication assets and priorities at once </li></ul><ul><li>You value strong governance, quality processes, audit readiness, and documentation </li></ul><ul><li>You enjoy spotting scientific communication opportunities, including at congresses </li></ul><ul><li>You are agile, collaborative and love to connect with colleagues at the local, regional and global level located in different time zones </li></ul><p><strong>To be considered</strong> </p><p>A <strong>PhD, MD, or PharmD</strong> is required, along with <strong>5+ years of Medical Communications experience</strong> including <strong>at least 3 years in Medical Information</strong>, and <strong>5+ years</strong> in biotech/pharma (Medical Affairs, Clinical R&D, or related fields). You’ll also need an <strong>advanced understanding of Switzerland’s healthcare regulatory environment</strong> relevant to medical practice and the pharmaceutical industry, plus strong knowledge of <strong>European medical information/scientific communications requirements</strong> (with a focus on <strong>Swissmedic</strong> and Nordic countries). Preferred qualifications include proficiency in <strong>English</strong> and at least one of <strong>German, French, or Italian</strong>, as well as depth in medical communication strategy, congress strategy, scientific content development, and medical education. </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - Mountain West]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48154]]></requisitionid>
    <referencenumber><![CDATA[R48154]]></referencenumber>
    <apijobid><![CDATA[r48154]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48154/neurology-account-director-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Minnesota]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: Mountain West (Minnesota, Iowa, Missouri, Kansas, Idaho, Colorado, New Mexico and Arizona)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Product Biochemistry]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46115]]></requisitionid>
    <referencenumber><![CDATA[R46115]]></referencenumber>
    <apijobid><![CDATA[r46115]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46115/associate-scientist-product-biochemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Our Product Biochemistry team is seeking a highly motivated <strong>Associate Scientist </strong>to join our growing team. A successful candidate will be responsible for performing protein purification, modification as well as providing in-depth characterization of therapeutic proteins to support research, pre-clinical and clinical assays. In this exciting role you will be part of method development and technology innovation efforts aimed to improve our understanding of biotherapeutic proteins/gene therapy reagents on a capillary based western systems.</p><p><strong> </strong></p><p><strong>A typical day as a Associate Scientist looks like:</strong></p><ul><li><p>Conducts biochemical and biophysical characterization experiments and analyze data to elucidate quality attributes of protein and gene therapy candidates</p></li><li><p>Develop methods/technologies to support both upstream and downstream functional groups</p></li><li><p>Perform protein purification and modification (labeling) as required to support therapeutic pre-clinical assay development and release testing</p></li><li><p>Document all analytical work in electronic laboratory notebook (ELN) according to a defined protocol accurately</p></li><li><p>Communicate any findings to supervisor</p></li><li><p>Summarize results in a concise format to support presentations and regulatory documents</p></li><li><p>Present findings at group, departmental, and cross-functional meetings</p></li><li><p>Maintain and troubleshoot essential instruments in lab</p></li></ul><p><strong> </strong></p><p><strong>This role may be for you if you have:</strong></p><ul><li><p>Experienced in the general operations of a laboratory and able to manage and organize data with manager’s supervision. </p></li><li><p>Fundamental technical competencies in key analytical protein methodologies such as Size Exclusion Chromatography (SEC), UV-Vis spectrophotometry, SDS-PAGE, Western blotting, CE-SDS, protein purification and basic chemistry skills as applied toward protein modifications.</p></li><li><p>Experience on capillary electrophoresis is a plus.</p></li><li><p>Strong organizational skills and ability to prioritize multiple tasks are required. Deep understanding of biophysical/biochemical characterization of proteins, experience on analytical method development is desirable.</p></li></ul><p><strong> </strong></p><p><strong>In order to be considered qualified for this role, </strong>you must have a either a Masters or Bachelors degree in Biochemistry, Biophysical Chemistry, Biomedical engineering or related field and a minimum of 0-2 years of relevant post-degree laboratory experience with an emphasis on protein characterization and conjugation.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - BUFFALO, NY]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48004]]></requisitionid>
    <referencenumber><![CDATA[R48004]]></referencenumber>
    <apijobid><![CDATA[r48004]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48004/medical-account-specialist-ii-neurology-buffalo-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Buffalo]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Buffalo (Metro), NY</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal External Manufacturing Specialist (Drug Product)]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47848]]></requisitionid>
    <referencenumber><![CDATA[R47848]]></referencenumber>
    <apijobid><![CDATA[r47848]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47848/principal-external-manufacturing-specialist-drug-product/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Principal External Manufacturing Specialist. The Principal External Manufacturing Specialist oversees all aspects of external manufacturing contract manufacturing operations (filling, assembly, packaging) including day-to-day operations, ensuring timely completion of associated operations/documentation and assisting in the monitoring of cGMP compliance. Additionally, the Principal Specialist provides guidance to other specialists as well as consults with management on all contract manufacturing operations and GMP compliance issues.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Serves as a Regeneron operational contact for contract manufacturing and/or business partner sites concerning day-to-day activities.</p></li><li><p>Coordinates external manufacturing activities at contract and/or business partner sites, including but not limited to: scheduling of all batches, supply of materials, providing direction on shipment of bulk or finished product, tracking and monitoring of cycle times, providing supporting documentation for manufacturing activities and enlisting support from others who will provide any required associated reports and technical expertise.</p></li><li><p>Coordinates/oversees multiple external manufacturing activities at multiple sites, as required.</p></li><li><p>Liaises between various departments within Regeneron including, but not limited to Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments, Legal, Regulatory, Strategic Sourcing and contract manufacturers or business partners.</p></li><li><p>Leads sub-teams in continuous process improvements, system/equipment implementation and/or strategy development.</p></li><li><p>Leads or supports all investigations which concern external manufacturing and associated shipping operations.</p></li><li><p>Ensures product integrity and company reputation monitoring of cGMP compliance at external manufacturing contract manufacturers and business partners.</p></li><li><p>Performs reviews of pre-production master batch records and executed batch records.</p></li><li><p>Authors documents and procedures.</p></li><li><p>Supports audit operations, both internal and external.</p></li><li><p>Analyzes data for trends and potential issues.</p></li><li><p>Travels 25% (target) or more (domestic and international), as required.</p></li></ul><p>This role might be for you if:</p><ul><li><p>Knowledge of external manufacturing from formulation through the final package.</p></li><li><p>Knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.</p></li><li><p>Proficient in Excel, PowerPoint, Visio, Word, Oracle etc. in addition to experience working within shared work environments.</p></li><li><p>Strong interpersonal, written and oral communication skills.</p></li><li><p>Exhibits confidence, has a high emotional IQ, and has strong interpersonal, written and oral communication skills for providing team updates.</p></li><li><p>Ability to impart understanding of provided instructions, develop instructions and sets and works towards goals with minimal supervision.</p></li><li><p>Exhibits a degree of ingenuity, creativity and resourcefulness in evolving and ambiguous environments.</p></li><li><p>Shows resiliency and flexibility in the face of challenges and adversarial situations.</p></li><li><p>Understands and listens to team members and stakeholders needs while supporting productive team environments toward a common objective.</p></li><li><p>Competent in German and/or French (oral and written) is a plus.</p></li></ul><p>To be considered for this role, you must have a BS/BA in a scientific discipline and the following years of experience in cGMP manufacturing operations (clinical and/or commercial external manufacturing), including experience collaborating with CMOs/CROs, or equivalent combination of education and experience, for each level:</p><ul><li><p>Sr Specialist - 5+ years</p></li><li><p>Principal Specialist - 8+ years</p></li></ul><p>Level to be determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Triage and Medical Review]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47768]]></requisitionid>
    <referencenumber><![CDATA[R47768]]></referencenumber>
    <apijobid><![CDATA[r47768]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47768/associate-director-triage-and-medical-review/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><div><p>As the Associate Director, Triage and Medical Review Team Lead, you will oversee the complete triage and medical review of Individual Case Safety Reports (ICSRs) from global development programs and selected globally marketed products within the India-based Global Patient Safety (GPS) POD. This role is responsible for ensuring end-to-end case quality, inspection readiness, and alignment with global pharmacovigilance standards while partnering closely with global GPS teams.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Overseeing the complete medical review of ICSRs, ensuring all medically relevant information is accurately captured in Argus</p></li><li><p>Leading and overseeing the triage team to ensure harmonization of triage and medical review activities</p></li><li><p>Developing innovative approaches to enhance core activities through integration of new technologies, including AI</p></li><li><p>Reviewing and updating case narratives, author analyses, company causality rationale, and ensuring documentation is clinically accurate and aligned with reporting decisions</p></li><li><p>Providing guidance and oversight on expectedness determinations in alignment with development programs, marketed products, and approved labeling documents</p></li><li><p>Overseeing MedDRA coding of adverse events and medical history to ensure clinical appropriateness and consistency with GPS standards</p></li><li><p>Collaborating across PV teams, RM leads, and clinical development teams to produce comprehensive case documentation prior to regulatory submissions</p></li><li><p>Serving as the medical resource for assigned Regeneron compounds within the GPS POD and resolving case-level issues as needed</p></li><li><p>Supporting SOP development, process improvements, and inspection readiness activities within GPS</p></li></ul><p><strong>This Role May Be for You If You Have:</strong></p><ul><li><p>Exceptional knowledge of ICH E2A, E2B, and E2D guidelines along with FDA/EMA pharmacovigilance regulations governing ICSR processing and expedited reporting</p></li><li><p>Strong expertise in independent medical review of ICSRs, including narrative authoring, causality assessment, and expectedness determination</p></li><li><p>Strong proficiency with Argus Safety or equivalent safety databases</p></li><li><p>Advanced MedDRA coding proficiency with consistent clinically appropriate term selection</p></li><li><p>Strong clinical judgment and the ability to assess complex cases and communicate rationale clearly in written documentation</p></li><li><p>Experience or interest in AI technologies within pharmacovigilance operations</p></li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li><p>10+ years of total industry experience, including a minimum of 7+ years of pharmacovigilance experience.</p></li><li><p>You must have an MD/MBBS degree with active registration or eligibility for registration with the relevant Indian professional regulatory body.</p></li><li><p>Hands-on experience in ICSR medical review, including narrative authoring, MedDRA coding, causality assessment, and expectedness determination</p></li><li><p>Experience supporting global development programs or marketed products preferred</p></li><li><p>Prior experience in a GPS POD or insourced PV model is an added advantage</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II-Ophthalmology-Ft. Worth, TX]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46891]]></requisitionid>
    <referencenumber><![CDATA[R46891]]></referencenumber>
    <apijobid><![CDATA[r46891]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46891/medical-specialist-ii-ophthalmology-ft-worth-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Fort Worth]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>MEDICAL SPECIALIST II - OPHTHALMOLOGY - FT. WORTH, TEXAS</strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.</p><p><strong>A typical day might include the following: </strong></p><p>The Ophthalmology Medical Specialist will report to the Regional Director and will be responsible for developing and managing relationships with retina specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The Medical Specialist will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you have:</strong></p><p>· Experience in biologics and buy and bill products</p><p>· Demonstrated history of high sales performance</p><p>· Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Buy and Bill experience. Ophthalmology with relevant retina experience is preferred. Must be based in or located in close proximity to the assigned territory, covering DFW, Waco, Midland/Odessa, Lubbock, and East Texas (relocation will not be provided). Ability to travel (40-60%)</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 16:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -RIVERSIDE, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48080]]></requisitionid>
    <referencenumber><![CDATA[R48080]]></referencenumber>
    <apijobid><![CDATA[r48080]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48080/medical-account-specialist-ii-neurology-riverside-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Riverside]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Riverside (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 18:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - KNOXVILLE, TN]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48023]]></requisitionid>
    <referencenumber><![CDATA[R48023]]></referencenumber>
    <apijobid><![CDATA[r48023]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48023/medical-account-specialist-ii-neurology-knoxville-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Knoxville]]></city>
    <state><![CDATA[Tennessee]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Knoxville (Metro), TN</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Patient Advocacy]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48571]]></requisitionid>
    <referencenumber><![CDATA[R48571]]></referencenumber>
    <apijobid><![CDATA[r48571]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48571/associate-director-global-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Global Patient Advocacy, Hematology-Oncology to cover International and US markets. In this role, you will lead the development and execution of patient advocacy strategies, building meaningful relationships with advocacy groups and professional societies to support patient needs and business objectives, while collaborating with cross-functional leaders (Medical Affairs, Market Access, Marketing, and Policy teams). This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><p>UK, Germany, Italy or Spain (Hybrid model)</p><p>Travel: 40%+</p><h3>Discover your role:</h3><ul><li><p>Lead advocacy and engagement strategy for Hematology-Oncology in Europe</p></li><li><p>Partner with senior cross-functional leaders to build advocacy strategies</p></li><li><p>Build and manage relationships with patient advocacy groups and professional societies</p></li><li><p>Oversee patient engagement initiatives, meetings, and communications</p></li><li><p>Develop frameworks to embed the patient perspective across organizational processes</p></li><li><p>Track and report outcomes of advocacy initiatives to senior leadership</p></li><li><p>You foster collaboration and consensus among diverse stakeholders</p></li><li><p>You drive a patient-centric culture and influence strategic decisions</p></li></ul><h3>This role requires:</h3><ul><li><p>Undergraduate degree required</p></li><li><p>10+ years of industry or relevant professional experience</p></li><li><p>5+ years of patient advocacy, stakeholder engagement, and issues management</p></li><li><p>European, international, or global advocacy experience and understanding of relevant regulations (e.g., EMA, HTA)</p></li><li><p>Proven leadership in developing and executing advocacy strategies</p></li><li><p>Country-level advocacy work experience preferred</p></li><li><p>Multilingual capabilities strongly preferred</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€81,300.00 - €135,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 03:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Patient Advocacy]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48572]]></requisitionid>
    <referencenumber><![CDATA[R48572]]></referencenumber>
    <apijobid><![CDATA[r48572]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48572/associate-director-global-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Global Patient Advocacy, Hematology-Oncology to cover International and US markets. In this role, you will lead the development and execution of patient advocacy strategies, building meaningful relationships with advocacy groups and professional societies to support patient needs and business objectives, while collaborating with cross-functional leaders (Medical Affairs, Market Access, Marketing, and Policy teams). This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><p>UK, Germany, Italy or Spain (Hybrid model)</p><p>Travel: 40%+</p><h3>Discover your role:</h3><ul><li><p>Lead advocacy and engagement strategy for Hematology-Oncology in Europe</p></li><li><p>Partner with senior cross-functional leaders to build advocacy strategies</p></li><li><p>Build and manage relationships with patient advocacy groups and professional societies</p></li><li><p>Oversee patient engagement initiatives, meetings, and communications</p></li><li><p>Develop frameworks to embed the patient perspective across organizational processes</p></li><li><p>Track and report outcomes of advocacy initiatives to senior leadership</p></li><li><p>You foster collaboration and consensus among diverse stakeholders</p></li><li><p>You drive a patient-centric culture and influence strategic decisions</p></li></ul><h3>This role requires:</h3><ul><li><p>Undergraduate degree required</p></li><li><p>10+ years of industry or relevant professional experience</p></li><li><p>5+ years of patient advocacy, stakeholder engagement, and issues management</p></li><li><p>European, international, or global advocacy experience and understanding of relevant regulations (e.g., EMA, HTA)</p></li><li><p>Proven leadership in developing and executing advocacy strategies</p></li><li><p>Country-level advocacy work experience preferred</p></li><li><p>Multilingual capabilities strongly preferred</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€79,800.00 - €133,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 03:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Medical Review]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47767]]></requisitionid>
    <referencenumber><![CDATA[R47767]]></referencenumber>
    <apijobid><![CDATA[r47767]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47767/senior-manager-medical-review/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Pharmacovigilance Medical Review, India to join our Global Patient Safety team, supporting our global development programs and marketed products in a hybrid role. In this role, you will lead the medical review of safety cases to ensure every report is scientifically sound and inspection-ready before health authority submission, while collaborating with triage, pharmacovigilance, risk management, and clinical development partners across India, the US, and the EU. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Hyderabad (Hybrid)</p><br><h3><strong>Discover your role:</strong></h3><ul><li><p>Act as team lead, owning end-to-end case quality from coding through causality to final company comment</p></li><li><p>Perform and oversee medical review of ICSRs within defined time standards, ensuring accuracy in Argus</p></li><li><p>Author and review case narratives, analysis of similar events, and company causality rationale</p></li><li><p>Code adverse events and medical history using MedDRA in line with global safety standards</p></li><li><p>Partner with triage, PV, risk management, and clinical development teams on inspection-ready documentation</p></li><li><p>Serve as the medical resource for assigned compounds, resolving and escalating complex case issues</p></li><li><p>Drive SOP development, process improvement, and integration of new technologies including AI</p></li><li><p>You mentor Managers and junior reviewers to ensure consistent application of medical and regulatory standards</p></li></ul><br><h3><strong>This role requires:</strong></h3><ul><li><p>MD or MBBS with active registration, or eligibility for registration, with the relevant Indian professional regulatory body</p></li><li><p>Minimum 8–10 years of pharmacovigilance experience with hands-on ICSR medical review, including narrative authoring, causality assessment, and expectedness determination</p></li><li><p>Strong knowledge of ICH E2A, E2B, and E2D guidelines and FDA/EMA pharmacovigilance regulations</p></li><li><p>Proficiency with Argus Safety or an equivalent safety database and MedDRA coding</p></li><li><p>Sound clinical judgment with the ability to assess complex cases and communicate reasoning clearly in writing</p></li><li><p>Experience within global development programs or on marketed products preferred</p></li><li><p>Exposure to AI or generative AI tools in pharmacovigilance or clinical documentation a plus</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 04:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43733]]></requisitionid>
    <referencenumber><![CDATA[R43733]]></referencenumber>
    <apijobid><![CDATA[r43733]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43733/senior-manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>***Please note this role is an onsite opportunity and is NOT eligible remote.</em></p><p>The <strong>Senior Manager Statistical Programming </strong>provides technical leadership and support to the project teams on all statistical programming matters according to the project strategies within therapeutic area(s). The incumbent manages the programming aspect of a project in collaboration with partnering functions, stakeholders, and external functional service providers for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards, regulatory safety reports, and other requests. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. The incumbent will lead or participate in process and methodology development for department goals and SME topics. Maybe responsible for goal setting and performance management.</p><p><strong>In this role, a typical day might include: </strong><strong>​</strong></p><ul><li>Manage and lead programming support within multiple studies/projects in various study activities to ensures timely and high-quality programming deliverables in assigned projects and areas. Lead and coordinate programming documentation including specifications, as appropriate, for multiple studies following programming standards and processes</li><li>Demonstrate company values and act as a role model by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability</li><li>Ensure the commitment and reinforcement of the roles and responsibilities of the statistical programming function</li><li>Proactive communication with study and project teams to clarify requirements and specifications, guide direct reports or support programmers on assignment status</li><li>Lead and support global regulatory authority submissions including preparing programming deliverable for submission and working closely with partnering functions to address health authority requests.</li><li>Lead and manage department goals and SME topics</li><li>May oversee development of direct reports by setting goals, managing performance, evaluating, and monitoring training needs, supporting development plans, mentoring, and coaching</li><li>May participate in screening and interviewing candidates for contractor and permanent positions.</li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li>MS (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 10+ (12+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience.</li><li>Advanced SAS programming skills in a clinical data environment with expertise in at least one, preferably multiple, therapeutic areas. Knowledge of other programming languages such as R, Python etc. is a plus.</li><li>Understanding of pharmaceutical clinical development across multiple therapeutic areas (i.e. understanding of statistical concepts, techniques and clinical trial principles) and good knowledge of regulatory submissions and requirements</li><li>Ability to work on global interdisciplinary teams. Good organizational, interpersonal, communication, and leadership skills. Establish and maintain effective working relationships with coworkers, managers, and clients</li><li>Ability to effectively manage multiple tasks and projects</li><li>Problem solving and innovative skills that demonstrate initiative and motivation</li><li>Ability to influence others, mentor, and coach junior programmers to achieve results</li></ul><p>#statprogramming</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Statistical Programming]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44857]]></requisitionid>
    <referencenumber><![CDATA[R44857]]></referencenumber>
    <apijobid><![CDATA[r44857]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44857/manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>***Please note this role is an onsite opportunity and NOT eligible remote. </em></p><p>A <strong>Manager Statistical Programming </strong>provides timely support to the study team on all programming matters according to the project strategies. As an integral </p><p>part of a study team, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan, programming specification or user requirements document using internal standards and guidelines. The incumbent provides guidance in implementing and executing the programming and project standards. The incumbent will be responsible for leading the programming aspect of a project, both internally or CROs, for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards and annual reports. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. Meets statistical ad hoc requests of senior management.<br> </p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Develop an expertise within a therapeutic area or standard tool. Work with minimal supervision to perform, coordinate and oversee the preparation, execution, reporting and documentation of a project</li><li>Function as a lead programmer in the development and QC of tables, listings, graphs, or systems in support of analysis requirements utilizing Regeneron tools and methodologies and current industry standards (i.e. CDISC SDTM / ADaM)</li><li>Manage the effort, including esubmssion deliverables, using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Provide programming support for complex presentations and more complex statistical ad-hoc requests. </li><li>Act as programming representative in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports.</li><li>If applicable, lead an application development and act as the programming representative to the user audience.</li><li>Work with management to determine resource requirements for therapeutic area or department function <br>responsibilities. </li><li>Review and select resumes, screen and interview candidates for contractor and permanent positions.</li><li>Provide feedback to management regarding team member’s contributions to the work effort for evaluating individual's performance and recommend yearly goals.</li><li>Advises all direct reports about the procedures surrounding retention of data, records, and information for <br>employees in their group.<br> </li></ul><p><strong>In order to be considered qualified for this role</strong></p><ul><li>Master’s Degree</li><li>8-10 years of relevant work experience</li><li>SAS Certification desirable.</li><li>Also acceptable - 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience with a Master’s Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.</li></ul><p>#statprogramming</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Associate Scientist, R&D Chemistry, Peptidomimetic Purification]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48140]]></requisitionid>
    <referencenumber><![CDATA[R48140]]></referencenumber>
    <apijobid><![CDATA[r48140]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48140/sr-associate-scientist-rd-chemistry-peptidomimetic-purification/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Sr. Associate Scientist (Peptidomimetic Purification), R&D Chemistry </strong></p><p>We are currently seeking a lab-centric peptide purification chemist to join the R&D (Research & Development) Chemistry group. In this position, they will play a key role in Regeneron’s peptidomimetic antibody-conjugate drug discovery capabilities to enable seamless combination with the company’s existing expertise in biologics and novel genetic medicines. The candidate will drive the purification of peptidomimetic payloads and linker payloads for antibody conjugate drug therapeutics across diverse research areas. Cultural fit with the Regeneron cross-functional teams will be a key driver for success. The R&D Chemistry team is primarily composed of synthetic organic, medicinal chemistry and bioconjugation scientists that work in a highly collaborative environment with other technology, biology and therapeutic area groups. Successful candidates will have a peptide/peptidomimetic purification background and will require a firm understanding of the latest techniques, strategies and instrumentation for HT peptide purification and isolation. We expect they will act as an inspiring and motivating colleague, effective communicator, and strong project team collaborator to help develop novel antibody-conjugated peptidomimetic therapeutics.</p><p><strong> </strong></p><p><strong>Build our future together:</strong></p><ul><li>Actively participate and collaborate in the day-to-day activities of the R&D Chemistry Peptidomimetic purification team.</li><li>Perform mass-triggered HPLC purification of novel peptidomimetic drug modalities, using modern purification instrumentation/detection and techniques</li><li>Troubleshoot and optimize peptide purification methods and enable high throughput purification and isolation.</li><li>Identify new strategies and technologies for peptidomimetic purification to improve on existing Regeneron techniques</li><li>Actively participate in departmental, cross-functional, leadership, and external meetings to contribute expertise and to represent the vision of the R&D Chemistry Peptidomimetic purification team.</li><li>Interact broadly and collaboratively with other Regeneron groups, forging relationships and active collaborations.</li></ul><p><strong> </strong></p><p><strong>Discover your role:</strong></p><ul><li>Passion and enthusiasm about the promise of peptidomimetic conjugated, antibody-targeted therapeutics and how peptide purification can enable their generation.</li><li>You enjoy applying and combining traditional methods and novel technologies to develop solutions for purification.</li><li>You are comfortable working in a cross-functional role and excel in a diverse team where egos are checked at the door.</li><li>You want to provide meaningful contributions to the development of an organizational culture that supports growth and development of its people and capabilities to drive forward the Regeneron pipeline.</li><li>You prefer to work in an organization that is modality agnostic, letting the data determine the best course forward.</li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required, Master’s degree preferred in peptide, peptidomimetic, small molecule purification</li><li>Minimum of 5 years of industry experience.</li><li>Extensive hands-on experience of the HPLC purification/detection and method troubleshooting of peptidomimetics</li><li>Hands-on experience with Waters and/or Agilent purifications systems preferred</li><li>Hands-on experience with mass-triggered collection preferred</li><li>Experience with high throughput purification</li><li>Extensive experience running modern purification/isolation equipment and instrumentation </li><li>A track record of success in the field of either peptidomimetics or small molecules purification is required. </li><li>Working collaboratively with both internal and external organizations (e.g., CROs) is essential.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 22 Jun 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Assurance Specialist (On the floor)]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48366]]></requisitionid>
    <referencenumber><![CDATA[R48366]]></referencenumber>
    <apijobid><![CDATA[r48366]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48366/quality-assurance-specialist-on-the-floor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Quality Assurance (QA) Specialist to join our QA Drug Product team. This position will support visual Inspection, assembly, and packaging operations performed at Regeneron’s internal Fill/Finish facility. They will provide floor support during production activities and contribute to establishing/updating procedures and policies to ensure assigned areas are operating to current FDA and International regulatory body requirements. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>Location: Rensselaer, New York, United States</li><li>Monday-Friday, 8am-4:30pm</li><li>Occasional flexibility may be requested for on-call schedule/weekend work</li></ul><p>What you’ll do:</p><ul><li>Oversee programs that support visual inspection, assembly, and packaging operations at the drug product facility</li><li>Ensure facilities, equipment, materials, processes, and procedures comply with good manufacturing practices, good documentation practices, safety, and Regeneron requirements</li><li>Develop, update, review, and approve standard operating procedures, specifications, and other documents supporting drug product operations</li><li>Provide quality oversight and guidance during on-the-floor manufacturing activities</li><li>Execute daily on-the-floor oversight to verify facilities, equipment, materials, and documentation comply with standard operating procedures and safety standards</li><li>Perform material quarantine and segregation and execute line clearance activities</li><li>Perform acceptable quality level sampling plan</li><li>Review and approve procedures, documents, and records, including batch production records and protocols</li><li>Ensure electronic and paper batch records are complete, accurate, and compliant with written procedures</li><li>Provide quality support for electronic batch record design, review, and approval</li><li>Author, review, and approve quality documents, including standard operating procedures, risk assessments, training materials and records, protocols, and reports</li><li>Support and represent quality assurance during audits and inspections, including direct interactions with regulatory agencies as needed</li></ul><p>Gowning and environment:</p><ul><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </li></ul><ul><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </li><li>Qualified applicants must be able to pass the following vision tests; Ishihara (colorblindness) and Jaeger (paragraphs of decreasing size) as part of the requirements of this role</li></ul><p>Let’s find out if we’re a fit:</p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>Assoc QA Specialist : 2+ years of experience</li><li>QA Specialist : 4 + years of experience</li><li>Sr. QA Specialist: 6+ years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p>Thrive today. Grow tomorrow.</p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Product Manager, Predictive Analytics]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48512]]></requisitionid>
    <referencenumber><![CDATA[R48512]]></referencenumber>
    <apijobid><![CDATA[r48512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48512/senior-product-manager-predictive-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated and skilled Senior Product Manager to join the Regeneron Genetics Center (RGC) to pioneer clinical use cases for proteomic and genomic data. In this role, you will develop products based on the world’s largest integrated datasets of genomics, proteomics, and electronic medical records. </p><p>The role involves partnering with cross-functional teams, including Business Development, Laboratory staff, and other scientific groups, to foster collaboration and advance key initiatives. Excellent communication and interpersonal skills are also required as this candidate will be encouraged to work efficiently in a collaborative, team working environment.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Mock up products based on proteomic, electronic medical record, and/or genomic datasets</p></li><li><p>Draft specifications for software to display disease risk predictions, use AI tools to implement the specifications, and evaluate the results</p></li><li><p>Turn disease prediction ideas from other teams and collaborators into concrete project/budget proposals</p></li><li><p>Stay informed on emerging market trends in disease prediction and applications of genomics data to continuously refine product directions</p></li><li><p>Deliver clear and concise presentations of genomics and proteomic use cases to leadership, ensuring alignment with organizational goals and priorities</p></li><li><p>Assist in the design of clinical validation programs for products</p></li><li><p>Leader partner and customer discussions to test hypotheses about the value of new products, and summarize this feedback to leadership </p></li></ul><p><strong>This role might be for you if have:</strong></p><ul><li><p>Demonstrated expertise in software engineering or product design </p></li><li><p>Proven skills for translating scientific results into product prototypes</p></li><li><p>Proven track record to independently lead and run research projects from conception to completion.</p></li><li><p>Excellent communication and collaboration skills, with a track record of working effectively in interdisciplinary teams</p></li><li><p>Proven ability to present data, insights, and recommendations effectively to stakeholders at all levels of the organization</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><ul><li><p>A bachelor's degree in a relevant field (software engineering, computational biology, etc.) with at least 13+ years of relevant industry experience (or a PhD and +7 years of experience as an equivalent)</p></li><li><p>Candidates with prior industry experience are preferred</p></li><li><p>Experience in software engineering or product design is preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Change Control Specialist (Technical Operations)]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48601]]></requisitionid>
    <referencenumber><![CDATA[R48601]]></referencenumber>
    <apijobid><![CDATA[r48601]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48601/change-control-specialist-technical-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Change Control Specialist position in our growing Technical Operations Compliance team. This position develops strategic plans related to change control and the implementation of robust corrective actions to support manufacturing operations by applying function expertise.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Craft business plans to independently advances change control initiatives to implement Corrective and Preventative Actions (CAPA’s) and process improvements in support of manufacturing operations</p></li><li><p>Assess sophisticated proposed change controls to evaluate if proposal satisfies company standards</p></li><li><p>Coordinate and prepare change control documentation that assesses and defines the scope, impact, risk, and regulatory impact associated with the change</p></li><li><p>Review, edit, and revise controlled documentation in accordance with cGMP standards</p></li><li><p>Coordinate and/or lead cross-functional meetings with multiple departments to drive change control implementation</p></li><li><p>Provide advice and mentorship to cross-functional teams to enable successful and GMP compliant change controls</p></li><li><p>Independently monitor and progress multiple projects concurrently – identifying, addressing, and/or raising potential obstacles in a timely manner</p></li><li><p>Present business critical and regulatory impactful change controls to senior leadership</p></li><li><p>Document all training</p></li><li><p>Assist with the training of new employees</p></li><li><p>May manage direct reports</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Excel in a quality driven organization.</p></li><li><p>Can manage multiple assignments and changing priorities through robust organizational, planning, and project management skills.</p></li><li><p>Have a strong attention to detail.</p></li><li><p>Have strong technical writing and interpersonal communication skills.</p></li><li><p>Enjoy working in a fast-paced environment.</p></li><li><p>Have experience navigating a controlled quality system (preferred but not required).</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Life Sciences, Engineering or related field and following minimum amounts of relevant experience for each level:</p><ul><li><p>Associate Specialist – 0-2 years</p></li><li><p>Specialist – 2+ years</p></li><li><p>Sr Specialist – 5+ years</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 19 Jun 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Pulmonology-Orlando, FL]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48730]]></requisitionid>
    <referencenumber><![CDATA[R48730]]></referencenumber>
    <apijobid><![CDATA[r48730]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48730/medical-specialist-i-pulmonology-orlando-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Orlando]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Orlando, FL</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups. </p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Affairs Senior Coordinator]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48298]]></requisitionid>
    <referencenumber><![CDATA[R48298]]></referencenumber>
    <apijobid><![CDATA[r48298]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48298/medical-affairs-senior-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Coordinator, International Medical Review Committee to join our Global Medical Affairs team, supporting our ex US, International locations. In this role, you will coordinate Medical Review Committee activities and support timely, compliant material review and approval while collaborating with material sponsors, submitters, management, customers, vendors, and partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Uxbridge, UK or Dublin, Ireland</p><p>Hybrid model</p><p><strong>Discover your role:</strong></p><ul><li><p>Coordinate International Medical Review Committee activities and approval workflows.</p></li><li><p>Manage materials from submission through final approval.</p></li><li><p>Create agendas and facilitate live Medical Review Committee meetings.</p></li><li><p>Prepare for and participate in quality checks and audits.</p></li><li><p>Maintain documentation, systems, and the Medical Reference Library.</p></li><li><p>Review submissions for appropriateness and completeness before routing.</p></li><li><p>Train sponsors and submitters on Medical Review Committee processes.</p></li><li><p>You collaborate clearly across teams to support timely decisions.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in a related field, or equivalent experience.</p></li><li><p>Minimum 5 years’ experience, or 7 years without a degree.</p></li><li><p>3 years’ Medical Review Committee or Medical Legal Review experience preferred.</p></li><li><p>Familiarity with local country regulatory requirements and guidelines.</p></li><li><p>Proficiency in Microsoft Office, Adobe Acrobat Professional, and Veeva Vault.</p></li><li><p>Strong project management, meeting facilitation, organization, and time management skills.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Control Analyst]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48359]]></requisitionid>
    <referencenumber><![CDATA[R48359]]></referencenumber>
    <apijobid><![CDATA[r48359]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48359/quality-control-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Quality Control Analyst to perform cell based and ELISA based potency assays to support release, stability programs, and lab operation within Quality Control. This role continuously strives to follow all pertinent regulatory agency guidelines to drive performance. </p><p>This position is a Tuesday – Saturday 8am-4:30pm schedule.<br><br>As a QC Analyst, a typical day might include the following:<br>• Executing potency testing for analytical test methods while complying with cGMP standards</p><p>• Supporting production, stability studies, and lab operations<br>• Performing laboratory support activities including equipment maintenance, reagent preparations, and review of associated documentation<br>• Maintaining and updating relevant procedures for testing and lab maintenance/support<br>• Collaborating with Development groups on new test methods<br>• Participating in all vital training activities<br><br>This role might be for you if:<br>• You are results-oriented and can problem solve</p><p>• You have a solid understanding of potency testing<br>• You can work efficiently as an individual as well as with others<br>• You are a strong communicator who is willing to build beneficial relationships with other peer groups<br><br>To be considered for this role, you must have a BS/BA in Biology or related field, and 2+ years of relevant experience. You must be willing and able to work Tuesday – Saturday 8am-4:30pm. </p><p>Level will be determined by demonstrated experience. </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 21:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Financial Analyst, SOX Compliance]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47488]]></requisitionid>
    <referencenumber><![CDATA[R47488]]></referencenumber>
    <apijobid><![CDATA[r47488]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47488/senior-financial-analyst-sox-compliance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Financial Analyst, SOX Compliance will be the dedicated contact in the Program Finance department providing support to our Global Development organization and relevant partners. This role ensures compliance with financial requirements and maintains and develops all appropriate guidelines and tools to guarantee an efficient and effective execution of financial activities in relation to Clinical Trials. We need someone who can maintain a validated command of all aspects of projects.</p><h3><strong>A typical day might include the following:</strong></h3><ul><li><p>Ensuring that financial controls are executed in accordance with Company SOX requirements</p></li><li><p>Partnering with the Head of Program Finance to present process changes/updates to the Company SOX committee and reflect these changes/updates in the SOX documentation (narrative)</p></li><li><p>Facilitating Audit SOX annual reviews: Lead process overview/walkthrough with external and internal auditors and prepare the requested documentation for Study Level Budget and Requisition approvals for key controls testing</p></li><li><p>Providing mentorship on SOX key controls for Clinical Start Up Budgets (CSUB), Blue Sheet Budgets (BSB) and Study Level Requisitions to Program Finance and Global Development</p></li><li><p>Performing ad-hoc reviews to ensure Program Trial Finance (PTF) analysts detail the budget control as appropriate within the requisition and maintain appropriate support. This will include identification of any gaps or weaknesses in the process and improvement opportunities to ensure adequate controls</p></li><li><p>Within the guardrails of the SOX environment, being a steward for operational improvements to eliminate any excess of work and streamline processes/controls execution</p></li><li><p>Adopt a continuous improvement approach to review existing processes and documentation to identify where additional controls and clarifications around Global Development Clinical Trials, Clinical Programs budgets and Study Level requisitions are required from a Finance stand-point; this includes but is not limited to:</p></li><li><p>Submission and updating of approved budget information in Hyperion.</p></li><li><p>Review of budget dashboards to ensure accurate reporting of approved budgets.</p></li><li><p>Review of custom hierarchies for clinical trials and required approvers</p></li><li><p>Administration and maintenance of BSB and CSUB workflows</p></li><li><p>Periodic review of CSUB and BSB values in Hyperion to ensure the most up-to-date budget amounts are reflected on the Finance dashboard</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have strong verbal and written communication skills to optimally interact with all levels of business partners and management</p></li><li><p>You can lead multiple projects in a fast-paced environment.</p></li><li><p>You demonstrate problem-solving, quantitative, and analytical skills</p></li><li><p>You have experience with a rapidly growing organization</p></li><li><p>You are organized, detail oriented and able to independently complete tasks and implement those tasks efficiently</p></li><li><p>You have validated analytical skills and the ability to translate analytical findings into impactful solutions and processes</p></li></ul><p>To be considered for this opportunity, you must have a bachelor’s degree in a Finance, accounting, or related quantitative field combined with MBA is helpful. 8+ years’ experience with forecasting, budgeting, and/or business partnering ideally in a science or research driven environment. The ideal candidate has a proven track record in both audit and finance functions.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Clinical Pharmacologist]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47532]]></requisitionid>
    <referencenumber><![CDATA[R47532]]></referencenumber>
    <apijobid><![CDATA[r47532]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47532/senior-clinical-pharmacologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>As a<strong> Senior Clinical Pharmacologist </strong>this individual is expected to plan, design, implement and analyze in-vivo and in-vitro pharmacokinetic & pharmacodynamic studies working with Clinical Pharmacology, Quantitative Pharmacology, Pharmacometrics/Pharmacodynamics (PK/PD), Toxicology, Bioanalytical, Therapeutic Focus areas and Clinical Development / Regulatory</p><p>Affairs teams.</p><p>This individual contributes to the scientific understanding of PK/PD for assigned projects, based on quantitative evaluation of the pharmacokinetic and pharmacodynamic profile for research programs, through the application of state-of-the-art knowledge in pharmacokinetics and pharmacodynamics.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Warren, NJ, Cambridge, MA</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Plans, designs, implements and analyzes routine Pharmacometrics (PMx) studies to advance scientific knowledge, in collaboration with other team members.</p></li><li><p>Performs analyses such as NCA, compartmental modeling, PopPK, translational modelling, disease modelling, Pop PK/PD, E-R analyses (or work closely with Research Specialist or PMx Stats Programming team) to deliver PMx results, interpretation and discussion.</p></li><li><p>Collaborates with Scientific Writing (and where appropriate with PMx Stats Programming team) to ensure TFLs for PMx reports are complete. Works in conjunction with Scientific Writing, Quality Control and QAA (as required) to issue study reports in support of IND/CTA submissions and other regulatory documents.</p></li><li><p>With close supervision from senior PMx staff, supports preparation of material to be used in regulatory interactions.</p></li><li><p>Contributes to preparation of PMx materials for regulatory background packages, e.g. for pre-IND, EOP2, and pre-BLA meetings.</p></li><li><p>Has understanding of advanced PMx concepts and techniques, such as advanced pharmacokinetics, advanced pharmacological principles, non-compartmental analysis methods, Exposure-Response analysis methods, translational modelling/pharmacology, Nonlinear Mixed Effects modeling, logistic regression, survival analysis, Bayesian approaches, disease modelling/QSP.</p></li><li><p>Is highly skilled in use of relevant software, including MS-Excel, R, R-Studio, Prism, Phoenix WinNonlin, NLME, STAN and NonMem, working in department computing environment to perform advanced PMx analyses.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A PhD in Biology, Pharmacology, Engineering or a Pharmacy (Pharm.D.), Medicine (MD) degree</p></li><li><p>3+ years of relevant Clinical Pharmacology experience</p></li><li><p>Able to communicate effectively with and influence team members from other functions.</p></li><li><p>Fully understand processes and are able to represent PMx on process initiatives.</p></li></ul><div><div><div><div><div><div><div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 11:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Dermatology *Iwate, Aomori Area]]></title>
    <date><![CDATA[Mon, 06 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48597]]></requisitionid>
    <referencenumber><![CDATA[R48597]]></referencenumber>
    <apijobid><![CDATA[r48597]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48597/medical-representative-mr-dermatology-stariwate-aomori-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative, Dermatology, Japan to join our ROW Commercial Team, supporting our Japan region in a hybrid work mode. In this role, you will achieve sales objectives in dermatology while collaborating with our alliance partners and internal teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Japan<br>Work model: Hybrid<br>Travel, evening, and weekend work will be required</p><br><p><strong>Discover your role:</strong></p><ul><li>Achieve sales objectives in dermatology for the assigned territory</li><li>Develop and implement annual territory business plans based on market insights</li><li>Manage territory budgets and expenses to optimize resource allocation</li><li>Utilize key data sources to strategically develop action plans</li><li>Perform all required administrative duties, including reporting and compliance</li><li>Attend local, regional, and national meetings as directed</li><li>You work collaboratively with alliance partners to deliver objectives</li><li>You adapt plans in response to changing market dynamics</li></ul><br><p><strong>This role requires</strong>:</p><ul><li>Bachelor’s degree (or equivalent experience)</li><li>Minimum five (5) years sales representative experience in the pharmaceutical industry</li><li>Superior customer engagement skills with a focus on delivering value</li><li>Excellent technical aptitude and ability to conduct disease/concept selling</li><li>Superb written, verbal, and presentation skills</li><li>Excellent planning and organizational skills</li><li>Ability to work independently and execute strategic plans under tight timelines</li><li>Computer literacy including word processing, spreadsheets, databases, and email software</li><li>Valid driver license and MR Certification</li><li>Therapy area knowledge (Dermatology) and sales experience in biologics desirable</li><li>Up-to-date clinical knowledge of therapy areas and competitor brands desirable</li><li>Established Key Opinion Leader relationships within dermatology desirable</li><li>Fluency in English is a plus but not essential for this role</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 06 Jul 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Sciences, Hematology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43418]]></requisitionid>
    <referencenumber><![CDATA[R43418]]></referencenumber>
    <apijobid><![CDATA[r43418]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43418/medical-director-clinical-sciences-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Medical Director, Clinical Sciences functions as clinical leader of a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase), under leadership of Program Lead Medical Director (Program Lead MD) or Sr. Medical Director.</p><p>A day in the life may include the following responsibilities:</p><ul><li><p>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program with minimal supervision from Program Lead MD. </p></li><li><p>Manages all operational aspects and drives execution of the section of the clinical program in partnership with global line functions, assigned Clinical Scientist and Clinical Operations associates.</p></li><li><p>Supports Program Lead MD (and/or Sr. MD) and frequently lead interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, HE&OR), and internal decision boards.</p></li><li><p>Serves occasionally as member for Global Clinical Development training programs, author or reviewer for clinical SOPs and may contribute to GCD strategy by serving on taskforces or other panels.</p></li></ul><p>This job may be for you if:</p><p>· You are passionate about impacting entire populations of patients</p><p>· You want to develop innovative new therapies</p><p>· You enjoy collaborating with team members towards a common goal.</p><p>In order to be considered for this position, you must have an MD or equivalent, ideally with Hematology Oncology fellowship training. More than 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV is strongly preferred. Medical/scientific expertise in disease area of assigned program is preferable. </p><p>#MDJOBS #heme</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$280,700.00 - $379,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44657]]></requisitionid>
    <referencenumber><![CDATA[R44657]]></referencenumber>
    <apijobid><![CDATA[r44657]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44657/manager-internal-medicine-clinical-scientist-immuneinflammatory/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>We are seeking a Manager, Clinical Scientist to join our team. The Manager Clinical Scientist assists in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Manager works in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to the Associate Director/Director Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p></div><div><div><div><div><div><div><div><div><p><strong>As a Manager within Clinical Sciences, a typical day may include the following:</strong></p><ul><li><p>Member of the Clinical Study Team and the Global Clinical SubTeam; regularly attends and actively participates in study team meetings</p></li><li><p>May contribute to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments</p></li><li><p>Develops/maintains basic understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and limited knowledge of disease and drug landscape</p></li><li><p>Applies basic scientific expertise to support execution of clinical research and development studies for early and/or late stage assets</p></li><li><p>May assist with preparation of documents related to trials, such as medical monitoring plans, SAPs, informed consents, clinical components of the Clinical Study Reports and regulatory documents; collaborate with others for scientific and foundational guidance</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>May contribute to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority)</p></li><li><p>Supports clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Supports identification of data trends and potential inconsistencies in data across assigned studies and raises</p></li><li><p>Exhibits basic research and analytical knowledge to understand how study objectives and design impact data analysis; supports identification of critical risks and mitigations to study</p></li></ul><p><strong>This role may be for you if: </strong></p><ul><li><p>Demonstrated basic knowledge of the drug development process, Good Clinical Practice, study design and clinical research methodology; beginner level medical writing skills</p></li><li><p>Demonstrate some ability to influence within study team</p></li><li><p>Independently resolves most issues and complex matters, requiring advanced analytical skill, training and/or education. Raises highly complex problems or out-of-policy issues</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven track record in clinical trial process improvements</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related area. Additionally, ≥ 6 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in immune/inflammatory related clinical trials. Basic knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Hearing Loss and Vestibular Disorders]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44687]]></requisitionid>
    <referencenumber><![CDATA[R44687]]></referencenumber>
    <apijobid><![CDATA[r44687]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44687/principal-scientist-hearing-loss-and-vestibular-disorders/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly skilled, motivated, and innovative Principal Scientist to lead the development of therapies to treat hearing loss and vestibular disorders. In this role, you will independently lead research projects and drive the development of novel therapies for inner ear disorders.</p><p><strong>A typical day in the life of a Principal Scientist on this team may include:</strong></p><ul><li><p>Lead the design of rigorous and appropriate experiments to address core questions of hearing biology, that can drive drug discovery and preclinical programs.</p></li><li><p>Develop and characterize novel animal models to better understand mechanisms of hearing loss and evaluate the potential of novel therapeutics to mitigate hearing phenotypes.</p></li><li><p>Design and execute <em>in vivo</em> and <em>in vitro</em> functional assays to understand the mechanisms of syndromic and non-syndromic hearing loss.</p></li><li><p>Work cross-functionally with a team to develop translationally relevant studies.</p></li><li><p>Carefully analyze and evaluate data.</p></li><li><p>Present data both internally and externally, and participate in discussions in our collaborative, cross-functional team environment.</p></li><li><p>Independently draft and review protocols and articles for publication.</p></li><li><p>Motivate, develop, and supervise junior scientists, research associates and other trainees.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You enjoy a dynamic, fast-paced environment</p></li><li><p>Can work well both independently and in a team, and communicate effectively with colleagues across all levels</p></li><li><p>Maintain a rigorous approach to scientific work</p></li><li><p>You are resilient in overcoming challenges and can adapt to shifting priorities</p></li><li><p>You are excited to learn on the fly and expand your areas of expertise</p></li></ul><p><strong>To be considered for this role, you must have the following</strong>:</p><p>Ph.D. with a strong record of innovation and publication and 5+ years of experience. Proven expertise in drug development is required. Managerial experience is highly desirable. In vivo experimental experience is desirable. Strong understanding of human and mouse genetics and/or auditory physiology is an advantage.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director,  Program Operations Leader - Ophthalmology/Renal]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45092]]></requisitionid>
    <referencenumber><![CDATA[R45092]]></referencenumber>
    <apijobid><![CDATA[r45092]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45092/director-program-operations-leader-ophthalmologyrenal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>For US Locations, this position is on-site 4 days per week and 1 day from home. A fully remote role is not possible for this position. </em></p><p>The Program Operations Leader (POL) is responsible for leadership of and setting and implementation of the operational strategy for delivery of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The POL is a member of the Clinical Trial Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. The POL is responsible for line management of clinical trial management staff (including AD POL), and has responsibility for staff recruitment, development, coaching, mentoring and performance management. Plays a key role in driving the functional strategy of Clinical Trial Management in partnership with Functional leadership. The Director POL is expected to operate with autonomy and high-degree of independence.</p><p>In a typical day, you will:</p><ul><li>Be responsible for the overall success of the clinical study team(s) within a program(s)</li><li>Maintain an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, timelines and/or budget; provide clinical program level updates to stakeholders as requested</li><li>Provide operational insight into feasibility, timeline and cost estimates during clinical program/study development</li><li>Oversee clinical study timelines within a clinical program(s)</li><li>Provide input and operational insight into Clinical Study Concepts (CSC)</li><li>Be responsible for development and implementation of operational strategy, driving early study planning budget and timelines from Clinical Study Concept through Final Protocol </li><li>Review plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies. Ensure consistency within the program and development of best practices within CTM</li><li>Oversee clinical study budgets within a program: ensures review, presentation and approval of initial study budget and manages the budget through the lifecycle of the program by communicating changes to TA Operations Leader, as appropriate</li><li>Ensure timely delivery of quality operational deliverables and accountable for ensuring consistency of process and approaches across clinical study teams within the clinical program(s). </li><li>Drive decision making and integrates all operational considerations for studies within a clinical program(s) to ensure goals are attainable prior to implementation</li><li>Act as point of contact for clinical program and study level escalation</li><li>Review key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study progress</li><li>Provide proactive creation and implementation of risk mitigation strategies</li><li>Provide innovative and flexible operational solutions and options to the cross functional and development teams; assists in preparing scenarios for creative solutions to operational challenges</li><li>Drives the strategy and oversight for vendor selection and management within a clinical program(s)</li><li>Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables and relationship with key CRO (functional and project) and vendor counterparts</li><li>May require up to 25% travel</li></ul><p>To be considered, you must possess a Bachelor's degree and a minimum of 12 years of related in-house sponsor-side pharmaceutical experience, with 8 years in clinical operations.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Change Communications]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45838]]></requisitionid>
    <referencenumber><![CDATA[R45838]]></referencenumber>
    <apijobid><![CDATA[r45838]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45838/manager-internal-change-communications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an internal communications pro at the Manager level to help develop and drive communications targeting our 15,000+ colleagues globally. The successful candidate will join a dynamic and high-performing Internal Communications team that thinks strategically and executes at a high level to support our fast-growing company -- where colleagues are passionate about their work and our mission to bring important new medicines to patients in need. Internal Communications is part of the Corporate Affairs organization, which is focused on strengthening Regeneron’s reputation by developing strategies and programs that (1) distinguish our science, medicines and patient focus, (2) sustain culture and drive employee engagement, and (3) advance and differentiate our corporate responsibility commitments.</p><p><em><strong>This role will require 4 days per week onsite at our Global HQ Campus in Westchester, NY. This is not available as a fully remote / hybrid work.</strong></em></p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li><p>Support the development and execution of global communications programs that advance the goals of our key corporate functions (HR, IT, etc.) that are advancing critical innovation and digital transformation programs across the company.</p></li><li><p>Serve as trusted internal communications partner to leaders within G&A functions, advising on communications approaches that support enterprise priorities and initiatives.</p></li><li><p>Plan and coordinate key internal communications initiatives, demonstrating project management know-how and creative approaches that effectively inform, inspire and engage employees.</p></li><li><p>Draft compelling messaging – including project briefs, key messages, talking points, FAQ and other materials – that connect to company goals and priorities.</p></li><li><p>Develop informative and creative ways to communicate and engage employees about critical enterprise change initiatives, including digital transformation, global expansion, culture storytelling, and more.</p></li><li><p>Build strong relationships with colleagues at all levels of the organization to support collaboration.</p></li><li><p>Measure the effectiveness of communications and translate insights into actionable recommendations to improve reach, clarity and impact. </p></li><li><p>Identify and implement opportunities to elevate the strategic focus of communications, streamline processes, and improve overall efficiency and effectiveness.</p></li></ul><h3><strong>This Role Might Be For You If You:</strong></h3><ul><li><p>Experienced in planning and executing communications initiatives, including storytelling and content management, that engage a busy, global employee base.</p></li><li><p>Knowledge and understanding of change communication principles that help employees navigate organizational change and connect to the opportunity that change presents.</p></li></ul><ul><li><p>Outstanding verbal and written communication skills, with the ability to translate complex topics into clear, accessible messaging tailored to diverse audiences.</p></li><li><p>Knowledge of and experience with channels, approaches and technologies that are used to communicate and connect with employees (intranets, enterprise social platforms, email distribution tools, etc.)</p></li><li><p>Ability to manage and prioritize multiple tasks and projects, adapt quickly to changing priorities and needs, and meet deadlines in a fast-paced environment.</p></li><li><p>Exceptional project management skills, strong attention to detail, sound judgment and curiosity to learn.</p></li></ul><p><strong>To be considered you must have a:</strong></p><ul><li><p>Bachelor's degree</p></li><li><p>Minimum 4+ relevant experience in internal communications and employee engagement.</p></li></ul><ul><li><p>Previous employment in a PR/Communications agency and/or the pharma/biotech industry preferred but not required.</p></li><li><p>Experience in a communications role supporting corporate or business functions, including HR, IT, etc.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, US Oncology Lung Cancer Marketing]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46333]]></requisitionid>
    <referencenumber><![CDATA[R46333]]></referencenumber>
    <apijobid><![CDATA[r46333]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46333/director-us-oncology-lung-cancer-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, US Oncology HCP Lung Cancer Marketing, is a member of the Oncology Business Unit with accountability for working closely with the Senior Director to develop commercial HCP promotion strategy and tactical plans for Non-Small Cell Lung Cancer (NSCLC) within the US. Also responsible for collaborating with the International team for Global commercialization and promotion.</p><p>This position will report directly to the Senior Director, US HCP Lung Cancer Marketing. The Director will work collaboratively across the Franchise Team, International teams, internal cross-functional colleagues, while effectively managing external agency partners to ensure alignment and to drive optimal integration and execution of personal and non-personal initiatives.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li>Lead HCP marketing for the NSCLC indications in the US. This includes defining US market opportunities, analyzing the competitive landscape, identifying key site of care and key account segmentation and needs, developing customer-focused and differentiated product and indication positioning, and customizing messages to key target audiences.</li><li>Works in close collaboration with Clinical, Medical Affairs and Field Medical to ensure alignment with Medical Education strategic plans.</li><li>Engage with physician experts and attend key congresses to support Scientific Marketing team efforts and assess important disease and treatment data.</li><li>Work closely with the Insights and Data Analytics team to design and implement promotional strategies, while tracking brand performance, share of voice, market dynamics and competitive actions & response. Provide business assumptions input to forecasting.</li><li>Oversee and collaborate with Digital/Media Strategy team for optimization and implementation of the multi-channel marketing mix, including omni-channel digital & media strategy and implementation, and creation and deployment of educational resources towards brand objectives and developing indicators/metrics for high-impact engagements with HCP key target audiences.</li><li>Develop and coordinate NSCLC HCP Marketing inputs and key sections of brand plan, identify and prioritize business opportunities.</li><li>Responsible for the development of the Field Plan of Action and training plan, national/regional sales meeting execution and Field communications in collaboration with internal and external partners/collaborators.</li><li>Maintain strong collaborative relationships with cross-functional areas and internal strategic partners (i.e., Field Sales, Training, Promotional Review Committee, Medical Affairs, Regulatory, Clinical, Legal, Compliance, Market Access etc.)</li><li>Ensures that the marketing processes, programs, and internal reports are developed, implemented, and effectively administered to be consistent with corporate guidance and all regulatory, legal, ethical guidelines.</li><li>Manages and develops a direct report to ensure their continued development and growth.</li><li>Works cross functionally to create, manage and track budget to ensure operating within the approved budget and phasing.</li></ul><h3><strong>This job might be for you if:</strong></h3><ul><li>You are effective collaborator and communicator both written and verbal</li><li>You can navigate regularly in ambiguity</li><li>You excel in a fast paced environment</li></ul><p>To be considered for this role, we expect you to have a Bachelors degree; 12+ years of pharmaceutical marketing focused on Oncology. Along with leading and developing long range brand plans, budgets and forecasts for commercial teams in the pharmaceutical/biotech industry. Lastly, this role requires you to travel 30% of the time and to be in the office in Sleepy Hollow, NY 4 days a week.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, Viral Delivery Technologies (AAV)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46365]]></requisitionid>
    <referencenumber><![CDATA[R46365]]></referencenumber>
    <apijobid><![CDATA[r46365]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46365/senior-associate-scientist-viral-delivery-technologies-aav/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Viral Delivery Technologies group is seeking a highly motivated Senior Associate<strong> </strong>Scientist to support development of an antibody-retargeted adeno-associated virus (AAV) delivery platform. This role will support the design, characterization, and in vitro/in vivo validation of novel AAVs, further expanding the company’s gene therapy vector delivery portfolio.</p><p><strong>As a Senior Associate Scientist within the Viral Delivery Technologies group, a typical day might include:</strong></p><ul><li><p>Design, execute, analyze, and troubleshoot in vitro experiments to characterize and validate antibody-retargeted viral vector designs, screening protocols, and performance.</p></li><li><p>Perform basic molecular biology and protein analysis techniques (e.g., cloning, SDS-PAGE, Western blotting, ELISA, DNA extraction, PCR, qPCR, protein chromatography).</p></li><li><p>Partner with the bioinformatics team to translate vector designs into screening platforms.</p></li><li><p>Execute rAAV production protocols and expand our understanding of AAV biology to inform novel vector optimizations.</p></li><li><p>Collaborate with cross-functional team members, collaborators in analytical groups, and core facilities across Research and Discovery.</p></li><li><p>Participate in team meetings and prepare regular updates and presentations for departmental forums.</p></li></ul><p><strong>This role may be a good fit if you:</strong></p><ul><li><p>Enjoy working in an innovation-driven, highly collaborative, fast-paced environment.</p></li><li><p>Have an affinity for bioengineering and technology-development projects.</p></li><li><p>Are highly motivated and seek continual improvement.</p></li><li><p>Are rigorous, have strong attention to detail, and can effectively balance multiple projects.</p></li><li><p>Have excellent presentation and communication skills.</p></li></ul><p><strong>To be considered for this role,</strong> you must have, at minimum, a B.A./B.S. and 5+ years of relevant industry or academic experience. An M.S. in cell biology, molecular biology, biochemistry, protein purification, and/or antibodies is preferred. Required experience includes mammalian cell culture; manipulation and purification of viruses and/or proteins; DNA isolation from tissues and cells; plasmid cloning; use of antibodies in various applications; and maintenance of accurate, up-to-date electronic lab records. Familiarity with key antibody properties, protein engineering, viral vector production, and relevant research software (e.g., Microsoft Office, GraphPad Prism, Benchling, MacVector) is desired. Level will be commensurate with experience.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QA Specialist (Oligonucleotides/VLPs)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46552]]></requisitionid>
    <referencenumber><![CDATA[R46552]]></referencenumber>
    <apijobid><![CDATA[r46552]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46552/qa-specialist-oligonucleotidesvlps/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Quality Assurance Specialist (Oligonucleotides/Virus-like particles (VLPs)) position. This position performs activities supporting dispositioning product and/or raw materials while ensuring compliance with Quality Assurance policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Reviewing and approving batch records from Contract Manufacturing Organizations (CMO) manufacturing bulk drug substance including VLPs and small interfering RNAs (si-RNA)</p></li><li><p>Representing Quality Assurance in support of sophisticated Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution</p></li><li><p>Providing consultation or advice in alignment with QA policies</p></li><li><p>Performing activities associated with disposition of raw materials and product (e.g. receipt, inspection, document review, shipping, etc.)</p></li><li><p>Reviewing, editing, or approving Regeneron controlled documents</p></li><li><p>Reviewing and approving of investigations associated with raw materials, product, laboratory, facilities, and materials</p></li><li><p>Performing status labeling of raw materials and product</p></li><li><p>Continually evaluating Regeneron processes and procedures with an eye toward continuous improvement</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Excel in a quality driven organization</p></li><li><p>Have an understanding of VLP or si-RNA manufacturing operations</p></li><li><p>Are organized and have an attention to detail</p></li><li><p>Can prioritize multiple assignments and changing priorities</p></li><li><p>Are able to learn and utilize computerized systems for daily performance of tasks</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree and the following amount of relevant experience for each level:</p><ul><li><p>Associate QA Specialist – 2+ years</p></li><li><p>QA Specialist – 4+ years</p></li><li><p>Sr QA Specialist - 6+ years</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Electrical Project Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46892]]></requisitionid>
    <referencenumber><![CDATA[R46892]]></referencenumber>
    <apijobid><![CDATA[r46892]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46892/senior-electrical-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Senior Electrical Engineer who will design, specify and commission new and renovated electrical systems. This individual will provide engineering support and problem solving for new capital projects, existing equipment and manufacturing processes and work in conjunction with the electrical maintenance team to ensure operational availability of electrical distribution networks. </p><p><strong>As a Senior Electrical Engineer a typical day might include the following:</strong></p><p>- Designing and maintaining LV (e.g. Lighting, General Services, UPS, Protection Settings incl. Arc Flash) and ELV (e.g. Fire Alarm, Data points, Building Automation) systems</p><p>- Managing small projects related to electrical systems infrastructure</p><p>- Assisting in the design review, site acceptance and installation of electrical equipment</p><p>- Preparing and maintaining electrical drawings and related documentation</p><p>- Designing and specifying cGMP E&I equipment and process controls</p><p>- Managing electrical systems residing on the business IT network</p><p>- Supporting validation department by preparation of design documents and assisting in protocol execution</p><p>- Assisting in investigations of equipment and control system anomalies, incl. power quality events</p><p>- Preparing engineering evaluations for and executing modification change control documentation</p><p>- Supervising electrical contractors and confirming works are to the required standard</p><p>- Preparing risk assessments, method statements and all aspects relating to Health and Safety on site</p><p>- Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</p><p>- Can safely operate and manage HV network</p><p>- Maintaining company reputation by enforcing compliance with all relevant laws, policies, standards and regulations</p><p><strong>This role may be for you if:</strong></p><ul><li><p>You have excellent technical and analytical skills</p></li><li><p>You are skilled at problem-solving and continuous improvement</p></li><li><p>You possess strong communication and collaboration skills</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><p>To be considered for this position, you must hold a Bachelors degree in Electrical Engineering or relevant discipline and have 5+ years' experience working in regulated industry. Level will be determined based on qualifications and experience relevant to the role</p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€63,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Neuroscience & Ophthalmology Genetics]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46973]]></requisitionid>
    <referencenumber><![CDATA[R46973]]></referencenumber>
    <apijobid><![CDATA[r46973]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46973/associate-director-neuroscience-ophthalmology-genetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Physician Scientist to join our Neuroscience and Ophthalmology Therapeutic Area Genetics (TAG) team. We see this role as a subject matter authority in the translation of human genetic evidence into actionable insights in neurological, psychiatric, ophthalmological, hearing- and aging-related diseases. You will work closely with other teams in the Regeneron Genetics Center and Regeneron at large and be primarily responsible for designing, contributing to the execution of, and interpreting large and complex human genetic studies in the therapeutic areas. We hope you are excited by the opportunity to play a role in the development and implementation of innovative translational sciences and identify new therapeutic targets through genetic approaches. </p><p>As a Physician Scientist in Neurology/Ophthalmology, a typical day might include the following:</p><ul><li><p>Applying human genetics to target discovery, selecting indications for drug programs, and identifying subgroups of patients who are more likely to respond to treatment through genetic analyses.</p></li><li><p>Working with a multidisciplinary genetics team consisting of human genetics scientists, bioinformaticians, statistical geneticists, and other team members to design, execute, and interpret genetics studies in ophthalmology.</p></li><li><p>Working in close collaboration with other Therapeutic Area Genetics team members and forming a strong partnership with Genome Informatics, Analytical Genomics, Clinical Informatics, and other RGC teams to deliver on complex, top-quality scientific endeavors in these Therapeutic Areas.</p></li><li><p>Generating, summarizing, and presenting results in internal and external meetings to a variety of audiences.</p></li><li><p>Leading or contributing to the writing of scientific reports and publications.</p></li><li><p>Representing the TAG team in cross-functional initiatives within RGC and Regeneron.</p></li><li><p>Collaborating with external industry and academic partners in scientific consortia.</p></li></ul><p>This job may be for you if:</p><ul><li><p>You have demonstrated the ability to design and lead human genetics studies delivering medically relevant findings in a team-based environment.</p></li><li><p>You use medical knowledge to define relevant phenotypes for genetic association studies and to formulate innovative and important research questions. You have familiarity with clinical genetics concepts and various genetic models of disease.</p></li><li><p>You have experience leading complex human genetics research endeavors, have knowledge of different study designs and analyses including GWAS, exome, or genome sequencing in cohort, case-control, or family-based studies, and have the ability to integrate different data resources to translate initial findings.</p></li><li><p>You have an interest in understanding the genetic basis and causes of Neurological, Psychiatric, Ophthalmological, Hearing- and Aging-related diseases and translating this knowledge into therapeutic insights. An outstanding candidate will have previous experience with phenotypes related to these diseases.</p></li><li><p>You thrive working in a highly interactive environment with a diverse team of colleagues.</p></li><li><p>You have outstanding communication skills and an ability to summarize and present the results of human genetic studies to a variety of audiences.</p></li></ul><p>To be considered for this opportunity, you must have an MD or MD/Ph.D. with a strong background in and knowledge of human genetics or genetic epidemiology. An outstanding candidate will be an MD/Ph.D. with training and experience in translational human genetics, genetic epidemiology (or related disciplines), and strong quantitative skills. Familiarity with the applications of statistical genetics to gain medically actionable insights including polygenic risk scores, quantitative traits analyses, and Mendelian randomization, and familiarity with command-line interface, programming languages, and statistical software (eg. Python, R) is preferred. The outstanding candidate will have experience with the use of genetics in combination with other “omics” technologies (eg. epigenetics, proteomics, RNA-seq).</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Medical Operations, Expanded Access Programs]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47170]]></requisitionid>
    <referencenumber><![CDATA[R47170]]></referencenumber>
    <apijobid><![CDATA[r47170]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47170/senior-manager-medical-operations-expanded-access-programs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Expanded Access Programs will be responsible for all operational aspects of multiple projects/programs such as Expanded Access Programs, individual patient expanded access, and post-trial access managed by Medical Affairs. Based on team assigned, this role may include supervision of staff. Additionally, this role will support other MA projects, as requested.</p><h3>As a Senior Manager, a typical day may include:</h3><h3>Program Management:</h3><ul><li><p>Operational responsibility across multiple projects/program(s) with minimal direction: Expanded Access Programs, individual patient expanded access, post-trial access</p></li></ul><h3>Meetings & Committees:</h3><ul><li><p>Participates in team review meetings, product team alignment meetings, and program budget & status update meetings as needed</p></li></ul><h3>Budget Management:</h3><ul><li><p>Accountable for financial forecasting accuracy of Managed Access Programs within span of responsibility</p></li><li><p>Maintenance of program budget trackers for each molecule/activity, ensuring all communicated actuals and accruals are captured, projections are reforested as necessary, and brand give back are fully assessed</p></li><li><p>Maintains financial forecast for programs for quarterly for reporting to Accounting & Finance, and responsible for ensuring issue resolution for all discrepancies</p></li></ul><h3>Drug Supply:</h3><ul><li><p>Responsible for managing drug supply for Expanded Access Programs and individual patient expanded access, as appropriate</p></li></ul><h3>Metrics & Reporting:</h3><ul><li><p>Responsible for ongoing analyses, tracking and reporting of projects/programs support, timelines for completion, expected or assessed delays, solutions for streamlining processes for greater efficiency, and other related metrics in support of program activities</p></li></ul><h3>Vendor Management:</h3><ul><li><p>Manages vendors and financial tracking as required per program</p></li></ul><h3>Essential Documents:</h3><ul><li><p>Ensures appropriate archiving of projects’/programs’ essential documents</p></li></ul><h3>Systems Management:</h3><ul><li><p>Utilizes appropriate systems to contribute to cross-functional communication, planning and transparency, including but not limited to:</p></li><li><p>Ensures ongoing QC of SharePoint document storage for completeness and audit readiness</p></li><li><p>Expertise required in the utilization of QlikSense, QlikView, SharePoint, Oracle and ESRA portal to support team needs</p></li></ul><h3>Process:</h3><ul><li><p>Adheres to all relevant processes, trainings, and SOPS to ensure consistency, efficiency, and compliance. Exercises' judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions; Continued process improvements</p></li></ul><h3>Organizational goals:</h3><ul><li><p>Development of objectives in order to quantify success and attainment of goals. Ensures optimal structure, procedures, and adequate resources supporting growth of multiple projects/programs. Knows when to escalate issues, and involve senior levels of management to obtain adequate resolution</p></li></ul><h3>Alliance Management:</h3><ul><li><p>Ensures financial transparency and alignment with both Alliance and internal stakeholders, supporting the product team financial reviews</p></li></ul><p>To be considered a bachelor’s degree is required and an advanced degree preferred. You are to have 5- 8 years’ experience working in clinical research or medical operations within the pharmaceutical or biotech industry. Active working experience and/or courses pertaining to clinical research and/or MA areas (such as GCP, Investigator Initiated Studies; medical/educational grants administration; medical information; registries; OIG/PhRMA guidance.). Compassionate Use or Managed Access programs preferred. We are seeking strong communication and presentation skills for senior management audiences.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director , Field Medical Affairs--Gastroenterology (GA, AL, KY, TN)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47174]]></requisitionid>
    <referencenumber><![CDATA[R47174]]></referencenumber>
    <apijobid><![CDATA[r47174]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47174/associate-director-field-medical-affairs-gastroenterology-ga-al-ky-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs, you will play a pivotal role as a field-based professional within Gastroenterology to support the clinical and business objectives across the product life cycle. We deliver strategic and operational support by establishing, developing and maintaining scientific exchange with medical specialists, health care professionals, and payers, aligned with our strategic objectives. We provide clinical and health economic information that enhances the value and appropriate use of Regeneron products. You will work with clinical research sites and investigators, and support of research activities as directed by the Global Medical Functional head.</p><p>Responsibilities of this role are to ensure accurate exchange and distribution of clinical and scientific information relevant to in-line and pipeline products in a timely, ethical and customer-focused manner.</p><p><strong>Territory:</strong> GA, AL, KY, TN</p><p><strong>A typical day may include:</strong><br>• Engaging in scientific discussions with medical and scientific specialists, including Healthcare Professionals and population health decision makers (“payers”) consistent with Medical Affairs objectives.<br>• Demonstrating deep scientific expertise related to assigned molecules/products and the associated therapeutic area to exchange relevant information and insights with specialists within a region.<br>• Building and developing relationships with key external scientific and medical specialists and organizations in a region to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape.<br>• Shaping and executing local medical strategy based on Global Medical Affairs strategy within planned timelines.</p><p><strong>This may be for you if you:</strong><br>• Enjoy working independently in the field, while having an impact on our mission.<br>• Are passionate about developing knowledge of and sharing clinical scientific data.<br>• Enjoy working collaboratively and building relationships in academic and clinical practice settings.<br>• Possess the innate ability to balance multiple initiatives, prioritize them and execute them independently, while excelling at keeping all partners advised and engaged.</p><p>To be considered for this position, you must have an advanced Clinical/Science Degree (e.g., MD, PharmD, PhD) with a minimum of 5 years related work experience (clinical, managed care, or industry experience). Experience as a Medical Science Liaison is required. Experience in Immunology is required; Gastroenterology experience is preferred. It is required to have the ability to communicate and disseminate scientific and clinical data.</p><p>Residency in the territory is required.</p><p>#msl #medicalscienceliaison</p><p>#i&i<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HCP Marketing - Oncology (Skin)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47350]]></requisitionid>
    <referencenumber><![CDATA[R47350]]></referencenumber>
    <apijobid><![CDATA[r47350]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47350/associate-director-hcp-marketing-oncology-skin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Oncology HCP Marketing will provide strategic & operational support for the US congresses and peer-to-peer education for the Non-Melanoma Skin Cancer (NMSC) indications. The Associate Director will work to increase brand equity and presence at key congresses, and will help build relationships & loyalty with customers. This role will provide an opportunity to gain marketing experience in a competitive space and make meaningful change in the ways we meet our business needs.</p><h3><strong>A Typical Day Might Look Like:</strong></h3><ul><li>Support & implement US congress & convention plans, creative vision, and communication strategy</li><li>Coordinate with marketing team, medical affairs, and thought leader liaisons (TLLs) to ensure cohesion across congress plans</li><li>Partner with Thought Leader Liaisons (TLLs) & Non-Small Cell Lung Cancer (NSCLC) congress point on Pan-tumor congress execution (eg. ASCO, ESMO)</li><li>Analyze the competitive landscape, identifying key promotions opportunities, and develop customer-focused and differentiated messages to key target audiences at congresses</li><li>Support all operational aspects for Peer-to-Peer education & Speaker Programs including content development/updates, new engagement tactics/formats, HCP contracting, training, logistics, communications, and act as key liaison with Commercial Operations group</li><li>Develop professional relationships with external medical experts & speakers</li><li>Contribute to US Advisory Board and Ad Council planning, including project management/timelines, content development, & contracting</li><li>Support management of promotional medical education, including content updates, execution, rollout of new promotional displays & tactics, pull-through with the sales team, vendor management, & budgets</li><li>Support management of agency involved in key projects with quarterly assessment and budget tracking</li><li>Support management of third party KOL programs</li><li>Planning & participation in relevant Brand Team Meetings</li><li>Ensuring marketing processes, programs, and internal reports are developed, implemented, and effectively administered to be consistent with corporate guidance and all regulatory, legal, ethical guidelines</li><li>Ensuring project timelines and expenses are kept on scope and budget</li><li>Ensuring cost effective delivery of all programs while tracking and monitoring metrics</li></ul><h3><strong>This Role Might Be For You If You:</strong></h3><ul><li>You can lead strategically, drive performance, and align across multiple functions</li><li>You bring strong project and process skills with attention to detail, proactivity, and ability to prioritize effectively</li><li>You are standout colleague with ability to navigate & collaborate cross-functionally</li><li>You thrive in a fast paced launch environment</li><li>You are innovative thinking and problem solving ability</li><li>You effectively communicate to a wide variety of scientific and commercially oriented individuals</li></ul><p>To be considered, you have 10 years of life science related marketing or slales experience along with a Bachelor's degree. We would like to see you have Oncology or Dermatology experience with a focus on Biologic products. We would prefer you to have Congress & Peer-to-Peer experience as well. Lastly, this will be a role that requires you to be onsite 4 days a week in Sleepy Hollow, NY.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Government Affairs Europe]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47381]]></requisitionid>
    <referencenumber><![CDATA[R47381]]></referencenumber>
    <apijobid><![CDATA[r47381]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47381/director-government-affairs-europe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. </p><p>We are looking for a <strong>Director, Government Affairs Europe</strong> to help shape and advance our public policy strategy across key European markets. In this role, you will lead government affairs activities, build trusted stakeholder relationships, and navigate complex healthcare systems to support business objectives. You will play a central role in aligning policy initiatives with organisational priorities while representing our interests externally. This is a unique opportunity to influence policy environments and drive meaningful impact across the region.</p><p><strong>Director, Government Affairs Europe</strong></p><p><strong>A Typical Day:</strong></p><ul><li>Leading government affairs and public policy activities across assigned European markets</li><li>Managing relationships with consultants to strengthen advocacy and policy influence</li><li>Developing advocacy strategies to support policy priorities and mitigate risks</li><li>Monitoring legislative developments and assessing impact on business operations</li><li>Representing the organisation in external forums and stakeholder engagements</li><li>Coordinating cross-functional teams to align policy activities with business goals</li><li>Supporting implementation of EU policies at national level to ensure compliance</li><li>Preparing policy analyses and briefing materials to inform strategic decisions</li></ul><p><strong>This Role may be for you:</strong></p><ul><li>You enjoy working across multiple countries and navigating diverse healthcare systems</li><li>You are comfortable influencing policy through stakeholder engagement and advocacy</li><li>You value building and maintaining strong external and internal relationships</li><li>You are motivated by translating complex legislation into strategic insights</li><li>You appreciate balancing strategic planning with operational execution</li><li>You thrive when coordinating with cross-functional and international teams</li><li>You are attentive to detail when tracking policy developments and compliance requirements</li><li>You enjoy representing an organisation in high-level external discussions</li></ul><p>To be considered, you must hold a Bachelor’s degree, with a minimum of <strong>7–10 years of experience in government affairs</strong>, public policy, or a related field within the pharmaceutical or healthcare industry. Demonstrated experience working with European healthcare systems and policy environments, along with managing external stakeholders or consultants, is required. Fluency in English is essential. An advanced degree in public policy, international relations, political science, law, or a related field is preferred, and proficiency in an additional European language such as German, French, Italian, or Spanish would be an advantage.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€119,900.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement - Direct Materials]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47496]]></requisitionid>
    <referencenumber><![CDATA[R47496]]></referencenumber>
    <apijobid><![CDATA[r47496]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47496/director-global-procurement-direct-materials/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As the Director, Global Procurement you will be developing and leading procurement strategies within the managed spend areas. You will work to build the foundation for continued success in Global Procurement by simplifying, accelerating, and clarifying ways of working. </p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li><p>Applying advanced judgement, planning, and independent thought leadership in order to influence positive business program outcomes and drive the procurement team deliverables</p></li><li><p>Either directly, or through a matrix, manages an organization of procurement professionals responsible for carrying out category management and sourcing projects</p></li><li><p>Developing and presenting functional strategy and objectives for procurement in alignment with the category business strategy and operational requirements</p></li><li><p>As part of a business team, influences the strategic direction of how Regeneron employs service providers</p></li><li><p>Directing a team responsible for activities associated with the development and execution of contracts covering spend under management</p></li><li><p>Liaising with finance to ensure all sourcing activities align with Regeneron’s financial controls, ensures ongoing engagement with finance throughout a program’s lifecycle for appropriate levels of contract, savings, and budgetary oversight</p></li><li><p>Providing mentorship, support, and overall leadership to the team to ensure goals are achieved</p></li><li><p>Advises, consults, and drives the global category management program for spend categories under management</p></li><li><p>Reviewing major contracts and acts as an expert resource for planning and leading complex negotiations using leader level mastery skills</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have strong interpersonal, cross-cultural, communication, negotiation, and problem-solving skills</p></li><li><p>You are committed to proactive resolution of issues with tact, diplomacy and composure</p></li><li><p>You demonstrate resilience and flexibility in a dynamic and fast-paced environment</p></li></ul><p>To be considered for this position you should have a BS/BA in a relevant area along with 12 years of relevant, progressive experience within procurement, preferably including 9 years directly in sourcing Pharma/Biotech. </p><p>Senior Manager: BS/BA plus 10 years experience</p><p>Associate Director: BS/BA plus 10 years experience</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Scientist, Drug Product Development]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47481]]></requisitionid>
    <referencenumber><![CDATA[R47481]]></referencenumber>
    <apijobid><![CDATA[r47481]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47481/sr-scientist-drug-product-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a highly skilled and motivated <strong>Senior Scientist </strong>to join our Drug Product Development and Technology (DPDT) Group. This Sr. Scientist position offers an exciting opportunity to work on various aspects of Drug Product development including high throughput formulation screening, characterization & development, lyophilization & other drug product process development activities for biologics, including monoclonal antibody (mAb), peptides, fusion proteins etc.</p><p><strong>A Typical Day In The Role Might Look Like:</strong></p><ul><li><p>Lead design and execution of high-throughput (HT) formulation studies to rapidly screen excipients for desirable physicochemical characteristics and stability for mAbs, peptides and fusion proteins etc. Perform HT analytical characterization and leverage statistical tools (e.g., JMP) to process large data sets efficiently.</p></li><li><p>Lead development and optimization of lyophilization cycles for various modalities across different phases of development</p></li><li><p>Perform biophysical and biochemical characterization of liquid and lyophilized formulations using techniques such as DSC, FDM, TGA, SE-UPLC, and others.</p></li><li><p>Support and lead process development, scale-up, technology transfer, and troubleshooting activities with Contract Manufacturing Organizations (CMOs) in collaboration with Industrial Operations & Product Supply (IOPS).</p></li><li><p>Collaborate cross-functionally with colleagues from Product, Analytical & Preclinical Development (PAPD) and IOPS organizations to advance the program needs.</p></li><li><p>Participate and contribute in cross-functional meetings to provide technical expertise and contribute to project planning and decision-making. Communicate effectively with stakeholders to ensure timely delivery of project milestones and objectives.</p></li><li><p>Draft and review protocols, technical reports, and supporting documents towards regulatory filings.</p></li><li><p>Stay abreast of advancements in DP Development technologies including novel process tools, HT methodologies, analytical tools and industry trends to drive innovation within the group.</p></li><li><p>Identify and implement process improvements to enhance efficiency, scalability, and quality in lyophilization and formulation development.</p></li></ul><p><strong>This Role Might Be for You If You Have:</strong></p><ul><li><p>Strong problem-solving skills and ability to address technical challenges in a fast-paced environment.</p></li><li><p>Ability to work independently and in team settings to drive the challenging task efficiently</p></li><li><p>Excellent technical writing, communication, and project management skills. Demonstrated ability to collaborate cross-functionally.</p></li></ul><p>This position requires a Ph.D. in Pharmaceutical Sciences, Biochemistry, Chemical and Biomolecular Engineering, or a related field with 0 - 3 years of relevant industry experience; OR M.S. with 8+ years of experience. Experience working with monoclonal antibodies and peptides is highly desirable with hands-on experience with biochemical and biophysical techniques for protein characterization using chromatography (SE-UPLC, IEX, RP-UPLC), electrophoresis (CE-SDS, MCE, cIEF, iCE), particle size (DLS, HIAC, MFI), UV-Vis, Viscosity and thermostability characterization (DSC, DSF). Expertise in lyophilization process development, including design, execution, and troubleshooting is desired as well. Experience with statistical software (e.g., JMP) for design of experiments and data analysis preferred. Ability to build efficient workflows for formulation screening and analytical testing and experience with automation tools is a plus.</p><p>This is a unique opportunity to contribute to cutting-edge drug product development initiatives and work on innovative technologies that will shape the future of the organization. You will join a dynamic and collaborative team committed to excellence and innovation in pharmaceutical development.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Commercial Launch & Project Management]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47535]]></requisitionid>
    <referencenumber><![CDATA[R47535]]></referencenumber>
    <apijobid><![CDATA[r47535]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47535/associate-director-commercial-launch-project-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>We are looking for an Associate Director of Commercial Launch & Project Management to lead product launches across our international markets, with a strong focus on the European Union. In this role, you’ll partner with global and regional teams to plan, coordinate, and deliver launches that bring innovative therapies to patients. You’ll play a key part in connecting teams, managing timelines, and ensuring launches stay on track from early planning through execution.</p><h3>A Typical Day:</h3><ul><li>Leading early planning for international product launches 12–18 months ahead</li><li>Defining launch scope, resources, and budgets with brand teams</li><li>Coordinating stakeholders across regions and functions</li><li>Building and managing launch timelines, tracking progress and dependencies</li><li>Running kick-off meetings and ongoing launch discussions</li><li>Monitoring progress, identifying risks, and keeping delivery on track</li><li>Driving problem-solving and escalating key issues when needed</li><li>Sharing clear updates on status, risks, and timelines with leadership</li></ul><h3>This Role May Be For You If You:</h3><ul><li>Enjoy organising complex projects across multiple markets</li><li>Like working with different teams and bringing people together</li><li>Stay focused and practical when plans shift or challenges arise</li><li>Build strong working relationships across regions and functions</li><li>Take ownership of timelines and follow through on delivery</li><li>Look for ways to improve how things are done</li><li>Are comfortable influencing decisions and moving things forward</li></ul><p>To be considered, you should bring at least 10 years of experience in commercial launch planning, ideally within pharma or biotech, along with a bachelor’s degree (master’s preferred). You’ll need strong experience with project management tools (including MS Project) and the Microsoft Office Suite. Experience managing international launches across matrix teams is essential, while a PMP certification and exposure to AI tools are a plus.</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€101,500.00 - €165,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Medical Study Operations]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47540]]></requisitionid>
    <referencenumber><![CDATA[R47540]]></referencenumber>
    <apijobid><![CDATA[r47540]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47540/manager-medical-study-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Manager, Medical Study Operations you are responsible for all operational aspects of Global Medical Affairs Oncology, including Investigator-Initiated Studies (IIS), Research Collaborations (RC), and Data Transparency requests across multiple products and new molecules. ensuring compliance with applicable standards and regulations. </p><p>This position will require you to be on-site 4 days/week at our Sleepy Hollow, NY offices. If eligible, we can offer relocation benefits. We cannot offer a remote work option. </p><p><strong>A typical may include the following: </strong><br>• Manage multiple projects/programs, including IIS, Research Collaborations, and Data Transparency, with moderate direction.<br>• Ensure proposals align with Areas of Interest, are complete, and reviewed by the appropriate governing bodies. Obtain all necessary approvals, including those from the Medical Affairs Review Committee (MARC), Collaborator/Partners, and Senior Management, for both original proposals and amendments.<br>• Facilitate meetings and committees, including setting agendas, driving goals, documenting outcomes, and ensuring follow-up on action items. Coordinate scientific meetings with external investigators and the Field Medical Team.<br>• Track and report study progress, data delivery, program impact, and other relevant metrics.<br>• Ensure collection, tracking, and archiving of all relevant documents, including regulatory submissions, IRB/EC approvals, and Health Authority communications.<br>• Ensure patent reviews, due diligence (e.g., OIG exclusion list, FDA debarment), and background checks for compliance.<br>• Collaborate with Site Budget & Contracting, Legal, Procurement, and Sponsor Institution to ensure agreement meets study requirements.<br>• Oversee study budgets, including Fair Market Value (FMV) analysis, approvals, and purchase orders (POs). Manage POs, achievements, invoicing, accruals, projections, and budget planning. Handle budget changes, reforecasts, and reconciliations while ensuring effective communication with partners.<br>• Plan and coordinate drug campaigns with Drug Supply Functions, ensuring compliance with packaging, labeling, and country-specific requirements.<br>• Manage drug shipments, resupply, expiry, quarantines, and destruction of unusable products.<br>• Ensures timely receipt and reconciliation of Serious Adverse Events (SAEs) and Investigator Alert Letters (IAL) in compliance with regulatory requirements.<br>• Coordinate internal review of publications, consolidate feedback, and document actions taken.<br>• Ensure data capture in study management tools and document repositories for audit readiness.<br>• Adhere to all relevant processes, training, and SOPs to ensure consistency, efficiency, and compliance.</p><p>To be considered a minimum of BA/BS degree in a related field with 7+ years of industry or relevant professional experience in clinical research. Experience in oncology and/or antibody research is a plus. Experience with Investigated Initiated Studies is preferred. <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Associate, Analytical Sciences: Synthetic and Bioconjugation Scale-Up Technologies (SBST) (1 of 2)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47642]]></requisitionid>
    <referencenumber><![CDATA[R47642]]></referencenumber>
    <apijobid><![CDATA[r47642]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47642/process-development-associate-analytical-sciences-synthetic-and-bioconjugation-scale-up-technologies-sbst-1-of-2/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Preclinical Manufacturing & Process Development (PMPD) organization in Tarrytown, NY is seeking a highly motivated <strong>Process Development Associate </strong>(PDA) to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics group. In this hands-on, lab-based role, you will generate high-quality, robust analytical data, support method development, and help characterize bioconjugates and critical intermediates to advance our growing and diverse bioconjugate pipeline. You will partner closely with cross-functional teams and external collaborators by generating key data to drive data-driven decisions that supports drug development in clinical to commercial stage.</p><p><em><strong>A Typical Day in the Role of Process Development Associate Might Look Like:</strong></em></p><ul><li><p>Perform hands-on analytical testing, method development, and characterization of bioconjugates and critical intermediate raw materials.</p></li><li><p>Analyze and present key data clearly to enable timely, data-driven decisions across a broad audience.</p></li><li><p>Partner with internal and external analytical groups to execute, establish and transfer fit-for-purpose analytical methods.</p></li><li><p>Communicate plans and results within cross-functional teams to enable program success.</p></li><li><p>Capture and document data in ELN entries in a timely manner to support program timelines.</p></li><li><p>Help with building business workflows to standardize sample and data management</p></li><li><p>Maintain compliance with lab and environmental safety requirements and promote a safe lab environment.</p></li><li><p>Be a responsible lab citizen by supporting equipment upkeep, maintaining an organized workspace, and proactively planning for lab resources.</p></li><li><p>Help with troubleshooting equipment and scheduling with Vendor service engineers</p></li></ul><p><em><strong>This Role May Be For You If You:</strong></em></p><ul><li><p>Enjoy working in the lab, and committed to generating high quality, reproducible data</p></li><li><p>Have strong initiative and aim to complete challenging tasks and learn new technologies in a timely manner.</p></li><li><p>Have strong fundamental understanding with analytical techniques and method development for antibody, bioconjugates, and/or small-molecule characterization.</p></li><li><p>Are capable of working in a fast-paced and collaborative environment involving cross-functional teams.</p></li><li><p>Communicate clearly (written and verbal) and build strong working relationships.</p></li><li><p>Can think critically and demonstrate problem-solving skills and comfortable navigating ambiguity.</p></li></ul><p>B.S. in chemistry, biochemistry, biology, chemical engineering, or a related field with 0–1 year of relevant laboratory experience (academic or industry); hands-on wet lab experience required. Fundamental knowledge of synthetic molecules (e.g., small molecules, PEG, peptides, and/or oligos) and/or protein analytical techniques. Strong communication skills (written and verbal) and the ability to present data clearly. Ability to work independently and collaboratively across cross-functional teams; strong attention to detail and documentation practices. Demonstrated initiative, learning agility, and a growth mindset in a fast-paced environment.</p><p><strong> </strong></p><p><strong>Preferred Qualifications</strong></p><ul><li><p>Experience with analytical characterization tools such as electrophoresis, HPLC separation, and UV spectroscopy.</p></li><li><p>Knowledge or experience in working with biological therapeutics, bioconjugates, or related modalities.</p></li></ul><p><strong> </strong></p><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III,  Analytical Science: Synthetic and Bioconjugation Scale-Up Technologies (SBST)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47644]]></requisitionid>
    <referencenumber><![CDATA[R47644]]></referencenumber>
    <apijobid><![CDATA[r47644]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47644/process-development-engineer-iii-analytical-science-synthetic-and-bioconjugation-scale-up-technologies-sbst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Preclinical Manufacturing & Process Development (PMPD) organization in Tarrytown, NY is seeking a highly motivated <strong>Process Development Engineer III</strong> to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics group. In this role, you will serve as the analytical lead to develop fit-for-purpose analytical methods, transfer, and provide troubleshooting support to advance diverse bioconjugate pipeline. You will lead and implement analytical deliverables working closely with bioconjugation teams and internal/external collaborators (CDMOs) to advance bioconjugate programs from development to commercialization.</p><p><em><strong>A Typical Day in the Role of Process Development Engineer III Might Look Like:</strong></em></p><ul><li><p>Independently design and execute analytical testing, method development and characterization to enable bioconjugate process development.</p></li><li><p>Serve as the subject matter expert to lead and design analytical deliverables: robust method development, method transfer to internal/external receiving labs, training, and troubleshooting to move program forward.</p></li><li><p>Connect, interpret, communicate complex results into clear actionable next steps to technical and non-technical audiences to persuade and drive timely decisions.</p></li><li><p>Author high-quality documentation (i.e., procedures, development and characterization reports, ELN entries) in a timely manner to support program timelines.</p></li><li><p>Drive, build and improve business workflows: documentation standardization, data digitization, and sample management.</p></li><li><p>Maintain compliance with lab and environmental safety requirements and promote a safe lab environment.</p></li><li><p>Proactively scout, evaluate, and implement new or improved technologies for high-throughput analytics and real-time decision making</p></li><li><p>Lead equipment upkeep, troubleshooting, maintain an organized workspace, and proactively plan for lab resources.</p></li><li><p>Mentor and support peers and junior team members (direct and/or indirect via matrix).</p></li></ul><p><em><strong>This Role May Be For You If You:</strong></em></p><ul><li><p>Enjoy working in the lab to advance exciting new drug modalities to patients</p></li><li><p>Posses strong initiative and aim to complete challenging tasks and learn new technologies quickly.</p></li><li><p>Possess strong hands-on experience and fundamental understanding of analytical techniques and method development for antibody, bioconjugates, and/or synthetic molecule (small molecule, peptides, and oligos) characterization, including relevant software.</p></li><li><p>Lead with customer centric mindset with providing analytical support to advance drug development in different phases of the program</p></li><li><p>Thrive in a fast-paced, highly collaborative environment working on complex problems.</p></li><li><p>Communicate clearly (written and verbal), simplify messages for impact, and build strong working relationships.</p></li><li><p>Think critically and apply strong problem-solving skills, and comfortable navigating ambiguity.</p></li></ul><p>This role requires a B.S. with 10+ years of relevant experience, or M.S. with 7+ years or recent PhD with 0-3 years of relevant experience in chemistry, biochemistry, biology, chemical engineering, or a related field. Hands-on experience with analytical method development for antibody, bioconjugate, and/or synthetic molecules (e.g., small molecule, PEG, peptides, and/or siRNA) such as electrophoresis, HPLCs, LC-MS, UV spectroscopy, plus associated software (e.g., Empower). Hands-on experience in transferring methods to internal/external labs, and troubleshooting. Demonstrated experience serving as an analytical lead for bioconjugate programs, collaborating effectively with internal teams and external CDMOs. Strong written and verbal communication skills, including the ability to present data clearly to diverse audiences. Experience drafting analytical methods, development and characterization reports to support regulatory filing. Ability to work independently and collaboratively across cross-functional teams to persuade and drive data-based decision. Demonstrated initiative, learning agility, and a growth mindset in a fast-paced environment.</p><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist - Analytical Development, Regeneron Cell Medicines (RCM)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47761]]></requisitionid>
    <referencenumber><![CDATA[R47761]]></referencenumber>
    <apijobid><![CDATA[r47761]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47761/scientist-analytical-development-regeneron-cell-medicines-rcm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Scientist, RCM Analytical Development, will support Regeneron Cell Medicines (RCM) cell therapy programs by developing, optimizing, and executing biophysical assays to characterize lentiviral vectors. In this exciting role you will be planning and performing experiments, developing new assay protocols, analyzing and interpreting data, and communicating results through presentations, protocols, and technical reports. This position also supports routine laboratory operations, instrument maintenance, and accurate electronic lab notebook documentation. The Scientist will partner cross-functionally to meet program timelines and deliver high-quality analytical data to support therapies for patients.</p><h3><strong>A Typical Day as Scientist Might Look Like</strong></h3><ul><li>Advance analytical development for cell therapy programs, with a primary focus on lentiviral vectors (LVVs).</li><li>Strengthen existing and establish new biophysical methods to characterize LVVs.</li><li>Analyze, interpret, and clearly present complex datasets to technical and cross-functional audiences.</li><li>Partner with cross-functional teams across RCM to troubleshoot challenges, align on priorities, and support program execution.</li><li>Author and review technical documentation, including assay protocols, method development reports, and data summaries.</li><li>Maintain complete, timely, and compliant electronic lab notebook records, support instrument upkeep, and independently troubleshoot equipment and assays.</li></ul><h3><strong>This Role May Be For You If:</strong></h3><ul><li>You thrive in a fast-paced, collaborative environment and consistently deliver results with efficiency and ownership.</li><li>You quickly learn new technologies, tackle complex problems, and have a passion for science.</li><li>You are self-motivated and proactive, prioritizing effectively, and driving work forward with minimal supervision.</li></ul><p>This role requires a Bachelors or Masters Degree in Biophysics, Biochemistry, Molecular Biology, or related field with 6-8+ years of proven experience with characterization and quantitative analysis of lentiviral vectors. This role requires the ability to work independently to design experiments, as well as interpret, document, and communicate results are required. Experience with biophysical characterization techniques for sizing and counting particles, such as DLS, MRPS, and fluorescent labeling assays, is preferred. Understanding and knowledge of viral vector biology, design, process, and gene delivery mechanisms is a plus.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Manager Workday]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42066]]></requisitionid>
    <referencenumber><![CDATA[R42066]]></referencenumber>
    <apijobid><![CDATA[r42066]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42066/sr-manager-workday/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a highly motivated Senior Functional Product Owner with expertise in Workday HCM solutions, particularly in Compensation, Advanced Compensation, and Benefits modules, to support both US and international operations. This role requires a combination of technical competence, functional product design expertise, and strong collaboration skills to deliver impactful solutions.</p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Act as the subject matter expert for Workday modules, focusing on Total Rewards (Compensation, Advanced Compensation), Benefits, and Time Tracking & Absence.</p></li><li><p>Collaborate with stakeholders to build product roadmaps and design innovative, scalable solutions that align with business needs.</p></li><li><p>Partner with business teams to capture requirements, document processes, and translate them into technical solutions.</p></li><li><p>Lead system-specific implementations, including integrations with third-party vendors for benefits solutions.</p></li><li><p>Be responsible for quality assurance testing, support user acceptance testing (UAT), and ensure timely delivery of solutions.</p></li><li><p>Provide hyper-care support after go-live, troubleshoot issues, and ensure smooth transitions.</p></li><li><p>Work closely with IT, boundary systems, and other technical teams to deliver effective solutions.</p></li><li><p>Identify gaps in existing processes and recommend improvements to enhance efficiency and scalability.</p></li><li><p>Build and maintain strong relationships with internal customers, keeping them informed of progress, risks, and delivery timelines.</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>8+ years of HR functional lead experience, with a strong background in Workday HCM.</p></li><li><p>6+ years of hands-on experience in Workday Compensation and Advanced Compensation modules, including supporting annual compensation cycles.</p></li><li><p>Experience with Workday Benefits modules, including integrations with third-party vendors.</p></li><li><p>Proficiency in creating advanced Workday reports and understanding security configurations for functional modules.</p></li><li><p>Exposure to other Workday modules like Time & Absence is a plus.</p></li><li><p>Strong understanding of system design, implementation, and integration processes.</p></li><li><p>Familiarity with ServiceNow or similar cloud-based applications is an advantage.</p></li><li><p>Experience documenting business processes, system flowcharts, and testing traceability (SIT, UAT).</p></li><li><p>Excellent communication and collaboration skills.</p></li><li><p>Analytical mindset with a proactive approach to problem-solving.</p></li><li><p>Ability to challenge and influence technical designs for simplicity and scalability.</p></li><li><p>Strong organizational skills with the ability to prioritize tasks and manage multiple priorities effectively.</p></li><li><p>Bachelor’s Degree is required.</p></li><li><p>Certifications in cloud-based technologies (e.g., Workday, AWS, ServiceNow) are a plus.</p></li></ul><p>Connect with us, so we can learn more about you, and you can learn more about our medicines. And join us in crafting the future of healthcare.</p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Specialist Third Party Risk Management]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48233]]></requisitionid>
    <referencenumber><![CDATA[R48233]]></referencenumber>
    <apijobid><![CDATA[r48233]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48233/sr-specialist-third-party-risk-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Specialist, Third Party Risk Management, India</strong> to join our <strong>Global Procurement</strong> team, supporting our <strong>enterprise Third Party Risk Management framework</strong> in a <strong>hybrid</strong> role. In this role, you will <strong>execute third-party risk activities accurately, consistently, and in line with the global framework</strong> while collaborating with <strong>Procurement, IP, Compliance, Legal, Information Security, and other risk domain teams</strong>. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>This role is based in Hyderabad, India, and follows a hybrid work model.</p><p><strong>Discover your role:</strong></p><ul><li><p>Implement third-party risk assessments across the full lifecycle.</p></li><li><p>Perform control reviews, risk tiering, and validation.</p></li><li><p>Track remediation actions and corrective plans through closure.</p></li><li><p>Maintain documentation, traceability, and audit readiness.</p></li><li><p>Support reporting of third-party risk KPIs and KRIs.</p></li><li><p>Partner with global teams to lead third-party risks.</p></li><li><p>You bring consistency and accuracy to risk operations.</p></li><li><p>You communicate clearly across global, matrixed stakeholder groups.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in engineering, risk management, compliance, information systems, or related field.</p></li><li><p>5–8+ years’ experience in third-party risk management, audit, procurement operations, or related roles.</p></li><li><p>Experience executing risk assessments, due diligence, or control-based operational processes.</p></li><li><p>Experience working in a regulated industry.</p></li><li><p>Hands-on experience with TPRM platforms, GRC tools, or supplier risk systems.</p></li><li><p>Exposure to automation, analytics, or AI-enabled tools in risk, compliance, or operations.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Scientist, Hematology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47872]]></requisitionid>
    <referencenumber><![CDATA[R47872]]></referencenumber>
    <apijobid><![CDATA[r47872]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47872/manager-clinical-scientist-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager to join our Clinical Scientist, Hematology department. You will lead in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. Leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to either Senior Manager, Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY, Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Member of the Clinical Study Team and Global Clinical sub-team; Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Develops/maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late-stage assets</p></li><li><p>Assists with development of the Expanded Synopsis and may author clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may authors/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Contributes to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority). Presents data and information to external investigators (SIV) and internal collaborators</p></li><li><p>Proven ability to influence within team and may influence across functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc)</p></li><li><p>≥ A minimum of 3 years of pharmaceutical clinical drug development experience</p></li><li><p>You have a basic knowledge of oncology or hematology therapeutic areas as well as a proven track in clinical trial process improvements</p></li><li><p>Proven leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs</p></li><li><p>Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Resolves novel problems requiring creative application of advanced skill, training, and education</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Los Angeles, CA]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47992]]></requisitionid>
    <referencenumber><![CDATA[R47992]]></referencenumber>
    <apijobid><![CDATA[r47992]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47992/medical-specialist-i-pulmonology-los-angeles-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Los Angeles]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Los Angeles, CA & Ontario, CA</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups. </p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Are confident in demonstrating strong and consistent sales performance that exceeds expectations related to goals</p></li><li><p>Are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>Can demonstrate a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>Collaborate effectively with internal and external partners</p></li><li><p>Share a passion and learning interest in science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Global Partnerships & Trial Optimization]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47900]]></requisitionid>
    <referencenumber><![CDATA[R47900]]></referencenumber>
    <apijobid><![CDATA[r47900]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47900/manager-global-partnerships-trial-optimization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[[Unknown]]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, to join our Global Partnerships & Trial Optimization team. You will lead study level activities, informing our clinical development strategy, clinical study concepts, study protocols and operational plans. We play a key role in developing and maintaining relationships with external experts facilitating a wide source of country and disease area intelligence used in study design and operational planning.<br>T</p><p>his position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>This is a US based remote position. </p><p><strong>Discover your role:</strong><br>• Partnering with teams during CRO led feasibility activities supporting validation of study and country level enrollment rates and study start up timelines to inform budget and baseline setting.<br>• Partnering with Data and Analytics function to review and identify central data sources and work with study teams to define assumptions for data curation and insight development<br>• Articulating our data story based o country level feasibility and centrally derived data to support data driven decisions to enhance protocol design<br>• Project management of study level country landscape assessment activities and the collection of targeted feasibility information supporting early assessment of operational feasibility for clinical trials.<br>• Provide functional input into the identification, qualification and relationship management of a range of vendors used in our processes<br>• Develop and maintain knowledge of external clinical trial environment and assess developments for impact on study design and execution<br>• Support Senior Managers in the development of study feasibility deliverables and Priority Investigator list.</p><p><strong>This role requires:</strong><br>• BS/BA required, Masters Preferred with 7+ years in Life Sciences industry or pharma consulting with a strong understanding and experience in operationalizing clinical development programs in a global setting from first-in-human to post-approval including feasibility<br>• Must be a compelling communicator with ability to translate sophisticated messages to a variety of audiences. Experience in using data to inform clinical strategy development<br>• Ability to understand sophisticated business questions and develop effective solutions<br>• Prior experience specifically managing feasibility strategy and execution of Hematology and/or oncology trials.<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Mid South]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47573]]></requisitionid>
    <referencenumber><![CDATA[R47573]]></referencenumber>
    <apijobid><![CDATA[r47573]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47573/regional-director-neurology-mid-south/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - North Carolina]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the [INSERT] Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Mid South (North Carolina, Virginia, South Carolina, Tennessee</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 18:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Administrative Coordinator]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48241]]></requisitionid>
    <referencenumber><![CDATA[R48241]]></referencenumber>
    <apijobid><![CDATA[r48241]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48241/senior-administrative-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are looking for a Senior Administrative Coordinator who is responsible for managing and providing administrative support to the Insights & Analytics Leadership team. This coordinator provides proactive support and administrative capabilities to 7 I&A sub-teams - Ophthalmology I&A, Oncology I&A, Immunology I&A, New Products/ Rare Disease I&A, Commercial Data Management, Field Enablement, and Market Access I&A.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Hybrid: 4 days per week on site </p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Submit procurement requirements: Confidential Disclosure Agreements (CDAs), Scope of Work (SOWs), Requisitions, Master Service Agreements (MSAs) and bid exceptions using REGN’s Icertis system</p></li><li><p>Track requisition approval status, assignment of Purchase Orders (POs), and invoice payments</p></li><li><p>Partner with cross-functional stakeholders — including Finance, Procurement, and Legal — to align on requirements, resolve dependencies, and drive initiatives forward</p></li><li><p>Monitor and manage department budget and monthly spend, ensuring expenditure remains aligned with forecast and financial targets</p></li><li><p>Partner with Finance to support the month-end close process, including timely submission and reconciliation of monthly accruals</p></li><li><p>Book internal and external meetings and trainings, including meeting invites, conference rooms, catering, directions, and security registration</p></li><li><p>Coordinate vendor site visits: introductions, capabilities meetings, and evaluations</p></li><li><p>Coordinate SurveyMonkey-type activities: detailing objectives and key questions, crafting and fielding surveys, and summary of results, as needed</p></li><li><p>Ensure the following materials are posted to SharePoint in a timely manner: final project reports, relevant vendor contact info, updated requisition templates, capabilities presentations, and other materials, as needed</p></li><li><p>Assist in on-boarding new employees and contractors using REGN’s NEMO system; help coordinate with IT on equipment (laptops, cellphones, monitors, etc.) that new personnel will require to be effective on day 1 of their joining, work with Executive Directors and VP, Insights & Analytics, in preparing Welcome Announcements</p></li><li><p>Process expense reports</p></li><li><p>Maintain master department calendar and non-Regeneron partner contact list</p></li><li><p>Consistent coordination and communication with Commercial staff regarding workload balance and coverage, facilities needs and issues, and companywide activities</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's Degree from an accredited college or university or at least 5 years of relevant administrative experience.</p></li><li><p>Strong Microsoft Office skills (Outlook, Excel, Word, PowerPoint) including knowledge of SharePoint</p></li><li><p>Detail-oriented, with the ability to manage multiple tasks and competing priorities effectively</p></li><li><p>Experience supporting/coordinating people and projects among multiple locations, a plus</p></li><li><p>Familiarity with contract management preferred (e.g. SOW, PO generation using a contract system like Icertis)</p></li><li><p>Strong written and verbal communication skills</p></li><li><p>Great teammate with the ability to work effectively with people at various locations and levels in the organization</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$33.80 - $52.93]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Assistant – Global Market Access]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48103]]></requisitionid>
    <referencenumber><![CDATA[R48103]]></referencenumber>
    <apijobid><![CDATA[r48103]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48103/executive-assistant-global-market-access/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Global Market Access Executive Assistant is primarily responsible for managing and providing administrative support to the Senior Vice President, Global Market Access, and their direct support team.</p><p>Responsibilities include, but are not limited to, heavy calendar management, coordination of in-house and offsite meetings (sourcing, planning, execution), expense reconciliation, and arranging US and international travel. The Executive Assistant should exercise considerable judgment and initiative with the ability to influence stakeholders and understand key relationships, while ensuring sensitive data is held in strict confidence.</p><p><strong>A typical day might look like this:</strong></p><ul><li>Proactively manage calendar for the SVP using a thorough understanding of department and leadership priorities. Ability to anticipate the needs of leadership and their teams to manage and problem solve when scheduling conflicts occur.</li><li>Arrange and coordinate travel logistics for the SVP which may include conference registrations, travel and meeting itineraries, air, hotel and ground transportation, along with reconciling corresponding expense reports.</li><li>Occasional domestic travel in support of the annual National Meeting, brand planning meetings, and various department team builders may be required.</li><li>Responsible for on and offsite meeting planning, including catering, rooming lists, audio visual requests, and team builders, while ensuring adherence to budgetary guidelines.</li><li>Work closely with our external collaborators to coordinate meetings and events.</li><li>Demonstrates a working knowledge of company policies, procedures, resources and where to find them.</li><li>Implements a highly organized and efficient administrative workflow. Identifies, develops, and/or supports administrative process improvements.</li><li>Process and submit purchase requisitions and enter SOW, CDA, MSA information into the contract management system including onboarding new vendors. Track requisitions approval status and assignment of purchase orders and ensure alignment with department budget.</li><li>Manage the ABAC Risk Assessment Platform for due diligence of new vendors - InfoSec, SSP New Supplier Intake.</li><li>Responsible for collaborating with Strategic Sourcing and Procurement to manage and negotiate contracts, entering and adhering to budgetary guidelines for off-site meetings, team builders and events.</li><li>Reconcile expenses for the SVP as well as expenses incurred for offsite meetings and department purchasing card.</li><li>Complete visitor pre-registration and provide internet access for attendees. Meet, greet, and escort guests to conference rooms.</li><li>Onboard new, in-house employees (including ordering preferred laptop and peripherals, seat assignment, supplies).</li><li>Any other ad hoc administrative assignments such as ordering birth/bereavement gifts, holiday field and inhouse gifts.</li></ul><p><strong>This role may be a fit for you if you:</strong></p><p><strong> </strong></p><ul><li>You are a collaborative teammate with proficient written and verbal communication skills, actively listens and builds relationships, demonstrates effective customer service, exhibits high attention to detail, has ability to interact with all levels of employees and maintain confidentiality.</li><li>You demonstrate strong initiative and drive to complete tasks, enjoy working independently and within teams on multiple tasks or projects simultaneously.</li><li>You anticipate and proactively adjust for challenges and roadblocks, understanding how/when to provide feedback and when to escalate to the right people.</li></ul><ul><li>Demonstrates strong organizational skills and ability to understand Commercial Business Unit priorities.</li><li>Adaptive learner who can shift gears with ease and make good decisions during change or ambiguity.</li><li>Exercises good judgement and be willing to go above and beyond; takes initiative.</li><li>Proficiency in MS Office is necessary. Knowledge in SharePoint, Concur, Oracle, iCertis and MS Teams are preferred but not required.</li></ul><p>This role requires an Associate or BA/BS, with BA strongly preferred. Minimum of –5-10 years of relevant administrative experience in a fast-paced environment. Collaborative team player with excellent oral and written communication skills. Advanced organizational skills with demonstrated attention to detail. Ability to learn new technologies and systems quickly and easily. Proficient in all MS Office applications.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$38.61 - $63.03]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Obesity, Muscle and Metabolism]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47998]]></requisitionid>
    <referencenumber><![CDATA[R47998]]></referencenumber>
    <apijobid><![CDATA[r47998]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47998/associate-scientist-obesity-muscle-and-metabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Obesity, Muscle and Metabolism group is seeking a highly motivated Associate Scientist to support the development of therapeutics for muscle diseases. This role involves joining a productive and collaborative team working on treatments for muscular dystrophies, myopathies, and myositis, with the opportunity to engage in cutting edge tissue engineering, disease modeling research as a part of our discovery efforts.</p><p>This is a lab-focused role suited for a bench scientist with a strong foundation in cell biology and physiology, as well as experience in cell culture and tissue engineering. You will be developing assays for validating molecular and functional readouts for our therapeutic programs.</p><p>As an Associate Scientist in the Obesity, Muscle and Metabolism group, your typical day might include:</p><ul><li><p>Maintaining, expanding, and modulating cells in vitro</p></li><li><p>Generation of engineered muscle tissue from primary or iPSC-derived progenitor cells</p></li><li><p>Optimization of cellular assays, and development of readouts for muscle function</p></li><li><p>Handling and caring for mice, including performing procedures such as blood and tissue sample collection</p></li><li><p>Processing of tissue samples for molecular and histological assessments</p></li><li><p>Close collaborative interactions with teams across the organization</p></li><li><p>Analysis of data using biological and statistical software such as ImageJ, Flowjo, Excel, Prism</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Enjoy working in an innovative and team-driven environment</p></li><li><p>Are highly organized, detail-oriented, and motivated, with a creative approach to problem-solving</p></li><li><p>Are adaptable, flexible, and enjoy learning new techniques or switching tasks as needed</p></li><li><p>Are excited to contribute to the development of novel therapeutics</p></li><li><p>Communicate openly and frequently with manager and team members</p></li></ul><p><strong>To be considered for this role, you should have</strong></p><ul><li><p>B.S. or M.S. degree in a relevant field with 1-2 years of experience in muscle biology or a related discipline</p></li><li><p>Experience in tissue culture, cell-based assays, flow cytometry, and histology (e.g. IHC, IF) is highly preferred</p></li><li><p>Experience in mouse handling is highly preferred</p></li><li><p>Proficiency in basic computer applications and experience with biological data collection and analysis is highly preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager International Payroll]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46479]]></requisitionid>
    <referencenumber><![CDATA[R46479]]></referencenumber>
    <apijobid><![CDATA[r46479]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46479/manager-international-payroll/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a International Payroll Manager, Europe and Asia to join our payroll function, supporting our Europe and Asia operations in a hybrid work mode. In this role, you will support payroll processing, reporting, compliance, and team management activities while collaborating with HR, Accounting, Tax, and Mobility teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><p>Hybrid - Dublin</p><p>Discover your role:</p><ul><li><p>Manage day-to-day payroll operations across multiple countries</p></li><li><p>Review payroll inputs and outputs prior to provider submission</p></li><li><p>Oversee payroll reconciliation processes ensuring accuracy and completeness</p></li><li><p>Lead payroll meetings with HR, Accounting, Tax, and Mobility teams</p></li><li><p>Drive process improvements and update payroll SOPs and training materials</p></li><li><p>Support implementation of new country payrolls during expansion</p></li><li><p>You collaborate across teams to resolve payroll queries and escalations</p></li><li><p>You prioritise tasks effectively to meet payroll deadlines</p></li></ul><p>This role requires:</p><ul><li><p>Degree in Business, Accounting or Finance</p></li><li><p>Minimum 5 years’ experience in payroll management with team responsibility</p></li><li><p>Strong Excel skills with analytical capability</p></li><li><p>Experience managing international payrolls across multiple countries</p></li><li><p>Experience working with external payroll providers</p></li><li><p>Experience with Workday and Oracle time tracking systems is advantageous</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€74,000.00 - €120,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Engineer]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47030]]></requisitionid>
    <referencenumber><![CDATA[R47030]]></referencenumber>
    <apijobid><![CDATA[r47030]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47030/senior-automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Our Automation Engineers keep our cutting-edge process controls and process monitoring systems running at peak efficiency. We provide unsurpassed expertise in designing, developing, implementing, and optimizing Regeneron’s sophisticated biopharmaceutical manufacturing processes.</p><p>As a Senior Automation Engineer, a typical day might include the following:</p><ul><li>Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures.</li><li>Using PLCs and HMIs to provide technical support and solutions to Manufacturing, Quality Control, and Facilities according to established SOPs and departmental practices.</li><li>Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems.</li><li>Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines.</li><li>Supporting small manufacturing, engineering, and validation projects.</li><li>Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action.</li><li>Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols.</li></ul><p>This job might be for you if you:</p><ul><li>Want to support our extraordinary team to produce the highest quality medicines for patients as efficiently as possible to change people’s lives.</li><li>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better.</li><li>Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly.</li><li>Have a knack for compiling documentation and enjoy it!</li><li>Don’t get frustrated with a meticulous process of change control, investigations and corrective actions.</li></ul><p>To be considered for this position, we prefer a BS in Engineering or a related field and 5+ years of relevant experience. Equivalent experience with process control systems and/or data acquisition systems may be considered in lieu of degree. </p><p>We look for experience in the design and maintenance of process control systems and/or data acquisition systems. We may consider candidates with limited experience programming and troubleshooting PLCs. Some experience in a regulated manufacturing environment is preferred. We use Allen-Bradley and Siemens control system products and video graphic chart recorders; specific knowledge with these products is ideal.​ Experience programming and troubleshooting with DeltaV DCS is desirable.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - GRAND RAPIDS, MI]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48049]]></requisitionid>
    <referencenumber><![CDATA[R48049]]></referencenumber>
    <apijobid><![CDATA[r48049]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48049/medical-account-specialist-ii-neurology-grand-rapids-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Grand Rapids]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Grand Rapids (Metro), Michigan </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - MINNEAPOLIS, MN]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48066]]></requisitionid>
    <referencenumber><![CDATA[R48066]]></referencenumber>
    <apijobid><![CDATA[r48066]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48066/medical-account-specialist-ii-neurology-minneapolis-mn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minneapolis]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Minneapolis (Metro), Minnesota</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - MILWAUKEE, WI]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48054]]></requisitionid>
    <referencenumber><![CDATA[R48054]]></referencenumber>
    <apijobid><![CDATA[r48054]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48054/medical-account-specialist-ii-neurology-milwaukee-wi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milwaukee]]></city>
    <state><![CDATA[Wisconsin]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Milwaukee (Metro), Wisconsin</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - LAS VEGAS, NV]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48077]]></requisitionid>
    <referencenumber><![CDATA[R48077]]></referencenumber>
    <apijobid><![CDATA[r48077]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48077/medical-account-specialist-ii-neurology-las-vegas-nv/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Las Vegas]]></city>
    <state><![CDATA[Nevada]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Las Vegas (Metro), NV</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 18:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -THOUSAND OAKS, CA - West]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48078]]></requisitionid>
    <referencenumber><![CDATA[R48078]]></referencenumber>
    <apijobid><![CDATA[r48078]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48078/medical-account-specialist-ii-neurology-thousand-oaks-ca-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Thousand Oaks]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Thousand Oaks (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - NEW ORLEANS, LA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48058]]></requisitionid>
    <referencenumber><![CDATA[R48058]]></referencenumber>
    <apijobid><![CDATA[r48058]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48058/medical-account-specialist-ii-neurology-new-orleans-la/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[New Orleans]]></city>
    <state><![CDATA[Louisiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: New Orleans (Metro), LA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs - Hematology - Ontario]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42140]]></requisitionid>
    <referencenumber><![CDATA[R42140]]></referencenumber>
    <apijobid><![CDATA[r42140]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42140/senior-manager-field-medical-affairs-hematology-ontario/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. </p></div><div><p>We are seeking a <strong>Senior Manager, Field Medical Affairs – Hematology</strong> to join our team and strengthen our partnerships with experts in hematologic malignancies. In this role, you will engage with key opinion leaders, healthcare providers, and investigators, serving as a trusted scientific resource and strategic partner. You’ll play a meaningful role in the understanding of Regeneron’s therapies, supporting clinical development and investigator-initiated research, and contributing to impactful new therapies. </p></div><div><p>We are looking for our next team member to join our passionate & dedicated Medical Affairs team in Canada. This is a remote, field-based role located in the Greater Toronto Area, Ontario, Canada.</p></div><div><p><strong>Senior Manager, Field Medical Affairs, Hematology</strong></p><p><strong>Greater Toronto Area, Ontario, Canada</strong></p></div><div><p><strong>A Typical Day:</strong> </p></div><div><ul><li><p>Building and maintaining relationships with KOLs in malignant hematology. </p></li></ul></div><div><ul><li><p>Acting as a primary clinical/scientific contact for HCPs and investigators. </p></li></ul></div><div><ul><li><p>Generating medical insights to advise strategy and development plans. </p></li></ul></div><div><ul><li><p>Supporting clinical trial execution by identifying investigators and trial sites. </p></li></ul></div><div><ul><li><p>Collaborating on abstracts, posters, and manuscripts to communicate data. </p></li></ul></div><div><ul><li><p>Contributing to investigator-initiated study programs and research collaborations. </p></li></ul></div><div><ul><li><p>Attending medical congresses to support scientific exchange. </p></li></ul></div><div><ul><li><p>Partnering cross-functionally with Medical Affairs, Commercial, and Market Access. </p></li></ul></div><div><p><strong>This Role May Be For You:</strong> </p></div><div><ul><li><p>You thrive on scientific exchange and are confident discussing complex data with KOLs. </p></li></ul></div><div><ul><li><p>You have established background in hematology and understand the oncology landscape. </p></li></ul></div><div><ul><li><p>You enjoy balancing independent field work with cross-functional collaboration. </p></li></ul></div><div><ul><li><p>You adapt easily to changing priorities and field-based challenges. </p></li></ul></div><div><ul><li><p>You are motivated by opportunities to contribute to country readiness and new research. </p></li></ul></div></div><div><div><ul><li><p>You value compliance and integrity while working with investigators and partners. </p></li></ul></div><div><ul><li><p>You are comfortable with frequent travel and engaging in high-level conversations. </p></li></ul></div><div></div><div></div><div><p>To be considered, you should bring at least 5 years of field medical or medical manager experience in biotech or pharma, with a strong background in hematology. Knowledge of malignant hematology is required, and experience in lymphoma or multiple myeloma is preferred. Country readiness experience and established KOL relationships are highly valued. You should also have solid knowledge of treatment guidelines, clinical research, and Canadian regulations. Strong communication, organizational skills, and the ability to travel up to 70% are essential. </p></div></div><ul></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (Skin) - North East]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46312]]></requisitionid>
    <referencenumber><![CDATA[R46312]]></referencenumber>
    <apijobid><![CDATA[r46312]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46312/sales-specialist-oncology-skin-north-east/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is growing its newly established International Oncology organisation and is seeking a Sales Specialist to join the UK sales team. This role focuses on engaging oncology healthcare professionals, supporting effective clinical practice through high‑quality scientific exchange, and representing Regeneron Oncology across the local healthcare system. The position offers the opportunity to contribute to a developing oncology portfolio while working closely with cross‑functional colleagues.</p><h3><strong>When and where</strong></h3><ul><li><strong>Location & work model:</strong> UK‑based, field‑facing role</li><li><strong>Travel:</strong> Frequent travel required, including attendance at meetings and congresses</li></ul><h3><strong>Discover your role</strong></h3><ul><li>Engage oncology healthcare professionals through compliant, scientific discussions</li><li>Understand local healthcare environments and account context</li><li>Communicate agreed brand messages to support objectives</li><li>Develop and implement territory and account plans using data and insights</li><li>Manage key accounts in line with regional and country guidance</li><li>Work closely with medical colleagues on regional activities</li><li>Represent Regeneron Oncology at national and international meetings</li><li>Report performance and market insights to UK leadership</li></ul><h3><strong>This role requires</strong></h3><ul><li>Comfort managing a defined territory and multiple accounts</li><li>A planned and structured approach to customer engagement</li><li>Flexibility to adapt activity based on account and market needs</li><li>Confidence using face‑to‑face, remote, and digital engagement channels</li><li>Consistent adherence to industry codes and company procedures</li><li>Professional conduct grounded in integrity and ethics</li></ul><h3><strong>Required qualifications</strong></h3><p>A Bachelor’s degree, or recognised equivalent for sales professionals, is required. The role requires experience in customer engagement and disease‑ or concept‑led selling, with the ability to present effectively to varied audiences. Strong planning and prioritisation capability and competence using CRM systems and multiple IT platforms are essential. Qualification in the relevant pharmaceutical industry Code of Practice (such as ABPI or EFPIA), fluency in English, and willingness to travel frequently are required.</p><p><strong>Preferred:</strong> Experience within the biotech or pharmaceutical sector, oncology sales exposure, and launch experience.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs - Neurology (Southeast)]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47896]]></requisitionid>
    <referencenumber><![CDATA[R47896]]></referencenumber>
    <apijobid><![CDATA[r47896]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47896/associate-director-field-medical-affairs-neurology-southeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>Job Description</div></div><div><div><div><div><div><div><div><div><div><p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. As a scientific expert in your territory, you will demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities to shape our medical strategy. You will be considered a scientific and clinical expert on our current and future Neurology assets. </p><p>Territory: GA, AL, FL, PR</p><p><strong>A typical day may include the following: </strong></p><ul><li><p>Establish, foster, cultivate and maintain peer relationships with KOLs in Neurology </p></li><li><p>Act as a primary clinical/scientific resource to HCPs for information pertaining to disease state and our products to ensure awareness and understanding. </p></li><li><p>Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans. </p></li><li><p>Support evidence generation (company sponsored trials and investigator-initiated studies) research initiatives. </p></li><li><p>Identify and report medical insights. </p></li><li><p>Identifies gaps in research and educational needs to inform medical strategy. </p></li><li><p>Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific and clinical data to appropriate audience in a compliant manner. </p></li><li><p>Performs disease management and therapeutic area education with identified practitioners, payers and researchers. </p></li><li><p>Attends conferences to collect and report relevant, scientific, clinical, & competitive intelligence. </p></li><li><p>Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally. </p></li></ul><p>To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) with a minimum 8 years of experience, including 4+ years working as a Medical Science Liaison in the pharmaceutical industry. Experience as a Neurology MSL or in Neurology is preferred. Demonstrated experience communicating complex data sets and the ability to be seen as a scientific peer while educating top KOLs is required. Established relationships with KOLs in neuromuscular centers is preferred, as is product launch experience. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. Capable of frequent business travel (approximately 70% of time), including air travel, ability to travel overnight and occasionally on weekends</p><p>#msl #medicalscienceliaison</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Purification Development (PMPD)]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48581]]></requisitionid>
    <referencenumber><![CDATA[R48581]]></referencenumber>
    <apijobid><![CDATA[r48581]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48581/process-development-engineer-iii-purification-development-pmpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking a hardworking <strong>Process Development Engineer III</strong>. The Purification Development (PD) group purifies reagents and candidates (novel molecules) to support pipeline and assay development and the release of the clinical and commercial products. PD's early and late stage development includes scalable speed-to-clinic processes and intended commercial processes, respectively. PD also evaluates viral clearance by the process to document safety in regulatory submissions. In this exciting role, you will use your domain expertise in liquid chromatography separations to design, lead, and react to experiments/projects independently and mentor less experienced direct reports and team members.</p><h3>A Typical Day in the Role of Process Development Engineer III Might Look Like:</h3><ul><li>Act as an established authority in chromatography-based separation techniques who can also demonstrate scientific acumen across Regeneron, proactively identify improvement opportunities, and determine strategies for improvements across Regeneron. Begin to lead technology development independently, drive results and onboard new technologies.</li><li>Skillfully write and review complex technical documents which are typically reviewed by senior leadership team.</li><li>Take calculated risks to achieve goals. Independently and accurately determine strategies/approaches to address gaps and implement them successfully and effectively.</li><li>Independently and expertly ask pointed questions to eliminate ambiguity and provide appropriate solutions to those questions.</li><li>Make science-based recommendations through novel incorporation of learning from internal and external (literature) references</li><li>Maintain and continuously improve lab operations and relevant data or knowledge management systems, within area of expertise.</li><li>Begin to anticipate customer needs at an organizational level and proactively shape internal workflows to meet them.</li><li>Work with supervisor to prepare and deliver effective oral presentations in internal and external professional meetings. Share cross-functional skills and knowledge at a wide variety of meetings.</li><li>Collaborate across Regeneron and external groups, with regular interactions with PMPD Senior Leadership.</li><li>Effectively represent PMPD in external PMPD multi-functional meetings.</li><li>Mentor directly or indirectly by leading, guiding, and assisting peers, direct reports, and PMPD personnel.</li></ul><h3>Other Duties and Responsibilities:</h3><ul><li>Contribute to lab equipment maintenance and safety to help create a safe, effective and efficient working environment.</li><li>Anticipate and recognize potential problems with laboratory supplies / equipment and takes action to prevent and solve problems.</li><li>Keep up with SOP training and/or compliance responsibilities.</li><li>Responsible for communicating relevant information to PMPD Senior Staff as departmental program team representative</li></ul><h3>This Role Might Be For You If You:</h3><ul><li>Have strong initiative and aim to complete challenging tasks and learn new technologies.</li><li>Are capable of multi-tasking, working both independently and within a team environment.</li><li>Have excellent interpersonal, verbal and written communication skills.</li><li>Can think critically and demonstrate problem-solving skills.</li></ul><p>This role requires a degree in an engineering discipline and 0-2+ (PhD), 3-5+ (MS) and 7-10+ BS years industrial experience. Industrial experience in Protein Purification required. Demonstrated ability to communicate complex messages clearly and credibly with widely multifaceted audiences while establishing multi-functional relationships that allow for proactive teamwork across the Regeneron organization required. Demonstration of innovative thinking by developing ideas, tools or techniques to solve problems or improve established procedures a plus. An experienced leader who can lead a team and effectively delegate tasks.</p><h3>Required Special Equipment and/or Programs:</h3><p>Akta Explorer/Avant, Akta Pilot, BioProcess Skid, Disc Stack Centrifuge, Depth filtration, Tangential flow filters, Normal flow filters, Chromatographic columns, HPLC, UPLC, Diafiltration skid, Raman Spectroscopy, Laminar Flow Hood, Chemical Fume hood, Empower, Unicorn, PI Historian, JMP, LIMS, Spotfire, RPES, ELN.</p><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 18 Jun 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Patent Attorney]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44376]]></requisitionid>
    <referencenumber><![CDATA[R44376]]></referencenumber>
    <apijobid><![CDATA[r44376]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44376/director-patent-attorney/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Director, Patent Attorney will act as legal counsel on matters related to the development, protection, and management of Regeneron’s valuable intellectual property pertaining to its manufacturing. The role will be responsible for patent activities relating to manufacturing and bioprocessing at all stages of the development pipeline including cell line technologies, purification, formulations, assay and media development. This position will partner closely with our world-class scientists and manufacturing development leaders around key strategies for our rapidly growing patent portfolio, patent filings, trade secret protection, and patent actions.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Identifying, capturing and prosecuting new inventions relating to manufacturing and bioprocessing; Preparing and prosecuting global patent applications relating to all aspects of manufacturing & bioprocessing including cell development, cell culture, purification, assay development, formulation, packaging and delivery; Leading outside counsel on various projects as appropriate;</p></li><li><p>Conducting patent landscape overviews, freedom-to-operate analyses, validity assessments and patentability assessments in relation to Regeneron pipeline products, and presenting the results and analyses to senior members of the Law Department and senior management;</p></li><li><p>Leading US and foreign administrative patent actions (e.g., oppositions, third party observations, inter partes reviews, etc.);</p></li><li><p>Supporting due diligence projects, agreements and other transactional work, administrative initiatives, and policy questions.</p></li><li><p>Advising on emerging legal issues, including monitoring and reviewing case law and legislative developments.</p></li><li><p>Possess strong interpersonal skills and the ability run multiple projects against competing priorities.</p></li><li><p>Excel at handling a large and sophisticated docket with minimal direction.</p></li><li><p>Have exceptional communication skills, including presentation, interpersonal, writing and conflict resolution.</p></li></ul><p><strong>This role requires:</strong></p><p>Ph.D. in the life sciences (e.g., biochemistry, molecular biology, cell biology, or related fields) is required with a Juris Doctorate from an accredited law school. Admitted to practice before the USPTO and licensed to practice law in at least one state (member of the NY bar or eligible for in-house licensure in NY); 5- 10 years of proven experience in a law firm setting (with or without corporate law department experience) preparing and prosecuting patent applications in the biological arts.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 23 Jun 2026 19:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Project Engineer]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48387]]></requisitionid>
    <referencenumber><![CDATA[R48387]]></referencenumber>
    <apijobid><![CDATA[r48387]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48387/project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Project Engineer </strong>to join our <strong>Project Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Designing and specifying cGMP process equipment, piping, and/or controls</li><li>Managing small projects related to process equipment and manufacturing</li><li>Assisting in the design review, site acceptance and installation of equipment</li><li>Preparing process and instrument drawings and other related drawings</li><li>Developing Process Flow Diagrams for manufacturing processes.</li><li>Supporting the validation department by preparing design documents and assisting in protocol execution</li><li>Assisting in investigations of process equipment and control system anomalies</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations for and executes modification change control documentation</li><li>Supervising mechanical, electrical, and automation contractors</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>You have excellent technical and analytical skills</li><li>Problem-solving and continuous improvement skills</li><li>You possess strong communication and collaboration skills</li><li>You are adaptable and can work in a fast-paced, regulated environment</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>To be considered for this opportunity you should have a BS/BEng or higher in Chemical/Process/Mechanical engineering with 2+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</li></ul><h3>Thrive today. Grow tomorrow.</h3><h3>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Statistical Programming - Pharmacometrics]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47328]]></requisitionid>
    <referencenumber><![CDATA[R47328]]></referencenumber>
    <apijobid><![CDATA[r47328]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47328/associate-director-statistical-programming-pharmacometrics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Associate Director Pharmacometrics Programming </strong>provides timely support to the study team on all programming matters according to the project strategies. Provides project leadership, resource planning/coordinating deliverables within project or across multiple projects. Lead programming support for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, clinical pharmacology report requirement and programming specifications using internal standards and guidelines. Providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. The incumbent is responsible for addressing administrative functions required for project management such as compilation of resource requirements and milestones, identifying/communicating changes in project requirements that may affect key deliverables at the project level, and working with the department head to develop resource strategies.</p><p><strong><em>This position requires 4 days onsite presence based out of our Tarrytown, NY or Warren, NJ location.</em></strong></p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Lead the programming and QC of analysis datasets, TFL's across multiple projects or standard tools following Regeneron standard data models or user requirements. Representation of PMX programming functions and coordination of activities with cross line functions and support planning/coordinating timelines in data exchange, deliverables. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.</p></li><li><p>Lead the integration of data across studies in support of Exposure-response, PopPK and PopPKPD analysis and 2.7.2.</p></li><li><p>Provide programming support for all PMX deliverable in HAR request, data driven analysis, publications, conference</p></li><li><p>Plan and lead the creation and validation of electronic submission requirements (i.e. annotated CRF, data export files, define documents).</p></li><li><p>Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Expert SAS programming skills (SAS (Base, Stat, Macro, graph) in a clinical data environment</p></li><li><p>Understanding of relational database structure and reporting systems utilizing multiple data delivery applications</p></li><li><p>Strong Experience/knowledge with implementing standardization methodology, creation of current CDISC data standards.</p></li><li><p>Comprehensive understanding of biostatistics, pharmaceutical clinical development (i.e. safety deliverables, efficacy analysis), experienced in data handling, process and analysis and able to understand/perform Pharmacokinetics, immunogenicity, exposure response analysis in timely manner</p></li><li><p>Mentor junior level staff in therapeutic area requirements. Develop collaborative work environment and be a positive role model.</p></li><li><p>Good Skilled in use of relevant software, including Window SAS, SAS studio (Base, Stat, Macro, graph), MS-Excel, R programming and/or Python.</p></li><li><p>Good knowledges in AI use case in statistical programming and data sciences.</p></li></ul><p><strong>To be considered for this opportunity</strong> you must have a Master in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline. 10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. Experience in project and people management, and expertise in one or more therapeutic areas is also preferred. SAS Certification desirable in statistics, computer science.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Clinical Data Reporting]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47785]]></requisitionid>
    <referencenumber><![CDATA[R47785]]></referencenumber>
    <apijobid><![CDATA[r47785]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47785/manager-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><p>As a Manager, Clinical Data Management Reporting, you will lead the development and delivery of high-quality clinical data reporting solutions that support efficient data review, operational oversight, and decision-making across clinical development programs. You will play a key role in transforming complex clinical and operational data into clear, actionable insights while ensuring consistency, accuracy, and compliance.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Leading the design, development, and maintenance of standardized clinical data reports and listings to support data review and clinical trial oversight</p></li><li><p>Partnering with cross-functional teams to gather reporting requirements and translate them into high-quality, accurate, and timely outputs</p></li><li><p>Delivering participant-level listings, exception reports, and reconciliation outputs to enable efficient data cleaning and review</p></li><li><p>Driving reporting solutions that provide actionable insights for operational performance and decision-making</p></li><li><p>Collaborating with data management and technology teams to leverage EDC systems, data lakes, and external data sources</p></li><li><p>Providing subject matter expertise in clinical data reporting, data structures, and reporting workflows</p></li><li><p>Identifying opportunities for automation and process improvement to enhance reporting efficiency and scalability</p></li><li><p>Monitoring data flows and troubleshooting issues related to data accuracy, completeness, and refresh cycles</p></li><li><p>Supporting inspection readiness by ensuring reporting outputs are compliant, traceable, and audit-ready</p></li><li><p>Delivering insights to identify risks, bottlenecks, and opportunities for operational improvement</p></li><li><p>Ensuring compliance with regulatory requirements such as GCP, ICH, and data privacy standards</p></li><li><p>Supporting training initiatives and development of reporting frameworks, standards, and documentation</p></li><li><p>Providing guidance and mentorship to team members and contributing to team development</p></li></ul><p><strong>This job may be for you if you have:</strong></p><ul><li><p>Strong experience in clinical data management, reporting, and data visualization</p></li><li><p>Good understanding of clinical trial processes, data standards (CDISC), and regulatory requirements</p></li><li><p>Experience working with EDC systems such as Medidata Rave</p></li><li><p>Proficiency in reporting and visualization tools such as SAS, R, Tableau, Power BI, Spotfire, or similar</p></li><li><p>Experience with data integration, data lakes, data pipelines, and automation frameworks</p></li><li><p>Strong knowledge of data lifecycle management and risk-based data review concepts</p></li><li><p>Excellent problem-solving, communication, and stakeholder management skills</p></li></ul><div><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Bachelor’s or Master’s degree in Data Science, Computer Science, Life Sciences, or a related field</p></li><li><p>7+ years of experience in clinical data, reporting, or related domains</p></li><li><p>Strong hands-on experience in clinical data reporting, analytics, and visualization</p></li><li><p>Experience working in a regulated clinical or pharmaceutical environment</p></li></ul></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42183]]></requisitionid>
    <referencenumber><![CDATA[R42183]]></referencenumber>
    <apijobid><![CDATA[r42183]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42183/associate-director-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><p>As an Associate Director, External Data Acquisition and Delivery (EDAD), you will provide strategic oversight and operational leadership for External Data Acquisition and Delivery activities across Regeneron’s clinical trial portfolio and initiatives. You will ensure readiness of external data collection platforms, data conformance tools, reconciliation processes, and the delivery of high-quality, compliant external data from third-party vendors including laboratory, biomarker, Digital Health Technologies, imaging, ECG, PK, genomics, and specialty data. You will partner closely with Clinical Data Management, CROs, external vendors, and cross-functional partners to drive external data strategy, operational excellence, vendor oversight, digital transformation initiatives, and process improvements.</p><p><strong>A Typical Day May Include:</strong></p><ul><li>Leading External Data Acquisition, integration, quality oversight, and delivery strategy across the clinical trial portfolio</li><li>Serving as a portfolio-level lead for external data quality and clinical-data operational strategy</li><li>Reviewing protocol requirements, vendor specifications, and operational data flows</li><li>Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents to ensure compliance with Regeneron standards and timelines</li><li>Providing expert mentorship on external data services including biomarker, eSource, eCOA, imaging, ECG, PK, genomics, and laboratory data</li><li>Driving external vendor oversight, onboarding, qualification, governance, and ongoing performance monitoring</li><li>Establishing and handling vendor KPIs, SLAs, and quality metrics</li><li>Governing reconciliation activities between EDC systems and vendor data platforms to ensure data integrity and consistency</li><li>Monitoring reconciliation metrics, discrepancy trends, and resolution timelines across studies</li><li>Collaborating with Database Development, Biostatistics, Study Data Managers, and external vendors to resolve complex data discrepancies</li><li>Leading process improvement initiatives, automation opportunities, and implementation of innovative external data solutions</li><li>Managing and developing a team of EDAD Managers, Specialists, and associates through coaching, mentoring, and performance management</li><li>Supporting SOP development, inspection readiness, audit activities, and regulatory compliance</li><li>Representing EDAD in leadership forums, governance committees, and technology discussions</li></ul><p><strong>This Role May Be For You If You Have:</strong></p><ul><li>Strong expertise managing multiple clinical external data types including biomarker, imaging, eCOA, ECG, PK, genomics, laboratory, and Digital Health Technology data</li><li>Advanced knowledge of external data reconciliation processes and EDC platforms such as Medidata Rave, Veeva, or Oracle Inform</li><li>Experience working with SAS, CSV, and XML data formats</li><li>Strong understanding of industry regulations including 21 CFR Part 11, ICH-GCP, and CDISC standards</li><li>Proven experience handling external vendor relationships and driving accountability for quality deliverables</li><li>Strong leadership, people management, coaching, and mentoring capabilities</li><li>Strategic thinking, creativity, problem-solving, and analytical skills</li><li>Strong project management and stakeholder management capabilities</li><li>Excellent verbal and written communication skills</li><li>Ability to work effectively in a fast-paced, matrixed, and global environment</li></ul><p><strong>To Be Considered For This Role, You Must Have:</strong></p><ul><li>Minimum 10+ years of experience in Clinical Data Acquisition/Management within biotechnology, pharmaceutical, or healthcare industries</li><li>Minimum 4+ years of people management experience</li><li>Demonstrated experience overseeing external data reconciliation activities between EDC systems and vendor platforms</li><li>Experience driving process improvements and vendor oversight in supervised environments</li><li>Bachelor’s degree in Science, Health, Mathematics, Computing, Information Systems, or a related field</li><li>Advanced degree preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,800.00 - $252,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, HR Technology - fixed term contract (12 months)]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48699]]></requisitionid>
    <referencenumber><![CDATA[R48699]]></referencenumber>
    <apijobid><![CDATA[r48699]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48699/associate-manager-hr-technology-fixed-term-contract-12-months/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a member of our HR Technology team, you will play a key role in shaping and supporting a world class digital employee experience for our people. Our team partners closely with HR Centers of Excellence (COE), HR Business Partners and our HR Operations team, to understand their challenges and strategic priorities.</p><p>We combine innovative HR process and operational support experience, with a strong appreciation of HR technology capabilities, to help these partners define their vision and business requirements. In collaboration with our IT partners, we support the introduction, optimization, and business support of our key enabling technologies.</p><p><strong>Where: </strong>Dublin (Ireland)</p><p><strong>Contract:</strong> Fixed term contract (12 months)</p><p><strong>Discover your role:</strong></p><p>The Associate Manager, HR Technology will provide business/functional analyst expertise and operational support across some of our key HR processes and platforms. In this role, you’ll act as a core part of the HR Technology team working across a wide variety of functional HR domains and partner with our Technology team to help design, deliver and support world-class technology enabled HR processes.</p><p>A key purpose of the role will be to shape the evolution of the employee experience in Workday particularly across our core business processes. This will involve working closely with our HR Operations and HRBPs to identity areas for process improvement, prioritizing these requirements/demands for Technology partner delivery, and managing operational support for end-users.</p><p>You will also play a key role in the delivery of broader projects across HR Technology, such as the identification and delivery of new tool tools to optimize our end-to-end employee experience.</p><p>Further, you will:</p><ul><li><p>Partner closely with HRBPs, HR Operations and Employee Services teams to understand their challenges, business priorities and associated prioritization.</p></li><li><p>Armed with this knowledge, develop clear and concise business requirements. Use this input to contribute to the prioritized backlog that can be transitioned to IT Product Managers for solution design and delivery. Support the outputs of this delivery via user acceptance testing, ensuring solutions meet the needs of the business. Partner with stakeholders to ensure change/comms/training materials are updated in line with process changes.</p></li><li><p>Support the delivery of successful and compliant business outcomes by applying business analyst capabilities (agile working, process design expertise, data analysis, critical thinking, problem solving, stakeholder communication, etc.) throughout project lifecycles. This could include identifying and implementing innovative new tools to support our workforce or extending the use of existing tools into new locations or new functional areas.</p></li><li><p>Provide end-user support for Workday, ensuring our processes are supporting the resolution of queries in a customer centric manner.</p></li><li><p>Manage the escalation process to our Technology partners for any technical issues/incidents. Use trends from ticket management to inform training/communication strategies and continuous improvement demands.</p></li><li><p>Establish and maintain strong relationships with the HRBPs and HR Operations team, both locally and globally. Develop a keen understanding of their operational demands, translating these into actionable plans and requirements. Oversee the end-to-end journey of these demands from idea to operational delivery to ensure key stakeholders are kept informed of progress.</p></li><li><p>Collaborate with our IT partners, in particular Product Managers, to ensure business and functional requirements are documented and understood. Ensure our prioritized demands are delivered within agreed timelines and to a level of quality expected by the business.</p></li><li><p>Stay abreast of the latest industry trends and thought leadership, to ensure that we are keeping an eye on the future and art of the possible with regards all roadmap planning and delivery.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's or Master’s degree in a related field; or equivalent related professional experience.</p></li><li><p>5+ years of experience working in HR, ideally with a focus on Core HR processes/technology in a global environment.</p></li><li><p>Hands-on business support of Workday HCM and Security.</p></li><li><p>Demonstrated ability to translate critical business demands into high quality business and functional requirements.</p></li><li><p>Extensive troubleshooting and communication skill, with the ability to understand business needs and distil and communicate complex details and data into consumable insights and recommendations.</p></li><li><p>Passion for and understanding of HR issues, data analytics and trends, as well as industry best practices and frameworks relating to people strategy, analytics, and candidate/employee experience.</p></li><li><p>Comfortable working with ambiguity, support diverse leaders, with diverse needs, in a unified direction.</p></li><li><p>Experience in managing numerous projects that have been delivered on time, meeting business requirements, with high customer and team satisfaction.</p></li><li><p>Experience of partnering with IT teams to ensure demands are understood and user-acceptance tested before deployment.</p></li><li><p>Intellectual curiosity with the ability to optimize business requirements and identify creative approaches to complex problems.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>63.200,00 € - 103.200,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 12:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs - Neurology (Mid South Region)]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46428]]></requisitionid>
    <referencenumber><![CDATA[R46428]]></referencenumber>
    <apijobid><![CDATA[r46428]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46428/associate-director-field-medical-affairs-neurology-mid-south-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. We expect you to demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities shaping our medical strategy. You will be considered a scientific and clinical expert on our current and future Neurology assets.</p><p><strong>Territory: </strong> Cincinnati OH, Southern VA, Eastern KY, WV, TN, NC, SC </p><p><strong>A typical day may include the following: </strong></p><ul><li><p>Establish, foster, cultivate and maintain peer relationships with KOLs in Neurology</p></li><li><p>Act as a primary clinical/scientific resource to HCPs for information pertaining to disease state and our products to ensure awareness and understanding.</p></li><li><p>Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans.</p></li><li><p>Support evidence generation (company sponsored trials and investigator initiated studies) research initiatives.</p></li><li><p>Identify and report medical insights.</p></li><li><p>Identifies gaps in research and educational needs to inform medical strategy.</p></li><li><p>Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.</p></li><li><p>Performs disease management and therapeutic area education with identified practitioners, payers and researchers.</p></li><li><p>Attends conferences to collect and report relevant, scientific, clinical, & competitive intelligence.</p></li><li><p>Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p></li></ul><p>To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) with a minimum 8 years of experience, including 4+ years working as a Medical Science Liaison in the pharmaceutical industry. Experience as a Neurology MSL or Neurology is preferred. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. Demonstrated experience communicating complex data sets and the ability to be seen as a scientific peer while educating top KOLs. Established relationships with KOLs in neurology and knowledge of institutions focused on myasthenia gravis (MG) preferred as is drug launch experience. Capable of frequent business travel (approximately 70% of time), including air travel, ability to travel overnight and occasionally on weekends</p><p>#msl #medicalscienceliaison</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Associate Scientist, Metabolic & Muscle Diseases]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48549]]></requisitionid>
    <referencenumber><![CDATA[R48549]]></referencenumber>
    <apijobid><![CDATA[r48549]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48549/sr-associate-scientist-metabolic-muscle-diseases/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated and experienced Sr Associate Scientist to join Obesity, Metabolism and Muscle Diseases Group. The individual will serve as a central histological resource, providing expert tissue processing and staining services to multiple Obesity, Metabolism and Muscle Diseases research programs simultaneously. The successful candidate will manage end-to-end histological workflows spanning a broad range of tissue types, maintain rigorous quality standards. This role demands both deep technical proficiency and strong interpersonal skills to navigate competing program demands and deliver high-quality data on time.</p><p><br> </p><p><strong>As a Sr Associate Scientist, a typical day may include:</strong></p><ul><li><p>Tissue processing, including tissue fixation, dehydration, clearing, embedding, and sectioning samples from multiple tissue types (e.g., liver, heart, brain, muscle, adipose).</p></li><li><p>Routine histological staining (e.g H&E, Sirius Red, PAS, Oil Red O) and special staining according to the program needs</p></li></ul><ul><li><p>Conduct immunohistochemistry (IHC) and immunofluorescence (IF); develop, optimize, and validate new IHC/IF protocols, antibody titrations, and antigen retrieval conditions.</p></li><li><p>Apply in situ hybridization (ISH/RNAscope) techniques for gene expression localization where required</p></li><li><p>Perform image aquation, using different scanning platforms (e.g. Aperio, Zeiss Axioscan), and manage image data repositories</p></li><li><p>Perform quantitative image analysis using platforms such as HALO, develop and apply customized image analysis algorithms</p></li></ul><ul><li><p>Generate high-quality figures and data summaries suitable for internal reports, regulatory packages, and peer-reviewed publications.</p></li></ul><ul><li><p>Maintain and communicate a dynamic workload tracker; proactively flag capacity constraints or scheduling conflicts to stakeholders.</p></li></ul><ul><li><p>Adapt rapidly to shifting program priorities and animal study schedules.</p></li><li><p>The candidate will be responsible for maintaining accurate and complete laboratory records. </p></li></ul><p><strong>This role may be for you if: </strong></p><ul><li><p>You enjoy working in a fast-paced environment</p></li><li><p>You are a fast learner and have desire to expand your skill set and learn new techniques</p></li><li><p>You are detail oriented, well-organized and can multi-task</p></li><li><p>You are a team player</p></li><li><p>You have strong communication skills</p></li></ul><p><strong> </strong></p><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>BS with 5+ years or MS with 2+ years of relevant experience</p></li><li><p>Proficiency in standard and special histochemical staining techniques across multiple tissue types.</p></li><li><p>Demonstrated IHC/IF assay development, optimization, and troubleshooting experience</p></li><li><p>Ability to optimize processing and staining protocols for challenging tissue types or low-abundance samples</p></li><li><p>Proficiency with whole-slide imaging systems and digital pathology image analysis software (e.g. HALO)</p></li><li><p>Experience with <em>in situ</em> hybridization platforms (RNAscope, BaseScope, FISH) is a plus </p></li><li><p>Strong organizational and record-keeping skills</p></li><li><p>Ability to manage and prioritize simultaneous requests from multiple stakeholders</p></li><li><p>Excellent oral and written communication skills</p></li><li><p>Ability to present data at lab meetings</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 16:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - HR Project Manager - 12 months contract]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48663]]></requisitionid>
    <referencenumber><![CDATA[R48663]]></referencenumber>
    <apijobid><![CDATA[r48663]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48663/temp-hr-project-manager-12-months-contract/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Project Manager, Human Resources will have primary responsibility for partnering with HR Operations leadership on global projects and establishing an operational excellence mindset within the Global HR function. This temporary position is responsible for defining, planning, and driving the team activities necessary to reach project objectives including the internal coordination of tasks with a project plan and ensuring that all tasks are completed on time and within budget.</p><p>Specifically, we are seeking a highly skilled and experienced HR Project Manager to lead the implementation of a new benefits platform across several locations.</p><p>The ideal candidate will have a strong background in HR project management and a proven track record of successfully managing complex HR system implementations.</p><p><strong>Where: </strong>Remote in Ireland</p><p><strong>Contract:</strong> Temporary, 12 months</p><p><strong>Essential Duties and Responsibilities</strong> include, but are not limited to, the following: </p><ul><li><p>Collaborate with HR and key Stakeholders on projects that support business and functional strategic objectives (project types include, but not limited to, People, Process and/or Technology).</p></li><li><p>Develop project work plans and revise as appropriate to meet business needs and requirements.</p></li><li><p>Collaborate with internal stakeholders in identifying strategic areas of opportunity to improve operational efficiency, customer experience or cost.</p></li><li><p>Create processes, tools and templates for the identification, execution, and successful handoff of projects within the HR function.</p></li><li><p>Provide regular project updates through a close working relationship with HR Operations and stakeholders.</p></li><li><p>Skillful delivery with an eye to strong change management for various personas, including employees, contingent workers, people managers, etc.</p></li><li><p>Coordinate the elements and document the progress of day-to-day project implementation through our standard processes and corresponding project plan. Provide regular implementation status updates to management.</p></li><li><p>Follow and apply the established methodologies and standards for project management and problem-solving techniques.</p></li><li><p>Support activities relating to HR Systems (i.e., HCMs, Workday, Oracle, Beeline, etc.) upgrades and new implementations, to include data gathering, input, testing, training, customer validation, and other support as needed.</p></li><li><p>Perform related duties as assigned or requested.</p></li><li><p>Collaborate with HR, IT and other departments to support the gathering of requirements and ensure alignment with business needs.</p></li><li><p>Support the design, configuration, and testing of the benefits platform.</p></li><li><p>Work closely with consultants and vendors to ensure best practices and optimal solutions are implemented.</p></li></ul><p>Note: Approx 10% travel will be required</p><p><strong>Education and Experience: </strong></p><ul><li><p>Bachelor’s degree in human resources, business, or related discipline required. </p></li><li><p>10+ years relevant experience with 5+ years of experience in a Project Management role preferred</p></li><li><p>Prior experience in applying these techniques within an HR function is highly preferred.</p></li><li><p>Project Management Certification (PMP) Required.</p></li><li><p>Proficiency with MS Office, MS Project, Visio</p></li><li><p>Or equivalent combination of education and experience.</p></li></ul><p><strong> Knowledge, Skills and Abilities:</strong></p><ul><li><p>Knowledge and application of project management techniques and tools.</p></li><li><p>Strong analytical skills with ability to develop solutions to unusually complex problems that impact business outcomes.</p></li><li><p>Understanding, application, and deployment of various problem-solving techniques and/or Continuous Improvement and Operational Excellence methodologies. </p></li><li><p>Proven ability to influence and communicate across multiple levels and regions of a global organization.</p></li><li><p>Ability to build and maintain strong relationships across the business with various stakeholder groups.</p></li><li><p>Working knowledge of change management strategies and tools.</p></li><li><p>Ability to be flexible, follow tight deadlines, independently organize, and prioritize work.</p></li><li><p>Ability to interact with all levels in an organization including executive management.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 13:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety Business Office]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47619]]></requisitionid>
    <referencenumber><![CDATA[R47619]]></referencenumber>
    <apijobid><![CDATA[r47619]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47619/senior-manager-global-patient-safety-business-office/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Senior Manager, Global Patient Safety Business Office to join our team!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Senior Manager, GPS Business Office will help support the execution and delivery of GPS’ overarching strategic plan, including the annual department operating plan, long-term roadmap, and key transformation initiatives for pharmacovigilance (PV) enablement (e.g., Global Capabilities Center (GCC)) </p><p>In partnership with the Director, GPS Business Office, this role supports business planning, execution and enablement of GPS initiatives, communication strategies, resource management, PV forecasting and capacity planning, talent calibration, and the PV functional-level vendor strategy. </p><p><strong>This role might be for you if can: </strong><strong>​</strong></p><ul><li><p>Partner directly with GPS LT to enable execution of GPS vision and strategic priorities </p></li><li><p>Support the facilitation of cross-functional coordination across GPS team to support execution of key priorities and initiatives </p></li><li><p>Track and report progress on GPS strategic initiatives and key priorities </p></li><li><p>Support the maintenance of strategy and governance activities for Global Capabilities Center (GCC) across GPS functions, including coordination of scope, resource planning, metrics tracking, and operational reporting aligned to GPS priorities </p></li><li><p>Support the development of annual department operating plans and strategic roadmaps for GPS </p></li><li><p>Coordinate and support delivery of key GPS functional meetings (e.g., GPS Leadership Team, All Hands, Mid-Year meetings) </p></li><li><p>Prepare and maintain regular delivery of GPS communications </p></li><li><p>Help to facilitate talent calibration processes and organizational planning activities </p></li><li><p>In partnership with RA GPS DQ Strategy and Operations and Portfolio Management, support establishment of operational portfolio forecasting for GPS </p></li><li><p>Support resource planning and operational portfolio coordination across GPS programs and initiatives </p></li><li><p>Collaborate cross-functionally with Development Services & Operational Excellence (DS&OE), Learning Center of Excellence (LCoE), and related stakeholder teams to support GPS priorities and initiatives </p></li><li><p>In partnership with the Director, GPS Business Office, support the development of innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li><li><p>Support scaling of the Business Office function and building a high-performing team </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Atleast 7+ years of related experience and minimum Bachelor’s Degree in business, preference for degree in life sciences or healthcare with 4-5 years of experience in pharmaceutical, biotech, or healthcare organizations, preferably within pharmacovigilance, drug safety, or global development operations.</p></li><li><p>Strong project and program management skills with the ability to manage multiple initiatives and stakeholders simultaneously </p></li><li><p>Demonstrated ability to work effectively in a matrixed environment and build partnerships across teams </p></li><li><p>Strong communication skills, with the ability to confidently present and interface with senior leadership </p></li><li><p>Strong organizational and problem-solving skills with the ability to adapt to evolving priorities and business needs </p></li><li><p>Ability to translate complex discussions into clear communications, summaries, and action plans </p></li><li><p>Experience supporting leadership governance and operational planning processes </p></li><li><p>Highly detail-oriented with strong focus on quality, accuracy, and consistency across deliverables </p></li><li><p>Preferred experience with PV operational and planning initiatives </p></li><li><p>Preferred experience with AI technologies </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development Quality Assurance (GCP)]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48482]]></requisitionid>
    <referencenumber><![CDATA[R48482]]></referencenumber>
    <apijobid><![CDATA[r48482]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48482/senior-manager-global-development-quality-assurance-gcp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Regeneron Senior Manager, Global Development Quality Assurance, is a key position in the supervising, guiding and leading for one of the Good Clinical Practice (GCP) audit programs. Responsibilities include managing direct reports while supporting the development and execution of departmental mission, vision and goals. As part of the role of people manager, you will be responsible for staff development & training and resourcing direct reports. You will create strategic partnerships and implement risk-based quality auditing activities. <br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>This is a United States based remote position. This role may require 20 – 30% travel (both domestic and international). </p><p><strong>Discover your role:</strong><br>• Manage, hire and develop direct reports by meeting with direct reports at least monthly and conducting performance assessments. <br>• Responsible for the training, resourcing, and individual staff development. <br>• Schedule, prepare, conduct, report, and follow-up on audits in support of routine and directed GxP audits as needed and in accordance with our standard operating procedures and quality policies. <br>• Audits include internal audits and external audits conducted globally. <br>• Represent the department by providing audit and compliance input in cross functional meetings <br>• Lead the identification of internal quality/compliance issues and act as a catalyst for process improvements to promote standardization and best practices. . <br>• Interpret and may assist in developing policies and standards, and evaluate potentially critical problems not covered by policies, standards, and regulations. <br>• Provides education and/or training to GDQA and other relevant Global Development departments. <br>• May participate in regulatory inspections by acting as part of the control and/or inspection room team </p><p><strong>This role requires:</strong></p><p>As Bachelor’s degree (Master’s degree preferred) with 8+ years of relevant industry experience Deep knowledge of the FDA and EU regulations and ICH guidance documents along with any other regulations that may affect drug development and/or post-authorization safety monitoring is required. 5+ years of both direct people management and GCP audit experience preferred Excellent communication and people management skills and ability to work with people in all levels of the organization and externally. Experience with FDA or other Regulatory Inspections of Investigator sites, Sponsors or CROs. <br>• Strong leadership with demonstrated ability to collaborate with both direct reports and senior leaders <br>• Good problem solving, written and verbal communication skills and uses professional concepts to evaluate problems and develop solutions for critical issues. <br>• Strong track record of project management, partner management, collaboration skills and negotiation of complex situations <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Finance Service Delivery Analyst]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47446]]></requisitionid>
    <referencenumber><![CDATA[R47446]]></referencenumber>
    <apijobid><![CDATA[r47446]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47446/finance-service-delivery-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Finance Service Delivery Analyst to join our Financial Shared Services team, supporting our global payroll and accounting operations in a hybrid work model. In this role, you will support standardized financial processes, ensure accurate reporting, and drive efficiency across global operations while collaborating with international teams and stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Perform reconciliations between enterprise systems and external vendor systems to ensure data accuracy</p></li><li><p>Prepare and reconcile payroll data templates supporting processing across multiple global countries</p></li><li><p>Implement established payroll and accounting procedures consistently to support centralized operations</p></li><li><p>Coordinate and support month-end, quarter-end, and year-end close processes, including preparation of schedules impacting reporting</p></li><li><p>Assist in preparing reports, audit documentation, and materials for compliance reviews</p></li><li><p>Collaborate with international teams to deliver operational support and ensure seamless service delivery across regions</p></li><li><p>Maintain process documentation, mappings, and Standard Operating Procedures (SOPs) while ensuring adherence to governance practices and internal controls</p></li><li><p>You proactively identify and drive opportunities to improve efficiency and consistency within financial operations.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in Accounting, Finance, Business, Data Analytics, or related field (B.Com or BBM preferred)</p></li><li><p>Minimum 2+ years of experience in payroll, accounting, or data analysis</p></li><li><p>Experience performing reconciliations between enterprise systems and external vendor systems</p></li><li><p>Experience preparing and reconciling payroll data templates across multiple global countries</p></li><li><p>Knowledge of accounting month-end close processes and financial reporting schedules</p></li><li><p>Experience supporting audit preparation and compliance documentation</p></li><li><p>Understanding of governance practices, internal controls, and regulatory compliance requirements</p></li><li><p>Strong customer service and stakeholder communication skills when addressing associate inquiries</p></li><li><p>Ability to collaborate effectively with international, cross-regional teams</p></li><li><p>Proactive approach to identifying process improvements and driving operational efficiencies</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Affairs Senior Coordinator]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48578]]></requisitionid>
    <referencenumber><![CDATA[R48578]]></referencenumber>
    <apijobid><![CDATA[r48578]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48578/medical-affairs-senior-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Coordinator, International Medical Review Committee to join our Global Medical Affairs team, supporting our ex US, International locations. In this role, you will coordinate Medical Review Committee activities and support timely, compliant material review and approval while collaborating with material sponsors, submitters, management, customers, vendors, and partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Uxbridge, UK or Dublin, Ireland</p><p>Hybrid model</p><p><strong>Discover your role:</strong></p><ul><li><p>Coordinate International Medical Review Committee activities and approval workflows.</p></li><li><p>Manage materials from submission through final approval.</p></li><li><p>Create agendas and facilitate live Medical Review Committee meetings.</p></li><li><p>Prepare for and participate in quality checks and audits.</p></li><li><p>Maintain documentation, systems, and the Medical Reference Library.</p></li><li><p>Review submissions for appropriateness and completeness before routing.</p></li><li><p>Train sponsors and submitters on Medical Review Committee processes.</p></li><li><p>You collaborate clearly across teams to support timely decisions.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in a related field, or equivalent experience.</p></li><li><p>Minimum 5 years’ experience, or 7 years without a degree.</p></li><li><p>3 years’ Medical Review Committee or Medical Legal Review experience preferred.</p></li><li><p>Familiarity with local country regulatory requirements and guidelines.</p></li><li><p>Proficiency in Microsoft Office, Adobe Acrobat Professional, and Veeva Vault.</p></li><li><p>Strong project management, meeting facilitation, organization, and time management skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Specialist, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48310]]></requisitionid>
    <referencenumber><![CDATA[R48310]]></referencenumber>
    <apijobid><![CDATA[r48310]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48310/senior-specialist-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist, External Data Acquisition and Delivery to join our Clinical Data Management team in a hybrid role. In this role, you will manage end-to-end non-Case Report Form data across assigned studies or Clinical Development Units - developing or amending Data Transfer Specifications of low to medium complexity with minimal supervision, performing external data reconciliation and ensuring vendor data is accurately transferred and cleaned in accordance with study protocols and Data Management Plan - while collaborating with external data vendors, CRO partners and cross-functional stakeholders. Ensure compliance with Regeneron SOPs, regulatory requirements, and industry best practices. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Develop Data Transfer Specifications (DTS) for assigned studies or Clinical Development Units as per study timelines.</li><li>Author and maintain DTS documents using standard templates and CDISC requirements, in collaboration with internal and external stakeholders.</li><li>Act as the primary technical point of contact between clinical data management and vendors.</li><li>Respond to vendor and stakeholder queries to ensure external data is complete, correctly structured and delivered in the required format.</li><li>Track DTS status, milestones and deliverables across data types and programs, escalating issues and following through to resolution.</li><li>Process change requests, support data structure issue resolution and facilitate the creation of new test codes where required.</li><li>Reconcile external vendor data against clinical database to ensure accurate transfer, completeness and consistency across all data sources.</li><li>Support data locking, archival, reconciliation documentation, eTMF maintenance and ensure inspection readiness standards.</li><li> Provide review of protocol requirements, vendor specifications, and operational data flows with minimal supervision.</li><li>You guide CROs, vendors and cross-functional partners with clear technical direction while identifying areas for process improvement.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Science, Health, Mathematics, Engineering, Computational or related field.</li><li>4+ years in external clinical data acquisition or management within biotechnology, pharmaceutical or a health-related industry.</li><li>Experience managing multiple clinical data types and formats such as biomarker, eCOA, imaging, ECG, PK, genomics and laboratory data.</li><li>Knowledge of 21 CFR Part 11, ICH-GCP guidelines and CDISC standards for data collection.</li><li>Proficiency extracting data into SAS, CSV and XML formats.</li><li>Experience with EDC platforms such as Medidata Rave, Veeva or Oracle Inform, and external data reconciliation and query processes between EDC and vendor systems.</li><li>Basic knowledge of database structures and protocol review as relevant to clinical data management is preferred.</li><li> Ability to draw from wide-ranging experience to resolve complex issues.</li><li> Strategic thinking, creativity, and problem-solving skills essential</li><li> Ability to work effectively with and motivate virtual teams in a matrix environment.</li><li>Good interpersonal, oral, and written communication skills.</li><li>Society of Clinical Data Management certification is recommended.</li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 05:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology – Washington DC / Baltimore]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48562]]></requisitionid>
    <referencenumber><![CDATA[R48562]]></referencenumber>
    <apijobid><![CDATA[r48562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48562/medical-specialist-ii-ophthalmology-washington-dc-baltimore/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Territory: Washington DC / Baltimore</strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets several medicines, including for eye diseases, and has product candidates in development in other areas of high unmet medical need.</p><p><strong>A typical day might include the following:</strong><br>The Medical Specialist II will report to the Regional Director and will be responsible for daily development and management of relationships with Retina Specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The primary focus on this role will be the approved indications suffered by patients as it relates to conditions of the eye. The Medical Specialist II will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you:</strong><br>• Have experience in biologics and buy and bill products<br>• Can demonstrate history of high sales performance<br>• Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Ophthalmology and/or Buy & Bill with relevant retina experience is preferred. Residency in the territory is required and occasional overnights expected.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 11:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Data Engineer]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43097]]></requisitionid>
    <referencenumber><![CDATA[R43097]]></referencenumber>
    <apijobid><![CDATA[r43097]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43097/principal-data-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Principal Data Engineer builds data infrastructure, leads technical initiatives, and mentors junior team members while driving data-driven solutions across the organization.</p><p>As a Principal Data Engineer, a typical day might include the following:</p><ul><li>Design complex data engineering solutions and define standards.</li><li>Architect and optimize secure, scalable pipelines (ETL/ELT) for real-time and batch processing. Integrate diverse data sources, implement fault-tolerant systems, and establish CI/CD practices.</li><li>Organize large datasets, ensure data quality, and design data lake/warehouse solutions for accessibility.</li><li>Monitor pipeline performance, troubleshoot issues, and implement observability and alerting systems. Leverage GenAI solutions to enhance team efficiency.</li><li>Document systems and ensure adherence to governance policies.</li><li>Mentor junior engineers and drive infrastructure innovation.</li></ul><p>This role may be for you if you have:</p><ul><li>Strong Python, Java, or Scala programming skills.</li><li>Deep SQL expertise and relational database experience.</li><li>NoSQL and big data technology experience (Hadoop, Spark, Kafka).</li><li>Proficiency in data modeling and schema design.</li><li>Knowledge of data security and compliance requirements in regulated environments.</li><li>Familiarity with Biotech Enterprise Systems (MES, LIMS, QMS).</li><li>Excellent communication skills.</li><li>Knowledge of MCP and Orchestration platforms related to AI/GenAI.</li><li>Proficiency in star schemas and data modeling tools.</li><li>Knowledge of industry regulatory requirements (CFR Part 11, GxP, CSA).</li><li>Stream processing experience (Kafka, Flink).</li><li>Cloud certifications.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Computer Science, Bioinformatics, or related field and</p><ul><li>Principal: 8+ years relevant experience with 1+ years experience in biotech, pharmaceutical, or other life sciences industries and 3+ years cloud platform experience (AWS, Azure).</li><li>Staff: 10+ years relevant experience with 3+ years experience in biotech, pharmaceutical, or other life sciences industries and 5+ years cloud platform experience (AWS, Azure).</li><li>Experience with workflow orchestration tools (Airflow, Luigi, Prefect, or similar), containerization technologies, scientific data management systems & using GenAI to enhance own work.</li><li>Master's degree in Computer Science, Bioinformatics, or related field preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€62,300.00 - €119,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - RALEIGH, NC]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48925]]></requisitionid>
    <referencenumber><![CDATA[R48925]]></referencenumber>
    <apijobid><![CDATA[r48925]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48925/medical-account-specialist-ii-hematology-raleigh-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Raleigh, NC</strong></p><ul><li><strong>Geography: </strong><strong>Raleigh, Wilmington, Fayetteville, Durham</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - COLUMBUS, OH]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48898]]></requisitionid>
    <referencenumber><![CDATA[R48898]]></referencenumber>
    <apijobid><![CDATA[r48898]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48898/medical-account-specialist-ii-hematology-columbus-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- Columbus, OH</strong></p><ul><li><strong>Geography: Columbus, Cincinnati, Dayton</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Tax]]></title>
    <date><![CDATA[Mon, 06 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48870]]></requisitionid>
    <referencenumber><![CDATA[R48870]]></referencenumber>
    <apijobid><![CDATA[r48870]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48870/manager-tax/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager Tax Compliance and Indirect Tax Operations India to join our Finance and Tax function, supporting our global tax operations in a hybrid work model. In this role, you will lead tax compliance and reporting activities across global value-added tax (VAT) and income tax processes while collaborating with finance, information technology, supply chain, procurement, operations teams, and external advisors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Support global VAT and international tax compliance through preparation, review, and filing activities delivered with external co-source partners.</p></li><li><p>Lead end-to-end VAT reconciliations, validate transactional data, investigate variances, and prepare audit-ready reporting files.</p></li><li><p>Maintain VAT ledgers by reconciling VAT accounts across returns, balance sheet, income statement, e-reporting, and Intrastat filings.</p></li><li><p>Monitor changes in global VAT legislation and assess the impact on business operations and compliance requirements.</p></li><li><p>Coordinate responses to VAT and income tax queries, provide practical guidance, and document tax positions through technical memos.</p></li><li><p>Ensure timely and accurate income tax calculations and reporting for statutory financial statements and corporate reporting obligations.</p></li><li><p>Support tax audits, inquiries, and regulatory notices by providing accurate documentation and responses.</p></li><li><p>Build strong cross-functional partnerships, mentor junior tax professionals, and foster a collaborative, process-driven tax function.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in Accounting, Finance, Taxation, or a related field.</p></li><li><p>CA, CPA, EA, or equivalent professional certification preferred.</p></li><li><p>7–9+ years of experience in tax compliance and tax operations.</p></li><li><p>Strong knowledge of global direct and indirect tax, including in-depth understanding of VAT legislation and statutory requirements.</p></li><li><p>Experience preparing and overseeing income tax reporting aligned with local statutory and corporate requirements.</p></li><li><p>Knowledge of cross-border transactions and related tax implications.</p></li><li><p>Experience working in multinational or global tax environments preferred.</p></li><li><p>Exposure to enterprise resource planning systems such as Oracle and tax reporting tools is desirable.</p></li><li><p>Strong analytical and problem-solving skills, with experience using artificial intelligence or automation technologies considered a plus.</p></li><li><p>Experience managing and developing teams.</p></li><li><p>Excellent communication and interpersonal skills, with the ability to engage effectively with diverse partners.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 06 Jul 2026 04:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Inspection Management (GCP)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R38901]]></requisitionid>
    <referencenumber><![CDATA[R38901]]></referencenumber>
    <apijobid><![CDATA[r38901]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r38901/associate-director-inspection-management-gcp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is responsible for the effective management of GCP, GVP and GLP inspections. The GDQIM IML will engage with key stakeholders, build strategic partnerships working and liaising with Clinical Study teams, relevant functions and other GDQ functions to support teams with inspection preparation activities on all Regeneron-sponsored clinical trials.</p><p><strong>In this role, a typical day might include the following:</strong></p><p>Ensuring and managing the notification of all relevant internal and external stakeholders of upcoming and/or anticipated regulatory inspections.<br>• Ensuring the preparation, management and integration of inspection management processes and training activities into the clinical development programs and all relevant stakeholders.<br>• Providing effective guidance, consultancy, and support to the Clinical Study Teams (and any other key stakeholders) in advance of an impending inspection.<br>• Assisting with the identification of opportunities to conduct mock inspections and/or Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.<br>• Identifying and discussing with the Clinical Study Teams potential issues and/or gaps, in advance of an impending inspection, that may require strategies to mitigate risk and/or provide additional clarification to an inspector.<br>• Ensuring the preparation, management and conduct of inspection preparation sessions which include mock inspections, trainings, and clinical site preparation visits working with GDQA team to identify and mitigate risks to clinical programs.<br>• Serving as the back room lead/co-lead or front room co-lead, responsible for explaining, managing,and ensuring the execution of all activities, including managing the tracking of requests and inquiries, and coordinating requests for responses from relevant personnel during any regulatory inspection conducted worldwide.<br>• Responsible for managing the preparation and provision of timely inspection updates and daily/end of inspection summaries to GD Executive and Senior Management, in addition to any other key relevant internal and external stakeholders.<br>• Responsible for managing inspection response development, and Corrective Actions/Preventive Actions (CAPA) follow-up activities alongside other GDQIM colleagues, cross-functional stakeholders, and process owners.<br>• Ensuring and managing the development, collection, reporting and analysis of inspection-related quality data, trends, and metrics.</p><h3><strong>This role may be for you if have:</strong></h3><p>• Advanced knowledge, understanding and application of GCP, and/or GVP <br>guidelines including the management of significant/complex quality issues <br>and compliance activities.<br>• Extensive experience with participating in, and supporting, Regulatory <br>Agency Inspections of Investigator Sites, Sponsors and Clinical Research <br>Organizations (CROs) in a GxP environment, including inspection <br>preparation, facilitation, and follow-up.<br>• Effective management of interpersonal relationships, stakeholder <br>engagement, and collaborations.<br>• Demonstrated ability to interface and collaborate effectively with other <br>Managers and Directors within, and external to, the organization.<br>• Extensive experience in providing training and presenting information on <br>key quality and regulatory compliance information.</p><p><strong>To be considered for this opportunity we are looking for:</strong></p><p>Bachelor's degree with a minimum of 10 years of relevant <br>healthcare/pharmaceutical industry experience.<br>• Experience working in either a quality/compliance role (e.g., Quality <br>Management, Quality Assurance etc.), or in a Clinical Development role <br>with expertise and/or transferable skills related to Good Clinical Practice <br>(GCP), and/or Good Pharmacovigilance Practice (GVP).<br>• Experience in training, supervising, line management, mentoring and <br>development of staff, and leading a small team</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Enterprise Integration]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44136]]></requisitionid>
    <referencenumber><![CDATA[R44136]]></referencenumber>
    <apijobid><![CDATA[r44136]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44136/associate-director-enterprise-integration/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of Enterprise Integration is a strategic and hands-on leader responsible for defining the integration vision, establishing governance, and delivering reliable, scalable, and secure integration capabilities across the enterprise. This role owns the integration platform and services as a product, sets design principles and leading practices, orchestrates work across application and corporate shared service teams, and ensures the portfolio delivers measurable business outcomes. They will inform technical and architecture strategy, stand up and qualify new technologies, and drive continuous improvement by reducing technical debt and standardizing work.</p><p>As an Associate Director, a typical day might include the following:</p><ul><li>Inform and define the technical and architecture strategy for enterprise integration (roadmaps, tools/technology selection, platforms, patterns, standards).</li><li>Establish design principles and leading practices for APIs, architecture, data movement, orchestration, and security.</li><li>Support standing up new technology and qualifying through proofs of concept, pilots, and vendor evaluations.</li><li>Lead decisions on “which bus to get on” (e.g., ESB, event bus, streaming backbone) aligned to use cases and scalability goals.</li><li>Create and maintain an Integration “Pattern” Decision Framework to guide synchronous vs. asynchronous, pub/sub vs. request/response, batch vs. streaming, ETL vs. ELT, and choreography vs. orchestration choices.</li><li>Establish and run governance processes including intake, prioritization & work management; create and maintain Standard Work (SOPs, playbooks, runbooks, checklists) for design, build, test, deploy, and support.</li><li>Maintain an authoritative Integration Catalog of APIs, events, integrations, schemas, SLAs, and ownership.</li><li>Serve as Product Owner for the Integration Platform and shared integration services, defining vision, roadmap, backlog, and success metrics.</li><li>Orchestrate work across application teams, corporate functions (security, compliance, finance), and programs to ensure alignment and remove blockers.</li><li>Provide project management oversight across the integration portfolio: scope, timeline, budget, dependencies, risk management, and status reporting.</li><li>Drive integration quality through design reviews, pattern adherence, testing standards, and observability.</li><li>Identify, prioritize, and remediate integration technical debt (legacy patterns, brittle point-to-point, insufficient observability, poor documentation).</li><li>Implement practices for reusability, versioning, deprecation, and lifecycle management of integrations.</li><li>Own integration financials: annual budgeting, forecasting, vendor/software costs, cloud consumption, and chargeback models.</li><li>Measure and communicate ROI, TCO, and value realization of integration investments.</li></ul><p>This role may be for you if you have:</p><ul><li>Proven experience with integration platforms (iPaaS, ESB, API gateway, event streaming), such as IBM MQ, MuleSoft, Boomi, Azure Integration Services, Kafka/Confluent, AWS/GCP integration suites, or similar.</li><li>Strong grasp of integration patterns (EDA, pub/sub, CQRS, SAGA, orchestration/choreography), data movement (ETL/ELT), and API lifecycle management; knowledge of integration platforms such as Oracle Integration Cloud (OIC), middleware, and APIs.</li><li>Familiarity with enterprise architecture frameworks (e.g., TOGAF), agile at scale (e.g., SAFe), and ITIL service management practices.</li><li>Solid understanding of security, compliance, privacy, identity, and data governance as they apply to integrations.</li><li>Demonstrated success in establishing governance, standard work, and cross-functional orchestration with measurable outcomes.</li><li>Familiarity of regulatory guidelines, including GxP compliance, Sox, and security.</li><li>Expertise in Oracle SQL, PL/SQL, and reporting tools like Oracle BI Publisher and OTBI.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field and</p><ul><li>Senior Manager: 8+ years in enterprise integration, middleware, or API/platform architecture; 4+ years in leadership roles.</li><li>Associate Director: 10+ years in enterprise integration, middleware, or API/platform architecture; 5+ years in leadership roles.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Device Development Engineer (Project Leadership)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44516]]></requisitionid>
    <referencenumber><![CDATA[R44516]]></referencenumber>
    <apijobid><![CDATA[r44516]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44516/sr-device-development-engineer-project-leadership/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Sr. Device Development Engineer to join our project lead team. The Sr. Device Development Engineer will drive the end-to-end development of a device combination product and/or platform delivery system, within a specific therapeutic area (Ophthalmic, Immunology/Inflammation, Cardiometabolic, etc.). They will provide comprehensive leadership in engineering product management, regulatory compliance (design controls), and multi-functional collaboration with internal and external partners, for the combination product device.</p><p>A typical day for a Sr. Device Development Engineer might include:</p><ul><li>Leads multidisciplinary engineering project teams (Human Factors, V&V Engineering, Manufacturing Engineer, Quality Engineering) through the complete device design and development lifecycle of a combination product development within the Regeneron Pipeline.</li><li>Defines detailed product requirements and specifications with commercial, clinical, and other development/strategy collaborators.</li><li>Defines technical specifications and design requirements in collaboration with engineering teams (manufacturing, verification, packaging etc.)</li><li>Responsible for all user needs and requirements to be validated through design and development.</li><li>Develops, manages, and communicates development program plans, risks, timelines, and budgets to internal and external team members.</li><li>Integrate device development activities with Chemistry Manufacturing Controls (CMC) and Global development timing and goals.</li><li>Supports global internal manufacturing and external manufacturing teams around relevant design and process development information transfers.</li><li>Leads all aspects of product testing and quality assurance processes for the specific device development.</li><li>Ensures comprehensive and compliant Design History File (DHF) is developed and ensures to meet regulatory and quality requirements (21CFR Part 3 and 21 CFR 820.30).</li><li>Supports management in related clinical and commercial regulatory activities that is related to the device development (ie: IND/IMPD, BLA Submission, Clinical Pharmacy Manuals etc.)</li><li>Understands design inputs and outputs of multiple delivery systems and how it can impact end users.</li><li>Supports management and/or therapeutic area device project leads, in strategic product launch and go-to-market plans for the device development.</li></ul><p>This role might be for you if you:</p><ul><li>Understand relevant FDA regulations, particularly 21 CFR Part 3 and 21 CFR 820.30.</li><li>Have experience with design history file management (21 CFR 820.30).</li><li>Possess strong project management and interpersonal skills and strong analytical and problem-solving capabilities.</li><li>Can balance business objectives with technical constraints.</li><li>Can work effectively across multiple functional teams.</li><li>Enjoy working in a fast-paced, multifaceted research and development environment.</li><li>Are willing and able to travel for partner meetings, audits, and project coordination activities.</li></ul><p>To be considered for the Device Development Engineer you must have a B.S in Engineering and 5+ years or relevant experience; or equivalent combination of education & experience. Previous experience in product management/project management/ and/or project leadership related activities is required. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$75,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45490]]></requisitionid>
    <referencenumber><![CDATA[R45490]]></referencenumber>
    <apijobid><![CDATA[r45490]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45490/manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager </strong>to join our<strong> Regulatory Affairs Advertising and Promotion</strong> team. In this role, you will apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). This individual will provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; in partnership with management, provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 2 total years relevant experience, preferably within Regulatory Advertising and Promotion</p></li><li><p>At minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences. An Advanced Scientific degree (i.e., Masters, PharmD, Ph.D) is preferred.</p></li><li><p>Knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and support launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs, Allergy & Respiratory (Asthma)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46160]]></requisitionid>
    <referencenumber><![CDATA[R46160]]></referencenumber>
    <apijobid><![CDATA[r46160]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46160/medical-director-medical-affairs-allergy-respiratory-asthma/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron seeks a dedicated Medical Director, Medical Affairs, who prioritizes patient care above all else. The successful candidate will drive the development and execution of medical strategies and activities related to Regeneron's strategic assets in the Allergy & Respiratory disease area, ensuring integrity and scientific accuracy. This role requires deep expertise in asthma and related diseases, and clinical trial execution.</p><p><strong>A typical day in the life of a Medical Director, Medical Affairs may include the following responsibilities: </strong></p><p>• Develops and oversees implementation of US and ex-US focused medical strategy and tactics, including scientific communications and publications, annual medical planning, field communications, and collaborations with experts.<br>• Supports the design, conduct, oversight, analysis, and reporting of Medical Affairs post-approval interventional and non-interventional respiratory clinical trials.</p><p>• Attends clinical study team meetings, data oversight review sessions, and works closely with CRO medical monitors in support of medical affairs clinical trials.</p><p>• Oversees and provides hands on support in management, generation and dissemination of clinical and non-clinical data that supports the medical strategy and results in high quality publications.</p><p>• Collaborates effectively within a multifunctional, matrix organization which includes field medical teams, medical operations, education, information, HEOR, publication management, and statistics.<br>• Develops and cultivates long-term strategic partnerships with clinical experts, societies, collaborative groups, advocacy groups, and other external stakeholders.</p><p>• Supports commercial activities such as promotional materials review, speaker training, colleague training, etc.</p><p><strong>This role may be for you if you have the following:</strong></p><p>• Physician (MD/MBBS or equivalent medical degree) with specialized training AND experience in pulmonology or allergy, specifically asthma</p><p>• 0-4 years of industry experience in Allergy/Respiratory Medical Affairs and/or Clinical Development (academic research experience will be considered)</p><p>• Demonstrated experience in clinical trial execution</p><p>• Experience working in an alliance setting is strongly preferred</p><p>• Lead complex business and technical discussions internally and externally and explain scientific/medical concepts to all levels<br>• Cultivate relationships and establish trust with internal and external Medical Experts in pulmonology.</p><p>• Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management.</p><p>• You thrive in a very dynamic environment in a therapeutic area with other competing treatment options.</p><p>#MDJobs, #MDJOBSMA, #GDMAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, US Oncology Skin Cancer Marketing]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46356]]></requisitionid>
    <referencenumber><![CDATA[R46356]]></referencenumber>
    <apijobid><![CDATA[r46356]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46356/director-us-oncology-skin-cancer-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, US Oncology HCP Skin Cancer Marketing, is a member of the Oncology Business Unit with accountability for working closely with the Senior Director to develop commercial HCP promotion strategy and tactical plans for Non-Melanoma Skin Cancer (NMSC) within the US. Also responsible for collaborating with the International team for Global commercialization and promotion.</p><p>This position will report directly to the Senior Director, HCP Skin Cancer Marketing. The Director will work collaboratively across the Franchise Team, International teams, internal cross-functional colleagues, while effectively managing external agency partners to ensure alignment and to drive optimal integration and execution of personal and non-personal initiatives<strong>.</strong></p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li>Lead HCP marketing for the NMSC indications in the US. This includes defining US market opportunities, analyzing the competitive landscape, identifying key site of care and key account segmentation and needs, developing customer-focused and differentiated product and indication positioning, and customizing messages to key target audiences.</li><li>Works in close collaboration with Clinical, Medical Affairs and Field Medical to ensure alignment with Medical Education strategic plans.</li><li>Engage with physician experts and attend key congresses to support Scientific Marketing team efforts and assess important disease and treatment data.</li><li>Work closely with the Insights and Data Analytics team to design and implement promotional strategies, while tracking brand performance, share of voice, market dynamics and competitive actions & response. Provide business assumptions input to forecasting.</li><li>Oversee and collaborate with Digital/Media Strategy team for optimization and implementation of the multi-channel marketing mix, including omni-channel digital & media strategy and implementation, and creation and deployment of educational resources towards brand objectives and developing indicators/metrics for high-impact engagements with HCP key target audiences.</li><li>Develop and coordinate NMSC HCP Marketing inputs and key sections of brand plan, identify and prioritize business opportunities.</li><li>Responsible for the development of the Field Plan of Action and training plan, national/regional sales meeting execution and Field communications in collaboration with internal and external partners/collaborators.</li><li>Maintain strong collaborative relationships with cross-functional areas and internal strategic partners (i.e., Field Sales, Training, Promotional Review Committee, Medical Affairs, Regulatory, Clinical, Legal, Compliance, Market Access etc.)</li><li>Ensures that the marketing processes, programs, and internal reports are developed, implemented, and effectively administered to be consistent with corporate guidance and all regulatory, legal, ethical guidelines.</li><li>Manages and develops a direct report to ensure their continued development and growth.</li><li>Works cross functionally to create, manage and track budget to ensure operating within the approved budget and phasing.</li></ul><h3><strong>This job might be for you if:</strong></h3><ul><li>You are effective collaborator and communicator both written and verbal</li><li>You can navigate regularly in ambiguity</li><li>You excel in a fast paced environment</li></ul><p>To be considered for this role, we expect you to have a Bachelors degree; 12+ years of pharmaceutical marketing focused on Oncology. Along with leading and developing long range brand plans, budgets and forecasts for commercial teams in the pharmaceutical/biotech industry. Lastly, this role requires you to travel 30% of the time and to be in the office in Sleepy Hollow, NY 4 days a week.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Assistant, Global Patient Safety]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46569]]></requisitionid>
    <referencenumber><![CDATA[R46569]]></referencenumber>
    <apijobid><![CDATA[r46569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46569/executive-assistant-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an Executive Assistant to join our Global Patient Safety Organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Global Patient Safety (GPS) Executive Assistant is a dynamic role that requires tenured experience in administrative support at Regeneron. The Executive Assistant will report to and support the Senior Vice President (SVP) of GPS who oversees a global leadership team and functions in their remit. The incumbent will provide advanced calendar management, travel and all associated logistics to the SVP of GPS to ultimately ensure leaders of Regeneron and associated teams can effectively carry out high level business objectives. Given business need, the incumbent will lead team event planning, cross functional team building and town halls, order department supplies, become involved with space planning and may take in additional client support in a highly proactive, professional, collaborative and efficient manner. The Executive Assistant should have advanced experience in Microsoft 365 applications, Concur, and is able to learn new technologies with ease for themselves and their client.</p><p><strong>This role might be for you if can: ​</strong></p><ul><li><p>Proactively manages and responsible for time management and calendars of Executive using thorough understanding of department and leadership priorities.</p></li><li><p>Ability to anticipate the needs of leaders and teams in order to manage and problem solve all logistics with a larger scope and greater impact if scheduling conflicts occur.</p></li><li><p>May lead all logistics/execution of internal meetings including but not limited to cross functional team buildings and town halls. Acts as the contact for external meetings and is responsible for collaborating with Strategic Sourcing and Procurement to manage and negotiate contracts for off-site meetings as well as managing meeting/event budgets within the approval limit. May act as point person to gather agenda items and may collect slides from multiple individuals in order to provide a complete slide deck and materials for meetings/events.</p></li><li><p>May assist with managing budgets within functional department supported.</p></li><li><p>Handles travel and expense reports for their client, and additional clients in the department if necessary. Assists guests with travel, where applicable. </p></li><li><p>Advanced knowledge of company policies, procedures and resources and acts as a point person for leader(s)/department(s) taking the lead to raise potential continuous improvement efforts to current processes. </p></li><li><p>Actively manages department contact lists/org charts. Proactively manages and updates content on department SharePoint sites and/or internal pages.</p></li><li><p>Responsible for proactively monitoring purchase order requests and may be responsible for gathering expense requests. May also submit requisitions and coordinate tracking of departmental deadlines. </p></li><li><p>May lead the preparation, onboarding and assimilation for new employees within GPS, including coordination with IT, Facilities, and Procurement. Assists with department space planning and may assist in headcount tracking. </p></li><li><p>Anticipate and make recommendations for catering for meetings and events scheduled over meal periods.</p></li><li><p>May act as SME for junior Administrative colleagues, create best practices and proactively works with other administrative coordinators to ensure coverage while Admins are out of the office.</p></li><li><p>All other duties as assigned.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Associates or BA preferred; 8+ years administrative experience with a minimum of 4 years of executive administrative experience desirable.</p></li><li><p>Years of experience may be considered in lieu of degree.</p></li><li><p>Highly collaborative within the department(s) of support as well as being sought out by peers cross-functionally. Skillful written and verbal communication skills are essential; ability to interact across all levels of employees and management while maintaining confidentiality. Demonstrated organizational knowledge and ability to understand department and leader priorities while potentially supporting groups with increasingly complex responsibilities.</p></li><li><p>Highly independent and shows advanced judgment and problem-solving skills. Comfortable leading projects. Ability to coordinate team members cross-functionally.</p></li><li><p>Is a quick learner, can cope and make good decisions despite change and ambiguity; skillfully handles risk and uncertainty with composure and shifts gears with ease. </p></li><li><p>Works comfortably with all levels in the organization including senior managers. Understands how senior leaders think and what they expect. </p></li><li><p>Advanced knowledge and proficiency in MS Office, SharePoint, Concur and teleconference systems with the ability to assist with more advanced troubleshooting. May be responsible for training new employees on internal systems</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$38.61 - $63.03]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Privacy Counsel: Digital, Cyber AI]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46433]]></requisitionid>
    <referencenumber><![CDATA[R46433]]></referencenumber>
    <apijobid><![CDATA[r46433]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46433/director-privacy-counsel-digital-cyber-ai/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>As a key member of the Privacy Office in Regeneron’s Law Department, this role will enable our rapidly growing and globally expanding business to develop and execute innovative data-driven strategies in accordance with data privacy law, and related cybersecurity and AI requirements. This role will support our Digital and Information Technology functions, including Information Security, AI, and Data Governance. This position will report to Regeneron’s Chief Privacy Officer.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY, Cambridge, MA</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Strategically assessing potential privacy risks associated with innovative new initiatives and developing appropriate controls, training and guidance to enable compliance with applicable regulations.</p></li><li><p>Providing legal advice on cybersecurity and information incidents and working with internal stakeholders to prepare for and respond to cyber/information incidents, including managing the incident response process</p></li><li><p>Providing legal guidance at the intersection of privacy and AI adoption including participation in AI use case assessments. </p></li><li><p>Drafting policies, procedures and guidance related to the foregoing subject matter areas in partnership with Law Department colleagues, Digital/IT and business functions.</p></li><li><p>Monitoring developments in the US and globally (including related legislation and industry practices) and supporting operationalization of compliance with regional and local laws such as CCPA/CPRA, NIS2 Directive, etc.</p></li><li><p>Advising on the application and solutions for complying with biometric and other emerging data-related laws.</p></li><li><p>Representing the Privacy Office as a member of Regeneron's technology-related committees and working groups.</p></li><li><p>Partnering with Privacy Office colleagues to contribute to the implementation and advancement of the Regeneron Privacy Program.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A JD and be licensed to practice law in New York State or eligible for licensure as a registered in-house counsel.</p></li><li><p>At least 12 years of legal experience at a law firm and/or in-house, with at least 5 years of experience of directly relevant experience. Biotechnology, pharmaceutical or related life science experience strongly preferred.</p></li><li><p>Strong knowledge of local and global privacy, cybersecurity and AI laws and familiarity with associated risk management frameworks and standards (e.g., NIST).</p></li><li><p>Excellent relationship building skills.</p></li><li><p>Demonstrated ability to work collaboratively and with all levels of the organization.</p></li><li><p>Exceptional oral, written, and presentation communication skills, with the ability to effectively communicate and translate complex legal analysis into practical guidance for a varied audience.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Precision Medicine (Cell Medicine)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46672]]></requisitionid>
    <referencenumber><![CDATA[R46672]]></referencenumber>
    <apijobid><![CDATA[r46672]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46672/director-precision-medicine-cell-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking to hire a Precision Medicine Scientific Lead to oversee the development and execution of biomarker strategies for novel cell therapies, cell transfer conditioning agents and combinations with bispecific antibodies across multiple disease areas (Oncology and Immunology). In this highly matrixed role, they will design, develop, communicate across levels and operationally implement clinical biomarker strategies to support selecet programs in early and late stage drug development. Clinical biomarker assays include pharmacokinetic assays, mechanism of action, patient stratification assays and pharmacodynamic assays. The candidate will collaborate with teams internal to RCM and more broadly Regeneron or with contract research organizations to develop and implement clinical biomarker assays.</p><p><strong>As a Director, a typical day may include the following:</strong></p><ul><li><p>Program-level Precision Medicine lead that develops and implements the strategic vision for pharmacokinetic, pharmacodynamic, and exploratory biomarkers for clinical studies enabling indication and/or patient selection, early indication of biological activity, and to identify potential novel combinations.</p></li><li><p>String collaboration with Biomarker and clinical operation teams to implement specific biomarker and exploratory sample collection and analyses in all relevant clinical studies in selected programs</p></li><li><p>Key individual contributor and precision medicine representative to development and Cell therapy characterization teams with a remit to integrate, influence and deliver biomarker strategies from initial concept to execution, data delivery and results interpretation.</p></li><li><p>Collaborate with internal Regeneron laboratories and groups (e.g. BioAnalytical, Clinical Pharmacology, Molecular Profiling, CDX, Discovery Research, Analytical Innovations, DMSQ etc.) to develop plan for validation and application of assays in the clinic.</p></li><li><p>Accountability for ensuring complex clinical assays used in programs are fit-for-purpose (whether developed and validated internally or externally)</p></li><li><p>Collaborate with Discovery Research and product development teams to facilitate appropriate incorporation of Precision Medicine biomarker strategies for molecules in discovery phases (leading to candidate molecule selection) through to the clinic.</p></li><li><p>Represent Regeneron externally thorough collaborations and/or presentations.</p></li><li><p>Contribute to Clinical Protocol, schedule of Assessments, clinical study reports, technical reports, data agreements, scientific publications and make recommendations to development teams and management</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>The ability to drive, manage, complete and deliver results for complex multi-functional projects</p></li><li><p>Excellent communication and presentation skills and high emotional intelligence, organizational skills and effective team skills</p></li></ul><p><strong>To be considered for this role, you must have a </strong>PhD and 10+ years of experience participating effectively on cross-disciplinary teams in pharmaceutical or biotech industry. Experience in clinical assay development, validation and implementation with strong experience in Immunology is preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Obesity]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46851]]></requisitionid>
    <referencenumber><![CDATA[R46851]]></referencenumber>
    <apijobid><![CDATA[r46851]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46851/medical-director-clinical-development-obesity/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Medical Director, Clinical Development, Obesity should be a qualified physician with pharmaceutical industry experience, preferably in the area of metabolism, in relevant areas such as obesity or Type 2 diabetes. The Director will serve as Medical Lead for clinical trials in the CDP and is responsible for the design of clinical study concepts leading to clinical trial protocols. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.</p><p><strong>A typical day in the life of a Medical Director may include the following responsibilities:</strong></p><ul><li><p>Acts as medical expert and leader in interactions with external stakeholders</p></li><li><p>Defines clinical trial-related Clinical Development Program (CDP) goals and objectives </p></li><li><p>Works closely with discovery teams to provide input on the next generation of targets in the field</p></li><li><p>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts </p></li><li><p>Reviews and finalizes clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings</p></li><li><p>Leads the Global Clinical Study Team to produce high quality program deliverables on schedule </p></li><li><p>Responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety </p></li></ul><p><strong>This job may be for you if you have the following: </strong></p><ul><li><p>An M.D. or equivalent with board eligibility or board certification in Pediatric Endocrinology preferred; relevant experience can be acceptable.</p></li><li><p>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</p></li><li><p>Experience in metabolic disorders drug development strongly preferred</p></li><li><p>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</p></li></ul><p>#MDJOBS, #MDJOBSCD#GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46894]]></requisitionid>
    <referencenumber><![CDATA[R46894]]></referencenumber>
    <apijobid><![CDATA[r46894]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46894/senior-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>We are seeking a Senior Project Engineer who will be responsible for designing, specifying and commissioning new and renovated biopharmaceutical process equipment. This position will provide engineering support and problem solving support for existing equipment and manufacturing processes.</div></div><div><div><div><div><div><div><div><div><div><p><strong>As a Sr Project Engineer, a typical day might include the following: </strong></p><ul><li><p>Designing and specifying cGMP process equipment, piping, and controls</p></li><li><p>Managing small-to-mid-sized projects related to process equipment and manufacturing</p></li><li><p>Assisting in the design review, site acceptance, and installation of equipment</p></li><li><p>Preparing piping and instrumentation diagrams (P&IDs) and other related drawings</p></li><li><p>Developing Process Flow Diagrams (PFDs) for manufacturing processes</p></li><li><p>Supporting the QA Validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Reviewing and approving lifecycle documentation, cleaning validation protocols, and summary reports</p></li><li><p>Assisting with investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</p></li><li><p>Assisting management with tracking of department throughput and efficiency</p></li><li><p>Representing the engineering department at cross-functional meetings</p></li><li><p>Supervising direct reports as needed</p></li><li><p>Implementing corrective/preventative actions for existing equipment and manufacturing processes</p></li><li><p>Preparing engineering evaluations and test plans, and executing change control documentation</p></li><li><p>Supervising mechanical, electrical, and automation contractors as needed</p></li><li><p>Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</p></li><li><p>Maintaining company reputation by ensuring compliance with all relevant laws, policies, and regulations</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You have excellent technical and analytical skills.</p></li><li><p>You are skilled at problem-solving and continuous improvement.</p></li><li><p>You possess strong communication and collaboration skills.</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><p>To be considered for this opportunity you should have a BS/BEng or higher in chemical/process/mechanical engineering with 5+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p><p>#LI-Onsite #JOBSIEPR #IRELIM #REGNIRLTO</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Data Governance and Contract Compliance, Regeneron Genetics Center (RGC)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47043]]></requisitionid>
    <referencenumber><![CDATA[R47043]]></referencenumber>
    <apijobid><![CDATA[r47043]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47043/director-data-governance-and-contract-compliance-regeneron-genetics-center-rgc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Data Governance and Contract Compliance lead and ensures compliance across a large portfolio of global data licensing collaborations involving genetic and associated health data. You will serve as RGC’s internal resource on data privacy, genomic data governance, and cross-border data transfer; partnering with RGC counsel, research and technology teams, and the Privacy Office, to uphold the highest standards of data stewardship. You will develop and implement operational policies, procedures, and risk mitigation strategies that enable scientific collaboration, while safeguarding individual data rights worldwide.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Lead compliance across approximately 150 global data licensing collaborations related to genetic and associated health data, including ongoing monitoring, risk assessment, and remediation.</p></li><li><p>Partner with counsel to interpret and ensure compliance with international privacy regulations (GDPR, HIPAA, CCPA/CPRA), and genomic data governance frameworks (NIH Genomic Data Sharing Policy, GA4GH), in data collaboration agreements and research operations.</p></li><li><p>Drive the development and operationalization of RGC data governance policies, procedures, consent frameworks, and data use agreements specific to genetic and health data.</p></li><li><p>Lead all aspects of data security stewardship practices, evaluating and integrating emerging privacy-preserving technologies with the IT Security team.</p></li><li><p>Monitor the evolving global regulatory landscape for genetic data governance, advising leadership on compliance risks and policy adaptations.</p></li><li><p>Lead, mentor, and develop a team of data governance and compliance professionals; championing a culture of accountability, transparency, inclusion, and continuous learning.</p></li><li><p>Collaborate cross-functionally with Legal, IT Security, Research, and Business Development to embed privacy-by-design into data collaboration workflows and initiatives.</p></li></ul><p><strong>This job might be for you if you have:</strong></p><ul><li><p>Experience with GDPR, HIPAA, CCPA/CPRA, and other applicable privacy regulations.</p></li><li><p>Solid understanding of genomic data governance frameworks, including the NIH Genomic Data Sharing Policy and GA4GH standards.</p></li><li><p>Clear written and verbal communication skills, with the ability to relay complex regulatory requirements to scientific and executive audiences.</p></li><li><p>Validated experience building and leading high-performing compliance teams.</p></li><li><p>IRB experience. Familiarity with federated learning, and secure multi-party computation technologies is preferred.</p></li></ul><p><strong> In order to be considered for this role, you must have:</strong></p><ul><li><p>A PhD in Genetics, Genomics, Bioethics, Life Sciences, or a related field; or a relevant degree with experience in data governance and compliance.</p></li><li><p>An equivalent combination of advanced education and 10+ years of experience in data governance, compliance, or regulatory affairs; with at least 5 years focused on genetic or health data in research, biopharmaceutical, or biotech settings.</p></li><li><p>CIPP/E or CIPP/US certifications are strongly preferred.</p></li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Legal Data Privacy Operations]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47119]]></requisitionid>
    <referencenumber><![CDATA[R47119]]></referencenumber>
    <apijobid><![CDATA[r47119]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47119/senior-manager-legal-data-privacy-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an experienced and forward-thinking Senior Manager Legal Data Privacy Operations to lead privacy program operations within the Law Dept. / Privacy Office. As a key member of the Privacy Office within Regeneron’s Law Department, you will play an important role in advancing our data privacy program. This includes managing complex privacy projects, delivering tactical operational support, and supporting governance initiatives. By leading well-designed and executed privacy operations, this role plays a central part in building the organizational foundation that enables Regeneron to manage data responsibly, maintain trust, and support the company's overall mission.</p><p><strong><em>A typical day might include:</em></strong></p><ul><li><p>Managing and identifying opportunities to improve core privacy operations, including PIA, ROPA, and DSAR processes across multiple business units, geographies, and regulatory frameworks.</p></li><li><p>Leading complex privacy program initiatives that involve coordinating and aligning privacy processes with other business functions and leveraging technology and AI to automate, find efficiencies, and enhance how privacy operations are managed and executed.</p></li><li><p>Documenting advice and implementation of online privacy notices and controls, tracking technologies, and privacy-enhancing tools.</p></li><li><p>Developing and maintaining privacy program metrics and KPIs.</p></li><li><p>Maintaining and developing internal policies, procedures, guidance documents, training and awareness, including our Intranet site.</p></li><li><p>Coordinating Privacy Steward engagement to advance enterprise-wide privacy initiatives in alignment with organizational objectives and regulatory requirements.</p></li><li><p>Managing vendor relationships by overseeing the execution of Statements of Work and ensuring timely processing of requisitions, purchase orders, and invoices.</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Knowledge of privacy laws and understanding of privacy risk management technologies</p></li><li><p>Demonstrated ability to critically evaluate privacy processes and implement innovative, practical improvements.</p></li><li><p>Experience collaborating with teams outside of privacy or legal function to integrate privacy requirements into business operations.</p></li><li><p>Strong project management skills and ability to manage multiple priorities and deliverables simultaneously</p></li><li><p>Excellent relationship building skills and demonstrated ability to work collaboratively</p></li><li><p>Exceptional oral, written, and presentation communication skills</p></li><li><p>AI literacy and experience leveraging technology to support or enhance privacy operations</p></li></ul><p><strong>To be considered for this role</strong>, you must have a bachelor's degree, advanced degree in a related field preferred. At least 8 years of experience in privacy, with a preference for at least 3 years managing privacy operations (including PIA, ROPA, and DSAR processes) within a legal or compliance privacy function.</p><p>Certified Information Privacy Manager (CIPM) or Certified Information Privacy Technologist (CIPT) Project Management Professional (PMP) or equivalent certification.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II, Advanced Therapy Project Management (ATPM)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47142]]></requisitionid>
    <referencenumber><![CDATA[R47142]]></referencenumber>
    <apijobid><![CDATA[r47142]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47142/process-development-engineer-ii-advanced-therapy-project-management-atpm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron, located in Tarrytown, NY, is seeking a Process Development Engineer II to support project management, technology transfer, and business operations for Regeneron Advanced Therapy Programs. This representative will work in the Advanced Therapy Project Management (AT-PM) group within Product, Analytical, and Process Development Operations (PAPD Ops) to help drive successful development and tech transfer of advanced therapies (e.g., AAV, bioconjugates, and synthetic chemistry programs) by enabling clear cross-functional ways of working, disciplined planning, and operational excellence with our internal partners and Contract Development & Manufacturing Organizations (CDMOs).</p><h3><strong>A Typical Day in This Role Might Look Like:</strong></h3><ul><li>Lead cross-functional tech transfer teams and independently own workstreams to establish production processes at CDMOs. Drive readiness for manufacturing start-up and execution by clarifying scope, securing inputs/approvals, tracking deliverables, and escalating risks/issues with proposed mitigations.</li><li>Own communication strategy and operating cadence for assigned programs (e.g., core team meetings, technical forums, and stakeholder updates). Provide concise, decision-ready status reporting (scope/timeline/cost/risk) tailored to different audiences, including senior stakeholders.</li><li>Build, maintain, and continuously improve integrated plans across development and transfer activities. Facilitate scenario planning and tradeoff discussions to protect key milestones and support portfolio-level prioritization.</li><li>Anticipate and address risks to manufacturing readiness related to process. Define mitigation plans and help ensure teams execute with rigor expected for successful CDMO campaign execution.</li><li>Lead recurring and ad-hoc technical forums to drive timely decisions, resolve issues, and capture lessons learned. Translate learnings into tools to improve repeatability across modalities and CDMOs.</li><li>Lead continuous improvement initiatives to mature AT-PM ways of working.</li><li>Partner with procurement, finance, legal, and internal stakeholders to support CDMO engagement (RFPs, scope alignment, contracting coordination, and invoice tracking).</li></ul><h3><strong>This Role Might Be For You If:</strong></h3><ul><li>You take initiative, reliably follow through, and thrive in non-structured environments, bringing energy, a strategic mindset, and an action-oriented approach while navigating ambiguity and changing priorities.</li><li>You enjoy and excel at problem solving and can break down complex technical and operational challenges, propose well-thought-out plans, and drive decisions.</li><li>You like building structure and scalable frameworks that help cross-functional teams execute efficiently and with the right balance of rigor and flexibility.</li><li>You proactively identify risks/roadblocks, communicate tradeoffs, and know when and how to escalate.</li><li>You are willing to try, learn, and iterate to keep programs moving forward and partners aligned.</li></ul><p>This role requires a B.Sc., with 5+, or M.Sc. with 3+ years of biochemistry/ chemical/biochemical engineering or a related field, including demonstrated ownership of cross-functional deliverables. A strong customer-service mindset is essential. The ideal candidate can independently facilitate team collaboration, build and maintain integrated plans, and design/improve repeatable business processes. Experience supporting CMC development and/or technology transfer to CDMOs (e.g., process development, analytics, documentation readiness) is preferred. Prior experience or knowledge of bioconjugation, gene therapy/AAV, or related advanced therapy process development is a plus.</p><p>If applicable, candidates may include GPA on their resume.</p><p>#pmpd</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Business Office]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47016]]></requisitionid>
    <referencenumber><![CDATA[R47016]]></referencenumber>
    <apijobid><![CDATA[r47016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47016/director-global-patient-safety-business-office/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Director, Global Patient Safety Business Office to join our organization!!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, GPS Business Office, serves as a strategic partner to the SVP of Global Patient Safety, driving execution of GPS’ overarching strategic plan, including the annual department operating plan, long-term roadmap, and key transformation initiatives for pharmacovigilance (PV) enablement (e.g., Global Capabilities Center (GCC)). This role leads business planning, execution and enablement of GPS initiatives, communication strategies, resource management, PV forecasting and capacity planning, talent calibration, and the PV functional-level vendor strategy.</p><p><strong>This role might be for you if can/have:</strong></p><ul><li><p>Define and communicate the GPS vision and strategy in alignment with enterprise goals and business priorities </p></li><li><p>Serve as a strategic thought partner to the SVP of Global Patient Safety regarding PV strategy, and operating model </p></li><li><p>Act as a strategic connector across GPS teams to enable execution of GPS vision, strategy and priorities </p></li><li><p>Lead strategy and governance for the Global Capabilities Center (GCC) across GPS functions, aligning scope, resourcing, and metrics to GPS priorities and enterprise objectives, to expand PV capacity and drive measurable outcomes </p></li><li><p>Lead development of annual department operating plans and strategic roadmaps for GPS </p></li><li><p>Drive operational excellence in collaboration with GPS leaders, through benchmarking and continuous improvement </p></li><li><p>Partner with GPS interfacing functions to enable PV operational alignment </p></li><li><p>Collaborate with GPS leadership on goal setting, initiative tracking, and performance dashboards </p></li><li><p>Lead delivery of key GPS functional meetings (e.g., GPS Leadership Team, All Hands, Mid-Year meetings). </p></li><li><p>Prepare and maintain regular delivery of GPS communications </p></li><li><p>Organize and manage mid-year and year-end talent calibration exercises in collaboration with stakeholders and HR Business Partners (HRBPs) </p></li><li><p>In partnership with RA GPS DQ Strategy and Operations and Portfolio Management, establish operational portfolio forecasting for GPS </p></li><li><p>Lead resource planning and optimization across GPS functions (internal staffing, GCC expansion, vendor utilization) in partnership with stakeholder functions (e.g., Vendor Relationship Management, GD Resource Management, RA GPS DQ Strategy Planning & Operations, and Portfolio Management) </p></li><li><p>Collaborate cross-functionally in support of GPS with Development Services & Operational Excellence (DS&OE) team, and Learning Center of Excellence (LCoE) functions. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum Bachelor’s Degree (Advanced Degree preferred) in business, strong preference for degree in life sciences or healthcare with 12+ years of relevant PV planning and operations experience in the pharmaceutical area and specific industry experience in managing and providing oversight of operations within a global patient safety organization highly preferred. </p></li><li><p>Proven ability to lead and develop a diverse remit in a constructive, goal-oriented environment, with continuous improvement and innovation mindset. </p></li><li><p>Demonstrated pharmacovigilance (PV) and Safety Risk Management (RM) expertise, including end-to-end safety processes, regulatory expectations, and cross-functional governance within a global patient safety organization </p></li><li><p>Demonstrated problem-solving with the ability to “flex” across different complexities, business situations and cross functional partners of GPS </p></li><li><p>Proven ability to drive results through strong cross-functional partnerships and stakeholder engagement </p></li><li><p>Demonstrated ability and track-record to lead PV operational and planning initiatives with excellence, including governance activities </p></li><li><p>Highly detail-oriented, ensuring accuracy, consistency, and quality across deliverables, documentation, and communications, while maintaining strategic perspective. </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Field Medical Affairs- Hematology (Western states)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47699]]></requisitionid>
    <referencenumber><![CDATA[R47699]]></referencenumber>
    <apijobid><![CDATA[r47699]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47699/director-field-medical-affairs-hematology-western-states/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Director, Field Medical Affairs you will be responsible for regional hiring, deployment, and leadership responsibilities for hematology focused Associate Directors – Field Medical (MSLs). In partnership with Senior Director, you will supervise team member development and evaluate performance. Responsible for providing oversight of all activities in accordance with current regulatory and health care guidelines. Other responsibilities include providing scientific exchange and collaboration with therapeutic area opinion leaders on disease and product information as well as research initiatives. Participates in the development and the management of company and investigator sponsored clinical trials.</p><p>Territory: Western US</p><p><strong>A typical may include the following: </strong></p><ul><li><p>Hematology Field Medical direct line leadership including, hiring, goal setting, performance evaluation and all other aspects related to direct report supervision. (Field visits, training, mentoring) </p></li><li><p>Execution of initiatives and other permissible field activities </p></li><li><p>Ensure team field activity level and field metrics. </p></li><li><p>Collaborate with internal team members in to ensure alignment and communication of goals and team value proposition. </p></li><li><p>Developing field strategies for healthcare professionals.</p></li><li><p>Participate in the development of the educational materials/evidence communication tools and champions the regulatory/legal/health care compliance approvals.</p></li><li><p>Create and implement of field collaborative strategies to ensure compliant partnership with other customer facing teams (e.g., sales).</p></li><li><p>Identifies gaps in research needs and strategies creating opportunities for the by collaborating with potential and existing investigators.</p></li><li><p>Assists with management of clinical data through support of abstracts, posters, presentations and manuscript development. </p></li><li><p>Engaging healthcare professionals and attends medical conferences to collect and report relevant medical insights.</p></li><li><p>Develop strategic plans and coordinates activities for Hematology scientific meetings and congresses.</p></li><li><p>Collaborating with Clinical and study staff to developing, implementing plans and strategies supporting Hematology Development Plans.</p></li><li><p>Develops strategies for maintaining lists of Hematology experts/investigator targets and plans of action.</p></li><li><p>Work with Medical Information to develop, plan, and review materials used for responses to scientific inquiries from health care professionals.</p></li><li><p>Ensures company policies, principles and financial controls are maintained with integrity and professionalism being displayed internally and externally.</p></li></ul><ul><li><p><strong>This may be for you if:</strong></p></li><li><p>• Can demonstrate establishing a highly functioning, customer centric, field medical organization.</p></li><li><p>• Want to be involved in pre-launch, launch and post launch activities. </p></li><li><p>• Have the ability to solve problems with innovative solutions along with strong organizational skills</p></li></ul><p>To be considered an Advanced medical and/or scientific degree required (e.g., MD/DO, PhD, PharmD, DVM) as well as 10+ years’ work experience in Field Medical Affairs. Oncology and/or Hematology experience is required (Lymphoma or Multiple Myeloma is preferred). Previous experience for 2+ years leading a team is required. Must have strong computer skills with a proficiency in Microsoft Word, Excel and PowerPoint and Veeva. Residency in the Western US is required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Facilities Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47620]]></requisitionid>
    <referencenumber><![CDATA[R47620]]></referencenumber>
    <apijobid><![CDATA[r47620]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47620/facilities-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Facilities Engineer, you will provide engineering support, troubleshooting, & subject matter expertise to the Facilities Operations, Utilities & HVAC teams.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li>Building and specifying cGMP clean/grey utilities, & HVAC equipment, piping, ducting and/or controls</li><li>Managing small-to-mid sized projects related to utilities & HVAC equipment & services</li><li>Conducting troubleshooting for complex issues with plant equipment issues and associated systems, identifying and recommending corrective actions</li><li>Assisting in the design review, site acceptance and installation of equipment</li><li>Supporting the QA Validation department by preparation of design documents and assists in protocol execution</li><li>Assisting in investigations of utility systems, and control system anomalies as well as safety incidents</li><li>Implementing corrective/preventative actions for existing equipment and maintenance processes</li><li>Preparing engineering evaluations and test plans for and executing modification change control documentation</li><li>Interpreting P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs</li><li>Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have strong analytical and interpersonal skills</li><li>You are able to prioritise and re-prioritise as needed and adapt to change</li><li>You are comfortable working in a fast-paced setting</li><li>You are adaptable and can work in a fast-paced, regulated environment</li></ul><p>To be considered for this position you should have a BS/BA in Mechanical Engineering or equivalent, with 5 years of relevant experience preferably in the Pharma/Biotech industry.</p><p>Senior Engineer: BS/BA in Mechanical Engineering with 5 years' minimum experience</p><p>Engineer: BS/BA in Mechanical Engineering with 2 years' minimum experience</p><p>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLTO</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Utilities Technician, 2nd shift Wednesday-Saturday]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47749]]></requisitionid>
    <referencenumber><![CDATA[R47749]]></referencenumber>
    <apijobid><![CDATA[r47749]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47749/utilities-technician-2nd-shift-wednesday-saturday/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a Utilities Technician to our growing team with a Wednesday-Saturday 2:00pm-12:30am shift. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Utility Technicians are responsible for operations and maintenance of High Purity Water/Steam systems and Plant Utility systems that support that manufacturing process. This is a diverse maintenance position with growth potential in a growing company.</p><p><strong>Please note training will take place Monday-Friday 7:00am-3:30pm for the first few weeks. Working hours thereafter will be Wednesday-Saturday 2:00pm-12:30am. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a Utilities Technician, a typical day might include the following:</p><ul><li>Maintaining water room and boiler room related equipment, including pumps, motors, clean and plant utilities pre-treatment systems, Water for Injection (WFI) stills, Clean Steam Generators, high pressure steam, plant steam boilers, boiler controls, condensate return, natural gas, domestic potable water, tepid water, wastewater, and related piping</li><li>Performing activities such as troubleshooting and hands on repairs on Clean Utility and Plant Utility equipment and systems</li><li>Following current good manufacturing practices (cGMPs)</li><li>Participating in rotational on-call schedule for site emergency work</li></ul><p>This role might be for you if you:</p><ul><li>Are adept at reading and/or understanding piping, electrical, and instrumentation drawings</li><li>Possess basic troubleshooting skills and mechanical aptitude as related to the utilities being maintained</li><li>Are capable of lifting, pushing, and/or pulling at least 50lbs</li><li>Are comfortable and flexible working in a changing environment</li><li>Can learn and follow routine procedures</li></ul><p>To be considered for the Utilities Technician position you must be willing and able to work Wednesday-Saturday 2:00pm-12:30am. Applicants ideally should have an AAS degree, preferably in an Engineering or Construction Technologies subject area and 2+ years of related experience or HSD/GED with 5+ years of related experience, preferably in a cGMP environment:</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Allergy) - Tampa N, FL]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47693]]></requisitionid>
    <referencenumber><![CDATA[R47693]]></referencenumber>
    <apijobid><![CDATA[r47693]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47693/medical-specialist-i-allergy-tampa-n-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tampa]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography– New Port Richey, Ocala, Lakeland, Jacksonville, Gainesville, Daytona</strong></p><p>The Medical Specialist (sales representative) Allergy will report to the District Manager, and will be responsible for engaging Allergists within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US</p><p>The MS is responsible for developing strategy and executing tactics within key allergists in the Dermatology and Respiratory therapeutic areas to generate product utilization. The MS will develop strong working relationships with experts and Allergists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>This role may be for you if:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory or Dermatology market and/or a similar subcutaneous self-injectable biologic specialty market. Ability to travel and cover large geographic territories</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[VP, Global Patient Safety Sciences, General Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47607]]></requisitionid>
    <referencenumber><![CDATA[R47607]]></referencenumber>
    <apijobid><![CDATA[r47607]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47607/vp-global-patient-safety-sciences-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>VP, Global Patient Safety Sciences – General Medicine</strong></p><p> <br>The VP, Global Patient Safety Sciences (GPS) – General Medicine serves as the primary point of contact for General Medicine safety strategy across clinical and post‑marketing assets. As the Therapeutic Area Head (TAH) and product subject matter expert (SME), you define safety strategy, establish the medical safety opinion, and provide the scientific point‑of‑view across GPS and non‑GPS interactions. You will advise senior leadership on safety strategies and processes, shape cross‑functional decisions, and serve on the GPS Leadership Team (GPS LT). This role also leads and develops a high‑performing team.</p><p><strong>In This Role, You Will:</strong></p><p><strong>Safety Strategy & Clinical Risk Assessment</strong></p><ul><li>Contribute senior‑level safety expertise to clinical programs across the assigned therapeutic area.</li><li>Serve as the medical review resource for complex Individual Case Safety Reports (ICSRs) and other data sources; act as point of escalation for ICSR causality assessments.</li><li>Oversee safety signal evaluations and deliver clinical interpretation of emerging safety issues.</li><li>Review benefit‑risk assessments (e.g., HHAs) and provide recommendations appropriate to asset lifecycle stage, including responses to health authority queries and safety documents (e.g., DSURs, PSURs).</li><li>Develop innovative approaches to core safety activities that integrate new technologies, including AI.</li></ul><p><strong>Governance Leadership</strong></p><ul><li>Influence cross‑functional leaders to align priorities and drive enterprise outcomes.</li><li>Approve and provide medical oversight for Risk Management Plans (RMPs).</li><li>Approve responses to medical and clinical health authority queries as needed.</li><li>Oversee cross‑functional Safety Monitoring Team (SMT) activities.</li><li>Represent GPS at governance forums, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT), and with external collaborators.</li></ul><p><strong>Talent Development & Organizational Leadership</strong></p><ul><li>Build, coach, and scale a high‑performing team; drive succession planning and talent pipelines.</li><li>Lead talent strategy and leadership development initiatives to strengthen organizational capabilities.</li></ul><p><strong>What You Need to Succeed</strong></p><p><strong>Required Qualifications</strong></p><ul><li>15+ years of pharmacovigilance (PV) or relevant clinical experience in the pharmaceutical/biotech industry.</li><li>8+ years of people leadership with demonstrated success leading teams; experience in a matrixed environment is a plus.</li><li>Proven ability to develop a deep understanding of product safety profiles to inform safety assessments, risk evaluations, and decision‑making.</li><li>Experience overseeing strategy within a global patient safety organization.</li><li>Strong leadership presence with excellent interpersonal, verbal, and written communication skills.</li><li>Advanced organizational and workload planning skills with the ability to manage multiple projects simultaneously.</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>Minimum 5 years of international pharmaceutical activities.</li><li>Advanced degree preferred: M.D., PA, or PharmD; Board Certification or equivalent in a relevant clinical specialty; MBA is an advantage.</li><li>Experience with AI technologies applied to safety science.</li></ul><p><strong>Work Model</strong></p><ul><li>This role requires 4+ days per week on‑site presence.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Study Start Up]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47995]]></requisitionid>
    <referencenumber><![CDATA[R47995]]></referencenumber>
    <apijobid><![CDATA[r47995]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47995/senior-manager-global-study-start-up/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Senior Manager, Global Site Start-Up Lead </strong>(SSU Lead) is responsible for driving the global execution of site activation for complex, high profile clinical trials, performing the role with high-degree of independence to ensure efficient and compliant processes aligned with Regeneron SOPs, ICH-GCP guidelines, and industry standards. Partnering closely with cross-functional teams and Clinical Research Organizations (CROs), this role balances strategic oversight with hands-on leadership to address challenges and deliver study objectives. The SSU Lead develops site activation projections, mitigates risks impacting site activation, and monitors CRO performance by analyzing metrics. Additionally, they lead all aspects of site start-up activities, including fast-track initiation, milestone tracking, and document collection, while ensuring timely submissions and leveraging country intelligence for informed decision-making. This person will also be responsible for direct line management and supporting development of their team.<strong> </strong></p><p><strong>A typical day in this role looks like:</strong></p><p>Site Start-up Strategy</p><ul><li>Develop the site start up strategy for each study assigned (complex, high profile), outlining all dependencies impacting site activation and actively mitigating and escalating risks. </li><li>Oversee the tracking and analysis of study metrics, including risks and mitigation strategies and to evaluate CRO performance and implement corrective actions.</li><li>Advocate for optimized site selection strategies, leveraging data-driven insights to guide cross-functional teams toward effective decision-making.</li><li>Lead the development, assessment, and alignment of site activation projections, ensuring cross-functional and CRO collaboration to meet strategic objectives.</li><li>Ensure comprehensive and compliant documentation of site start-up materials in the Trial Master File (TMF) to maintain inspection readiness.</li></ul><p>Country Start-up</p><ul><li>Partner with cross functional and CRO partners (where applicable) to develop a comprehensive global country start up strategy, outlining all dependencies impacting country start up and actively mitigating and escalating risks cross functionally. </li><li>Monitor and maintain country intelligence data to support informed decision-making and develop accurate startup projections and strategic plans.</li><li>Support regulatory submissions as needed, including activities such as: providing required site documentation, coordinating submissions to Central Institutional Review Boards (CIRBs), supporting sites with Local Institutional Review Board (LIRB) submissions, and handling or supervising Clinical Research Organization (CRO) insurance requests, etc.</li><li>Ensure timely country submission deliverables (ensure task completion; all roles clarity, identification of critical path items, effective communication pathway). </li></ul><p>Site Start up Management</p><ul><li>Lead and oversee all aspects of site start-up activities for complex, high profile studies, including fast-track site initiation, site calls, document collection, and milestone tracking, ensuring timely and efficient completion of processes.</li><li>Serve as the subject matter expert for essential site documents, providing training, guidance, and support to teams and sites on regulatory requirements, document management, and TMF filing.</li><li>Oversee CRO site start up management or in house site facing regional SSU team, where applicable</li><li>Lead the collection and analysis of site intelligence to support strategic site selection and site start-up.</li><li>Oversee the preparation and approval of site regulatory package, ensuring compliance with country-specific requirements, TMF standards, and ICH-GCP guidelines, while supporting inspection readiness and maintaining high-quality site documentation.</li></ul><p>Team Interactions</p><ul><li>Represent SSU on cross-functional teams, providing updates, escalating challenges, and proposing mitigation strategies for site start-up issues.</li><li>Act as the escalation point for CRO and internal team to ensure timely SSU issue resolution </li></ul><p>Process Improvement</p><ul><li>Recommends and drives cross functional and department process improvements.</li></ul><p>Line Management</p><ul><li>Responsible for direct supervision of SSU staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</li><li>May require up to 25% travel</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Strong interpersonal and leadership skills</li><li>Ability to provide and implements operational strategic direction and guidance for respective clinical trials</li><li>Demonstrates strong knowledge and a data driven approach to planning, executing, and problem solving</li><li>Strong communication skills via verbal, written and presentation abilities</li><li>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</li><li>Ability to influence and negotiate across a wide range of stakeholders</li><li>Ability to lead and develop productive study teams and collaborations</li><li>Applies advanced negotiation and interpersonal skills to vendor management</li><li>Strong technical proficiency in trial management systems (CTMS, TMF) and MS applications including (but not limited to) Project, PowerPoint, Word, Excel</li><li>Extensive experience in the clinical drug development process, including study start-up</li><li>Knowledge and understanding of ICH/GCP and regulatory guidelines/directives</li><li>Strong project management skills, cross-functional team interaction and organizational skills</li><li>Line management experience preferred</li></ul><p><strong> </strong></p><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelor's degree and 8+ years of relevant industry experience is required. Preference in a sponsor Site Start-Up role preferred.</p><p><br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Boundary Systems & Integration Readiness]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48116]]></requisitionid>
    <referencenumber><![CDATA[R48116]]></referencenumber>
    <apijobid><![CDATA[r48116]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48116/director-boundary-systems-integration-readiness/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, you will be part of a collaborative environment driving critical enterprise transformation initiatives. This role offers the opportunity to influence global ERP strategy, work across diverse functional domains, and play a key role in ensuring seamless integration across complex systems supporting life-changing therapies.</p><p>The Director, Boundary Systems & Integration Readiness is accountable for the strategy, governance, and end-to-end readiness of boundary applications that connect to the Oracle Fusion Cloud ERP landscape across a multi-phase, global transformation program.</p><p>This role ensures boundary systems are defined per deployment wave, aligned to target state architecture, and operationally ready for design, testing, cutover, and stabilization while maintaining compliance with regulatory requirements (e.g., SOX, GxP, 21 CFR Part 11) and ensuring continuity of business operations.</p><p><strong>In This Role, a Typical Day May Include:</strong></p><p>Boundary Strategy & Roadmap:</p><ul><li><p>Develop and maintain a comprehensive Boundary Systems roadmap aligned to Oracle Fusion program waves and enterprise priorities</p></li><li><p>Define and manage wave-by-wave boundary scope, including dependencies, sequencing, and impact assessment</p></li><li><p>Maintain capability matrices outlining current state, target state, and system gaps</p></li></ul><p>Governance & Intake Management</p><ul><li><p>Establish and lead governance processes for boundary system intake, ensuring enterprise-wide alignment and visibility</p></li><li><p>Own and maintain a Boundary Systems portfolio dashboard</p></li><li><p>Drive cross-functional alignment across Finance, Procurement, Supply Chain, and other business domains prior to implementation decisions</p></li></ul><p>Discovery, Impact Assessment & Readiness</p><ul><li><p>Lead enterprise-wide boundary system inventory and impact assessments across processes, data flows, integrations, and compliance requirements</p></li><li><p>Identify and proactively mitigate capability gaps, risks, and readiness blockers</p></li><li><p>Provide clear recommendations and escalation paths to program leadership</p></li></ul><p>Design Readiness & Solution Assurance</p><ul><li><p>Partner with Business Process Owners, Product Leads, and System Integrators in a “3-in-a-box” model</p></li><li><p>Review and validate functional and technical designs impacting boundary systems</p></li><li><p>Define and enforce readiness and acceptance criteria across design, testing, reconciliation, and cutover phases</p></li></ul><p>Integration Readiness (Non-Build Ownership)</p><ul><li><p>Drive cross-system dependency management and integration readiness across APIs, middleware, and file-based patterns</p></li><li><p>Ensure clear role separation: accountable for business readiness while technical integration ownership resides elsewhere</p></li><li><p>Incorporate boundary considerations into testing, defect prioritization, and cutover planning</p></li></ul><p>Testing, Cutover & Stabilization</p><ul><li><p>Supervise boundary readiness for SIT/UAT, validation, and reconciliation activities</p></li><li><p>Ensure successful cutover execution, including sequencing, runbooks, and rollback planning</p></li><li><p>Lead boundary-specific hypercare activities and ensure operational stabilization post launch</p></li></ul><p>Vendor & Delivery Management</p><ul><li><p>Support vendor engagement, SOW development, resource planning, and delivery tracking</p></li><li><p>Partner with internal functions (Security, Quality, Data, Architecture) to ensure consistent standards and compliance</p></li><li><p>Supervise performance of system integrators and external partners</p></li></ul><br><p><strong>To Be Considered for This Role, You Must Have:</strong></p><ul><li><p>Bachelor’s degree in Computer Science, Information Systems, Engineering, or related field (or equivalent work experience)</p></li><li><p>12+ years of validated experience with enterprise ERP and integrated business applications</p></li><li><p>Proven leadership in large-scale transformation programs (Oracle Fusion Cloud preferred)</p></li><li><p>Strong understanding of Finance and Supply Chain processes and supporting application ecosystems</p></li><li><p>Working knowledge of integration technologies (APIs, middleware, file-based interfaces)</p></li><li><p>Experience operating in regulated environments (e.g., SOX, GxP, 21 CFR Part 11) preferred</p></li><li><p>Experience building governance models, capability frameworks, and portfolio roadmaps</p></li><li><p>Consistent track record of leading cross-functional initiatives and influence executive stakeholders</p></li><li><p>Experience managing vendors and system integrators</p></li><li><p>Familiarity with enterprise boundary platforms (e.g., CLM, treasury, MES, APS, LIMS, T&E)</p></li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Clinical Trial Services, India]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47672]]></requisitionid>
    <referencenumber><![CDATA[R47672]]></referencenumber>
    <apijobid><![CDATA[r47672]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47672/director-global-clinical-trial-services-india/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Global Clinical Trial Services, India to join our Global Clinical Trial Services team, supporting our India operations. In this role, you will provide operational leadership for clinical trial delivery in India as part of the senior leadership team, ensuring high-quality and compliant execution while collaborating with global functional leaders, site management, and vendor partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Hyderabad, India.</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Lead clinical trial services in India, from feasibility through to site close.</p></li><li><p>Manage and develop India-based staff and Functional Service Provider (FSP) teams.</p></li><li><p>Partner with global functional leaders to align India operations with worldwide standards.</p></li><li><p>Build relationships with local sites, investigators, and regulatory authorities.</p></li><li><p>Champion clinical trial infrastructure development in India alongside site management.</p></li><li><p>Oversee FSP resource planning, contracts, and vendor performance.</p></li><li><p>You connect regional and global teams through clear, cross-cultural communication.</p></li><li><p>You drive process improvements and standard methodologies while upholding compliance.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Deep understanding of the Indian clinical research landscape and regulatory environment.</p></li><li><p>Knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and Indian regulations.</p></li><li><p>Proven leadership in a matrix organisation with dotted-line reporting.</p></li><li><p>Strong experience in resource planning, vendor management, and operational budgeting.</p></li><li><p>Familiarity with site management, site start-up, trial optimisation, and central monitoring.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - CHICAGO South, IL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48051]]></requisitionid>
    <referencenumber><![CDATA[R48051]]></referencenumber>
    <apijobid><![CDATA[r48051]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48051/medical-account-specialist-ii-neurology-chicago-south-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Chicago South (Metro), Illinois </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II Neurology - DETROIT South, MI]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48048]]></requisitionid>
    <referencenumber><![CDATA[R48048]]></referencenumber>
    <apijobid><![CDATA[r48048]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48048/medical-account-specialist-ii-neurology-detroit-south-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Detroit]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Detroit South (Metro), Michigan </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - DALLAS, TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48059]]></requisitionid>
    <referencenumber><![CDATA[R48059]]></referencenumber>
    <apijobid><![CDATA[r48059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48059/medical-account-specialist-ii-neurology-dallas-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dallas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Dallas (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - HOUSTON (SOUTH), TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48061]]></requisitionid>
    <referencenumber><![CDATA[R48061]]></referencenumber>
    <apijobid><![CDATA[r48061]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48061/medical-account-specialist-ii-neurology-houston-south-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Houston]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><p><strong>When & where: </strong> </p><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Houston South (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II -  NEUROLOGY -SAN DIEGO, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48081]]></requisitionid>
    <referencenumber><![CDATA[R48081]]></referencenumber>
    <apijobid><![CDATA[r48081]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48081/medical-account-specialist-ii-neurology-san-diego-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[San Diego]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: San Diego (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PITTSBURGH, PA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48005]]></requisitionid>
    <referencenumber><![CDATA[R48005]]></referencenumber>
    <apijobid><![CDATA[r48005]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48005/medical-account-specialist-ii-neurology-pittsburgh-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Pittsburgh]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Pittsburg (Metro), PA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Health Economics & Outcomes Research (Immunology)]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47988]]></requisitionid>
    <referencenumber><![CDATA[R47988]]></referencenumber>
    <apijobid><![CDATA[r47988]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47988/senior-manager-health-economics-outcomes-research-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a Senior Manager will support the execution of our global and regional HEOR strategies and programs, aiming to inform, support and strengthen commercialization activities, including clinical development, marketing, and market access.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>This is located in Sleepy Hollow, NY and is on-site 4 days/week. <br>Discover your role:<br>• Partner with cross functional and business partners to develop and support compelling product value propositions with aim to optimize access, reimbursement and uptake.<br>• Identify HEOR evidence requirements and gaps, and design, conduct, and deliver studies and tools to support relative value demonstration and product differentiation. These will include: prospective and retrospective observational studies, real world data analyses, registry studies, PRO studies, cost effectiveness and budget impact analyses, modeling studies.<br>• Conduct population and disease state analyses and epidemiology studies to inform clinical development and life-cycle management.<br>• Oversee and guide the development and implementation of Patient Reported Outcomes (PRO) strategies ensuring PRO end points in product labeling and support product differentiation. <br>• Develop and validate PRO endpoints for integration in pivotal studies. <br>• Responsible for including patient-reported outcomes studies into NDA/MAA dossiers and labels, and interacting with Agencies.<br>• Report, publish and disseminate HEOR data and study results in compliance with company, industry and regulatory requirements.<br>• Deliver HEOR presentations to customers to support reimbursement decisions across the portfolio.<br>• Collaborate with Alliance partners on HEOR plans, studies and deliverables; build and maintain constructive and productive relationships . </p><p><strong>This role requires</strong>:<br>• Advanced graduate degree (PhD, MS, or PharmD) in HEOR-related field (e.g. health economics, epidemiology, healthcare/data analytics, health services research, public health) with at least 2 year post-graduate experience.<br>• For PharmD, a 3+ years fellowship training, pharma or consulting experience in health economics and outcomes research is required; For MS, at least 3 years experience is required.<br>• Strong technical expertise required in design and conduct of HEOR studies and models;<br>• Excellent written and verbal communication skills required.<br>• Ability to interact with and present to Senior Management.<br>• Experience in immunology therapeutic areas a plus.<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior ManagerThird Party Risk Management]]></title>
    <date><![CDATA[Thu, 21 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47552]]></requisitionid>
    <referencenumber><![CDATA[R47552]]></referencenumber>
    <apijobid><![CDATA[r47552]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47552/senior-managerthird-party-risk-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. As we continue to scale globally, strong governance, risk management, and compliance frameworks are critical to supporting sustainable growth and operational excellence.</p><p>As a Senior Manager – Third Party Risk Management (TPRM), you will play a key role in establishing and strengthening enterprise-wide third-party risk programs. You will lead risk assessment activities, drive governance frameworks, and partner with cross-functional teams to ensure third-party relationships align with regulatory, operational, and ethical standards</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li><p>Lead and manage third-party risk management activities across the supplier lifecycle, including onboarding, due diligence, monitoring, and offboarding</p></li><li><p>Perform risk assessments and due diligence on vendors to identify, evaluate, and mitigate potential risks</p></li><li><p>Collaborate with cross-functional teams including Legal, Compliance, Information Security, Quality, and Procurement to embed TPRM into business processes</p></li><li><p>Establish and support governance frameworks to ensure consistent risk management practices across the organization</p></li><li><p>Monitor supplier performance and risk using defined KPIs/KRIs and provide insights to leadership</p></li><li><p>Support implementation and management of TPRM tools and systems for risk tracking and reporting</p></li><li><p>Ensure compliance with internal policies, regulatory requirements, and audit expectations related to third-party engagements</p></li><li><p>Partner with internal and external auditors and support audit activities related to third-party risk</p></li><li><p>Track and manage remediation actions to ensure timely risk mitigation and closure</p></li><li><p>Prepare and present risk reports, dashboards, and insights to senior leadership</p></li><li><p>Drive continuous improvement of TPRM processes, frameworks, and governance models</p></li><li><p>Lead and mentor team members, providing guidance and support to build capability and consistency.</p></li></ul><p><strong>This Job May Be for You If You Have:</strong></p><ul><li><p>Strong experience in third-party risk management, vendor risk, or enterprise risk management programs</p></li><li><p>Solid understanding of risk assessment methodologies, internal controls, and compliance frameworks</p></li><li><p>Experience working in a global or regulated environment (pharma/biotech preferred)</p></li><li><p>Ability to assess risk, interpret data, and provide practical and actionable recommendations</p></li><li><p>Strong analytical, problem-solving, and decision-making skills</p></li><li><p>Effective stakeholder management and ability to influence across functions</p></li><li><p>Experience working with cross-functional and global teams</p></li><li><p>Ability to operate in a fast-paced environment and manage competing priorities</p></li><li><p>Experience driving process improvements and transformation initiatives.</p></li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li><p>8–12+ years of experience in <strong>Third Party Risk Management</strong>, Risk, Compliance, or related areas</p></li><li><p>Bachelor’s degree in a relevant field; advanced degree preferred</p></li><li><p>Experience working in global environments and managing third-party risk programs</p></li><li><p>Experience in pharma/biotech or regulated industries is an advantage</p></li><li><p>Familiarity with <strong>TPRM tools or risk management</strong> platforms preferred</p></li><li><p>Proven experience in <strong>stakeholder management</strong> and influencing decision-making</p></li><li><p>Prior experience in team leadership or mentoring roles is preferred</p></li><li><p>Proficiency in Microsoft Office tools (Excel, PowerPoint, Word)</p></li><li><p>Fluency in English and ability to work in a global environment</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 22 May 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences - Rare Disease]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48141]]></requisitionid>
    <referencenumber><![CDATA[R48141]]></referencenumber>
    <apijobid><![CDATA[r48141]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48141/executive-director-global-patient-safety-sciences-rare-disease/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Executive Director, Global Patient Safety Sciences, Rare Disease is the first point of contact for all Rare Disease strategy-related responsibilities across clinical, and post-marketed drugs in the portfolio. As the product subject matter expert (SME) and Therapeutic Area Head (TAH) for the Rare Disease portfolio, this role defines the product safety strategy, establishes the medical safety opinion, and provides the safety scientific POV across both GPS and non-GPS interactions. In addition, the position acts as a trusted advisor to senior management regarding safety strategies/processes while developing organizational objectives and, importantly, understanding the impact of decisions across functional areas. The ED Global Patient Safety Sciences Rare Disease is responsible for the development of their team, which is comprised of GPS Leads. They will serve as a member of the GPS Leadership Team (GPS LT). </p><p><strong>When & where:</strong> ​​</p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>Hybrid: 4 days per week on-site</p></li><li><p>25% travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Contribute senior-level safety expertise to clinical projects across assigned therapeutic area </p></li><li><p>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds and serves as point of escalation for ICSR causality assessments </p></li><li><p>Provide oversight for safety signal evaluations & deliver clinical interpretation of emerging safety issues </p></li><li><p>Review benefit-risk assessments (e.g., HHAs) written by Safety Sciences Delivery and recommendations for the product safety profile as appropriate for the stage of the asset lifecycle for safety responses to regulatory agency queries and safety documents (e.g., DSURs, PSURs) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Governance Leadership </em></p><ul><li><p>Influence cross-functional leaders to align priorities and drive enterprise results </p></li><li><p>Approve and provide medical oversight for Risk Management Plans (RMPs) </p></li><li><p>Approve responses to medical & clinical health authority queries as needed </p></li><li><p>Oversee cross-functional Safety Monitoring Team (SMT) activities </p></li><li><p>Represent GPS at cross-functional governance meetings including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT), and with other parties external to Regeneron (e.g., collaborators) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty preferred; MBA is an advantage</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required</p></li><li><p>6+ years of leading a team and people management experience, added benefit if in a matrixed environment </p></li><li><p>Preferred 1-3 years of international pharmaceutical activities </p></li><li><p>Proven track record in developing a deep understanding of the products’ safety profile, supported by in-depth product knowledge to inform safety assessments, risk evaluations, and decision-making </p></li><li><p>Experience with oversight of strategy within a global patient safety organization </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li><li><p>Preferred experience with AI technologies </p></li></ul><p>#GDPSJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - INDIANAPOLIS, IN]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48052]]></requisitionid>
    <referencenumber><![CDATA[R48052]]></referencenumber>
    <apijobid><![CDATA[r48052]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48052/medical-account-specialist-ii-neurology-indianapolis-in/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Indianapolis]]></city>
    <state><![CDATA[Indiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Indianapolis (Metro), Indiana </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PHOENIX N, AZ]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48071]]></requisitionid>
    <referencenumber><![CDATA[R48071]]></referencenumber>
    <apijobid><![CDATA[r48071]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48071/medical-account-specialist-ii-neurology-phoenix-n-az/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Phoenix]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Pheonix (North Metro), AZ</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - SALT LAKE CITY, UT]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48073]]></requisitionid>
    <referencenumber><![CDATA[R48073]]></referencenumber>
    <apijobid><![CDATA[r48073]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48073/medical-account-specialist-ii-neurology-salt-lake-city-ut/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Salt Lake City]]></city>
    <state><![CDATA[Utah]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Salt Lake City (Metro), UT</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director Applied AI]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48511]]></requisitionid>
    <referencenumber><![CDATA[R48511]]></referencenumber>
    <apijobid><![CDATA[r48511]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48511/executive-director-applied-ai/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron’s Enterprise Data & AI organization is newly established and moving fast — built to drive AI transformation and adoption at scale across every part of the enterprise. This is a high-visibility, high-velocity position where the work is directly tied to business and scientific impact.</p><p>As a key member of our AI Technology, Innovation & Delivery team, this role leads Regeneron’s enterprise applied AI strategy and innovation agenda, accountable for translating frontier AI capabilities into production-grade solutions that advance the company’s scientific and business priorities. The Executive Director, Applied AI sets direction across four interconnected domains — Agentic AI Strategy and Platform Evaluation, Enterprise AI Product Management, Emerging Technology and Industry Intelligence, and Forward Deployment Engineering — and is responsible for moving from opportunity to architecture to deployed solutions. The role works in close partnership with the Data & AI Engineering leader in Regeneron’s Global Capability Center (GCC) in India, where build and operate resides. Together, they ensure that what is designed is architected for platform-scale delivery and built to last.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>Hybrid; 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Sets enterprise direction for agentic AI, evaluating and selecting platforms, frameworks, and architecture patterns. Strategy and platform selection reside in this role; build and operate sit within the GCC.</p></li><li><p>Leads a team of product managers and product owners accountable for Regeneron’s portfolio of enterprise AI capabilities. Each capability has a defined owner, a roadmap, and adoption metrics — ensuring AI solutions are treated as products, not projects: with clear business sponsors, measurable outcomes, and a path to sustained value.</p></li><li><p>Tracks the AI frontier across models, platforms, agentic frameworks, and methods — and translates that intelligence into concrete recommendations tied to Regeneron’s business and scientific priorities.</p></li><li><p>Maintains a clear view of how AI is advancing across biopharma and life sciences and identifies where emerging capabilities can solve real problems or unlock new opportunities. Runs structured pilots with clear adoption criteria.</p></li><li><p>Leads a team that embeds directly with business and scientific stakeholders to activate AI solutions at speed. Operates in two modes: rapid deployment of configured GenAI and low-code/no-code solutions and structured prototype-to-handoff engagements for higher-complexity problems requiring GCC production engineering.</p></li><li><p>Set the technical and architectural direction for applied AI at Regeneron. Translate business problems into solution blueprints, architecture patterns, and integration pathways. Own design decisions from concept through prototype with the rigor required for production.</p></li><li><p>Lead the agentic AI strategy — defining where Regeneron builds, buys, or partners; and ensuring strategic alignment with GCC for build-and-operate execution.</p></li><li><p>Lead the Enterprise AI Product Management function — ensuring every enterprise AI capability has a defined roadmap, a business sponsor, and measurable adoption outcomes.</p></li><li><p>Lead the Forward Deployment Engineering function — maintaining a clear operational distinction between rapid-deployment mode and build-to-scale mode.</p></li><li><p>Connect emerging technology intelligence to specific business problems and scientific opportunities across all departments. Run disciplined pilots with clear adoption criteria.</p></li><li><p>Partner with GCC engineering leadership to ensure solutions are buildable, scalable, and maintainable at platform level. Define and govern handoff standards between applied AI prototypes and GCC production engineering.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree (Master's or advanced degree preferred) with 17+ years leading applied AI/ML organizations through the full lifecycle — opportunity identification, architecture, prototype, and production handoff.</p></li><li><p>Demonstrated experience building and leading AI product management organizations — establishing product ownership, roadmaps, and adoption accountability for enterprise AI capabilities.</p></li><li><p>Strong product mindset paired with hands-on solution architecture depth; able to operate as both strategist and technical leader — not a pure people-manager.</p></li><li><p>Deep appreciation for the life sciences context — an understanding of how AI is reshaping drug discovery, clinical development, regulatory, and commercial functions in biopharma, and a genuine appetite to engage with Regeneron’s science. Candidates without this orientation will struggle to earn credibility with Regeneron’s scientific and operational leadership.</p></li><li><p>Deep familiarity with the current AI landscape: generative AI, agentic systems, LLM application architecture, retrieval and reasoning patterns, and modern AI/ML platforms.</p></li><li><p>Hands-on familiarity with low-code/no-code AI deployment and configured GenAI platforms; able to recognize when a business problem calls for rapid configuration versus custom engineering and build a team that executes both modes with equal discipline.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - WASHINGTON, DC]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48016]]></requisitionid>
    <referencenumber><![CDATA[R48016]]></referencenumber>
    <apijobid><![CDATA[r48016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48016/medical-account-specialist-ii-neurology-washington-dc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Washington]]></city>
    <state><![CDATA[District of Columbia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Washington, DC (Metro)</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp EHS specialist]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48472]]></requisitionid>
    <referencenumber><![CDATA[R48472]]></referencenumber>
    <apijobid><![CDATA[r48472]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48472/temp-ehs-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Temporary Environmental, Health and Safety Specialist to join our <strong>Environmental, Health and Safety </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Developing, implementing and monitoring environmental, health & safety programs to ensure compliance with all applicable government regulations and company standards and values</li><li>Establishing, maintaining and auditing the Environmental and Health & Safety Management System</li><li>Determining and addressing site EHS issues and employee concerns</li><li>Performing incident management activities including injury management investigations and associated recordkeeping</li><li>Identifying, implementing and tracking corrective actions to prevent recurrence</li><li>Performing Environmental, Health and Safety risk assessments and makes recommendations to control hazards</li><li>Creating, implementing and maintaining Environmental, Health and Safety training program for health, safety and the environment</li><li>Responsible for developing appropriate emergency plans and response capabilities</li><li>Staying abreast of new Environmental, Health and Safety government regulations as they are promulgated as well as new developments in industry (best practices)</li><li>Building relationships with key departments to foster support for Environmental, Health and Safety programs</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>A thorough knowledge of Environmental, Health and Safety legislation for a pharmaceutical facility operating within Ireland/Europe</li><li>Knowledge of behavioural based safety programs</li><li>Operational Safety Experience: Safe Systems of Work - Environmental, Health and Safety permitting, Fatality Prevention Programme - EHS Control of Hazardous Energy – Lock Out Tag Out</li><li>The ability to lead and direct others and work as part of a team</li><li>Logical problem solving skills</li><li>Excellent interpersonal and communication skills coupled with good ability to produce technical reports</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>For this opportunity you should have a BS/ BA in Health and Safety or related field with 5+ years of experience working in an Environmental, Health and Safety role within the pharmaceutical industry or similar industry.</li></ul><h3>Thrive today. Grow tomorrow.</h3><p>#IRELIM #JOBSIEST #LI-Onsite #REGNIEEHS</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 05:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Patient Advocacy (m/f/d)]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48568]]></requisitionid>
    <referencenumber><![CDATA[R48568]]></referencenumber>
    <apijobid><![CDATA[r48568]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48568/associate-director-global-patient-advocacy-mfd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Global Patient Advocacy, Hematology-Oncology to cover International and US markets. In this role, you will lead the development and execution of patient advocacy strategies, building meaningful relationships with advocacy groups and professional societies to support patient needs and business objectives, while collaborating with cross-functional leaders (Medical Affairs, Market Access, Marketing, and Policy teams). This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><p>UK, Germany, Italy or Spain (Hybrid model)</p><p>Travel: 40%+</p><h3>Discover your role:</h3><ul><li><p>Lead advocacy and engagement strategy for Hematology-Oncology in Europe</p></li><li><p>Partner with senior cross-functional leaders to build advocacy strategies</p></li><li><p>Build and manage relationships with patient advocacy groups and professional societies</p></li><li><p>Oversee patient engagement initiatives, meetings, and communications</p></li><li><p>Develop frameworks to embed the patient perspective across organizational processes</p></li><li><p>Track and report outcomes of advocacy initiatives to senior leadership</p></li><li><p>You foster collaboration and consensus among diverse stakeholders</p></li><li><p>You drive a patient-centric culture and influence strategic decisions</p></li></ul><h3>This role requires:</h3><ul><li><p>Undergraduate degree required</p></li><li><p>10+ years of industry or relevant professional experience</p></li><li><p>5+ years of patient advocacy, stakeholder engagement, and issues management</p></li><li><p>European, international, or global advocacy experience and understanding of relevant regulations (e.g., EMA, HTA)</p></li><li><p>Proven leadership in developing and executing advocacy strategies</p></li><li><p>Country-level advocacy work experience preferred</p></li><li><p>Multilingual capabilities strongly preferred</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€106,875.00 - €178,125.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 03:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Control Data Reviewer]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48360]]></requisitionid>
    <referencenumber><![CDATA[R48360]]></referencenumber>
    <apijobid><![CDATA[r48360]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48360/quality-control-data-reviewer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is looking for a QC Data Reviewer to perform data review to support release, stability programs, and lab operation within Quality Control. This role continuously strives to follow all pertinent regulatory agency guidelines to drive performance. This position is a <strong>Tuesday – Saturday 8am-4:30pm schedule.</strong><br><br>As the QC Data Reviewer, a typical day might include the following:<br>• Executing detailed data review for analytical test results generated by QC for compliance with cGMP, internal SOPs and Specifications<br>• Supporting production, stability studies, and lab operations<br>• Reviewing release and stability data, trend charts of reference standards, lab equipment calibration records and logbooks<br>• Performing detailed data review for analytical test results created by contract testing labs to assure correctness and accuracy<br>• Maintaining and updating relevant SOPs for data review and reporting<br>• Collaborating with Stability and other groups to support stability report writing and regulatory updates<br>• Participating in all vital training activities<br><br>This role might be for you if:</p><ul><li>You have a solid understanding of data reviewing and regulatory agency guidelines</li><li>You are results-oriented and can optimally analyze data trends</li><li>You can work efficiently as an individual as well as with others</li><li>You are a strong communicator who is willing to build beneficial relationships with other peer groups</li></ul><p>To be considered for this role, you must have a BS/BA in Chemistry, Biology, or related field. You must be willing and able to work Tuesday – Saturday 8am-4:30pm. Level will be determined by demonstrated experience. </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Assistant (Temporary)]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48432]]></requisitionid>
    <referencenumber><![CDATA[R48432]]></referencenumber>
    <apijobid><![CDATA[r48432]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48432/executive-assistant-temporary/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we pair science with technology to accelerate the discovery and delivery of life‑changing medicines. We are searching for an Executive Assistant to support Digital Technology and AI executives who oversee and interact with multiple functional teams within our business, including Research, Global Development, Commercial, and G&A. This role requires advanced understanding of the Digital Technology and AI team and its business clients, including key relationships.</p><p>We're looking for someone who brings strategic thinking, technological fluency, and genuine curiosity to the work of a fast-moving, high-impact legal team. The Executive Assistant will exercise considerable judgment and initiative, with the ability to influence stakeholders and understand key relationships.</p><p><strong>Build our future together:</strong></p><ul><li>Managing complex calendars, expenses, and time commitments for executives.</li><li>Anticipating the needs of leaders and teams before they arise, resolving scheduling conflicts with minimal direction.</li><li>Triaging incoming requests and inquiries, raising time-sensitive or significant matters with good judgment and discretion.</li><li>Identifying, developing, and implementing process improvements, bringing new tools or approaches to the team proactively, while maintaining highly organized and efficient administrative workflows and independently delivering solutions.</li><li>Using AI tools (such as Microsoft CoPilot) to draft communications, summarize information, and streamline administrative workflows.</li><li>Planning and managing internal and external meetings end‑to‑end, including team meetings, large offsites, live trainings, and cross-functional gatherings, with attention to gathering agendas, logistics, coordination with attendees, catering decisions, materials and follow up.</li><li>Building polished PowerPoint presentations by synthesizing inputs from multiple contributors into organized, executive-ready decks.</li><li>Submitting requisitions, tracking of deadlines, monitoring purchase orders and renewals.</li><li>Collaborating cross‑functionally and serving as a trusted partner to peers.</li><li>Communicating effectively across all levels while maintaining confidentiality.</li><li>Demonstrating organizational knowledge and understanding leader priorities, including support for increasingly complex responsibilities.</li><li>Handling travel arrangements and expense reports for executives including managing complex international travel (typically VP+), visas and expense reporting.</li><li>Maintaining departmental SharePoint, Teams and Intranet sites, keeping them current, organized and useful as working resources.</li></ul><p><strong>When and Where:</strong></p><ul><li>Location will be Tarrytown, NY. We are four days per week on site with 1 day of work from home flexibility.</li><li>This is a contract position, with an initial contract expectation of 3 months and potential for extension and/on conversion to full time.</li></ul><p><strong>Discover your role:</strong></p><ul><li>Are highly collaborative and adept at coordinating across teams to develop and implement solutions and operate under minimal guidance.</li><li>Exhibit discretion, independence, and sound judgment.</li><li>Adapt well to change, ambiguity, and shifting priorities, and can embrace AI and modern productivity tools as a part of how you work.</li><li>Work comfortably with senior leaders and understand how they think and what they expect.</li><li>Possess advanced knowledge or ability to readily learn company and Digital Technology and AI team policies, practices, and resources and act as a point person for supported leaders and departments.</li><li>Proactively highlight opportunities for continuous improvement to current processes.</li><li>Communicate exceptionally well, whether orally or in writing</li></ul><p><strong>This role requires:</strong></p><ul><li>Eight (8) or more years of administrative experience required, with at least four (4) years supporting senior leaders in a business or legal environment.</li><li>Associate or bachelor’s degree preferred.</li><li>Advanced proficiency in Microsoft 365 (Outlook, PowerPoint, Excel, Word, Teams), SharePoint, Concur, and collaboration platforms; ability to troubleshoot and train others.</li><li>Proven track record managing complex calendars, orchestrating senior‑level meetings and events, and coordinating domestic/international travel with precision.</li><li>Exceptional organization, prioritization, and follow‑through.</li><li>Flexibility to support after‑hours needs tied to executive travel, global time zones, and critical events.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48748]]></requisitionid>
    <referencenumber><![CDATA[R48748]]></referencenumber>
    <apijobid><![CDATA[r48748]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48748/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials, including Phase IV/Real World Evidence studies, from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions</p></li><li><p>Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution</p></li><li><p>Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials</p></li><li><p>Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work</p></li><li><p>Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies</p></li><li><p>Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics</p></li><li><p>Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and have at least six years of relevant industry experience</p></li><li><p>Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience</p></li><li><p>Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC</p></li><li><p>Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li><li><p>Experience with Phase IV /RWE preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs- Hematology (Houston/Dallas)]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48605]]></requisitionid>
    <referencenumber><![CDATA[R48605]]></referencenumber>
    <apijobid><![CDATA[r48605]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48605/associate-director-field-medical-affairs-hematology-houstondallas/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>BUILD OUR FUTURE TOGETHER:</strong><br>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><br>W<strong>HEN & WHERE:</strong><br>Territory: Texas with a focus on Houston and Dallas, New Mexico, Louisiana. Residency in the territory is required with a preference for Houston or Dallas</p><p><br><strong>DISCOVER YOUR ROLE:</strong><br>- Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.</p><p>- Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies</p><p>- Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.</p><p>- Participates in the development and management of company sponsored clinical trials including.</p><p>- Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.</p><p>- Identifying relevant insights on research developments, treatment landscape to shape medical strategy</p><p>- Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.</p><p>- Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.</p><p>- Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.</p><p>- Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally</p><p><br><strong>THIS ROLE REQUIRES</strong>:<br>To be considered a terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required. 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. </p><p><br><strong>ADDITIONAL REQUIREMENTS: </strong><br>- Residency in the assigned territory</p><p>- Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><p>- Possesses and maintains a valid driver’s license and clean driving record.</p><p><br><strong>PREFERRED EXPERIENCES INCLUDE:</strong> <br>- Established relationships with KOLs and institutions focused on Hematologic Malignancies</p><p>- Drug launch experience.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 22 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist – Protein Expression Sciences (Antibody Discovery)]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48393]]></requisitionid>
    <referencenumber><![CDATA[R48393]]></referencenumber>
    <apijobid><![CDATA[r48393]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48393/senior-scientist-protein-expression-sciences-antibody-discovery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated <strong>Senior Scientist</strong> to join our Antibody Discovery team within the Protein Expression Sciences department. This role is at the forefront of early therapeutic discovery, where you will drive ongoing programs and analyze complex datasets to enable the selection of next-generation therapeutic antibodies.</p><p>The ideal candidate will thrive in a collaborative, cross-functional environment and will coordinate screening campaigns, interpret high-throughput data across multiple concurrent projects, and clearly communicate key findings to internal stakeholders. Strong analytical skills, attention to detail, and the ability to translate data into actionable insights are essential for success in this role.</p><p><strong>As a Senior Scientist, a typical day may include:</strong></p><ul><li>Managing multiple projects simultaneously within a cross-functional team environment</li><li>Establishing and communicating timelines across research teams, both within and outside the department</li><li>Analyzing primary screening data using a variety of software tools and selecting antibodies with desired functional properties</li><li>Ensuring accurate and complete capture of experimental data in internal databases and repositories</li><li>Presenting results from antibody discovery campaigns to team members, cross-functional partners, and senior leadership</li><li>Staying current with scientific advances in the field and contributing to team strategy</li><li>Mining and summarizing data to support process improvements and enhance discovery pipelines</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Enjoy working in a high-throughput environment focused on discovering innovative therapies for serious medical conditions</li><li>Bring a collaborative, agile mindset and leverage technology creatively to accelerate drug discovery</li><li>Have experience using modern data analysis and visualization tools (e.g., advanced Excel, GraphPad Prism, Spotfire, Power BI, or similar platforms) to explore datasets, generate insights, and communicate results</li><li>Have familiarity with basic scripting or automation tools (e.g., Python, R, or workflow tools), which is a plus but not required</li><li>Demonstrate strong project management, analytical, and organizational skills</li><li>Have experience with laboratory automation and data management systems (e.g., LIMS), which is a plus</li><li>Possess a strong publication record in peer-reviewed journals (preferred)</li></ul><p><strong>Requirements:</strong></p><ul><li>Ph.D. in Molecular Biology, Cellular Biology, Biochemistry, Immunology, or a related field with 2–4 years of relevant experience.</li></ul><p><strong>Additional qualifications:</strong></p><ul><li>Working knowledge of immunology, including antibody generation, structure, and characterization (strongly preferred)</li><li>Proven experience analyzing large datasets and synthesizing results into clear conclusions</li><li>Experience with multi-well assays used in drug screening and high-throughput data analysis (preferred)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Payroll Service Delivery Analyst]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47445]]></requisitionid>
    <referencenumber><![CDATA[R47445]]></referencenumber>
    <apijobid><![CDATA[r47445]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47445/payroll-service-delivery-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Payroll Service Delivery Analyst to join our Global Capability Center, supporting our global payroll operations in a hybrid work model. In this role, you will support accurate and timely payroll processing across multiple countries while collaborating with Global Payroll, Human Resources, Finance teams, and external vendors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Prepare and process payroll for assigned international countries by collecting, validating, and entering employee data with oversight</p></li><li><p>Perform audit checks, reconciliations, and data reviews to ensure payroll accuracy and compliance across regions</p></li><li><p>Maintain payroll calendars, checklists, and documentation to support timely and standardized operations</p></li><li><p>Partner with Global Payroll, Human Resources, and Finance teams to ensure employee data integrity and timely submission of payroll inputs</p></li><li><p>Coordinate with external payroll vendors to submit data, track deliverables, and resolve basic inquiries</p></li><li><p>Develop statutory updates and support the implementation of required payroll changes while maintaining adherence to internal controls</p></li><li><p>Support payroll reporting by generating standard reports and assisting with month-end activities, while contributing to process improvements and system updates</p></li><li><p>You demonstrate strong attention to detail, confidentiality, and a collaborative, service-oriented perspective in a fast-paced environment.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in Business, Human Resources, Accounting, Finance, or related field (or equivalent experience)</p></li><li><p>Proficiency in Microsoft Excel and ability to learn new systems</p></li><li><p>Strong attention to detail and ability to work accurately with numbers and data</p></li><li><p>Ability to operate in a fast-paced, deadline-driven environment</p></li><li><p>Strong communication, organizational, and teamwork skills</p></li><li><p>Understanding of payroll operations, data validation, and compliance requirements</p></li><li><p>Customer service orientation and ability to handle inquiries effectively</p></li><li><p>Interest in global operations, payroll, or human resources shared services</p></li><li><p>Experience in payroll, HR operations, accounting, or shared services (2+ years preferred)</p></li><li><p>Exposure to Human Resource Information Systems (HRIS) or payroll systems such as Workday, SAP, or ADP is a plus</p></li><li><p>Multilingual skills or experience working across cultures is an advantage</p></li><li><p>Ability to maintain confidentiality, demonstrate learning agility, and apply problem-solving in day-to-day operations.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Pathologist]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47855]]></requisitionid>
    <referencenumber><![CDATA[R47855]]></referencenumber>
    <apijobid><![CDATA[r47855]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47855/associate-director-clinical-pathologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>Associate Director of Pathology has primary responsibility to support drug molecule efficacy and safety studies in a variety of therapeutic focus areas (TFAs). The successful candidate will also provide Clinical Pathology support for GLP toxicology and PK studies of Regeneron molecules. The Associate Director will be expected to manage Clinical Pathology support to selected TFAs, and mentor junior Pathologists. </p></div><div></div><div><p><strong>A Typical day in this role may look like:</strong> </p></div><div><ul><li><p>Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas. </p></li></ul></div><div><ul><li><p>Work both independently and as a part of integrated discovery and development teams to interpret pharmacologic and toxicity related findings and help advance promising therapeutics through Regeneron’s pipeline. </p></li></ul></div><div><ul><li><p>Determining and evaluating clinical pathology-related endpoints in pharmacology and toxicology studies and guiding decision making. </p></li></ul></div><div><ul><li><p>Collaborate closely with anatomic pathologists, toxicologists, and researchers within Regeneron. </p></li></ul></div><div><ul><li><p>Partner with our CRO partners in providing scientific peer review of nonclinical safety studies. </p></li></ul></div><div></div><div><p><strong>This job might be for you if you have:</strong> </p></div><div><ul><li><p>Experience with integrating clinical and anatomic pathology data </p></li></ul></div><div><ul><li><p>Experience with animal models of human diseases </p></li></ul></div><div><ul><li><p>Clear, concise oral and written communication skills </p></li></ul></div><div><ul><li><p>Demonstrated ability to contribute to cross functional teams </p></li></ul></div><div><ul><li><p>Ability to contribute to scientific strategy, problem solving, and the broader understanding of pathology-related issues that influence drug development outcomes. </p></li></ul></div><div></div><div><p><strong>In order to be considered for this role, you must have</strong>: </p></div><div><ul><li>DVM (or equivalent) with ACVP certification in Clinical Pathology required, (strong preference for PhD in Pathology, Immunology, or related ) </li></ul></div><div><ul><li>Minimum 3 years of industry experience interpreting GLP and non GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/ biotech or CRO setting. </li><li>Additional certification in Anatomic Pathology nice to have</li></ul></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 14:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47957]]></requisitionid>
    <referencenumber><![CDATA[R47957]]></referencenumber>
    <apijobid><![CDATA[r47957]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47957/associate-director-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>Job Description</p></div><div><div><div><div><div><div><div><div><div><p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p></div></div></div></div></div></div></div></div></div><p>As an Associate Director, External Data Acquisition and Delivery (EDAD), you will provide strategic oversight and operational leadership for External Data Acquisition and Delivery activities across Regeneron’s clinical trial portfolio and initiatives. You will ensure readiness of external data collection platforms, data conformance tools, reconciliation processes, and the delivery of high-quality, compliant external data from third-party vendors including laboratory, biomarker, Digital Health Technologies, imaging, ECG, PK, genomics, and specialty data. You will partner closely with Clinical Data Management, CROs, external vendors, and cross-functional partners to drive external data strategy, operational excellence, vendor oversight, digital transformation initiatives, and process improvements.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Leading External Data Acquisition, integration, quality oversight, and delivery strategy across the clinical trial portfolio</p></li><li><p>Serving as a portfolio-level lead for external data quality and clinical-data operational strategy</p></li><li><p>Reviewing protocol requirements, vendor specifications, and operational data flows</p></li><li><p>Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents to ensure compliance with Regeneron standards and timelines</p></li><li><p>Providing expert mentorship on external data services including biomarker, eSource, eCOA, imaging, ECG, PK, genomics, and laboratory data</p></li><li><p>Driving external vendor oversight, onboarding, qualification, governance, and ongoing performance monitoring</p></li><li><p>Establishing and handling vendor KPIs, SLAs, and quality metrics</p></li><li><p>Governing reconciliation activities between EDC systems and vendor data platforms to ensure data integrity and consistency</p></li><li><p>Monitoring reconciliation metrics, discrepancy trends, and resolution timelines across studies</p></li><li><p>Collaborating with Database Development, Biostatistics, Study Data Managers, and external vendors to resolve complex data discrepancies</p></li><li><p>Leading process improvement initiatives, automation opportunities, and implementation of innovative external data solutions</p></li><li><p>Managing and developing a team of EDAD Managers, Specialists, and associates through coaching, mentoring, and performance management</p></li><li><p>Supporting SOP development, inspection readiness, audit activities, and regulatory compliance</p></li><li><p>Representing EDAD in leadership forums, governance committees, and technology discussions</p></li></ul><p><strong>This Role May Be For You If You Have:</strong></p><ul><li><p>Strong expertise managing multiple clinical external data types including biomarker, imaging, eCOA, ECG, PK, genomics, laboratory, and Digital Health Technology data</p></li><li><p>Advanced knowledge of external data reconciliation processes and EDC platforms such as Medidata Rave, Veeva, or Oracle Inform</p></li><li><p>Experience working with SAS, CSV, and XML data formats</p></li><li><p>Strong understanding of industry regulations including 21 CFR Part 11, ICH-GCP, and CDISC standards</p></li><li><p>Proven experience handling external vendor relationships and driving accountability for quality deliverables</p></li><li><p>Strong leadership, people management, coaching, and mentoring capabilities</p></li><li><p>Strategic thinking, creativity, problem-solving, and analytical skills</p></li><li><p>Strong project management and stakeholder management capabilities</p></li><li><p>Excellent verbal and written communication skills</p></li><li><p>Ability to work effectively in a fast-paced, matrixed, and global environment</p></li></ul><p><strong>To Be Considered For This Role, You Must Have:</strong></p><ul><li><p>Minimum 10+ years of experience in Clinical Data Acquisition/Management within biotechnology, pharmaceutical, or healthcare industries</p></li><li><p>Minimum 4+ years of people management experience</p></li><li><p>Demonstrated experience overseeing external data reconciliation activities between EDC systems and vendor platforms</p></li><li><p>Experience driving process improvements and vendor oversight in supervised environments</p></li><li><p>Bachelor’s degree in Science, Health, Mathematics, Computing, Information Systems, or a related field</p></li><li><p>Advanced degree preferred</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager - Full Stack Developer- Clinical Data Operation]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47963]]></requisitionid>
    <referencenumber><![CDATA[R47963]]></referencenumber>
    <apijobid><![CDATA[r47963]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47963/senior-manager-full-stack-developer-clinical-data-operation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>About Regeneron</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>As a Senior Manager – Clinical Data Solutions & Insights, you will be responsible for designing, building, and handling a centralized clinical reporting platform that consolidates reporting outputs across Data Management and external vendor reconciliation activities into a single governed reporting layer. This role will be responsible for the end-to-end reporting lifecycle including data ingestion, analytical dataset development, dashboard creation, automated reporting, and self-service analytics applications using modern visualization and web technologies. You will work closely with Clinical Sciences, Data Management, Pharmacometrics, Precision Medicine, Safety, and multi-functional collaborators to deliver intuitive, audit-ready reporting solutions that support data-driven decision making, regulatory compliance, and operational perfection.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong></p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Owning the design and delivery of a centralized clinical reporting platform consolidating EDC listings, exception reports, and vendor reconciliation outputs</p></li><li><p>Building and maintaining Clean Patient Tracker applications providing real-time access to CRF completion, visit status, data queries, freeze/lock status, and PI signature status</p></li><li><p>Developing executive-level dashboards highlighting portfolio-wide KPIs such as query aging, protocol deviations, data entry lag, and study completion achievements</p></li><li><p>Partnering with Data Management Reporting teams and external vendor delivery teams to establish structured data ingestion pipelines for EDC and reconciliation reports</p></li><li><p>Collaborating with Clinical Sciences, Biostatistics, Safety, and Precision Medicine teams to develop validated self-service analytical tools and reporting applications</p></li><li><p>Designing and implementing data visualization standards, UX/UI guidelines, and reporting procedures for non-technical stakeholders</p></li><li><p>Building curated analytical datasets and semantic layers connected to clinical data lakes and vendor reconciliation feeds</p></li><li><p>Running the full reporting lifecycle including requirements gathering, UX wireframing, development, validation, UAT coordination, and production deployment</p></li><li><p>Driving automation across routine reporting workflows including scheduled data ingestion, reconciliation report generation, and alert-based notifications</p></li><li><p>Supporting GCP compliance, inspection readiness, report governance, version control, and audit trail management</p></li><li><p>Driving adoption of reporting tools through stakeholder engagement, training, and change management initiatives</p></li><li><p>Serving as an SME for clinical data reporting, embedded analytics, and emerging visualization technologies</p></li></ul><p><strong>This Role May Be For You If You Have:</strong></p><ul><li><p>Demonstrable experience in Clinical Data Management, clinical trial reporting, analytics, or reporting platform development</p></li><li><p>Hands-on experience with Medidata Rave EDC including query management workflows and dataset structures</p></li><li><p>Solid understanding of CDISC CDASH/SDTM standards and GxP/CSV validation principles</p></li><li><p>Experience developing reporting applications using Python frameworks such as Dash, Streamlit, or Flask</p></li><li><p>Demonstrable experience with Power BI, Tableau, SQL, and analytical dataset development</p></li><li><p>Experience working with clinical data sources, clinical metrics, and external vendor reconciliation outputs</p></li><li><p>Strong UX/UI design sensibility for building intuitive reporting tools for non-technical users</p></li><li><p>Excellent stakeholder management, communication, and presentation skills</p></li><li><p>Strong analytical thinking and problem-solving capabilities</p></li><li><p>Ability to work optimally in a fast-paced, matrixed, and multi-functional environment</p></li></ul><p><strong>To Be Considered For This Role, You Must Have:</strong></p><ul><li><p>8+ years of experience in Clinical Data Management or clinical trial operations</p></li><li><p>Minimum 3+ years focused on clinical data reporting, analytics, or reporting tool development</p></li><li><p>Experience with clinical reporting applications, dashboards, and data visualization tools</p></li><li><p>Bachelor’s or Master’s degree in Computer Science, Data Science, Bioinformatics, or a related field</p></li><li><p>Advanced degree (MBA/MS) preferred</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Global Procurement]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44844]]></requisitionid>
    <referencenumber><![CDATA[R44844]]></referencenumber>
    <apijobid><![CDATA[r44844]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44844/manager-global-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we are passionate about transforming science into life-changing medicines. As a leading biotechnology company, our mission is to improve lives through groundbreaking research and innovative solutions. We are looking for a <strong>Manager, Global Procurement – International Markets: Japan</strong> to join our Tokyo-based team and play a vital role in enabling our international expansion and local market priorities.</p><p>As part of our Global Procurement team, you will collaborate with international stakeholders and category teams to address Japan’s unique regulatory, cultural, and commercial requirements. This is your opportunity to make a meaningful impact, drive strategic sourcing initiatives, and contribute to Regeneron’s vision of building a procurement capability that serves as a competitive advantage.</p><p><strong>A Typical Day:</strong></p><ul><li>Partner with stakeholders and the Global Procurement organization to align global priorities with local needs.</li><li>Implement global category strategies within Japan to ensure consistency in sourcing, contracting, and supplier relationship management.</li><li>Provide input to global strategies to incorporate Japan’s market-specific requirements effectively.</li><li>Execute sourcing, negotiation, and contracting activities to support business objectives.</li><li>Collaborate with country stakeholders to understand strategy, budgets, and annual spend requirements.</li><li>Analyze local contracts and monitor spend trends to identify opportunities for efficiency.</li><li>Leverage data for decision-making and to drive successful category projects.</li><li>Foster relationships with suppliers and stakeholders to deliver cost savings, improve cash flow, and enhance operational efficiency.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You thrive in a collaborative environment and enjoy working closely with international teams.</li><li>You have a keen understanding of Japan’s unique regulatory, legal, and cultural landscape.</li><li>You are passionate about driving value through strategic procurement and supplier engagement.</li><li>You excel at analyzing data to identify trends and inform decision-making.</li><li>You are an effective communicator and can build influential relationships with stakeholders and suppliers.</li><li>You are adaptable, focused, and able to navigate ambiguity to drive change and improvement.</li><li>You are committed to maintaining the highest ethical standards and delivering excellence in all you do.</li></ul><p><strong>To Be Considered:</strong></p><p>The ideal candidate will have a bachelor’s degree in a relevant field and at least 5 years of experience in indirect procurement, preferably in the Pharma/BioPharma industry. Experience in Commercial, Corporate/Indirect, and R&D categories is highly desirable, along with a proven ability to lead global category teams and processes. Proficiency with sourcing and contracting tools (e.g., Oracle, Zycus, GEP, Ariba) and standard business applications (Word, Excel, PowerPoint) is required.</p><p><strong>Why Join Regeneron?</strong></p><p>At Regeneron, we lead with science and are committed to fostering a culture of integrity, excellence, and innovation. Our Global Procurement team is at the forefront of enabling our scientific advancements and driving value for the organization. Join us to be part of a dynamic team that is shaping the future of procurement while making a difference in the lives of patients worldwide.</p><p>This job ad has been crafted to align with the provided guidelines, ensuring clarity, inclusivity, and a professional tone while strictly adhering to the job description.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Regulatory Submission Project Management]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48684]]></requisitionid>
    <referencenumber><![CDATA[R48684]]></referencenumber>
    <apijobid><![CDATA[r48684]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48684/associate-director-regulatory-submission-project-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director</strong> to join our <strong>Regulatory Affairs </strong>team. This individual will be responsible for providing senior leadership in the strategic planning and execution of regulatory milestones from IND Project Approval (IPA) through post marketing. They will serve as the Reg PM lead for assigned therapeutic area(s) (TA) and drives organizational excellence and consistency across regulatory programs within the function.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site </p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrates independent and strategic thinking, serves as a subject matter expert, and provides leadership and direction to the Reg PM team. Acts as a key decision-maker and escalation point, partnering closely with senior management to shape and advance the regulatory project management function.</p></li><li><h3>Provides strategic oversight and leadership across therapeutic area(s), directing team members responsible for project managing regulatory milestones such as pre-IND or Scientific Advice, INDs and CTAs, BLAs, sBLAs, MAAs and Type II variations, and BLA annual reports; accountable for functional quality and consistency across the portfolio</h3></li><li><h3>Partners with senior Regulatory Affairs leadership to drive program teams to successfully meet regulatory milestones, influencing strategy and prioritization across assigned therapeutic areas</h3></li><li><p>Leads and facilitates Global Regulatory Sub-team meetings with Regulatory Affairs liaison as the meeting chair; drives alignment and resolution of complex cross-functional issues</p></li><li><p>Conducts working group meetings to monitor and track progress of major submissions</p></li><li><p>Conducts kickoff meetings for major submissions, including those for INDs, CTAs, BLAs, sBLAs and MAAs and variations</p></li><li><p>Reviews and owns regulatory portfolio slides for complete and accurate milestone dates; presents to cross-functional and senior/executive management stakeholders and drives informed decision-making</p></li><li><p>Creates submission timelines and responsibility matrices through cross-functional discussions</p></li><li><p>Maintains accurate program timelines for cross-reporting with other functional groups</p></li><li><p>Communicates program projections and progress and serves as the key contact for coordinating regulatory activities and milestones</p></li><li><p>Serves as the senior escalation point and strategic advisor for team members and cross-functional groups, resolving complex issues related to timelines, submission documents, or regulatory matters impacting the timeliness or quality of submissions; establishes best practices and process improvements to enhance functional effectiveness</p></li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li><p>Minimum<strong> </strong>Bachelor’s Degree with 10+ years of combined industry and relevant experience</p></li><li><p>Requires strong knowledge of applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH, etc).</p></li><li><p>Requires eCTD knowledge.</p></li><li><p>Microsoft Project skills required.</p></li><li><p>Project management skills required; PMP certification or equivalent preferred.</p></li><li><p>Working knowledge with MS Office applications and Adobe Acrobat is required. Working knowledge of electronic document management systems (eg, SharePoint) is desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Medical Affairs-Strategic Business Planning & Execution,]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48688]]></requisitionid>
    <referencenumber><![CDATA[R48688]]></referencenumber>
    <apijobid><![CDATA[r48688]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48688/associate-director-medical-affairs-strategic-business-planning-execution/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Associate Director, Medical Affairs Strategic Business Planning & Execution provides project management support to the Global Medical Affairs Head and Medical Directors within our Neurology Franchise. As the key operational member you will seamlessly interact cross-functionally with all related Product Committees for information sharing, issue escalation, and resolution. <br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where</strong>:</p><p>This is located in Sleepy Hollow, NY and will require you to be on-site 4 days/week. If eligible, we can offer relocation benefits. </p><p><strong>Discover your role:</strong><br>• Drive the execution of Global and US Medical Affairs tactics as defined in the Medical Product Plans<br>• Schedule and facilitate team meetings for decision making, achieving project goals and updating the current status of projects within the desired timeline, resources, and budget. <br>• Create and maintain strong collaborations with internal and external partners; including but not limited to: Global Development, Medical Operations and Commercial. <br>• Owns integrated medical tactical plans, track progress and reports out status on progress. Ensures ownership for completion of all tactics on time, scope and within budget<br>• Facilitates the identification and resolution of risks, delays and or changes on the tactical execution<br>• Oversight of all Ph IV, Registry, IIS & Strategic Collaboration Studies in terms respective progress per timelines and budget<br>• Manage operational plans and associated budgets working in collaboration with Finance.<br>• Provide project-related process support for implementation and execution of publication and communication plans, advisory boards, expert consultations, steering committees and management of vendors.<br>• Serve as a key liaison between Medical Affairs and external vendors. <br>• Develop and drive new processes and tools to ensure vertical and horizontal integration across functional areas.<br>• Identify new tools and resources, and act as an ambassador for all systems and tools, including AI.<br>• Identifies and communicates business process enhancement needs or technical issues to management and Global Development Systems.<br>• Ensures compliant execution of medical affairs activities. Assists with reviewing and developing departmental procedural documents in accordance with SOPs, regulations and guidance’s. </p><p><strong>This role requires:</strong><br>A Bachelor’s Degree with 10+ years experience, an MBA with 8 years or an advanced degree with 5+ years experience (preferred). Active working experience in the pharmaceutical/biotechnology field as a project manager in Clinical Development is required. Experience with medical affairs or launch experience is preferred. <br>• Requires strong knowledge of applicable regulatory agency regulations, guidelines and/or specifications (FDA, EMA, ICH).<br>• Ability to initiate and lead large, cross-function projects and see it through to completion.<br>• Demonstrated project management skills.</p><p>• PMI Certification preferred</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Reimbursement Business Manager-Lexington, KY]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48672]]></requisitionid>
    <referencenumber><![CDATA[R48672]]></referencenumber>
    <apijobid><![CDATA[r48672]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48672/reimbursement-business-manager-lexington-ky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p><strong> </strong></p><p>The Field Access & Reimbursement environment for specialty biologics has proven to be highly challenging for HCPs and Patients. Payer Formularies and restrictive Utilization Management Criteria including: Prior Authorization Processes, Step Edits, Appeals, detailed Clinical Documentation, Peer to Peer reviews etc. requires dedicated and focused customer facing support through the Reimbursement Management Team.</p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. The primary purpose of this role is to support Health Care Practitioner offices in obtaining appropriate access to Regeneron products for patients. Ensuring optimal access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron product portfolio. Support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate across multiple internal stakeholders, sales teams, Payer teams, Alliance partners, HUBs, etc. The Field Reimbursement Management reports to the District Manager of Field Market Access. </p><p><strong>When & where: </strong></p><ul><li><p>Field Role</p></li><li><p>Location: Lexington-Fayette, KY </p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</p></li><li><p>Execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</p></li></ul><ul><li><p>Execute against established performance parameters and monitor personal performance against these agreed parameters:</p></li></ul><ul><li><p>Work closely with REGN and Sanofi partners as assigned; REGN and Sanofi District Sales Managers, Medical Specialists, other FRM, Reimbursement, Marketing and Access team members in assigned geographical areas to insure optimal coverage and customer knowledge of this process and all REGN patient services within defined accounts</p></li></ul><ul><li><p>Provide appropriate process, payer, and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products, in efforts to streamline the coverage and specialty pharmacy processes to obtain alliance products</p></li><li><p>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</p></li><li><p>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that complies with Regeneron policies, processes, and standard operating procedures</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimal educational requirement: Bachelor’s Degree</p></li><li><p>Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience</p></li><li><p>Experience working with products delivered through a Specialty Pharmacy network is critical</p></li><li><p>Reimbursement experience a plus</p></li><li><p>Experience in self-injectable biologic products a plus</p></li><li><p>Strong collaboration and proactive communication skills required</p></li><li><p>Background in leadership and effective cross functional teamwork a plus</p></li><li><p>Established ability to work within an Account Management based structure</p></li><li><p>Demonstrate excellent interpersonal and collaboration skills</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Supply Planning and Reporting Analyst - Advanced Therapies]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48755]]></requisitionid>
    <referencenumber><![CDATA[R48755]]></referencenumber>
    <apijobid><![CDATA[r48755]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48755/principal-supply-planning-and-reporting-analyst-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Supply Planning Analyst to join our Manufacturing Supply Chain team, supporting Commercial and Clinical programs in a cross-functional environment. In this role, you will own end-to-end supply planning across advanced therapy modalities — including siRNA, AAV-based gene therapies, LNP platforms, and CRISPR-based medicines — while collaborating with Manufacturing, Quality, Regulatory, Clinical Operations, and Commercial teams. This position offers the opportunity to shape supply chain strategies and analytics infrastructure for some of the most innovative medicines in development today.</p><p><br><strong>When & where:</strong><br>Location: Troy, New York | Work Model: Monday – Friday 8am – 4:30pm | Travel: 0%</p><p><br><strong>Discover your role:</strong></p><ul><li>Lead end-to-end supply planning for assigned Clinical and Commercial programs, ensuring uninterrupted supply across advanced therapy modalities.</li><li>Execute master production scheduling (MPS), material requirements planning (MRP), demand management, and inventory management for assigned programs and sites.</li><li>Build and maintain inventory reports accounting for complex manufacturing requirements, shelf-life constraints, and cold-chain considerations.</li><li>Design and implement statistical models, simulations, and algorithms to forecast and quantify operational and supply chain performance metrics.</li><li>Generate dashboards, data visualizations, and advanced Excel tools that communicate analytical insights and drive informed planning decisions.</li><li>Support Sales, Inventory & Operations Planning (SIOP) processes by consolidating data and facilitating information flow across demand, supply, and integration functions.</li><li>Partner with cross-functional teams to ensure compliant, disciplined planning in alignment with GMP requirements and audit readiness standards.</li></ul><p><strong>This role requires:</strong></p><ul><li>Senior Analyst: Bachelor's degree in business, Supply Chain Management, or a science discipline and 5+ years of supply chain experience.</li><li>Principal Analyst: Bachelor's degree in business, Supply Chain Management, or a science discipline and 8+ years of supply chain experience with demonstrated leadership experience.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li></ul><p><strong>Preferred qualifications:</strong></p><ul><li>Strong working knowledge of MPS, MRP, demand management, and inventory management principles.</li><li>Experience in pharmaceutical, biotechnology, or advanced therapy manufacturing.</li><li>Familiarity with the regulatory and supply chain considerations specific to advanced therapy modalities (siRNA, AAV, LNP, CRISPR).</li><li>Experience with Kinaxis Maestro, Oracle ERP, Access Database, or SharePoint </li><li>Master's degree (MBA, MS Supply Chain, or life sciences).</li><li>APICS certification (CPIM, CSCP) or Lean/Six Sigma knowledge. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 11:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead Warehouse Associate | Nights]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48765]]></requisitionid>
    <referencenumber><![CDATA[R48765]]></referencenumber>
    <apijobid><![CDATA[r48765]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48765/lead-warehouse-associate-nights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Warehouse & Inventory Team Lead to join our plant operations team, supporting materials management and logistics in an on-site, floor-based role. In this role, you will provide hands-on leadership to a team responsible for the receipt, documentation, and movement of inventory within the plant and from outside sources, while collaborating with Quality Assurance, Manufacturing, and Supply Chain teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>East Greenbush, New York <strong>| Work Model: </strong>2nd 4x10 | Sun-Wed | 12:00p-10:30p <strong> | Travel: </strong>0%</p><p><strong>Discover your role:</strong></p><ul><li>Lead and support a warehouse team on the floor, overseeing receipt, documentation, labeling, and movement of inventory and non-inventory items throughout the plant</li><li>Unload trucks, inspect incoming goods against purchase orders and packing slips, and transfer materials to QA Release, storage, or process areas</li><li>Maintain accurate paper and electronic records of received goods, inventory transfers, and material disbursements to production</li><li>Generate and apply labels to received inventory; schedule deliveries of incoming raw materials and coordinate outbound shipments per SOPs</li><li>Examine, stock, and distribute materials to manufacturing; fill requisitions manually and electronically for production workers</li><li>Support shipping and receipt of finished products in coordination with fillers, labelers, and distribution partners</li><li>Ensure the warehouse environment is clean, organized, and compliant with cGMP safety practices and established SOPs</li><li>Monitor employee training completion and timesheets; conduct monthly performance feedback meetings and escalate issues to management or HR as needed</li></ul><p>This role requires:</p><ul><li>Lead Warehouse Associate I: High school diploma or GED and 0 – 2 years of experience</li><li>Lead Warehouse Associate II: High school diploma or GED and 2+ years of experience</li><li>Lead Warehouse Associate III: High school diploma or GED and 4+ years of experience</li><li>Lead Warehouse Associate IV: High school diploma or GED and 6+ years of experience</li><li>Associate’s degree and/or dedicated warehouse experience in a cGMP environment preferred</li><li>Ability to perform physical tasks including unloading trucks, lifting heavy items, and operating a forklift</li><li>Forklift certification, handheld scanner experience, and/or CDL a plus</li><li>Shift Requirements (Schedule): 2nd 4x10 | Sun-Wed | 12:00p-10:30p</li><li>Shift Requirements (Physical): Role involves regular lifting of heavy items, standing, and operating material handling equipment</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.49 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Indirect Category Management]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48238]]></requisitionid>
    <referencenumber><![CDATA[R48238]]></referencenumber>
    <apijobid><![CDATA[r48238]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48238/manager-indirect-category-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Indirect Category Management Procurement to join our Global Procurement team, supporting our India operations in a hybrid work model. In this role, you will lead category management enablement, transform data and market intelligence into actionable insights, and support global indirect category strategies while collaborating with global procurement teams, data and analytics partners, and key collaborators. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead a team of associates and specialists transforming internal and external analytics into insights that enable global indirect category management strategies.</p></li><li><p>Support the definition and implementation of global indirect category strategies aligned to regional and global business needs.</p></li><li><p>Deliver micro and macro market analysis, spend analysis, supplier evaluation, and risk insights to support strategy development and partner engagement.</p></li><li><p>Partner with data and analytics teams to demonstrate internal and external data sources to identify trends, opportunities, and forecast future strategy direction.</p></li><li><p>Facilitate sourcing processes by preparing RFPs, RFQs, and RFIs and managing response collection, analysis, and comparative evaluation across sourcing and SRM events.</p></li><li><p>Maintain, standardize, and optimize category management templates, strategy decks, and stage-gate materials while improving procurement tools and repositories.</p></li><li><p>Lead contract management activities, oversee team execution, and track and report category management enablement requests in line with engagement plans.</p></li><li><p>You build strong relationships, lead through influence, and operate with integrity and clarity in a global, matrixed, and evolving environment.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field with progressive procurement experience; Pharma/Biopharma experience preferred.</p></li><li><p>Proven experience leading teams, processes, and suppliers across a breadth of categories in a multinational environment.</p></li><li><p>Strong expertise in category management principles including market analysis, spend analysis, supplier evaluation, and risk management.</p></li><li><p>Experience transforming data and market intelligence into actionable insights to enable category strategies.</p></li><li><p>Experience managing and developing associate and specialist-level professionals, including performance management, coaching, and career development.</p></li><li><p>Ability to build influential relationships with collaborators and suppliers to get results .</p></li><li><p>Experience in contract management and supporting sourcing and supplier relationship management activities.</p></li><li><p>Working knowledge of ERP systems such as Oracle and Source-to-Pay platforms (Oracle, Zycus, GEP, Ariba, or similar) preferred.</p></li><li><p>Proficiency in standard business applications (Word, Excel, PowerPoint).</p></li><li><p>Ability to operate with integrity, focus, and clarity in ambiguous environments and inspire change and continuous improvement .</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers)]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45310]]></requisitionid>
    <referencenumber><![CDATA[R45310]]></referencenumber>
    <apijobid><![CDATA[r45310]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45310/medical-director-clinical-development-oncology-lung-breast-colorectal-gastric-cancers/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Director, Clinical Development, Oncology</strong></p><p><strong>Build our future together:</strong></p><p>The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials.</p><div><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>4 days a week on-site in Tarrytown, NY or Warren, NJ</p><p><strong>Discover your role: </strong></p><ul><li><p>You define clinical trial-related goals and objectives.</p></li><li><p>You conduct literature and database research on clinical trials as needed</p></li><li><p>You are responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts</p></li><li><p>You are responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety</p></li><li><p>You lead and supervise the Global Clinical Study Team to produce high quality program deliverables on schedule</p></li><li><p>Maintains and develops relationship with key study investigators</p></li></ul><p><br><strong>This role requires: </strong></p><ul><li><p>An MD or MD/PhD with Oncology clinical fellowship training strongly preferred</p></li><li><p>At least 3-5 years of translational and/or clinical research experience</p></li><li><p>This role has a 4-day onsite minimum requirement in Tarrytown, NY or Warren, NJ</p></li></ul><p>#MDJOBSCD, #MDJOBS, #GDTher, #Oncology</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 17:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Sr Associate Scientist]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48701]]></requisitionid>
    <referencenumber><![CDATA[R48701]]></referencenumber>
    <apijobid><![CDATA[r48701]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48701/temp-sr-associate-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Auditory group is seeking a Senior Associate Scientist to support the development of therapies to treat hearing loss. This is a hands-on, in vivo-focused role in which you will be central to our preclinical studies that drive our discovery and development efforts toward new medicines.</p><p><strong>As a Senior Associate Scientist in the auditory group, your typical day might include:</strong></p><p>· Performing a broad range of in vivo procedures in mice, including survival and terminal blood collection.</p><p>· Carrying out systemic dosing and delivery via intravenous, intraperitoneal, subcutaneous.</p><p>· Performing specialized inner ear procedures such as perilymph collection and other microsurgical techniques.</p><p>· Handling and caring for mice, including performing procedures like tissue sample collection.</p><p>· Harvesting and collecting a range of tissues for downstream molecular and histological analysis.</p><p>· Ex vivo tissue processing, including dissection, fixation, decalcification, embedding, and cryosectioning.</p><p>· Supporting the planning and execution of in vivo studies and helping train and guide junior team members on procedures</p><p>· Maintaining detailed, accurate documentation of in vivo procedures and study records in compliance with IACUC protocols</p><p>· Collaborating closely with study directors, veterinary staff, and cross-functional research teams</p><p><strong>This role may be for you if you:</strong></p><p>· Enjoy hands-on in vivo work and thrive in a fast-paced, team-driven environment</p><p>· Are highly organized and thorough, with a strong commitment to animal welfare and ethical research practices</p><p>· Are adaptable and comfortable learning and refining new surgical and procedural techniques</p><p>· Communicate openly and frequently with study directors, your manager, and team members</p><p><strong>To be considered for this role, you should have:</strong></p><p>· B.S. with relevant experience or M.S. degree in Animal Science, Physiology, Neuroscience, Cell Biology, or a related discipline</p><p>· Proven hands-on experience with rodent in vivo techniques, including bleeds, systemic dosing, and tissue collection.</p><p>· Familiarity with post-mortem tissue processing (perfusion, dissection, fixation, sectioning) is preferred.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Finance Service Delivery Analyst]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47692]]></requisitionid>
    <referencenumber><![CDATA[R47692]]></referencenumber>
    <apijobid><![CDATA[r47692]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47692/senior-finance-service-delivery-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Finance Service Delivery Analyst to join our Financial Shared Services team in a hybrid role. In this position, you will support global payroll and accounting operations by performing reconciliations, maintaining data accuracy, supporting month-end close activities, and ensuring compliance with established financial controls and processes. You will collaborate with internal team members and external partners to drive operational excellence and deliver a high standard of service across multiple regions. This role offers an excellent opportunity to build expertise in global finance operations within a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Perform reconciliations between enterprise systems and external vendor platforms to ensure financial and payroll data accuracy.</p></li><li><p>Prepare, validate, and reconcile data templates supporting payroll processing across multiple global countries.</p></li><li><p>Execute accounting and payroll processes in accordance with established procedures and service delivery standards.</p></li><li><p>Provide exceptional customer service by responding to employee and stakeholder inquiries in a timely and professional manner.</p></li><li><p>Collaborate with global Finance, Payroll, and Shared Services teams to support operational activities across regions.</p></li><li><p>Prepare schedules and supporting documentation impacting the accounting month-end close and financial reporting processes.</p></li><li><p>Support month-end, quarter-end, and year-end close activities while ensuring adherence to timelines.</p></li><li><p>Assist in the preparation of reports, audit documentation, and compliance-related deliverables.</p></li><li><p>Maintain process documentation, mappings, and Standard Operating Procedures (SOPs) to support operational consistency and governance.</p></li><li><p>Identify opportunities to enhance efficiency, improve processes, and optimize service delivery within the Shared Services organization.</p></li><li><p>Ensure compliance with internal controls, financial policies, governance requirements, and regulatory standards.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Accounting, Finance, Commerce, Business Administration, or a related discipline (B.Com or BBM preferred).</p></li><li><p>5+ years of experience in payroll operations, accounting, finance shared services, financial reporting, or related analytical roles.</p></li><li><p>Experience performing reconciliations between enterprise systems and third-party vendor platforms.</p></li><li><p>Strong analytical and quantitative skills with exceptional attention to detail.</p></li><li><p>Proficiency in Microsoft Excel and experience working with large datasets.</p></li><li><p>Ability to manage multiple priorities and meet deadlines in a fast-paced environment.</p></li><li><p>Strong customer service, communication, and stakeholder management skills.</p></li><li><p>Experience supporting month-end, quarter-end, and year-end close processes.</p></li><li><p>Knowledge of financial controls, governance practices, compliance requirements, and audit support activities.</p></li><li><p>Ability to proactively identify process improvement opportunities and drive operational efficiencies.</p></li><li><p>Experience working in a global shared services environment is preferred.</p></li><li><p>Demonstrated ability to collaborate effectively across functions, geographies, and cultures.</p></li><li><p>Strong organizational, problem-solving, and interpersonal skills.</p></li></ul></div><ul><li></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  ALBANY, NY]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48916]]></requisitionid>
    <referencenumber><![CDATA[R48916]]></referencenumber>
    <apijobid><![CDATA[r48916]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48916/medical-account-specialist-ii-hematology-albany-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>ALBANY, NY</strong></p><p><strong>Geography: </strong><strong>Albany Area, Western MA</strong></p><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Precision Medicine Operations]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48614]]></requisitionid>
    <referencenumber><![CDATA[R48614]]></referencenumber>
    <apijobid><![CDATA[r48614]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48614/manager-precision-medicine-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><div><div><div><div><div><div><div><div><div></div></div></div></div></div></div></div></div></div><p>The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Immuno-Oncology. In this role, you will be a key driver of precision medicine operational execution partnering with Precision Medicine Strategy Lead (PMSL), clinical study teams, data management (DM), Samples, Kits, Data, Logistics (SKDL), Clinical Laboratory Study Manager (CLSM), and Clinical Laboratory Project Management (CLPM) groups to deliver high-quality samples and data. Through strong cross functional collaboration and operational excellence, you will help ensure biomarker and non-biomarker strategies are executed seamlessly, enabling the translation of innovative science to medicines for patients.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Armonk, NY, Warren, NJ</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Works with project manager and set-up manager of central/specialty lab and clinical study team to build lab database to address clinical trial sample collection needs, kits, testing and logistics</p></li><li><p>Monitor’s acquisition of clinical trial samples (including human tissue, bone marrow aspirate, whole blood, plasma, serum, etc.) and ensure compliance with ICF permissions</p></li><li><p>Supports individual clinical study teams as required for all technical and operational sample-related matters for assigned projects by liaising with internal stakeholders working on ICF and other trial documents impacting samples and testing </p></li><li><p>Work closely with central lab and/or specialty lab project managers, clinical trial management team, and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries.</p></li><li><p>Oversees Study start up, closeout and overall life-cycle activities for assigned studies at central lab/specialty labs to support all samples and testing</p></li><li><p>Provides input on sample-related section in clinical trial-related (e.g. protocols and ICF) and other supporting documents</p></li><li><p>Works closely with data management lead and SKDL to determine how sample and testing data will be captured, blinded and transferred for clinical trials.</p></li><li><p>Enables transfer of sample/testing data from vendors through development and review of appropriate data transfer specification and related documents in collaboration with SKDL.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor's degree with a minimum of 8 years of pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams.</p></li><li><p>Minimum of 5 years' experience with Clinical Trials, focus on clinical sample collection</p></li><li><p>Extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested.</p></li><li><p>Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - NEW ORLEANS, LA]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48930]]></requisitionid>
    <referencenumber><![CDATA[R48930]]></referencenumber>
    <apijobid><![CDATA[r48930]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48930/medical-account-specialist-ii-hematology-new-orleans-la/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Louisiana]]></city>
    <state><![CDATA[Louisiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>New Orleans, LA</strong></p><ul><li><strong>Geography: </strong><strong>New Orleans, Baton Rouge, Lake Charles, Shreveport, Biloxi</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Nurse Educator - Hematology - Ohio Valley]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48934]]></requisitionid>
    <referencenumber><![CDATA[R48934]]></referencenumber>
    <apijobid><![CDATA[r48934]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48934/associate-director-nurse-educator-hematology-ohio-valley/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Michigan]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Nurse Educator (NE) provides education to health care providers (HCPs) in support of relevant disease states that align with Regeneron’s hematology business unit for our bispecific antibody for Multiple Myeloma (MM). This role will focus on education regarding product dosing and administration and potential adverse event and adverse event management to support proper usage of our Multiple Myeloma bispecifc antibody. This position will report to the Director of Nurse Educators who reports into the Executive Director of Strategic Customer Engagement for Oncology.</p><p>The NE is a field-based position that collaborates with other field teams and cross-functional partners to identify educational needs within accounts and delivers on-label education to targeted customers to support their usage of our Multiple Myeloma bispecific antibody. The NE role includes delivering on-label presentations to APPs and Nurses and supporting other external groups as appropriate with approved educational initiatives. The NE will deliver education in a compliant manner with a high degree of integrity, strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. The nurse educator is a support role that provides education to prescribers and relevant staff once a prescriber or office has decided to use Regeneron products. It is not a sales or marketing role, is not compensated on sales performance and does not promote Regeneron products.</p><h3>When & where:</h3><p>Ohio Valley- MI, IN, OH, KY, TN and Western PA and need to have the ability to travel and must live within the geographic area of the assigned territory and hold a valid driver's license.</p><h3>Discover your role:</h3><ul><li>Provides educational support to HCPs, nurses, and APPs regarding dosing/administration, adverse event and adverse event management regarding our approved Multiple Myeloma bispecific antibody when a clear educational need has been identified.</li><li>Appropriately collaborates with internal cross-functional partners, including field sales, training, marketing, thought leader liaisons, oncology key account leaders, and medical affairs</li><li>Coordinates and implements strategic plans to support educational responsibilities</li><li>Interacts with HCPs, such as APPs (i.e., NP, PA), nurses, pharmacists, and other key stakeholders in the assigned geography to ensure they are informed on current, key information about Regeneron’s Multiple Myeloma bispecifc antibody</li><li>Conducts educational and in-service programs through 1:1 HCP and group presentations</li><li>Consistently works to improve disease state/product clinical knowledge/account management via ongoing approved NE training curriculum and appropriate cross-functional collaboration at POA meetings.</li><li>Completes all training requirements and proactively seeks to strengthen ongoing scientific knowledge regarding disease-state, competitive products, and healthcare trends</li><li>Maintains the highest level of integrity and acts per company compliance/legal guidelines at all times</li></ul><h3>This role requires:</h3><ul><li>A minimum of BSN is required; a graduate-level degree (i.e., MSN, NP, DNP) is preferred</li><li>Oncology Certified Nurse (e.g., OCN, AOCN, CBNC, etc.) is preferred</li><li>Minimum 5+ years of clinical experience in oncology with expertise in hematology-oncology and bone marrow transplant, a strong plus</li><li>Demonstrated ability to access and understand challenges and educational needs of key HCPs and accounts within the assigned geography</li><li>Excellent oral and written communication skills</li><li>Demonstration of strong Presentation/Platform skills</li><li>Superior clinical skills and business acumen with the proven ability to excel in a technically complex and ambiguous environment</li><li>Exceptional collaborator who can effectively develop and work with internal functional partners and external customers</li><li>Experience in the pharmaceutical/biotechnology industry is preferred</li><li>Working knowledge of pharmaceutical regulatory and compliance required</li><li>Ability to travel and cover large geographic territories</li></ul><p>Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - PITTSBURGH, PA]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48946]]></requisitionid>
    <referencenumber><![CDATA[R48946]]></referencenumber>
    <apijobid><![CDATA[r48946]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48946/medical-account-specialist-ii-hematology-pittsburgh-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- Pittsburgh</strong></p><ul><li><strong>Geography: Pittsburgh</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ERP Reporting and Analytics Lead (Oracle Fusion)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44208]]></requisitionid>
    <referencenumber><![CDATA[R44208]]></referencenumber>
    <apijobid><![CDATA[r44208]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44208/director-erp-reporting-and-analytics-lead-oracle-fusion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oracle Fusion ERP Reporting and Analytics Lead oversees the reporting and analytics strategy for the Oracle Fusion Cloud implementation. This role partners closely with SI partners, GPOs, Product Leads, Data Engineering, and Business SMEs to rationalize reporting requirements and guide the design and development of reporting solutions across Oracle Fusion Cloud reporting tools and Fusion Data Intelligence (FDI). The role ensures that reporting architecture, data sourcing, and analytics approaches align with enterprise standards, support phased modernization—from Oracle EBS to Oracle Cloud—and comply with data governance and AI policies, including the responsible use of Oracle AI Agents.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Provide leadership and subject-matter expertise across Oracle Fusion Cloud reporting tools, including OTBI, BI Publisher, Fusion Data Intelligence (FDI), OAC within FDI, Financial Reporting Center, Account Inspector/Monitor, Smart View, and embedded dashboards/KPIs.</p></li><li><p>Work closely with the SI partner to guide reporting design, validate deliverables, and ensure solutions meet business requirements and align with Oracle Cloud capabilities.</p></li><li><p>Lead the report rationalization strategy, determining the appropriate placement of reporting across Fusion-native tools, FDI, the Data Lake, or external BI platforms.</p></li><li><p>Support reporting strategy across a phased implementation, where some functions transition to Oracle Fusion Cloud while other modules remain in Oracle EBS.</p></li><li><p>Ensure reporting continuity during Chart of Accounts (CoA) redesign, including mapping, harmonization, and alignment of reporting structures across EBS and Oracle Cloud during coexistence.</p></li><li><p>Guide reporting solutions that require combined data from Fusion Cloud and external systems, determining where best to perform data blending (FDI vs. Data Lake).</p></li><li><p>Oversee Data Lake extract designs and data sourcing strategies, ensuring required datasets from Oracle Cloud and legacy systems are modeled accurately and consistently.</p></li></ul><h3><strong>This Job Might Be For You If You Have:</strong></h3><ul><li><p>Deep expertise with Oracle Fusion Cloud reporting tools: OTBI, BIP, Fusion Data Intelligence (FDI), OAC within FDI, Financial Reporting Center, Account Monitor/Inspector, Smart View, and embedded KPIs.</p></li><li><p>Strong ability to rationalize reporting requirements and determine appropriate placement across Fusion-native tools, FDI, Data Lake, or external BI platforms.</p></li><li><p>Ability to guide SI partner designs and influence architectural decisions.</p></li><li><p>Knowledge of key business domains including P2P, R2R, O2C, Plan to Make, PLM/PDH, WMS, OTM/GTM.</p></li><li><p>Experience designing, reviewing, and governing Standard and Custom Oracle AI Agents for reporting and analytics use cases.</p></li><li><p>Strong knowledge of SOX, audit controls, data integrity, and security/role-based access models.</p></li></ul><h3><strong>To be considered for this role, you must have:</strong></h3><ul><li><p>Bachelor’s degree in Information Systems, Data Analytics, Computer Science, Engineering, or related field.</p></li><li><p>15+ years of experience in enterprise reporting and analytics.</p></li><li><p>10+ years of experience with Oracle Fusion Cloud reporting tools.</p></li><li><p>3+ years of experience with Oracle AI Agents.</p></li><li><p>Experience supporting large-scale ERP transformations and phased modernization (EBS → Fusion)</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety - General Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44959]]></requisitionid>
    <referencenumber><![CDATA[R44959]]></referencenumber>
    <apijobid><![CDATA[r44959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44959/senior-manager-global-patient-safety-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager</strong> to join our <strong>Patient Safety</strong> team.The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment.</p><div><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Complete signal detection activities in line with approved safety surveillance plan</p></li><li><p>Perform signal evaluation for any identified signals and author the safety evaluation reports</p></li><li><p>Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries</p></li><li><p>Prepare and deliver presentations at Signal Management Team (SMT) meetings; participate in clinical study team meetings for assigned compounds</p></li><li><p>Participate in other risk management activities as appropriate for assigned compounds</p></li><li><p>We may ask you to represent GPS on cross-functional teams, including Regeneron Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC) and other teams with members external to Regeneron</p></li><li><p>Actively participate in process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents</p></li></ul><p><strong>This role requires:</strong>​</p><ul><li><p>Minimum a Master's, PhD, or PharmD</p></li><li><p>Offers 7+ years of relevant risk management experience in the pharmaceutical/ biotech industry or health authority</p></li><li><p>Ability to apply relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments</p></li><li><p>Ability to work with a safety system database for purposes of medical case review and simple queries</p></li><li><p>Able to be proactive and self-disciplined, you can meet deliverables, and effectively use your time and prioritize</p></li><li><p>Ability to effectively communicate (verbal and written) safety findings</p></li></ul><p>#GDPSJobs </p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Procurement- Advanced Therapies]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46026]]></requisitionid>
    <referencenumber><![CDATA[R46026]]></referencenumber>
    <apijobid><![CDATA[r46026]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46026/senior-manager-global-procurement-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Senior Manager, Global Procurement-Advanced Therapies, with experience in end-to-end procurement strategies/processes and with proven successful global category execution in Contract Development and Manufacturing Operations. Regeneron is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. Founded and led for 36 years by physician-scientists, Regeneron's unique ability to translate science repeatedly and consistently into medicine has led to numerous FDA-approved treatments and products in development, almost all of which were homegrown in Regeneron's laboratories.</p><p>A typical day might include the following:</p><ul><li><p>Accountable for supporting the definition and implementation of the global CMO Category strategy to serve global and regional business needs as assigned</p></li><li><p>Works closely with partners to manage discussions related to the CMO Categories and aligns category priorities with Procurement management and business partners</p></li><li><p>Manage negotiations, supplier management activities, and partner engagement activities for the Packaging Category as assigned</p></li><li><p>Takes direction to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities</p></li><li><p>Supports Global Procurement by participating in organizational decisions in the CMO categories with critical short and long-term impact on the success, efficiency, growth, and results of the category team</p></li><li><p>Demonstrates knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities</p></li></ul><p>The Role Might be for you if have:</p><ul><li><p>Experience leading category activities to ensure compliance with appropriate GxPs and other applicable regulations</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements</p></li><li><p>Managed teams of professional level employees responsible for performing category management tasks (if applicable.)</p></li><li><p>Uses data to drive decision-making for successful category projects.</p></li><li><p>Working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li></ul><p>We are looking for someone with a bachelor's degree in a relevant field of study plus relevant, progressive experience in procurement, including experience in Pharma/BioPharma or science in general.</p><ul><li><p>Sr Manager level: 8+ years of experience in relevant functions or industries, demonstrating growth in experience, scale, and development throughout.</p></li></ul><p>*This role requires working onsite 5 days per week</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Scientific Communications - Oncology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46231]]></requisitionid>
    <referencenumber><![CDATA[R46231]]></referencenumber>
    <apijobid><![CDATA[r46231]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46231/director-scientific-communications-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Scientific Communications- ONCOLOGY- will assume a pivotal role in leading and aligning strategic, integrated medical communications efforts, The Director will be responsible for the development of the global scientific communication platform(s), which will serve as the foundational resource(s) for cross-functional teams to harmonize and deliver evidence-based internal and external communications. Ensuring content is accurate, concise and accessible, the Director will drive and create meaningful scientific communications tailored to diverse audience needs and lead the collation of Integrated Medical Communications Plans (IMCP). Together, these collective efforts will position the Director, Scientific Communications at the heart of galvanizing stakeholder engagement, advancing medical knowledge, and ultimately improving clinical care for patients.</p><p>This position requires on-site presence 4 days a week in Warren, NJ or Sleepy Hollow, NY, with occasional travel between sites. If eligible, we can offer relocation benefits. </p><p>A typical day may include the following:</p><ul><li>For the asset/program(s) under the purview of responsibility, the Director, Scientific Communications will:</li><li>Lead the development and alignment of a comprehensive Integrated Medical Communication Plan(s)</li><li>Establish and effectively communicate clear Scientific Communication objectives and goals to internal stakeholders, and formulate a tactical plan for compliant execution</li><li>•Partner with Medical Director(s) and other key internal stakeholders to devise an overarching Congress strategy and align on Congress presence and key deliverables for Tier 2 congresses.</li><li>Drive the creation and development of Scientific and Digital Communications materials with a focus on:</li><li>Scientific Communication Platform, Lexicon and Narrative</li><li>Congress Presence: Coordinate and Collaborate with the Congress Strategy and Planning team on Tier 1 medical booth design and content/material; Tier 2 end-to-end planning & execution.</li><li>Program and Scientific Slides</li><li>Disease-State Education materials</li><li>Data/Publication updates</li><li>In collaboration with the therapeutic area medical directors and Field Medical Leads, assess medical education gaps and needs of external stakeholders</li><li>Identify and prioritize scientific educational opportunities to reach targeted stakeholders in an impactful manner</li><li>Address knowledge gaps, or Clinical Impact Opportunities, with tailored, targeted and timely content creation which can be adapted for engagement across geographic regions as well as multiple platforms, including digital</li><li>Lead projects within the scope of responsibility through medical review committees, facilitating the endorsement of appropriate materials</li><li>Ensure medical and scientific integrity and accuracy of created content and ensure materials have a fair and balanced representation</li><li>Work with Project Manager to supervise all materials are delivered within the allocated budget, and tracks budget spend in a systematic manner</li><li>Maintain adherence to rigorous ethical and compliance standards, upholding an uncompromising level of personal ethics rooted in a “patient first” value framework.</li></ul><p>To be considered it is required to have a PhD, MD, or PharmD with at least 8 years of relevant medical communication experience with Oncology is required. . Demonstrated expertise in medical communication strategies, congress planning, scientific content development, and medical education is required. Strong project management skills, ethical integrity, and the ability to work in a matrix organization are essential. <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Material & Supplier Quality]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46568]]></requisitionid>
    <referencenumber><![CDATA[R46568]]></referencenumber>
    <apijobid><![CDATA[r46568]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46568/manager-material-supplier-quality/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role you will lead all aspects of a team of QA employees within the Material and Supplier Quality area. You will be responsible for ensuring quality standards and excellence internally and externally.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li><p>Responsible for review and approval of the following types of documents, relating to area functions including QC test data, specifications, failure investigations, change controls, SOPs, validation protocols and summary reports and SCAR records (Supplier Corrective Action Request)</p></li><li><p>Coordinating QA resources assigned to functional area to meet goals and timings; coordinates prioritization of activities with area management</p></li><li><p>Performing compliance monitoring of area operations, including trending of SCARS/MARS and evaluating effectiveness of corrective actions</p></li><li><p>Generating monthly trend data on release cycle times and SCAR/MAR cycle times</p></li><li><p>Supporting Supplier Quality Group</p></li><li><p>Reviewing customer requirements and implementing required processes to meet customer expectations regarding Quality</p></li><li><p>Participating in regulatory and customer audits</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Demonstrate excellent people management experience</p></li><li><p>Have a strong quality mindset</p></li><li><p>Enjoy working in a dynamic and fast-paced environment</p></li><li><p>Can collaborate and build successful partnerships internally and externally</p></li></ul><p>To be considered for this role, you should hold a Requires BSc/BEng in scientific discipline or related field with 8+ years of relevant work experience in pharmaceutical or related industry. Supervisory experience required.</p><p>Manager: Minimum 7 years of experience</p><p>Senior Manager: Minimum 8 years of experience</p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€74,000.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist: Bispecifics and Antibody Engineering]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47480]]></requisitionid>
    <referencenumber><![CDATA[R47480]]></referencenumber>
    <apijobid><![CDATA[r47480]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47480/senior-scientist-bispecifics-and-antibody-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a results-driven Senior Scientist to join Regeneron’s Antibody Engineering team within the Bispecifics and Antibody Engineering Department. In this fast-paced, innovative group, you will design, produce, and characterize next-generation antibody and protein therapeutics across multiple therapeutic areas with a focus on myeloid cell biology. Your work will directly contribute to the pipeline and help build new platform capabilities at a pivotal time for antibody engineering.</p><p><strong> </strong></p><p><strong>As a Senior Scientist, a typical day could require the following:</strong></p><ul><li><p>Apply molecular and structural biology expertise to independently design innovative multi-specific antibodies with desired potency, selectivity and developability.</p></li><li><p>Perform molecular and structural-guided design, high-throughput construct generation, and vector engineering using modern software and tools.</p></li><li><p>Produce and purify novel and logic-gated alternative format antibodies using mammalian expression systems utilizing an assortment of molecular biology & biochemical techniques (i.e. AKTA systems and other chromatographic columns).</p></li><li><p>Characterize binding affinities, binding kinetics & stability. </p></li><li><p>Design and implement high-throughput and properly controlled biochemical and cell-based assays (ELISA and AlphaLISA, flow cytometry binding, phagocytic assays, cell activation and cytolytic assays).</p></li><li><p>Troubleshoot bioanalytical and cell-based assay data to inform subsequent iterations.</p></li><li><p>Engage program stakeholders to communicate biologic designs with data updates to meet program objectives. </p></li></ul><ul><li><p>Clearly convey results to management during cross-departmental meetings and maintain timely, accurate entries using Benchling and research ELN.</p></li></ul><p><strong>This role may be a strong fit If You:</strong></p><ul><li><p>Have expertise in myeloid, molecular, and protein biology.</p></li><li><p>Learn new skills quickly and troubleshoot antibody production and functional assays effectively.</p></li><li><p>Excel in data analysis and interpretation while supporting multiple projects simultaneously.</p></li><li><p>Competently prioritize efforts to quickly adapt to evolving program directions.</p></li><li><p>Possess exemplary organizational, communication, and presentation skills.</p></li><li><p>Enjoy collaborating across diverse, cross-functional teams. </p></li></ul><p><strong>To be considered for this role you must have </strong>a PhD in molecular biology, cell biology, biochemistry, immunology or a related field with at least one year of relevant experience in academia or industry. Core hands-on experience with cloning, antibody expression in mammalian cell lines, antibody purification (i.e., using AKTA systems), and comprehensive protein characterization is desired; however, we’re excited to train motivated learners. Familiarity with cell-free expression and structural AI/ML-design is preferred but not required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-West]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47572]]></requisitionid>
    <referencenumber><![CDATA[R47572]]></referencenumber>
    <apijobid><![CDATA[r47572]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47572/regional-director-neurology-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - California]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the West Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: West (California, Oregon Washington)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Immunology & Inflammation]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47657]]></requisitionid>
    <referencenumber><![CDATA[R47657]]></referencenumber>
    <apijobid><![CDATA[r47657]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47657/associate-scientist-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a highly motivated Associate Scientist to join our Immunology and Inflammation team. In this role, you will contribute to the discovery and development of novel therapies for inflammatory bowel disease and autoimmune diseases, working at the intersection of innovative science, translational research, and drug discovery. You will join a collaborative, fast-paced research environment and work closely with cross-functional partners to generate high-quality data, apply diverse in vivo and in vitro approaches, and help advance programs from early discovery toward clinical translation.</p><p>The ideal candidate will bring strong experimental skills, careful attention to detail, and enthusiasm for working on complex immunology questions.</p><p><strong>As an Associate Scientist in the Immunology and Inflammation group, your typical day might include:</strong></p><ul><li><p>Handling and caring for mice, including performing procedures such as blood and/or tissue sample collection or injections (IP, IV and subcutaneous)</p></li><li><p>Processing of organs for immune cell isolation and analysis</p></li><li><p>Maintaining, expanding, and/or modulating cells in vitro</p></li><li><p>Evaluating cell phenotypes and function using ex vivo or in vitro assays such as flow cytometry and immunoassays.</p></li><li><p>Analysis of data using biological and statistical software such as Flowjo, Excel, Prism</p></li><li><p>Close collaborative interactions with teams across the organization</p></li><li><p>Documentation of experimental procedures and results</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Enjoy working in an innovative and team-driven environment</p></li><li><p>Are highly organized, detail-oriented, and motivated, with a creative approach to problem-solving</p></li><li><p>Are adaptable, flexible, and enjoy learning new techniques or switching tasks as needed</p></li><li><p>Are excited to contribute to the development of novel therapeutics</p></li><li><p>Communicate openly and frequently with manager and team members</p></li></ul><p><strong> </strong></p><p><strong>To be considered for this role, you should have</strong></p><ul><li><p>B.S. or M.S degree in a relevant field with 0-2 years of experience in immunology or a related discipline.</p></li><li><p>Experience in tissue culture, cell-based assays, flow cytometry, or immunoassays (e.g. ELISA, MSD, Luminex), as well as proficiency in basic computer applications and experience with biological data collection and analysis highly preferred</p></li><li><p>Experience in mouse handling is highly preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist, Immunology & Inflammation]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47494]]></requisitionid>
    <referencenumber><![CDATA[R47494]]></referencenumber>
    <apijobid><![CDATA[r47494]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47494/senior-scientist-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Senior Scientist to join a highly collaborative Immunology & Inflammation team. This individual will have the opportunity to support a broad pipeline in allergic and inflammatory diseases by validating targets, assessing the efficacy of therapeutic candidate molecules in vitro and in vivo, and interrogating mechanisms of pathology that inform therapeutic strategies. Candidate should have prior Immunology experience and prefer working in a team-driven environment, possess organizational skills and communicate openly and frequently with manager and team members.</p><h3><strong>As a Senior Scientist, a typical day may include:</strong></h3><ul><li><p>Contributes to project advancement by developing new methods and technologies. Troubleshoots methodological and technical issues, interprets experimental data and literature, and communicates results to supervisor, department, or project team.</p></li><li><p>Executes experiments based on projects/protocols provided and works towards independently developing project.</p></li><li><p>Collaborates and communicates efficiently with team members to coordinate complex in vivo experiments, and with other departments to facilitate cross-functional efforts.</p></li><li><p>Experience with proper handling and care of mice, general surgical techniques and the collection of blood and tissue samples.</p></li><li><p>Develops and optimizes relevant disease mouse models and the subsequent analysis of associated disease-related pathologies by flow cytometry, histology and ELISA.</p></li><li><p>Develops and executes cell-based assays to screen candidate antibodies for various research programs. Performs ELISAs and or MSDs to measure cytokine levels and determine antigen binding for various research programs.</p></li><li><p>Contributes to lab and equipment maintenance and orders supplies/reagents to help create a safe, effective and efficient working environment.</p></li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li><p>You enjoy working in a fast-paced environment</p></li><li><p>You are a fast learner and have desire to expand your skill set and learn new techniques</p></li><li><p>You are detail oriented, well-organized and can multi-task</p></li><li><p>You are a great teammate</p></li><li><p>You have strong communication skills</p></li></ul><h3><strong>To be considered, you must have the following: </strong></h3><ul><li><p>Ph.D + 0-2+ years experience. The ideal candidate will be skilled in the design of complex studies to interrogate the in vivo efficacy of novel therapeutics and thus, will have experience with developing and optimizing mouse models of inflammatory diseases and analysis of associated disease-related pathologies by flow cytometry, histology and ELISA.</p></li><li><p>Qualified applicants will preferably have minimum of 5-8 years of relevant research experience in immunology. Ph.D. in Biology, Immunology, or Cellular and Molecular Biology preferred but not required.</p></li><li><p>Extensive experience with multi-parameter flow cytometry, panel design and data analysis is required.</p></li><li><p>Basic computer literacy and experience collecting and analyzing biological data on the computer is a necessity. Preferred experience with the following data analysis programs:</p></li><li><p>GraphPad PRISM, Softmax Pro, FlowJo analysis, HALO, DIVA software.</p></li><li><p>Knowledge of allergic and inflammatory diseases, with emphasis in skin and/or lung biology is preferred.</p></li><li><p>Preferred experience developing and optimizing primary cell assays used to characterize cytokine and immunoreceptor pathways and screen antibody candidates.</p></li><li><p>Must have a record of high-quality publications in scientific literature.</p></li><li><p>The candidate is expected to have effective verbal communication and written skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Digital Health Technologies Manager]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47926]]></requisitionid>
    <referencenumber><![CDATA[R47926]]></referencenumber>
    <apijobid><![CDATA[r47926]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47926/digital-health-technologies-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Di<strong>gital Health Technologies (DHT) Manager</strong> is accountable for the implementation of digital tools and technologies (e.g. electronic COA (eCOA), econsent, wearables, sensors, spirometry, ECG, etc.) in individual clinical research studies from study design to close out in collaboration with the study team. In this role, a typical day may include: Accountability for all supported digital tool and technology project timelines, training development, translation, specifications, executing UAT, and ensuring collection of such data is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight of digital technologies will vary accordingly. Responsible for enforcing digital tools and technology system standards, managing vendor performance, and supporting training & education of stakeholders. This position will participate in process improvement and strategy development initiatives in global development.</p><p><em>***Please note this role is an onsite position and is NOT eligible remote.</em></p><br><p><strong>A typical day in this role looks like:</strong></p><ul><li>Responsible & accountable for the successful implementation of digital tools and technologies for one or more clinical research trials with quality and compliance</li><li>Applies patient technology expertise on day-to-day activities, cross-functional and departmental process improvements, supplier selection, and escalations.</li><li>Provides input into protocol development as it relates to digital tools and technologies</li><li>May participate in creation of digital tools and technology standards</li><li>Define and support study level strategy for the implementation, validation, and maintenance of various digital tools and technologies</li><li>Oversee or support license acquisitions and purchasing of digital tools and technologies</li><li>Oversee vendor performance at the clinical trial level, including oversight of KPI, performing root cause analysis and identifying corrective actions, and serving as point of escalation for supported translations, digital tools and technology issues.</li><li>Uses interpersonal, negotiating, and project management skills to perform the following tasks as related to digital tools and technologies project implementation:<ul><li>Project plan development, execution, and change control. Coordinates resolution & risk mitigation of all supported technology systems related issues and end of study vendor deliverables</li><li>Project documentation management</li><li>Risk management planning</li><li>Communication planning, information distribution, performance reporting, and project closure.</li><li>Performing lessons learned</li></ul></li><li>Monitor financial components related to digital tools and technologies for each study</li><li>Provides training and mentor new staff</li><li>Drive strategy & processes for expansion of eSource modalities to enable data availability in a virtual clinical trial environment</li><li>Support strategy for implementation of innovative clinical trial technologies and disruptive innovations for both stakeholders and the broader organization.</li><li>Provide consultation on digital tool modality benefits, risks, costs and process</li><li>May require up to 25% travel</li></ul><p><br> </p><p><strong>This role may be for you if you have:</strong></p><ul><li>Demonstrate knowledge of some digital tools and technologies. Specifically, eCOA systems development processes</li><li>Demonstrated interpersonal & leadership skills</li><li>Ability to understand and implement the strategic direction and guidance for respective clinical studies</li><li>A data driven approach to planning, executing, and problem solving</li><li>Effective communication skills via verbal, written and presentation abilities</li><li>Ability independently perform and manage multiple tasks at one time and meet deadlines in a complex environment working both internal to Regeneron and external vendors</li><li>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</li><li>Ability to influence and negotiate</li><li>An awareness of relevant industry trends</li></ul><p><strong>In order to be considered qualified for the this role</strong>, a minimum of a Bachelors degree and 6+ years or relevant industry related experienced in required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison  - Neurology (Southeast)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48123]]></requisitionid>
    <referencenumber><![CDATA[R48123]]></referencenumber>
    <apijobid><![CDATA[r48123]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48123/associate-director-thought-leader-liaison-neurology-southeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Florida]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Neurology Marketing team. It will be focused on enhancing and improving interactions with key external US Neurology thought leaders at academic centers and leading community practices for our neurology product.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Neurology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><p><strong>The typical day may include the following:</strong></p><ul><li>The Neurology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You possess a strong science background with deep knowledge of rare neurology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p><strong>To be considered for this opportunity, you will possess the following:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10years of relevant work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in Neurology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry. Launch experience preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li><li>Must have a valid driver’s license</li><li>Must be able to travel 60%-80% of time </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Internal Audit]]></title>
    <date><![CDATA[Wed, 20 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47892]]></requisitionid>
    <referencenumber><![CDATA[R47892]]></referencenumber>
    <apijobid><![CDATA[r47892]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47892/senior-manager-internal-audit/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization focuses on inventing, developing, and commercializing medicines that help people with serious diseases. As we continue to expand globally, strong governance, internal controls, and risk management frameworks are critical to ensuring compliance and supporting sustainable business growth.</p><p>As a Senior Manager – Internal Audit, you will play a key role in strengthening the organization’s internal control environment and risk management practices. You will lead audit engagements, support SOX and compliance programs, and partner with cross-functional teams to provide insights that improve business processes and maintain a strong governance framework.</p><h3><strong>A Typical Day May Include the Following</strong></h3><ul><li><p>Lead and implement internal audit engagements, including planning, fieldwork, and reporting</p></li><li><p>Drive SOX 404 compliance activities and support internal control frameworks across business processes and systems</p></li><li><p>Evaluate risks and assess the effectiveness of financial, operational, and IT controls</p></li><li><p>Partner with cross-functional teams to identify control gaps and recommend process improvements</p></li><li><p>Review audit findings and provide clear, actionable insights to collaborators</p></li><li><p>Coordinate with internal and external auditors for audit activities and compliance requirements</p></li><li><p>Monitor remediation actions and ensure timely closure of audit findings</p></li><li><p>Prepare audit reports and present key insights to leadership teams</p></li><li><p>Support development and enhancement of audit methodologies, governance frameworks, and policies</p></li><li><p>Leverage data analytics to improve audit effectiveness and reporting insights</p></li><li><p>Oversee quarterly audit reporting, compliance tracking, and management updates</p></li><li><p>Support risk-based audit planning and execution across global operations</p></li><li><p>Collaborate with stakeholders to strengthen compliance culture and internal control awareness</p></li><li><p>Lead and mentor team members, providing guidance, performance feedback, and development support</p></li></ul><h3><strong>This Job May Be for You If You Have</strong></h3><ul><li><p>Strong experience in internal audit, SOX compliance, or risk and compliance functions</p></li><li><p>Good understanding of internal controls, audit methodologies, and governance frameworks</p></li><li><p>Experience working in a global or regulated environment (pharma/biotech preferred)</p></li><li><p>Ability to assess risk, analyze data, and provide practical recommendations</p></li><li><p>Strong analytical, problem-solving, and decision-making skills</p></li><li><p>Effective communication and stakeholder management skills</p></li><li><p>Experience working with cross-functional and global teams</p></li><li><p>Ability to manage multiple priorities in a dynamic environment</p></li><li><p>Experience in driving process improvements and control enhancements</p></li></ul><h3><strong>To Be Considered for This Role</strong></h3><ul><li><p>8–12+ years of experience in Internal Audit, Risk, Compliance, or Public Accounting</p></li><li><p>Bachelor’s or Master’s degree in Accounting, Finance, or related field (MBA preferred)</p></li><li><p>Professional certifications such as CPA, CA, CIA, ACCA, or equivalent preferred</p></li><li><p>Strong experience in SOX compliance and internal control frameworks</p></li><li><p>Experience in pharma/biotech industry or Big 4 audit firms is an advantage</p></li><li><p>Proven team management and leadership experience</p></li><li><p>Proficiency in English and ability to work in a global environment</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 21 May 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-St. Louis, MO/Springfield , IL]]></title>
    <date><![CDATA[Tue, 19 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47790]]></requisitionid>
    <referencenumber><![CDATA[R47790]]></referencenumber>
    <apijobid><![CDATA[r47790]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47790/medical-specialist-i-pulmonology-st-louis-mospringfield-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Springfield]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Springfield, IL</strong></p><p>The Medical Specialist (MS) will report to the District Manager and be responsible for engaging customers in the Pulmonary therapeutic area within an assigned geographical universe, presenting clinically focused selling messages to create and drive growth, and consistently delivering product goals.<br><br><strong>A Typical Day Might Look Like This:</strong></p><ul><li><p>Demonstrate strong and consistent sales performance related to product goals in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p></li><li><p>Develop strategy and execute tactics within key accounts in the Pulmonary therapeutic area to generate product utilization.</p></li><li><p>Develop strong working relationships with Pulmonologists and Midlevel experts in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p></li><li><p>Collaborate with their regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography.</p></li><li><p>Participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p></li></ul><p><strong>This Position Might Be For You If:</strong></p><ul><li><p>Demonstrate advanced clinically based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li></ul><p>To be considered for this role you must have a Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Pulmonary market or a similar subcutaneous self-injectable biologic specialty market. Ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 27 May 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Worldwide Operations Office - Pharmacovigilance]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48216]]></requisitionid>
    <referencenumber><![CDATA[R48216]]></referencenumber>
    <apijobid><![CDATA[r48216]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48216/executive-director-worldwide-operations-office-pharmacovigilance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Regeneron is seeking an Executive Director, Worldwide Operations Office to join our PV Organization!</p></div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><p>The Executive Director, Worldwide Operations Office serves as the single point of accountability for Regeneron’s global-to-local pharmacovigilance model. This role ensures consistency, compliance and operational excellence across all regions and countries by defining the scope and governance of regional PV Hubs, establishes clear boundaries between global, regional, and local responsibilities, and translates regional insights into strategic guidance for GPS leadership. This role drives a unified, patient-centered approach to safety across Regeneron’s global footprint while enabling appropriate local adaptation to meet regional regulatory requirements. </p><p><strong>This role might be for you if can: ​</strong></p><ul><li><p>Partner with cross-functional US and International teams to embed a patient safety mindset across Regeneron’s global operations (e.g., gather feedback from regional leaders, establish knowledge sharing forums) </p></li><li><p>Provide functional oversight of WWOO and regional PV Hubs, ensuring operational performance, quality standards, regulatory compliance, and consistent application of global processes across markets </p></li><li><p>Define execution scope for regional PV Hubs, determining which processes require localization to meet requirements versus which can be executed through centralized global processes, including clear delineation of responsibilities between GPS and affiliate teams </p></li><li><p>Establish governance framework for local process adaptation, defining clear standards for when and how global PV processes may be tailored to meet local regulatory requirements </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li><li><p>Aggregate insights and potential risks from regional and country-level activities to shape, influence, and prioritize objectives for the PV system </p></li><li><p>Coordinate across key GPS functions (e.g., QPPV, Case Management, Quality & Compliance) on matrixed activities, regional priorities, and global to local interdependencies </p></li><li><p>Adapt the international model to fit changing business needs, including assessing future needs for additional PV Hubs based on portfolio expansion, geographic growth, and regulatory landscape changes </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that raise capabilities across the organization </p></li><li><p>Influence cross-functional leaders to align priorities and drive enterprise results </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Advanced degree (PharmD, MD, MS, or MBA) in life sciences, healthcare, or related field preferred; Bachelor's degree required</p></li><li><p>17+ years of experience in pharmacovigilance, international operations within the life sciences industry </p></li><li><p>Minimum 7 years in leadership roles with demonstrated experience managing international or multi-regional operations </p></li><li><p>Proven ability to develop relationships and influence key decision making with GPS and Non-GPS functions (e.g., QPPV, Med Affairs, Regulatory), regions, and senior stakeholders </p></li><li><p>Strong background in PV compliance, inspection readiness, and quality oversight across multiple markets </p></li><li><p>Strategic mindset with the ability to translate regional complexity into clear governance, decisions, and executive-level insights </p></li><li><p>Preferred experience with AI technologies </p></li></ul><p>#GDPSJobs</p></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 11:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - South Central]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48156]]></requisitionid>
    <referencenumber><![CDATA[R48156]]></referencenumber>
    <apijobid><![CDATA[r48156]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48156/neurology-account-director-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: South Central (Texas, Arkansas and Louisiana)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - COLUMBUS, OH]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48007]]></requisitionid>
    <referencenumber><![CDATA[R48007]]></referencenumber>
    <apijobid><![CDATA[r48007]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48007/medical-account-specialist-ii-neurology-columbus-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbus]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Columbus (Metro), OH</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - LITTLE ROCK, AR]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48057]]></requisitionid>
    <referencenumber><![CDATA[R48057]]></referencenumber>
    <apijobid><![CDATA[r48057]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48057/medical-account-specialist-ii-neurology-little-rock-ar/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Little Rock]]></city>
    <state><![CDATA[Arkansas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Little Rock (Metro), AR</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - CHARLOTTE, NC]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48022]]></requisitionid>
    <referencenumber><![CDATA[R48022]]></referencenumber>
    <apijobid><![CDATA[r48022]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48022/medical-account-specialist-ii-neurology-charlotte-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Charlotte]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p><br>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.<br>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.<br> </p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Charlotte (Metro), NC</li></ul><p><strong> </strong></p><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - MANCHESTER, NH]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48000]]></requisitionid>
    <referencenumber><![CDATA[R48000]]></referencenumber>
    <apijobid><![CDATA[r48000]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48000/medical-account-specialist-ii-neurology-manchester-nh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Manchester]]></city>
    <state><![CDATA[New Hampshire]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Manchester, NH</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -OAKLAND, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48075]]></requisitionid>
    <referencenumber><![CDATA[R48075]]></referencenumber>
    <apijobid><![CDATA[r48075]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48075/medical-account-specialist-ii-neurology-oakland-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Oakland]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Oakland (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 17:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Dermatology *Okayama, Hiroshima Area]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47551]]></requisitionid>
    <referencenumber><![CDATA[R47551]]></referencenumber>
    <apijobid><![CDATA[r47551]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47551/medical-representative-mr-dermatology-starokayama-hiroshima-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong></p><p>You will primarily work in the Okayama and Hiroshima area.</p><p>Your residence is expected to be in Okayama or Hiroshima.</p><p>Are you ready to make a meaningful impact in the pharmaceutical industry? At Regeneron, we’re committed to putting patients first, and we’re looking for a passionate Sales Representative to join our Dupixent ROW Commercial Team in Japan. This role is your opportunity to drive dermatology sales objectives while working with a team dedicated to innovation and excellence. With a focus on delivering value to healthcare professionals and patients alike, this position offers the chance to grow your career while making a difference in people’s lives.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Achieve sales objectives by effectively managing territory budgets and resources.</p></li><li><p>Develop and implement an annual territory business plan that incorporates market insights and aligns with marketing strategies.</p></li><li><p>Regularly update business plans to adapt to changing market dynamics.</p></li><li><p>Utilize key data sources to create strategic action plans for the territory.</p></li><li><p>Conduct disease and concept selling to engage healthcare professionals and deliver tailored solutions.</p></li><li><p>Perform administrative tasks, including expense reporting, marketing feedback, and call reporting.</p></li><li><p>Collaborate with alliance partners to meet overall objectives and ensure compliance with regulatory guidelines.</p></li><li><p>Attend local, regional, and national meetings as required, and complete all training programs provided by Regeneron.</p></li><li><p>Maintain company property in good order and adhere to safe driving practices.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You excel at building strong relationships with customers and delivering value-driven solutions.</p></li><li><p>You have a knack for strategic thinking and can manage your time effectively to achieve goals.</p></li><li><p>You thrive in independent work environments and can execute plans under tight timelines.</p></li><li><p>You’re organized, detail-oriented, and comfortable with administrative responsibilities.</p></li><li><p>You enjoy collaborating with others to achieve shared objectives.</p></li><li><p>You’re adaptable and willing to travel, including evenings and weekends, as needed.</p></li></ul><p><strong>To Be Considered:</strong></p><p>Candidates must have a Bachelor’s degree (or equivalent) and at least five years of sales representative experience in the pharmaceutical industry. A valid driver’s license and MR certification are required. While fluency in English is a plus, it is not essential for this role. Preferred qualifications include therapy area knowledge in dermatology, sales experience in biologics, and established relationships with key opinion leaders in dermatology.</p><p>Join us at Regeneron, where your expertise and dedication can make a real difference. Apply today to become a part of a team that’s revolutionizing healthcare and improving lives worldwide.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[MEDICAL REPRESENTATIVE (MR) – ONCOLOGY *TOKYO AREA]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48621]]></requisitionid>
    <referencenumber><![CDATA[R48621]]></referencenumber>
    <apijobid><![CDATA[r48621]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48621/medical-representative-mr-oncology-startokyo-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist, Oncology to join our Oncology Sales team, supporting our oncology business area in a field-based role. In this role, you will drive the adoption of our oncology product portfolio while collaborating with healthcare professionals and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>You will be responsible for the Tokyo area.</p><p>While we assume living within Tokyo's 23 wards, we are also open to discussion regarding those living outside of Tokyo's 23 wards, Saitama, Chiba, and Kanagawa prefectures, depending on the specific area.</p><br><p><strong>Discover your role:</strong></p><ul><li>Drive sales and adoption of the oncology product portfolio within assigned territory</li><li>Develop and execute territory business plans to achieve sales targets</li><li>Build and maintain relationships with healthcare professionals and key accounts</li><li>Deliver approved scientific and clinical information to support customer decisions</li><li>Identify and engage new business opportunities in the oncology space</li><li>Collaborate with cross-functional teams to support customer needs</li><li>You adapt to evolving priorities and thrive in a results-driven environment</li><li>You demonstrate strong communication and relationship-building skills</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in life sciences, business, or related field</li><li>Proven sales experience in the pharmaceutical, biotech, or healthcare industry</li><li>Knowledge of oncology or related therapeutic area</li><li>Strong communication, presentation, and negotiation skills</li><li>Ability to travel within assigned territory as required</li><li>Driver license and MR certification</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Commercial Procurement]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48237]]></requisitionid>
    <referencenumber><![CDATA[R48237]]></referencenumber>
    <apijobid><![CDATA[r48237]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48237/manager-commercial-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Commercial Category Management Procurement to join our Global Procurement team, supporting our India operations in a hybrid work model. In this role, you will lead category management enablement, transform data into actionable insights, and support global category strategies while collaborating with global procurement teams, data and analytics partners, and key collaborators. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead a team of associates and specialists to transform market intelligence and analytics into actionable insights that enable global category management strategy development.</p></li><li><p>Support the definition and implementation of global commercial category strategies aligned to regional and global business needs.</p></li><li><p>Deliver micro and macro market analysis, spend insights, supplier evaluation, and risk assessments to support strategy and partner engagement.</p></li><li><p>Partner with data and analytics teams to demonstrate internal and external data sources to identify trends, opportunities, and future strategy direction.</p></li><li><p>Facilitate sourcing processes by supporting RFP, RFQ, and RFI development and managing response collection, analysis, and comparative evaluations</p></li><li><p>Maintain and optimize category management templates, strategy decks, and stage-gate materials, ensuring consistent tools and repository governance.</p></li><li><p>Track and report internal requests handled by the category management enablement team in line with engagement plans and delivery commitments.</p></li><li><p>You foster collaboration, lead through influence, and operate with clarity and integrity in a global, matrixed, and evolving environment.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field with progressive experience in procurement, preferably in Pharma/Biopharma</p></li><li><p>Proven experience leading teams, processes, and suppliers across multiple categories in a global or multi-national environment</p></li><li><p>Strong knowledge of category management principles, including market analysis, spend analysis, supplier evaluation, and risk management</p></li><li><p>Demonstrated expertise in transforming data and market intelligence into actionable category insights and strategies</p></li><li><p>Experience leading and developing associate- and specialist-level professionals, including performance management, coaching, and career development.</p></li><li><p>Ability to build influential relationships with partners and suppliers to drive business outcomes.</p></li><li><p>Working knowledge of ERP systems and Source-to-Pay (S2P) platforms (e.g., Oracle, Zycus, GEP, Ariba) preferred.</p></li><li><p>Proficiency in standard business applications (Word, Excel, PowerPoint).</p></li><li><p>Ability to operate effectively with integrity, focus, and clarity in ambiguous environments and inspire change and improvement.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Ophthalmology]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48582]]></requisitionid>
    <referencenumber><![CDATA[R48582]]></referencenumber>
    <apijobid><![CDATA[r48582]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48582/associate-director-clinical-scientist-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Scientist, Internal Medicine team supporting Ophthalmology. In this role, you will contribute to the development, evaluation, planning and execution of Internal Medicine clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. Work in a matrix environment as part of a cross-functional team (with internal and external vendor representation) and may contribute to candidate development projects through early and/or late phase development. You will report to the Sr Dir/Director, Clinical Science, Internal Medicine and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY, Warren, NJ, Cambridge, MA</p><p><strong>Hybrid: </strong>4 days per week on site</p><p><strong>Discover your role:</strong></p><ul><li><p>May function as Clinical Scientist for program, and/or as delegate of Therapeutic area Clinical Scientist</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Utilizes proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late-stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Contributes to planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal collaborators</p></li><li><p>Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A bachelor’s Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/PharmD/MSc)</p></li><li><p>≥ 10 years of pharmaceutical clinical drug development experience, including basic knowledge of Ophthalmology</p></li><li><p>Proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills</p></li><li><p>Experience in all aspects of conducting global clinical trials and execution of clinical programs</p></li><li><p>We need an individual who is a strong team-player; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements</p></li><li><p>You possess strong cross-functional management, interpersonal skills, and strong attention to detail</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 19 Jun 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager - GA]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48661]]></requisitionid>
    <referencenumber><![CDATA[R48661]]></referencenumber>
    <apijobid><![CDATA[r48661]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48661/field-reimbursement-manager-ga/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Macon]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Reimbursement Business Manager (RBM) is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. We are seeking someone to support HCP offices in acquiring appropriate access to Regeneron products for patients. Ensuring efficient access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron Alliance product portfolio. You will drive and support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate and across multiple internal stakeholders, sales teams, Payer teams, and Alliance partners.</p><h3>A typical day may include the following:</h3><ul><li>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</li><li>Build and execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</li><li>Provide appropriate process, payer and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products (Dupixent).</li><li>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</li><li>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that aligns with Regeneron policies, processes, and standard operating procedures</li><li>Ensure individual training and knowledge is maintained to the level required to guarantee that personnel are seen as the most knowledgeable team in the industry as it pertains to access and reimbursement across Alliance therapeutic areas as well as future product markets</li></ul><br><h3>This role may be for you if:</h3><ul><li>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</li><li>You are an ethical, standout colleague and have can grow in a cross-functional team environment - contributing creative ideas and positive energy to the group.</li><li>You possess excellent organizational, project management, and communication skills.</li></ul><p>To be considered for this opportunity, you will possess the following:</p><ul><li>A bachelors' degree and Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience.</li><li>Experience working with products delivered through a Specialty Pharmacy network is essential.</li><li>Collaboration and proactive communication skills required.</li><li>Background in leadership and effective cross functional partnership a plus.</li><li>Established ability to work within an Account Management based structure.</li><li>Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors.</li><li>Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 08:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - Discovery Research, Regeneron Cell Medicines]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48687]]></requisitionid>
    <referencenumber><![CDATA[R48687]]></referencenumber>
    <apijobid><![CDATA[r48687]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48687/senior-associate-scientist-discovery-research-regeneron-cell-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated and innovative <strong>Senior Associate Scientist</strong> to join our discovery research team at Regeneron Cell Medicines. You will be performing immunological functional assays for analyzing genetically engineered human primary T cells (CAR-T or TCR T cells) from both early discovery programs as well as late-stage development programs' nonclinical studies that support regulatory submissions. We hope you are excited to be in a hands-on laboratory role in a fast-paced environment.</p><p><strong>As a Senior Associate Scientist, a typical day might include:</strong></p><ul><li>Contributing to preclinical research and development of CAR/TCR T cell therapies in solid tumor indications</li><li>Characterizing genetically modified primary human T cells via immunophenotyping using multi-color flow cytometry and molecular assays (PCR, library preps for NGS, RNA-Seq)</li><li>Developing and performing immunological functional assays to assess immune cell activation, anti-tumor cytotoxicity, proliferation, and cytokine secretion to evaluate the efficacy of CAR and TCR-based T-cell therapeutics</li><li>Designing experiments independently and contributing to the project direction</li><li>Maintaining an electronic lab notebook and documenting experiment results</li><li>Reviewing and presenting research data to the functional team</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Have a can-do attitude, are curious, and excel in creative problem solving</li><li>Can multi-task and manage time well </li><li>Can quickly adapt to new research areas and implement new techniques independently</li><li>Are scientifically rigorous, highly organized, and a self-starter with excellent attention to detail</li><li>Have strong verbal and written communication skills</li><li>Are self-motivated and enthusiastic about working in an interdisciplinary, collaborative research environment</li></ul><p><strong>In order to be considered for this role, you must have at least a </strong>BS/MS in immunology, cell biology or related field and 3+ years of relevant experience. Must have experience working in a biotech/pharmaceutical industry. We need someone with a strong understanding of immunology and cancer biology. Must have extensive experience in primary human immune cell isolation techniques and mammalian cell culture, including cell culture of primary human T lymphocytes. Experience working on in-vitro immunological studies and development of functional T cell assays using techniques such as multi-color flow cytometry, ELISA and cytotoxicity assays is required. Gene delivery into T cells or tumor cells using lentiviral vector transduction, CRISPR/Cas9 editing, and mRNA electroporation a plus. Experience with standard molecular biology techniques, including but not limited to PCR, qPCR, Westerns, and library preps for NGS, RNA-Seq also advantageous.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 25 Jun 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Oncology]]></title>
    <date><![CDATA[Fri, 26 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42074]]></requisitionid>
    <referencenumber><![CDATA[R42074]]></referencenumber>
    <apijobid><![CDATA[r42074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42074/medical-director-clinical-development-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials. This role may work on studies in melanoma, lung, breast, gastric, or colorectal cancers.</p></div><div><p><strong>As a Medical Director, a typical day may include the following:</strong></p><ul><li><p>Defines clinical trial-related goals and objectives.</p></li><li><p>Conducts literature and database research on clinical trials as needed</p></li><li><p>Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and with the Therapeutic Area Program Manager</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings.</p></li><li><p>Leads and supervises the Clinical Team to produce high quality program deliverables on schedule</p></li><li><p>Maintains and develops relationship with key study investigators</p></li></ul><p><br><strong>This role may be for you if:</strong></p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p><br><strong>To be considered for this role</strong>, you must have a MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience. Oncology clinical fellowship training with translational and/or clinical research experience is strongly preferred.</p><div><p><em>This role has a 4-day onsite minimum requirement in Tarrytown, NY or Warren, NJ.</em></p></div><div><div><div><div></div></div></div></div><p>#MDJOBSCD, #MDJOBS, #GDTher, #Oncology</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$280,700.00 - $379,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 15:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist Auditory Research]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48673]]></requisitionid>
    <referencenumber><![CDATA[R48673]]></referencenumber>
    <apijobid><![CDATA[r48673]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48673/associate-scientist-auditory-research/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Auditory group is seeking an associate scientist to support the development of therapies to treat hearing loss. You will have the opportunity to engage in cutting edge research as part of our discovery efforts and to contribute to the development of new medicines. </p><p><strong>As an Associate Scientist in the auditory group, your typical day might include: </strong></p><p>· Processing of tissue samples for molecular and histological assessments</p><p>· Conduct follow-up analysis of tissues from <em>in vivo</em> studies using qPCR, western blotting, immunohistochemistry and ELISA.</p><p>· Handling and caring for mice, including performing procedures such as blood and/or tissue sample collection or injections.</p><p>· Documentation of experimental procedures and results </p><p>· Data processing and statistical analysis using software such as FIJI, Excel, and Prism. </p><p>· Close collaborative interactions within and across research teams in the organization </p><p><strong>This role may be for you if you: </strong></p><p>· Enjoy working in an innovative and team-driven environment </p><p>· Are highly organized, detail-oriented, and motivated, with a creative approach to problem-solving. </p><p>· Are adaptable, flexible, and enjoy learning new techniques or switching tasks as needed. </p><p>· Are excited to contribute to the development of novel therapeutics </p><p>· Communicate openly and frequently with manager and team members </p><p><strong>To be considered for this role, you should have </strong></p><p>· B.S. or M.S. degree in Cell Biology, Neuroscience, Molecular Biology or a related discipline. </p><p>· Experience in protein readouts (ELISA, Western) is highly desirable. </p><p>· Experience in mouse handling is preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager QA Auditor GCP Strategy]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48491]]></requisitionid>
    <referencenumber><![CDATA[R48491]]></referencenumber>
    <apijobid><![CDATA[r48491]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48491/senior-manager-qa-auditor-gcp-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong></p></div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, GCP Audit Strategy, Global Development to join our Global Development Quality Assurance (GDQA), supporting our Global Development organization in a remote work mode. In this role, you will lead risk-based audit strategy programs and oversee compliance across therapeutic areas, studies, and audit activities while collaborating with Global Development teams, auditors, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p></div><div><p><strong>When & where: </strong></p></div><div><p>UK Remote - Ireland Remote </p></div><div><p><strong>Discover your role: </strong></p></div><div><ul><li><p>Lead risk-based audit planning across therapeutic areas and studies </p></li><li><p>Drive strategic audit programs using risk indicators from study teams </p></li><li><p>Ensure audits align with approved programs and scheduled timelines </p></li><li><p>Manage audit outcomes to identify trends and communicate risks </p></li><li><p>Represent quality assurance on complex cross-functional initiatives </p></li><li><p>Deliver reports and metrics to Global Development leadership </p></li><li><p>You collaborate effectively with stakeholders across global functions </p></li><li><p>You navigate ambiguity while prioritizing multiple complex activities </p></li><li><p>10-20% travel might be required </p></li></ul></div><div></div><div><p>This role requires: </p></div><div><ul><li><p>Bachelor’s degree with 8+ years of relevant industry experience </p></li></ul></div><div><ul><li><p>5+ years of GCP audit strategy or audit experience </p></li></ul></div><div><ul><li><p>Knowledge of FDA, EU, and ICH GCP regulations and guidance </p></li></ul></div><div><ul><li><p>Experience supporting or participating in regulatory inspections </p></li></ul></div><div><ul><li><p>Strong project management and stakeholder management capabilities </p></li></ul></div><div><ul><li><p>Excellent written and verbal communication skills with senior audiences </p></li></ul></div></div><div></div><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 22 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Internal Audit]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48400]]></requisitionid>
    <referencenumber><![CDATA[R48400]]></referencenumber>
    <apijobid><![CDATA[r48400]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48400/senior-manager-internal-audit/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our Quality Assurance internal auditing team. They are responsible for providing professional expertise, leadership, oversight and assisting with strategic planning for the Regeneron Industrial Operations and Product Supply (IOPS) Quality Auditing function. Quality (GMP) Auditing is responsible for maintaining the internal and external audit programs and performing internal and external audits for Regeneron IOPS, with primary emphasis on GMP, IT and Quality audits that may impact GMP operations and/or products. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>Location: Troy, New York, United States</li><li>Monday-Friday, 8am-4:30pm</li><li>25-30% travel domestic & occasionally international</li></ul><p>Discover your role:</p><ul><li>Maintain up-to-date expertise in global GxP regulations and standards (Chapter 21 of the Code of Federal Regulations, Eudralex Volume 4 and associated Annexes, ISO Standards, and ICH, WHO and IPEC Guidelines, etc ) and internal policies; track and communicate industry trends, agency expectations, and warning letters</li><li>Lead enterprise audit programs (internal and external) across GMP, IT, and quality: set strategy, build schedules, plan, assign, and personally lead/participate in audits; ensure inspection readiness</li><li>Manage cross-functional and supplier relationships (procurement, manufacturing, quality, external manufacturing, quality assurance, operations, audit clients) to meet audit schedules, quality deliverables, and organizational goals</li><li>Provide leadership and subject-matter guidance to auditors; recruit, select, train, and assess external proxy auditors; coach, mentor, and develop internal GMP auditing staff; maintain robust training and qualification programs</li><li>Ensure auditing processes meet regulatory and industry requirements; carry out adherence to procedures; document and assess deviations and changes per IOPS processes; uphold safety and operational standards</li><li>Develop, maintain, and present metrics and targets (including RTO) to senior leadership to measure strategy execution and the health of quality auditing systems</li><li>Drive continuous improvement by periodically reassessing auditing processes; translate ambiguity into actionable plans; proactively solve problems to prevent deviations and operational issues</li><li>Accountable for team performance and outcomes of internal/external audit programs, including managing leaders where applicable; support inspections as needed</li></ul><p>This role requires:</p><ul><li>BS/BA in Life Sciences; or equivalent combination of education and 8+ years of relevant experience</li><li>Experience with quality systems and auditing</li><li>Previous leadership/supervisory experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Predictive Analytics]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45118]]></requisitionid>
    <referencenumber><![CDATA[R45118]]></referencenumber>
    <apijobid><![CDATA[r45118]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45118/senior-manager-predictive-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated and talented Senior Manager of Predictive Analytics to join the Regeneron Genetics Center (RGC) to pioneer clinical use cases for proteomic and genomic data. In this role, you will develop and apply predictive models on the world’s largest integrated datasets of genomics, proteomics, and electronic medical records. </p><p>The role involves partnering with cross-functional teams, including Business Development, Laboratory staff, and other scientific groups, to foster collaboration and advance key initiatives. The candidate must have the ability to influence, with strong interpersonal skills. Excellent communication and interpersonal skills are also required as this candidate will be expected to work productively in a collaborative, team working environment.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Plan, develop, and execute large-scale analyses of proteomic and genomic datasets, with an emphasis on aging and age-related diseases.</p></li><li><p>Develop and implement methods for data harmonization and normalization across distinct cohorts to ensure consistency and reproducibility of results.</p></li><li><p>Evaluate statistical methods for disease risk prediction, and if necessary, develop new methods</p></li><li><p>Turn disease prediction needs from other teams and collaborators into concrete project/budget proposals</p></li><li><p>Stay informed on emerging market trends in disease prediction and applications of genomics data to continuously refine research directions</p></li><li><p>Deliver clear and concise presentations of genomics and proteomic findings to leadership, ensuring alignment with organizational goals and priorities</p></li><li><p>Ability to provide data to internal, external, and non-scientific audience </p></li><li><p>Design, implement, and optimize data pipelines for high-throughput genomic and proteomic workflows, ensuring efficient processing of large-scale proteomic datasets.</p></li><li><p>Develop and integrate robust quality control (QC) measures at multiple stages of analysis pipelines to ensure data accuracy, consistency, and reproducibility.</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Demonstrated expertise in statistics, machine learning and predictive analytics applied to biological data.</p></li><li><p>Demonstrated aptitude for translating research results into products or prototypes</p></li><li><p>Proven ability to independently lead and manage research projects from conception to completion.</p></li><li><p>Excellent communication and collaboration skills, with a track record of working effectively in interdisciplinary teams</p></li><li><p>Demonstrated ability to present data, insights, and recommendations effectively to stakeholders at all levels of the organization</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><ul><li><p>A PhD in a relevant field (e.g., human genetics, statistics, computational biology, or related disciplines) and at least five years of experience analyzing large-scale genomics data, or a bachelor's degree with at least 8 years of relevant experience.</p></li><li><p>Candidates with prior industry experience are preferred</p></li><li><p>Experience in exploratory data analysis, applied statistics, or software engineering is preferred in one or more of these domains</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager EDC Development]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47771]]></requisitionid>
    <referencenumber><![CDATA[R47771]]></referencenumber>
    <apijobid><![CDATA[r47771]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47771/senior-manager-edc-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>About Regeneron</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>As a Senior Manager, EDC Development & UAT, you will lead Clinical Database Development and User Acceptance Testing (UAT) activities across the global clinical trial portfolio. You will be responsible for ensuring high-quality, compliant EDC system delivery from design through release and post-production, while driving standardization, innovation, and continuous improvement across EDC processes.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong></p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Leading and developing a team of Managers and specialists across EDC Development, UAT, and QC functions, including performance management and career development</p></li><li><p>Overseeing resource planning, workload allocation, and capacity management across a global portfolio</p></li><li><p>Driving end-to-end EDC database development, including eCRF design, database build, edit check programming, and post-production change management</p></li><li><p>Providing oversight of UAT activities including planning, execution, defect management, and release readiness assessments</p></li><li><p>Establishing UAT standards, templates, and quality benchmarks to ensure consistency across internal and CRO-delivered systems</p></li><li><p>Partnering with CROs and cross-functional team members to ensure alignment on database development strategy and quality results</p></li><li><p>Driving innovation by evaluating and implementing new EDC technologies and automation tools</p></li><li><p>Leading SOP development, process standardization, and continuous improvement initiatives across EDC Development and UAT functions</p></li><li><p>Acting as an escalation point for complex technical, operational, and stakeholder challenges</p></li></ul><p><strong>This job may be for you if you have:</strong></p><ul><li><p>Extensive experience with Medidata Rave, including database design, edit check programming, and platform administration</p></li><li><p>Strong expertise in EDC development, UAT methodologies, and quality management processes</p></li><li><p>Solid understanding of regulatory requirements including 21 CFR Part 11, ICH-GCP, and CDISC standards</p></li><li><p>Proven leadership experience leading teams and driving performance in a matrix environment</p></li><li><p>Experience handling CRO/vendor relationships and ensuring high-quality deliverables</p></li><li><p>Strong strategic thinking, problem-solving, and stakeholder management skills</p></li><li><p>Ability to influence without authority and collaborate effectively with senior leadership and cross-functional teams</p></li><li><p>Good to have Medidata Builder Certification, TrialGrid experience and Exposure to programming (e.g., C#)</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Bachelor’s degree in mathematics, science, information systems, or a related field (advanced degree preferred)</p></li><li><p>Minimum of 8+ years of experience in biotechnology, pharmaceutical, or healthcare industry</p></li><li><p>At least 4+ years of direct EDC development experience</p></li><li><p>Minimum 3+ years of people management experience</p></li><li><p>Proven experience leading UAT and QC functions for EDC systems</p></li><li><p>Experience building governance frameworks, SOPs, and driving process improvements in regulated environments</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Data Management Process, Quality & Inspection Readiness]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48439]]></requisitionid>
    <referencenumber><![CDATA[R48439]]></referencenumber>
    <apijobid><![CDATA[r48439]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48439/director-data-management-process-quality-inspection-readiness/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Director, Data Management Process, Quality, and Inspection Readiness provides strategic leadership for Data Management quality, inspection readiness, and process excellence. This role is accountable for establishing and driving standardized approaches to Data Management quality, process frameworks, governance, compliance, and operational execution while ensuring compliance with global regulatory requirements, GCP, and industry best practices. The position serves as the primary Data Management lead for health authority inspections and audits, accountable for inspection preparation, response coordination, functional representation, and ensuring teams are prepared to effectively represent the function during regulatory inspections. In addition, the role also owns and drives the development, governance, and continuous improvement of Data Management processes, training programs, and operational frameworks to support standardized, scalable, compliant, and inspection-ready execution across the Data Management organization. </p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Warren, NJ, Tarrytown, NY or Armonk, NY</p></li><li><p>Hybrid; 4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><p><em>Data Management Quality and Inspection Readiness</em></p><ul><li><p>Provide strategic leadership for Data Management quality and compliance, ensuring consistent application of quality standards and resolution of complex and systemic issues.</p></li><li><p>Develop Data Management quality frameworks, including CRO oversight, issue management, escalation pathways, and quality oversight processes to support proactive identification and management of operational quality issues and compliance gaps.</p></li><li><p>Ensure Data Management quality frameworks and operational activities are aligned with GCP, ICH guidelines, global regulatory requirements, and company quality standards.</p></li><li><p>Lead quality event and CAPA management activities, including root cause analysis, and implementation of sustainable corrective and preventive actions. Leverage insights to strengthen controls, improve processes, and enhance inspection readiness.</p></li><li><p>Collaborate with CRO partners and internal stakeholders on quality events, issue escalation, remediation activities, and CAPA implementation.</p></li><li><p>Lead Data Management inspection readiness and audit support; direct preparation, coordination, and response for health authority inspections.</p></li><li><p>Lead and conduct independent, risk-based reviews of study documentation and operational conduct at defined and ad hoc timepoints to identify gaps, strengthen compliance, and ensure sustained inspection readiness.</p></li><li><p>Establish Data Management quality review processes to identify process gaps and deficiencies, training needs, and the documentation of risks, enabling early remediation.</p></li><li><p>Establish and leverage Data Management KPI & KQI frameworks to provide visibility into performance, data quality, & compliance trends, driving proactive decision-making, continuous improvement, & innovation across the portfolio.</p></li><li><p>Define, monitor, and perform effectiveness checks measures for Data Management quality, compliance, inspection readiness, training and process performance to drive continuous improvement and operational excellence.</p></li><li><p>Lead impact assessments for new and evolving regulatory requirements, ensuring appropriate updates to Data Management processes, quality standards, and operational practices.</p></li><li><p>Educate and guide the Data Management organization on quality standards, regulatory expectations, and inspection readiness practices.</p></li><li><p>Establish and maintain strong partnerships with Inspection Management and Quality stakeholders to ensure alignment on inspection readiness activities, quality standards, compliance expectations, and remediation strategies.</p></li><li><p>Oversee Data Management SharePoint repositories to support centralized access to current quality and inspection readiness documentation.</p></li></ul><p><em>Data Management Process and Training</em></p><ul><li><p>Own and drive the development, governance, and continuous improvement of Data Management processes to support scalable, standardized, compliant, and inspection-ready execution.</p></li><li><p>Develop and execute robust implementation and change management plans for new and revised Data Management processes to ensure consistent adoption, operational effectiveness, and sustainable execution.</p></li><li><p>Establish & maintain training frameworks to support consistent implementation through development, maintenance, and delivery of role-based training and guidance.</p></li><li><p>Lead the Data Management SME network to ensure designated subject matter expertise, process ownership, and functional support coverage across Data Management.</p></li><li><p>Oversee Data Management SharePoint repositories to support centralized access to current process and training documentation.</p></li><li><p>Serve as a Data Management representative in the Global Development Process Owner Network.</p></li><li><p>Establish and maintain strong partnerships with the Process & Procedures, Learning Center of Excellence, Change Management functions to ensure alignment on Data Management processes and training.</p></li><li><p>Lead and contribute to cross-functional process improvement initiatives as required.</p></li></ul><p><em>People Management</em></p><ul><li><p>Responsible for line management and performance of direct reports, including the development of competencies, coaching, and assessment of annual performance.</p></li><li><p>Provide leadership, mentorship, and guidance to direct reports, fostering skill development, knowledge sharing, and operational excellence.</p></li><li><p>Foster a culture of accountability, collaboration, continuous improvement, and quality.</p></li><li><p>Support prioritization and workload management to ensure effective utilization.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum Bachelor's Degree (Science, Health, Computing, or related field) with 12+ years in Clinical Data Management within the biotechnology, pharmaceutical or health related industry.</p></li><li><p>5+ years of people management, leadership, and mentoring</p></li><li><p>Expert knowledge of clinical data management principles, processes, quality frameworks, and inspection readiness practices within a global clinical development environment.</p></li><li><p>Deep understanding of global regulatory requirements and industry standards, including GCP, ICH guidelines, 21 CFR Part 11, ALCOA+ principles and inspection readiness expectations.</p></li><li><p>Demonstrated experience leading Data Management quality, compliance, inspection readiness, audit support and process governance activities.</p></li><li><p>Demonstrated experience developing, implementing, and continuously improving departmental processes, quality standards and frameworks, and operational controls.</p></li><li><p>Strong knowledge of quality management systems, CAPA processes, issue management, escalation frameworks, and continuous improvement methodologies.</p></li><li><p>Demonstrated experience supporting multiple health authority inspections across different health authorities (e.g., FDA, PMDA, MHRA, EMA, etc..) including inspection preparation, response coordination, remediation activities, and functional representation during regulatory inspections.</p></li><li><p>Experience establishing and leveraging KQI / KPI frameworks, effectiveness measures, and operational metrics to drive quality oversight, compliance monitoring, and process improvement.</p></li><li><p>Demonstrated ability to lead organizational change management initiatives, including implementation of new processes, quality standards, and operational frameworks.</p></li><li><p>Demonstrated success in solving complex business problems through strategic and critical thinking.</p></li><li><p>Proven ability to lead and influence within a matrix organization, driving alignment and outcomes with cross-functional stakeholders without direct authority</p></li><li><p>Proven ability to build strong collaborative relationships and influence alignment across key internal and external stakeholders.</p></li><li><p>Strong understanding of cross-functional activities and management of multiple and varied tasks with enthusiasm and attention to detail.</p></li><li><p>Excellent interpersonal, oral, and written communication skills.</p></li><li><p>Demonstrated ability to effectively lead and prioritize within a fast-paced, evolving, and highly regulated environment.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, Clinical Data Reporting]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48587]]></requisitionid>
    <referencenumber><![CDATA[R48587]]></referencenumber>
    <apijobid><![CDATA[r48587]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48587/specialist-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Specialist, Clinical Data Reporting to join our Data Management team, supporting clinical trial oversight and study-level data review in a hybrid role. In this role, you will produce accurate and consistent reporting outputs that drive data cleaning, medical review, and operational decision-making, while collaborating with clinical data management, technology partners, and cross-functional teams to deliver study-level reports on schedule. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Hyderabad, India (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Program and maintain standardized clinical data reports and listings used for participant-level data review, data cleaning, and operational oversight</p></li><li><p>Translate study reporting requirements into technical specifications and implement outputs using established frameworks and data standards</p></li><li><p>Build and validate data review listings, exception reports, reconciliation outputs between EDC and external data, and operational performance reports</p></li><li><p>You communicate clearly with cross-functional partners to clarify reporting needs and deliver outputs on schedule</p></li><li><p>Partner with clinical data management and technology teams to leverage data sources including the Scientific Data Lake, EDC systems, and external data streams</p></li><li><p>Monitor routine data refreshes, troubleshoot issues with accuracy, completeness, and integration, and contribute to automation and workflow streamlining</p></li><li><p>Keep reporting documentation, specifications, and outputs audit- and inspection-ready in line with GCP, ICH, GDPR, SOPs, and internal quality standards</p></li><li><p>You stay curious about reporting tools and methodologies, sharing knowledge of standards and processes to support team learning and continuous improvement</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's or Master's degree in Data Science, Computer Science, Life Sciences, or a related field</p></li><li><p>2+ years of experience in clinical data, data visualization, or related disciplines, with a background in building interactive reporting solutions, KPIs, and metrics to support clinical trial oversight</p></li><li><p>Proficiency in EDC systems (e.g., Medidata RAVE) and analytics, reporting, and data visualization tools such as SAS, R, Python, JReview, elluminate, Tableau, Power BI, or Spotfire</p></li><li><p>Strong understanding of clinical trial processes, clinical data standards (e.g., CDISC), and regulatory requirements (GCP, GDPR, HIPAA)</p></li><li><p>Experience with risk-based data review concepts, data quality standards, and data lifecycle management in a regulated environment</p></li><li><p>Experience with data lakes, data pipelines, data integration, automation, and reporting and analytics in a clinical research environment</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement - Third Party Risk Management]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48762]]></requisitionid>
    <referencenumber><![CDATA[R48762]]></referencenumber>
    <apijobid><![CDATA[r48762]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48762/director-global-procurement-third-party-risk-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Global Procurement - Third Party Risk Management to join our Global Procurement team, supporting the regional execution of our enterprise third-party risk management (TPRM) programme in a remote work mode. In this role, you will ensure third-party risks across suppliers, service providers, and external partners are identified, assessed, mitigated, and raised in line with the global TPRM framework, while collaborating with Procurement, Legal, Compliance, IP, Information Security, and other risk domain owners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a significant difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Uxbridge, UK (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Provide regional oversight and execution of the enterprise TPRM programme, ensuring consistent, risk-based application of third-party risk processes and acting as the escalation point for material or emerging risks.</p></li><li><p>Oversee the end-to-end third-party risk lifecycle: onboarding, due diligence, ongoing monitoring, issue management, and offboarding.</p></li><li><p>Maintain regional alignment with regulatory and industry standards, and partner with Compliance and risk domain owners on supplier assessments, issue remediation, and corrective action plans.</p></li><li><p>Support global governance bodies with regional insights and reporting, and define and monitor KPIs and KRIs to drive risk visibility.</p></li><li><p>Drive adoption of automation, AI, analytics, and data-driven tools within approved TPRM platforms to improve efficiency, scalability, and the quality of risk screening, monitoring, analysis, and reporting.</p></li><li><p>Partner with Procurement, Legal, Compliance, IP, Information Security, and other risk domain owners to manage third-party risks holistically, and act as a trusted regional advisor to business partners.</p></li><li><p>Develop the third-party risk team's capabilities, judgement, and partner engagement skills, and contribute to broader talent development across Global Procurement.</p></li><li><p>You operate with integrity, clarity, and focus through change and ambiguity, influencing cross-functional partners in a matrixed environment.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in a relevant field; advanced degree or certifications preferred.</p></li><li><p>12+ years of dynamic experience in Third Party Risk Management, preferably within pharmaceutical, biotech, or other regulated industries.</p></li><li><p>Previous people management experience.</p></li><li><p>Experience managing regional or multi-country risk management programmes.</p></li><li><p>Strong understanding of third-party risk domains, regulatory expectations, and governance models.</p></li><li><p>Experience with TPRM technologies and risk monitoring platforms, including application of automation and AI-enabled tools within risk or compliance processes, strongly preferred.</p></li><li><p>Proven ability to influence cross-functional partners, operate effectively in a matrixed environment, and work with integrity, clarity, and focus in conditions of change and ambiguity.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Accounting (Cost/Manufacturing) - Contract]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47511]]></requisitionid>
    <referencenumber><![CDATA[R47511]]></referencenumber>
    <apijobid><![CDATA[r47511]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47511/manager-accounting-costmanufacturing-contract/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This contractor role leads hands-on accounting support and systems enablement during a multi‑year ERP implementation, preparing and reviewing critical schedules and deliverables across inventory, cost accounting, fixed assets, leases, collaborations, and general ledger. In addition to core close and reporting activities, the role partners cross‑functionally with Manufacturing, Supply Chain, IT, Engineering, Facilities, and Finance to strengthen internal controls, drive standardization and automation, and ensure accurate, timely financial reporting.</p><p>This is a contract, on-site position based in our Rensselaer, NY facility. We anticipate the role running through end of November, 2027.</p><p><strong>A day in the life may look like:</strong></p><ul><li><p>Own preparation and review of monthly close deliverables across GL.</p></li><li><p>Contribute to standard cost establishment and maintenance in Oracle Process Manufacturing (OPM), including materials, labor, and overhead; perform variance analysis and actionable commentary</p></li><li><p>Analyze batch completions, production variances, inventory levels, and inventory status; partner with Manufacturing and Supply Chain to investigate and resolve issues</p></li><li><p>Support CMO inventory accounting and end‑to‑end reconciliations across the external supply chain</p></li><li><p>Assist with annual physical inventories and cycle counts for internal warehouses, CMOs, and 3PLs; track and resolve count differences and control gaps</p></li><li><p>Prepare and review journal entries, account reconciliations, and close checklists to meet deadlines with high quality</p></li><li><p>Manage fixed asset activities: capitalization, disposals, depreciation, reconciliations, and fixed asset register integrity</p></li><li><p>Analyze lease agreements to ensure accurate accounting under ASC 842; coordinate with Corporate Accounting on policy and complex arrangements</p></li><li><p>Support collaboration accounting (e.g., deferred inventory, COGS, partner reporting) and align with contractual terms and policies</p></li><li><p>Partner with Finance on budgets, forecasts, and manufacturing/operations variance analysis, linking operational drivers to P&L and balance sheet impacts</p></li><li><p>Develop and maintain accounting policies, procedures, and internal controls that meet SOX requirements; document and remediate issues</p></li><li><p>Serve as an accounting systems partner for Oracle OPM, Inventory, Order Management, and Financial modules; liaise with IT to troubleshoot issues and stabilize close</p></li><li><p>Identify and implement automation and process improvements; translate business needs into functional builds, use cases, and testing documentation</p></li><li><p>Implement end‑to‑end testing for ER improvementsts, upgrades, and new processes, including impact assessments, data validation, and UAT sign‑offs</p></li><li><p>Deliver executive‑ready outputs: reconciliations, bridges, variance analyses, KPI dashboards, and issue logs with root‑cause, risk, and remediation plans</p></li></ul><p><strong>This may be the right role for you if you:</strong></p><ul><li><p>Thrive in a contractor capacity that supplements FTEs during major ERP change, bringing structure, urgency, and calm to fast‑paced environments</p></li><li><p>Drive automation of recurring close tasks, reconciliations, exception monitoring, and data quality checks to reduce cycle time and error rates</p></li><li><p>Define data structures, hierarchies, and master data standards across OPM, Inventory, Order Management, and Financials to enable consistent reporting</p></li><li><p>Standardize processes and cross‑module controls for inventory, fixed assets, leases, and GL to improve accuracy and audit readiness</p></li><li><p>Translate ambiguous requests into clear options with assumptions, effort, risks, and recommendations for decision‑makers</p></li><li><p>Communicate crisply with cross‑functional partners and influence outcomes without direct authority</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><p>BS/BA in Accounting, Finance, Information Systems, or related field</p><p>Typically 7+ years of progressive accounting experience, with strong inventory and cost accounting; manufacturing experience required, biotech/pharma preferred</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - TACOMA, SPOKANE, WA]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48959]]></requisitionid>
    <referencenumber><![CDATA[R48959]]></referencenumber>
    <apijobid><![CDATA[r48959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48959/medical-account-specialist-ii-hematology-tacoma-spokane-wa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialist - Hematology- </strong><strong>Tacoma, Spokane, WA</strong></p><ul><li><strong>Geography: </strong><strong>Tacoma, Spokane, Montana</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Masters degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (West)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48128]]></requisitionid>
    <referencenumber><![CDATA[R48128]]></referencenumber>
    <apijobid><![CDATA[r48128]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48128/field-reimbursement-manager-neurology-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Los Angeles]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Los Angeles, (Metro) CA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (New York, Metro)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48126]]></requisitionid>
    <referencenumber><![CDATA[R48126]]></referencenumber>
    <apijobid><![CDATA[r48126]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48126/field-reimbursement-manager-neurology-new-york-metro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: New York, (Metro) NY</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager - Neurology (Mid South)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48132]]></requisitionid>
    <referencenumber><![CDATA[R48132]]></referencenumber>
    <apijobid><![CDATA[r48132]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48132/field-reimbursement-manager-neurology-mid-south/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Richmond]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Austin (Metro), TX, Jackson (Metro), MS, Little Rock (Metro), AR New Orleans (Metro), LA, Dallas (Metro), TX, Houston (Metro), TX, Austin (Metro), TX, Fort Worth (Metro), TX, San Antonio (Metro), TX<br> </li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Integration Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44508]]></requisitionid>
    <referencenumber><![CDATA[R44508]]></referencenumber>
    <apijobid><![CDATA[r44508]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44508/senior-automation-integration-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>We are seeking a highly skilled, experienced software Integration Engineer with experience in real-time data collection and analysis to join a diverse team of engineers, developers, analysts, and administrators to design, implement and support Data Acquisition and Analysis Systems. </p></div><div><p>As a Senior Automation Systems Integration Engineer<strong>,</strong> a typical day might include the following: </p></div><div><ul><li><p>Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures. </p></li></ul></div><div><ul><li><p>Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems. </p></li></ul></div><div><ul><li><p>Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines. </p></li></ul></div><div><ul><li><p>Supporting small manufacturing, engineering, and validation projects. </p></li></ul></div><div><ul><li><p>Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action. </p></li></ul></div><div><ul><li><p>Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols. </p></li></ul></div><div><ul><li><p>Reviewing cyber security vulnerabilities and risk pertaining to automation systems, software, and infrastructure </p></li></ul></div><div><ul><li><p>Creation, modification, and maintenance of automation system documentation </p></li></ul></div><div><p>This role might be for you if you: </p></div><div><ul><li><p>Have experience with OT applications, including SCADAs, HMIs, Historians, etc. </p></li></ul></div><div><ul><li><p>Are familiar with standing up large systems at the enterprise level </p></li></ul></div><div><ul><li><p>Have core knowledge related to ISE S95 and S88 principles and IT/Automation integration </p></li></ul></div><div><ul><li><p>Have familiarity with PLC communication, HMIs, computerized system design and maintenance of automation process control infrastructure </p></li></ul></div><div><ul><li><p>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better </p></li></ul></div><div><ul><li><p>Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly </p></li></ul></div><div><ul><li><p>Can balance changing priorities with increasing workload by making/communicating timely decisions </p></li></ul></div><div><p>To be considered for the Senior Automation Systems Integration Engineer position you ideally should have a bachelor's degree in Computer Science, Chemical, Mechanical, or Electrical Engineering and the following minimum years of relevant experience for each level: </p></div><div><ul><li><p>Senior Engineer: 5+ years </p></li></ul></div></div><div><div><ul><li><p>Principal Engineer: 8+ years</p></li></ul></div><div><p>Level will be determined based on qualifications relevant to the role</p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Precision Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44954]]></requisitionid>
    <referencenumber><![CDATA[R44954]]></referencenumber>
    <apijobid><![CDATA[r44954]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44954/director-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Precision Medicine group at Regeneron is responsible for designing, implementing, executing, analyzing and interpreting the overarching clinical biomarker strategies for therapeutic candidates during clinical development. We are seeking to hire a hands-on Precision Medicine Strategy Lead (PMSL) roles at the director level, with backgrounds in one or more therapeutic areas within the group. We are seeking someone to independently oversee the development and execution of biomarker strategies across one (or more) therapeutic areas depending on their areas of expertise, with a preference in obesity / metabolism pharmaceutical development.. The following therapeutic areas are in scope: Neurodegenerative Disorders, Cardiovascular Disease, Muscle and Metabolism Disorders, and/or Rare Genetic Diseases). In this highly matrixed role, they will design, develop, communicate at senior levels and operationally implement clinical biomarker strategies to support key programs in early and late stage drug development. Clinical technologies applied include biomarker assays, pharmacogenetic assessments, as well as other clinical and physiological testing devices. </p><p><strong>A typical day may include:</strong></p><ul><li><p>Enhancing our understanding of indications at a cellular and molecular level</p></li><li><p>Conducting novel biomarker discovery, qualifying new biomarkers/approaches to expedite proof-of-concept for new drug candidates.</p></li><li><p>Optimizing label claims for later stage candidates, enabling personalized medicine principles to be applied, as appropriate, in full development. </p></li><li><p>With a focus in therapeutic areas outside of Oncology, broad understanding of disparate biomarker technologies, and deep experience in biomarker assay development and validation in clinical drug development </p></li><li><p>Responsible for conducting in-depth literature and technology reviews pertinent to assigned clinical development programs within the TFA, identifying and pulling in experts in multiple disease areas, navigating and supporting the logistical and regulatory factors pertaining to clinical technologies.</p></li></ul><p><strong>This role may be for you if have experience with the following:</strong></p><ul><li><p>TA--level lead for implementation of strategic vision for clinical biomarkers in one or more therapeutic areas across multiple programs with multiple studies that will broadly enable advances in target identification, indication selection, early indication of biological activity and patient stratification/selection</p></li><li><p>Serve as an individual contributor and senior-level representative of Precision Medicine on development teams and deliver biomarker strategies to key programs from initial concept to execution, data delivery and results interpretation</p></li><li><p>Collaborate with Discovery Research and product development teams to facilitate appropriate incorporation of Precision Medicine and clinical biomarker strategies for molecules in discovery phases (leading to candidate molecule selection)</p></li><li><p>Represent Regeneron and work with colleagues from allied companies to develop and implement strategies for partnered alliances</p></li><li><p>Collaborate with clinical operations teams to implement specific biomarker and exploratory sample collection and analyses in all relevant clinical studies in selected programs</p></li><li><p>Design, oversee and manage internal and external research collaborations in areas of clinical technologies and translational research</p></li><li><p> Accountability for ensuring complex clinical assays used in programs in the TFA portfolio of clinical development are fit-for-purpose (whether developed and validated internally or externally)</p></li><li><p>Collaborate with internal Regeneron laboratories (e.g. Discovery Research, Molecular Profiling, Regeneron Genetics Center, DNA core, BioAnalysis, etc.) to develop plan for validation and application of research assays</p></li><li><p>Ensure timely delivery of results across selected programs, consistent with program team and senior management expectations in a way that increases the potential impact of Precision Medicine deliverables on Global Development programs</p></li><li><p> Contribute to and ensure the quality of Precision Medicine technical reports, study memos and clinical study reports, data reviews and interpretations, scientific publications and recommendations to development teams and management.</p></li></ul><p><strong>To be considered for this role</strong>, you must have a PhD and 10+ years of experience driving, managing, executing and delivering results for complex multi-functional projects. You have excellent communication and presentation skills and high emotional intelligence, organizational skills and effective team skills. Strong track record in mentorship and development of direct reports.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Medical Affairs, MASH]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45729]]></requisitionid>
    <referencenumber><![CDATA[R45729]]></referencenumber>
    <apijobid><![CDATA[r45729]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45729/senior-medical-director-medical-affairs-mash/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>The Senior Medical Director, Medical Affairs – MASH, will play a pivotal and highly visible strategic leadership role within the organization, reporting directly to the VP, Medical Affairs, General Medicine. This role is responsible for driving the medical strategy and execution for MASH assets, with a strong focus on strategic planning, cross-functional leadership, and external engagement. The Senior Medical Director will ensure all medical affairs activities are delivered with scientific excellence, integrity, and patient-centricity.</div></div><div><div><div><div><p><strong>A typical day in this role might look like: </strong></p><ul><li>Provides visionary leadership in the development, execution, and continuous refinement of medical strategy and tactics for assigned assets, ensuring alignment with corporate and global objectives. Champions the integration of scientific communications, publications, annual medical planning, and field communication strategies in partnership with key internal and external stakeholders.</li><li>Apply deep therapeutic area expertise and strategic business acumen to proactively identify and address evolving medical needs in clinical practice. Ensures the medically appropriate use of investigational medicines and anticipates future trends impacting patient care, policy, and access.</li><li>Directs and oversees the generation, management, and dissemination of robust clinical and non-clinical data. Drives high-impact publication strategies and ensures scientific content supports both the medical strategy and external stakeholder needs, maintaining the highest standards of accuracy and scientific rigor.</li><li>Leads cross-functional and cross-alliance teams with a focus on strategic alignment, collaboration, and excellence in execution. Fosters a culture of innovation and accountability, ensuring seamless coordination across medical, commercial, regulatory, and alliance partners.</li><li>Serves as a key strategic advisor and leader on global and US cross-functional teams, providing authoritative scientific and medical perspectives that inform and shape organizational strategy and decision-making.</li><li>Oversee the design, conduct, and reporting of Medical Affairs studies, ensuring scientific integrity, regulatory compliance, and alignment with strategic priorities. Provides mentorship and guidance to teams executing these initiatives.</li><li>Cultivates and expands long-term, strategic partnerships with clinical experts, societies, collaborative groups, advocacy organizations, payers, policy makers, and other external stakeholders. Acts as the primary ambassador for Regeneron, building trust and advancing shared goals in the MASH therapeutic area.</li><li>Leads prioritization and support for investigator-initiated studies, serving as a key decision-maker and member of internal Scientific Review Committees. Ensuring alignment with overall medical strategy and organizational objectives.</li><li>Overseas and ensures the scientific accuracy and compliance of all medical materials, including promotional and non-promotional content. Provides final approval and guidance to uphold the highest standards of scientific and ethical integrity.<br> </li></ul><p><strong>This role might be for you if: </strong></p><ul><li>Must have an MD or MD equivalent with a preference for specialized fellowship training in Gastroenterology or Hepatology</li><li>5 years of related industry experience in global or US medical affairs</li><li>Solid background and experience in drug development and life-cycle management</li><li>Experience with working in an alliance setting strongly preferred</li><li>Ability to lead technical and business discussions internally and externally and explain scientific/medical concepts to all levels</li><li>Ability to cultivate and maintain relationships with leading medical/scientific experts in the relevant fields</li><li>Ability to establish trust through the consistent demonstration of scientific expertise and satisfactory follow-through on requests from key opinion leaders</li><li>Strong leadership and management skills</li><li>Attention to detail in analyses, deliverables, and communications</li><li>Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management</li><li>A proactive self-starter who can lead work and manage others independently, with the ability to see the next step and take actions without prompting</li><li>Ability to juggle multiple projects</li><li>Thorough understanding of the healthcare environment including all external stakeholders</li></ul><p>#MDJOBSMA, #MDJOBS, #GDMAJobs</p></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, IT Applications - Laboratory Informatics]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45565]]></requisitionid>
    <referencenumber><![CDATA[R45565]]></referencenumber>
    <apijobid><![CDATA[r45565]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45565/senior-manager-it-applications-laboratory-informatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This position manages a team responsible for the day-to-day maintenance, support, and development of Regeneron's IT Applications portfolio, including but not limited to Empower CDS, SDMS, and other business supporting applications. Responsible for managing the application portfolio and associated support staff, driving audit readiness and compliance, and ensuring systems are maintained in a validated and compliant state — with particular emphasis on data integrity and 21 CFR Part 11 requirements. The role contributes to the strategic direction of the IOPS IT Applications function and collaborates closely with peer managers overseeing complementary application portfolios.</p><p>As an IT Applications Manager, a typical day might include the following:</p><ul><li>Manages a team of FTEs responsible for supporting and maintaining IT Applications, encompassing performance management, mentoring, coaching, and staff development.</li><li>Works with staff in the development of annual goals; performs monthly performance reviews and develops annual performance evaluations.</li><li>Works in close collaboration with peer managers overseeing different application portfolios to ensure alignment, shared best practices, and coordinated delivery across the broader IOPS IT Applications function.</li><li>Collaborates with global counterparts to support and maintain globally deployed QC systems in a consistent and compliant manner.</li><li>Drives audit readiness across the application portfolio; serves as a key point of contact during FDA inspections and internal audits, ensuring systems, audit trails, and documentation are inspection-ready at all times.</li><li>Ensures all supported applications are maintained in a compliant and validated state; proactively identifies and resolves data integrity and compliance issues in accordance with 21 CFR Part 11, applicable DI principles, SOPs, and policies.</li><li>Maintains responsibility for the accuracy of system documentation, including User Requirement Specifications, Design Specifications, Configuration Specifications, Test Plans, for validated systems.</li><li>Manages relationships with vendors, including vendor performance, contract adherence, and ensuring delivery of services in line with business and regulatory compliance requirements.</li><li>Develops and implements operational rigor using metrics and other operational controls; drives continuous improvement initiatives that enhance workflows, system reliability, and team efficiency.</li><li>Contributes to and supports the strategic vision and direction of the IOPS IT Applications function in collaboration with key stakeholders, including IT leadership, QA, and business units.</li></ul><p>This role may be for you if you:</p><ul><li>Recognize the importance of ALCOA+ principles and Data Integrity in Bio-pharmaceutical production, should display a high level of integrity in the performance of his/her work.</li><li>Passionate about quality / right first time.</li><li>Proven ability to support Applications in a highly regulated environment.</li><li>Knowledge of cGMP, GAMP, 21 CFR Part 11, Annex 11.</li><li>Knowledge of Regulatory Asset Manager Systems advantageous.</li><li>Excellent written and oral communication skills.</li><li>Possess excellent customer facing skills allowing comfortable traversing of cross departmental levels</li></ul><p>In order to be considered for this position, you must hold a Bachelor's degree in Information Technology, Science/Engineering, Computer Science or related field and</p><ul><li>Manager: 7+ years of experience, 3+ years of managing teams.</li><li>GMP Laboratory/IT setting preferred.</li><li>Senior Manager: 8+ years of experience, 4+ years of managing teams.</li><li>GMP Laboratory/IT setting preferred.</li><li>May consider experience in lieu of education. Level is determined based on qualifications relevant to the role.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Scientific Communications- General Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46059]]></requisitionid>
    <referencenumber><![CDATA[R46059]]></referencenumber>
    <apijobid><![CDATA[r46059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46059/director-scientific-communications-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Join our passionate team as the Director of Scientific Communications for General Medicine. In this pivotal role, you will lead the creation and alignment of our integrated medical communication strategies to advance medical knowledge and improve clinical care for patients. Collaborating with cross-functional teams, we develop evidence-based scientific communication platforms, ensuring content accuracy, accessibility, and impact. With a focus on innovation and collaboration, this role offers the opportunity to make meaningful contributions to partner engagement and patient outcomes.<br>This position requires on-site presence 4 days a week in Warren, NJ or Sleepy Hollow, NY, with occasional travel between sites. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong> <br>• Lead the development and execution of comprehensive Integrated Medical Communication Plans. <br>• Establish and communicate clear scientific communication of our objectives and tactical plans<br>• Partner with medical directors and key collaborators to devise congress strategies and oversee deliverables. <br>• Drive the creation of scientific and digital communication materials, including scientific communication platforms, lexicons, narratives, and disease-state education.<br>• Collaborate with the Congress Strategy and Planning team to ensure impactful booth designs and materials.<br>• Assess medical education gaps and find opportunities to create tailored, targeted, and timely content for diverse platforms and regions.<br>• Oversee the medical review process to ensure scientific accuracy, compliance, and ethical integrity of all materials.<br>• Manage project budgets and timelines in collaboration with the project manager.</p><p>T<strong>his may be for you if you: </strong><br>• Thrive in a collaborative, cross-functional environment. <br>• Can manage multiple projects, vendors, and priorities in a fast-paced environment. <br>• Are committed to ethical and compliance standards and have a “patient-first” value framework. <br>• Bring critical thinking and analytical skills to assess data and inform strategic decision-making. </p><p>To be considered it is required to have a PhD, MD, or PharmD with at least 8 years of relevant medical communication experience. Demonstrated expertise in medical communication strategies, congress planning, scientific content development, and medical education is required. Strong project management skills, ethical integrity, and the ability to work in a matrix organization are essential. <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Consumer Marketing (Ophthalmology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46178]]></requisitionid>
    <referencenumber><![CDATA[R46178]]></referencenumber>
    <apijobid><![CDATA[r46178]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46178/associate-director-consumer-marketing-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Marketing will contribute to the financial success of the Ophthalmology franchise. Main area of responsibility will be to implement and manage key elements of the U.S. Consumer Marketing plan, ultimately to drive demand for the product.</p><p>Specifically, this will include omnichannel campaign implementation including, Television, Print/Mail, digital and social media marketing execution, patient engagement tool/material development, patient education plan development and implementation, strategic content creation, Agency collaboration, materials and inventory management, budget management, management of review materials schedule and process.</p><p><strong>A Typical Day Might Look Like This:</strong></p><ul><li><p>Contributing to, and implementing consumer strategy, communications planning and tactical plans</p></li><li><p>Implementation of consumer initiatives and tactical plans</p></li><li><p>Delivering against omnichannel strategy and optimizing performance media programs against business goals and priorities</p></li><li><p>Manage & provide strategic input to Agency-led media planning that delivers against the goals of the business</p><ul><li><p>Evaluate, and provide feedback to, performance of media buys in an ongoing way ensure alignment with brand objectives</p></li><li><p>Work with internal Insights & Analytics Teams to expand our approach to measurement of campaigns and other omnichannel initiatives</p></li></ul></li><li><p>Developing innovative digital and social media programs that accelerate brand awareness and drive consumer action</p></li><li><p>Extend omnichannel strategies through an understanding of technical, data, and media system integration points and underlying platforms in a way that delivers incremental value to our customers, patients, and prospects</p><ul><li><p>Expand on compliant first-party data strategy that enriches our customer experience and drives value for our brand</p></li><li><p>Continue to refine our view of our customer, personas, segmentation, and related – business-critical user journeys</p><ul><li><p>Mature our approach to customer journeys in a way that delivers data, insights, and an evolution of our marketing activities</p></li></ul></li><li><p>Develop SEO-inspired content planning that delivers on the needs of our customers in a way that ladders up to critical success factors for our brand</p><ul><li><p>Content development in various formats including: long form, short form, video, social channel specific (Reddit vs Facebook vs LinkedIn), and email</p></li></ul></li><li><p>Develop a seamless holistic digital experience that fulfills on tactical goals including key site actions, engagement, and customer registrations for CRM programs</p></li><li><p>Enrich existing CRM strategy to be more inclusive of additional user needs, journeys, and conversion stages</p></li></ul></li><li><p>Driving selection of patient ambassadors and developing patient testimonials and videos</p></li><li><p>Implementing targeted communication programs</p></li><li><p>Representing promotional tactics for medical, legal, and regulatory team reviews and ensuring final deliverables are accurate and compliant.</p></li><li><p>Working closely with the cross functional marketing team</p></li><li><p>Managing budgets and closely monitoring performance, ensuring cost effective delivery of all programs while tracking and monitoring KPIs</p></li><li><p>Developing and managing patient education and engagement tools and materials- and related promotion through personal and digital distribution channels</p></li></ul><p><strong>If This Looks Like You:</strong></p><ul><li><p>Demonstrated competency in managing consumer/patient marketing programs</p></li><li><p>Demonstrated digital and social marketing experience</p></li><li><p>Demonstrated ability to work effectively, efficiently, and collaboratively with team members and across departments to develop and execute programs and materials</p></li><li><p>Demonstrated competency in agency management and budget management</p></li><li><p>Proven ability to work within regulatory, legal, and compliance guidelines</p></li><li><p>Demonstrated project management skills</p></li></ul><p>To be considered you have a Bachelor's Degree, MBA a plus. Demonstrated experience in marketing of biologics preferred. You have 10+ years of progressive marketing experience including at least 5 years in the Consumer space in pharmaceutical marketing. Demonstrated omnichannel digital marketing experience. Demonstrated Consumer marketing competencies in the pharmaceutical/biotech areas. Prior U.S. launch experience a plus. Strong interpersonal & presentation skills. Ability to communicate with all levels of the organization. Must be willing to travel ~10% (including weekend travel as needed). This is an office-based role, and the expectation will be to work in the office 4-days a week.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Operational Technology (OT) Data]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46099]]></requisitionid>
    <referencenumber><![CDATA[R46099]]></referencenumber>
    <apijobid><![CDATA[r46099]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46099/process-development-engineer-iii-operational-technology-ot-data/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Data Enablement and Analytics (DEA) team drives the future of digitalization within the Product, Analytics and Process Development (PAPD) organization. By making data usable, useful, and impactful DEA accelerates process development, supporting Regeneron’s mission to use the power of science to bring new medicines to patients over and over again.</p><p>In this role, you will drive the design, evolution, and governance of Operational Technology (OT) data systems, platforms, and tools that deliver high-quality data to lab specialists for real-time decision-making and offline analysis. You’ll implement value-focused data management solutions that increase asset value, meet immediate business needs, and build scalable data capabilities for the future.</p><h3>Responsibilities:</h3><ul><li>Provide technical leadership for OT data platforms by defining architecture principles, reference designs, and best practices that improve reliability, availability, and usability for manufacturing process development teams.</li><li>Ensure OT data availability, integrity, quality, security and accessibility by establishing and enforcing standards, controls, and audits that reduce incidents and outages.</li><li>Coach and mentor distributed data managers and junior engineers; set technical direction, review designs, and drive consistent execution against objectives and key results (OKRs).</li><li>Partner with lab specialists and IT to integrate process control and data acquisition systems into a unified architecture to advance data analytics capabilities and digital maturity.</li><li>Lead IT/OT convergence initiatives to align cybersecurity posture, compliance requirements, and network segmentation.</li><li>Communicate progress and decisions to stakeholders and leadership—create clear technical narratives, roadmaps, and status updates that enable informed decisions.</li></ul><h3>What A Typical Day in the Role Might Look Like:</h3><ul><li>Continuous Improvement: Translate user requests into prioritized backlog items; run grooming and planning sessions to deliver high-impact features.</li><li>Project Management: Design, lead, and implement cross-functional DEA programs (agile and waterfall); coach junior resources, unblock teams, ensure delivery against commitments.</li><li>Administration: Standardize and automate equipment onboarding; systematize access management with role-based controls; delegate routine tasks while instituting guardrails.</li><li>Support & Maintenance: Perform software updates and patching. Proactively monitor system health issues. Drive incident triage and root-cause remediation.</li><li>Knowledge Sharing: Serve as OT subject matter expert to PAPD and partner functions; lead evaluations of new applications and platforms; present proof-of-concept outcomes with clear recommendations.</li></ul><h3>This Role May Be for You If:</h3><ul><li>You are a champion for data-driven decision making and can articulate trade-offs across performance, security, compliance, and cost.</li><li>You uphold high standards for accuracy, quality and attention to detail.</li><li>You balance near-term delivery with long-term platform health, managing technical debt deliberately.</li><li>You enjoy mentoring, growing talent, and building repeatable processes that elevate team capabilities and outcomes.</li><li>You thrive in cross-functional environments—communicating clearly with technical and non-technical partners, and translating complex requirements into secure, scalable, maintainable data solutions.</li></ul><br><p>This role requires BS in Computer Science, Information Systems, Biomedical/Chemical/Electrical Engineering, or related field with 10+ years of proven experience, or MS with 7+ years or a PhD with 0-3 years. Preferably, with 5+ years with AVEVA PI System (Data Archive, Asset Framework) and Ignition SCADA, including high-availability design, data modeling, and integrations. Other preferred experience: SQL experience in a database owner role, demonstrated proficiency in design, deployment, and lifecycle management of OT data systems across high-availability industrial architectures, and familiarity with control systems architecture, industry standards and communication protocols (ISA-95, S88, OPC, MQTT). A working knowledge of continuous and batch manufacturing processes, associated data sources, software integration, consumption and data analytics tools and a foundational knowledge of lab-based automation software (e.g. Unicorn, Biobrain Supervise, FactoryTalk, Empower) is a plus. Growing proficiency in Python for automation, data pipelines, and tooling. Familiarity with the concepts of Industry 4.0, digitalization, and IT systems that drive IT/OT convergence</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - AAV (CDMS) - Analytical and Biological Mass Spectrometry (ABMS)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46347]]></requisitionid>
    <referencenumber><![CDATA[R46347]]></referencenumber>
    <apijobid><![CDATA[r46347]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46347/senior-scientist-aav-cdms-analytical-and-biological-mass-spectrometry-abms/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Pharmaceutical's Analytical and Biological Mass Spectrometry Group (ABMS), located in Tarrytown, NY, is seeking a highly motivated Sr. Scientist. In this role, you will work in an innovative mass spectrometry (MS) lab and develop LC-MS methods for characterizing biotherapeutic products to support all stages of drug development, from early-stage candidate selections to late-stage regulatory submissions. You will conduct and develop innovative technologies to support a diverse Regeneron's R&D pipeline. </p><p><strong>A Typical Day in the Role Might Look Like:</strong> </p><ul><li><p>Design, execute, and clearly communicate analytical characterization for biotherapeutics, including adeno-associated virus (AAV), monoclonal and bispecific antibodies, Fc-fusion proteins, and other modalities, to support drug development. </p></li></ul><ul><li><p>Lead and execute characterization activities to evaluate and elucidate critical quality attributes such as charge variants, size variants, and post-translational modifications, with an emphasis on charge detection mass spectrometry (CDMS) and related native-MS approaches. </p></li></ul><ul><li><p>Provide analytical support for cross-functional teams, including formulation development, upstream/downstream process development, and manufacturing to solve drug development challenges. </p></li></ul><ul><li><p>Proactively advance LC-MS characterization of biotherapeutics by developing innovative techniques that address evolving developmental needs and improve operational efficiency. </p></li></ul><ul><li><p>Independently conduct sample preparation and LC-MS analyses in compliance with SOPs, and document experimental procedures and results in electronic laboratory notebook (ELN). </p></li></ul><ul><li><p>Author and review regulatory submission documents, including IND, comparability, and BLA reports, and contribute to manuscripts for peer-reviewed publications. </p></li></ul><ul><li><p>Represent analytical development on project teams, provide subject matter expertise, and communicate results at internal and external meetings.<strong> </strong> </p></li></ul><p><strong>This Role Might Be For You If You:</strong> </p><ul><li><p>You thrive in a fast-paced, collaborative environment and consistently deliver results with efficiency and ownership. </p></li></ul><ul><li><p>You quickly learn new technologies, tackle complex problems, and have a passion for science. </p></li></ul><ul><li><p>You are self-motivated and proactive, prioritizing effectively, and driving work forward with minimal supervision. </p></li></ul><p><strong>To be considered for this role, you must have</strong> a BS (10+ years), MS (7+ years) or PhD degree (0-3+ years) in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a closely related field. Experience with charge detection mass spectrometry (CDMS) is strongly preferred. Experience applying LC-MS to extended characterization of AAV and monoclonal antibodies to support product and process development is a plus. Extensive experience with advanced mass spectrometers (Q Exactive Plus, Q Exactive UHMR, Q-TOF, etc.), liquid chromatography, and data processing software (Protein Metrics, Skyline, UniDec etc.) is desired. Experience with experimental design and data analysis (e.g., molecular modeling, graphing, and statistical analysis) is a plus. Please copy and paste the desired job description for this role here. If you need a copy of an existing job description please reach out to TA or work with your HR Business Partner to develop one for a new role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Manager QA Drug Product (Filling)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46662]]></requisitionid>
    <referencenumber><![CDATA[R46662]]></referencenumber>
    <apijobid><![CDATA[r46662]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46662/sr-manager-qa-drug-product-filling/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently seeking a Sr Manager Quality Assurance to join our internal QA Drug Product Manufacturing team. This role is responsible for quality floor oversight of the filling (i.e. equipment prep, formulation, and filling) operations for SA12.</p><p>As a Sr. Manager QA, a typical day might include the following:</p><ul><li>Provide leadership to multiple teams under your supervision, including being responsible for</li><li>Quality oversight of all equipment prep, formulation, and filling (multiple lines)</li><li>Responsible for programs that support the department, for example: area walkthroughs</li><li>Support development and growth of team, including your people leaders</li><li>Leadership point of contact for escalation of events, process updates, etc.</li></ul><p>This role might be for you if you have:</p><ul><li>Proven leadership in cGMP environments, including experience speaking and preparing for regulatory inspections and audits.</li><li>Strong collaboration and communication cross-functionally</li><li>Ability to think critically, and continuously improve processes</li><li>Ability to lead a department through a fast-paced and dynamic environment</li></ul><p>Gowning and Environment </p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </p></li></ul><p>To be considered for the Sr. Manager Quality Assurance you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS/BA in Life Sciences or related field and 8+ years of experience. Experience in fill/finish manufacturing is preferred. Previous supervisory/ people leadership experience is required. May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Automation Integration Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47031]]></requisitionid>
    <referencenumber><![CDATA[R47031]]></referencenumber>
    <apijobid><![CDATA[r47031]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47031/principal-automation-integration-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly skilled, experienced software Integration Engineer with experience in real-time data collection and analysis to join a diverse team of engineers, developers, analysts, and administrators to design, implement and support Data Acquisition and Analysis Systems. </p><p>As a Principal Automation Systems Integration Engineer<strong>,</strong> a typical day might include the following: </p><ul><li><p>Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures. </p></li></ul><ul><li><p>Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems. </p></li></ul><ul><li><p>Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines. </p></li></ul><ul><li><p>Supporting small manufacturing, engineering, and validation projects. </p></li></ul><ul><li><p>Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action. </p></li></ul><ul><li><p>Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols. </p></li></ul><ul><li><p>Reviewing cyber security vulnerabilities and risk pertaining to automation systems, software, and infrastructure </p></li></ul><ul><li><p>Creation, modification, and maintenance of automation system documentation </p></li></ul><p>This role might be for you if you: </p><ul><li><p>Have experience with OT applications, including SCADAs, HMIs, Historians, etc. </p></li></ul><ul><li><p>Are familiar with standing up large systems at the enterprise level </p></li></ul><ul><li><p>Have core knowledge related to ISE S95 and S88 principles and IT/Automation integration </p></li></ul><ul><li><p>Have familiarity with PLC communication, HMIs, computerized system design and maintenance of automation process control infrastructure </p></li></ul><ul><li><p>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better </p></li></ul><ul><li><p>Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly </p></li></ul><ul><li><p>Can balance changing priorities with increasing workload by making/communicating timely decisions </p></li></ul><p>To be considered for this position you ideally should have a bachelor's degree in Computer Science, Chemical, Mechanical, or Electrical Engineering and the following minimum years of relevant experience for each level: </p><ul><li><p>Senior Engineer: 5+ years </p></li></ul><ul><li><p>Principal Engineer: 8+ years</p></li></ul><p>Level will be determined based on qualifications relevant to the role</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - Bioanalytical & Biomarker Technologies]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47134]]></requisitionid>
    <referencenumber><![CDATA[R47134]]></referencenumber>
    <apijobid><![CDATA[r47134]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47134/senior-associate-scientist-bioanalytical-biomarker-technologies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a dynamic <strong>senior associate scientist</strong> to join bioanalytical & biomarker technologies group. The candidate will design and execute analytical and bioanalytical method to support biotherapeutics discovery and preclinical development. The individual should be experienced in executing HPLC and/or LC-MS based methods from sample preparation, instrument operation to data analysis. The successful candidate will be expected to work cross-functionally in a collaborative, fast-paced, multidisciplinary team environment and have the opportunity to explore new technologies while growing technical depth.</p><p><strong>A Typical day in this role looks like:</strong></p><div><ul><li>Design, execute, and troubleshoot LC‑MS and HPLC methods for analytical characterization of bioconjugates and bioanalytical quantification of therapeutics.</li><li>Support a range of modalities—including monoclonal antibodies (mAbs), antibody–drug conjugates (ADCs), siRNA/oligonucleotides, and endogenous biomarkers—across diverse biological matrices.</li><li>Perform end‑to‑end sample preparation (e.g., LLE, SPE, affinity capture, enzymatic digestion, homogenization) and operate LC‑MS/MS workflows from instrument setup to data analysis.</li><li>Analyze and interpret results; summarize findings, propose next steps, and present data at internal meetings.</li><li>Document experiments, methods, and results in electronic lab notebooks (ELNs) with clarity and rigor; contribute to SOPs and method documentation.</li><li>Maintain instruments and general lab readiness; troubleshoot systems and ensure data integrity and instrument uptime.</li><li>Evaluate and implement new platforms, workflows, and automation to improve throughput, sensitivity, and robustness.</li><li>Prioritize effectively across multiple projects and timelines, collaborating closely with colleagues in discovery biology, DMPK/PK‑PD, and process/analytical teams.</li></ul></div><p><strong>This role may be for you, if you have experience: </strong></p><ul><li>BS or MS degree in Chemistry, Biochemistry, Pharmaceutical Science or a related discipline with 3+ years hand-on experience.</li><li>Experience in liquid chromatography and/or mass spectrometry is preferred, with the ability to execute, qualify and optimize analytical methods.</li><li>Hands on experience in sample preparation techniques (LLE, SPE, affinity capture, enzymatic digestion, homogenization, etc.); experience with automation platforms is a plus.</li><li>Detail-oriented, good interpersonal and effective technical communication skills (written and verbal).</li><li>Ability to manage multiple projects in a fast-paced environment.</li><li>Collaborative team player with a growth mindset to quickly adapt to evolving priorities and continuously learn to embrace new challenges.</li><li>Previous exposure in bioanalysis of LC-MS based small molecule, oligonucleotides, biomarkers and biotherapeutics assay development is beneficial.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47175]]></requisitionid>
    <referencenumber><![CDATA[R47175]]></referencenumber>
    <apijobid><![CDATA[r47175]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47175/senior-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an experienced Engineer to join our growing Project Engineering team. Our team designs, specifies and commissions new and renovated biopharmaceutical process and clean utility equipment. We provide engineering support and lead deviation investigations for existing equipment and manufacturing processes to support the production of our life-changing medications.</p><p>As a Senior Project Engineer, a typical day might include the following:</p><ul><li>Designing and specifying cGMP process equipment, piping, and/or controls including development and review of engineering documentation</li><li>Managing mid-to-large sized projects related to process equipment and clean utilities including start-up and commissioning</li><li>Leading the design review, site acceptance and installation of equipment</li><li>Preparing piping and instrumentation diagrams and other related drawings</li><li>Developing Process Flow Diagrams for manufacturing processes</li><li>Supporting QA/Validation department by preparing design documents and assisting in protocol execution</li><li>Assisting in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations and test plans for executing modification change control documentation</li><li>Supervising mechanical, electrical, and automation and engineering contractors</li><li>Traveling up to 10% of the time, both domestically and internationally</li></ul><p>This position might be for you if you:</p><ul><li><p>Are interested in having a broad scope with a variety of tasks, seeing the entire process, not just specific equipment or processes</p></li><li>Enjoy solving puzzles and challenges, supporting investigations across the business</li><li>Have a desire to contribute to elements of design work by helping to specify and translating customer needs into equipment</li><li>Want to do more than just project management or troubleshooting, balancing your technical and project management skills</li><li>Have a solid understanding of process control systems and automation</li><li>Are skilled at planning and tracking project activities and schedules</li><li>Are thoroughly knowledgeable with engineering documentation required for cGMP process equipment as well as sanitary equipment design requirements</li><li>Have working knowledge of biopharmaceutical equipment</li><li>Have demonstrated strengths with strong interpersonal, cross-cultural communication</li><li>Are adept at building and maintaining relationships and leading without direct authority</li><li>Show resiliency and flexibility in the face of challenging situations</li></ul><p>Qualified candidates must have a Bachelor's degree Chemical Engineering or Biochemical Engineering (or another relevant Engineering discipline) and the following minimum years of experience in project/process engineering or an equivalent combination of education and experience. Direct experience with biopharmaceutical process equipment is preferred.</p><ul><li>Senior Project Engineer: 5+ years</li><li>Principal Project Engineer: 8+ years</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Sample Management Specialist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47257]]></requisitionid>
    <referencenumber><![CDATA[R47257]]></referencenumber>
    <apijobid><![CDATA[r47257]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47257/sr-sample-management-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A Sr. Sample Management Specialist independently supports biobanking operations efficiently and effectively while managing sample data processes. Possesses expertise in the understanding of clinical and non-clinical study protocols and associated documentation. Manages biospecimen operations for assigned clinical/non-clinical studies and research initiatives, demonstrating strong program and data management skills and decision-making abilities with limited guidance. Works closely with clients and thoroughly understands client processes to ensure deliverables are met. The incumbent is proactive in assessing and investigating new opportunities that will lead to increased efficiencies and improved productivity with regards to biobanking operations.</p><p><strong>In this role a typical day might include the following:</strong></p><ul><li>Responsible for the interpretation of clinical/non-clinical study protocols and associated study documentation as it pertains to biospecimen management. Independently executes study reference file creation by interpreting protocols and other applicable data inputs.</li><li>Manages biosample operations for assigned clinical/non-clinical studies to ensure company deliverables are met and objectives are achieved under limited guidance.</li><li>Manages the execution of reconciliation and data cleaning of biospecimens to drive deliverables forward.</li><li>Collaborates with Data Management to draft and review Data Transfer Specifications.</li><li>Liaises with Global Clinical Development and Central Laboratories to provide input, planning, and integration of biosample operations and data transfers.</li><li>Creates and/or reviews sample collection instructions to be incorporated in the study lab manual.</li><li>Independently assigns and coordinates sample management activities for assigned programs to support high demand tasks.</li><li>Independently collaborates with internal and/or external stakeholders to facilitate data discrepancy resolution.</li><li>Proactively identifies and troubleshoots issues in area of technical expertise or assignment appropriately.</li><li>Independently handles high priority and high-volume tasks within the appropriate timeframe while maintaining accuracy. Operates effectively in ambiguous and complex situations. Anticipates changing priorities and initiates actions with the appropriate parties.</li><li>Leads efforts to improve both physical and electronic inventory management systems. Pro-actively brings external cutting-edge technology and/or ideas to the department. Sought out for advice in area(s) of specialization.</li><li>Provides cross-functional support to other sample management teams, as needed.</li><li>Facilitates data reporting needs for clinical/non-clinical/research study queries surrounding sample inventory.</li><li>Actively contributes to meetings. May lead team meetings to discuss deliverables, resourcing, and sample management related issues.</li><li>May supervise individual contributors, including responsibility for goal setting, performance evaluations and development.</li><li>Trains and provides leadership and guidance to other laboratory staff.</li><li>Facilitates sample transfer documentation and review, as applicable.</li><li>May participate in software validation and/or change control activities.</li><li>Works closely with Quality Control (QC) to address findings and ensure data is captured appropriately in LIMS.</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Has advanced knowledge of LIMS software. Executes LIMS functions to support sample management activities.</li><li>Has an advanced knowledge of Microsoft Excel and can independently analyze and interpret discrepancies in sample metadata with high quality.</li><li>Works closely with Quality Control (QC) to address findings and ensure data is captured appropriately in LIMS.</li><li>Has an advanced knowledge of the ELN and uses it for data documentation.</li><li>Proactively ensures a state of audit readiness. Actively participates in the preparation of supporting documents for Quality Assurance & Auditing (QAA), as applicable. Participates in study audit activities.</li><li>Maintains effective verbal and written communication both internally and with external collaborators and vendors. Communicates with CRO’s and third-party vendors to support sample management responsibilities.</li><li>Ensures compliance and proper documentation in accordance with working instructions, SOPs, and applicable regulations.</li><li>Conducts him /herself with professionalism and integrity while consistently driving results forward.</li><li>Pro-actively collaborates and leverages relationships within and across departments.</li><li>Operates effectively in the face of ambiguity and change.</li><li>Communicates and collaborates effectively across levels and groups in different settings, conveying information in a compelling and articulate way.</li><li>Drives conversation and actively seeks out and/or creates opportunities to develop their skills and/or knowledge base to further grow their depth and breadth</li><li>Responsible for his/her own safety in the laboratory, as well as for the safety of co-workers and visitors.</li></ul><p><strong>To be considered for this role</strong>, you must have a Bachelor’s degree with 6 years of relevant post-degree laboratory experience or a Master’s degree with 4 years of relevant post-degree laboratory experience.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Preclinical & Translational PK/PD]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47275]]></requisitionid>
    <referencenumber><![CDATA[R47275]]></referencenumber>
    <apijobid><![CDATA[r47275]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47275/associate-director-preclinical-translational-pkpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of Translational/Preclinical Modeling develops and implements quantitative and mechanistic PK/PD models to aid in the understanding of target biology, therapeutic modality selection/optimization, and contributes to early clinical trial dose selection and/or design and advancement and strategic direction of modeling and simulation sciences.</p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Independently develops and implements quantitative and mechanistic mathematical PK/PD models that inform preclinical-to-early clinical translation, including human efficacious dose predictions and first-in-human dose selection.</p></li><li><p>Actively contributes to the advancement and strategic direction of modeling and simulation sciences</p></li><li><p>Provides expert support to pre-clinical PK/PD project representatives and R&D project teams to design, execute and interpret in vitro and in vivo quantitative pharmacology studies. This included working with the Research PK group to optimize use of mouse PK data to inform translation to nonhuman primate and human PK.</p></li><li><p>Effectively integrates and summarizes modeling and simulation analyses into useable information for multidisciplinary project teams.</p></li><li><p>Remains apprised of emerging science and literature, and effectively collaborates with subject matter experts in Clinical Pharmacology, Quantitative Pharmacology and R&D to advance modeling and simulation sciences.</p></li><li><p>Presents work at internal/external scientific meetings and publishes work in scientific journals</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>Experience using one or more modeling and simulation platforms (e.g., Phoenix NLME, NONMEN, Monolix, ADAPT, MATLAB, SimBiology, etc.)</p></li><li><p>Strong theoretical and practical foundation in pharmacokinetics, including non-compartmental, compartmental, PK/PD and PBPK.</p></li><li><p> Effectively work in a fast-paced, highly-matrixed team-based environment and leverages scientific reasoning to influence key stakeholders.</p></li><li><p>Ability to learn new areas of biological sciences to develop quantitative and mechanistic PK/PD models for emerging therapeutic modalities.</p></li><li><p>Familiarity with biotherapeutic modalities, including monoclonal and bispecific antibodies, gene therapy, CAR-T, siRNAs and other targeting agents preferred</p></li></ul><p><strong>To be considered for this position, you must have:</strong></p><p>Ph.D. or M.S. in pharmacokinetics, pharmaceutical sciences, engineering, applied mathematics or related disciplines with a track record of applying quantitative and mechanism-based PK/PD modeling and simulation approaches to advance the discovery and development of therapeutics. Greater than 6 years of pharmaceutical industry or related experience in developing and applying mechanism-based PK/PD models to guide R&D teams from early discovery to IND-stage clinical development.</p><p><strong> </strong></p><p><strong> </strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-South Central]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47577]]></requisitionid>
    <referencenumber><![CDATA[R47577]]></referencenumber>
    <apijobid><![CDATA[r47577]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47577/regional-director-neurology-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the South Central Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: South Central (Texas and Louisiana)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, PV Innovation]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47621]]></requisitionid>
    <referencenumber><![CDATA[R47621]]></referencenumber>
    <apijobid><![CDATA[r47621]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47621/director-pv-innovation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Director of PV Innovation to join our Patient Safety Organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, PV Innovation is responsible for leading the development, implementation, and governance of AI capabilities that deliver measurable operational value and align to broader pharmacovigilance (PV) technology strategy. They are the primary point of contact for translating PV business needs into scalable digital solutions, while ensuring responsible, compliant, and secure adoption of AI technologies. </p><p><strong>This role might be for you if can/have: ​</strong></p><ul><li><p>Define and communicate the AI function vision, strategy and governance structure in alignment with business goals </p></li><li><p>Identify opportunities to leverage AI across PV processes to improve efficiency, insights, and scalability </p></li><li><p>Support the definition and execution of the GPS digital innovation strategy, providing AI expertise and technical input to the Executive Director, PV Innovation, GPS </p></li><li><p>Translate PV business requirements into scalable AI-enabled solutions and digital capabilities </p></li><li><p>Establish and maintain architecture, data, security, and Responsible AI standards and guardrails for PV AI initiatives </p></li><li><p>Oversee the implementation and scaling of AI solutions across GPS, ensuring solutions are fit-for-purpose and deliver measurable value </p></li><li><p>Ensure AI-enabled solutions comply with GxP, validation, data integrity, privacy, and regulatory requirements </p></li><li><p>Partner with key technology teams (e.g., GD IT, Cloud, Dev Ops, AI & Digital, Compliance) to ensure technology alignment, platform integration, and scalable deployment </p></li><li><p>Provide operational insights and emerging technology opportunities to inform the broader PV digital innovation roadmap </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum Bachelor's degree with 12+ years (Or MS with 10+) of experience in pharmacovigilance, safety systems, digital innovation, data science, or AI-enabled technology within the life sciences industry </p></li><li><p>Proven hands on AI expertise can be considered as a substitute for total years of required experience. </p></li><li><p>Demonstrated experience working at the intersection of safety operations and technology </p></li><li><p>Strong knowledge of AI and advanced analytic applications within regulated environments </p></li><li><p>Strong understanding of pharmacovigilance processes and safety systems (e.g., safety databases, signal detection tools, reporting platforms) </p></li><li><p>Knowledge of AI governance, Responsible AI frameworks, and data security standards </p></li><li><p>Ability to lead cross-functional initiatives across Safety, IT, and digital teams </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Project Manager, External Manufacturing (CMO Site Selection)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47617]]></requisitionid>
    <referencenumber><![CDATA[R47617]]></referencenumber>
    <apijobid><![CDATA[r47617]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47617/project-manager-external-manufacturing-cmo-site-selection/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Project Manager position within our External Manufacturing organization. Using strong project management experience and knowledge of external manufacturing, the Project Manager is responsible for evaluating and leading technology transfer projects from IND Project Approval (IPA) through Contract Manufacturing Organization (CMO) selection, as well as providing flexible project management support across the External Manufacturing portfolio. This role collaborates with cross-functional departments and CMOs to plan, manage, and drive project activities within agreed quality, scope, budget, and time. Builds and maintains productive relationships with a wide variety of internal and external stakeholders and ensures superior quality and timeliness of project deliverables.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Leads the evaluation and execution of technology transfer projects from IND Project Approval (IPA) through CMO selection, ensuring alignment with the overall life cycle management strategy.</p></li><li><p>Manages the planning and execution of deliverables for assigned External Manufacturing projects related to molecule-specific programs, including Technical Transfers, Process Validation, new CMO selection, and CapEx.</p></li><li><p>Acts as single point of contact for assigned project-related communications with CMOs and internal Regeneron stakeholders, including the CMC Program Manager.</p></li><li><p>Leads cross-functional teams and prioritizes project activities using excellent organizational, communication, and time management skills.</p></li><li><p>Ensures teams and stakeholders are aligned on one single External Manufacturing project plan.</p></li><li><p>Plans and tracks project activities, coordinating contingency and risk mitigation planning throughout the project lifecycle.</p></li><li><p>Facilitates regular project-focused meetings with CMOs and working teams (technical transfer, validation, new product launch, etc.).</p></li><li><p>Ensures meeting minutes and weekly/monthly reports are completed and distributed accurately.</p></li><li><p>Provides flexible project management support across the External Manufacturing portfolio as business needs evolve.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Strong project management, interpersonal, cross-cultural communication, negotiation, and problem-solving skills.</p></li><li><p>Ingenuity, creativity, and resourcefulness in a sometimes evolving and ambiguous environment.</p></li><li><p>Ability to provide clear direction to others in ambiguous situations and environments.</p></li><li><p>Ability to drive proactive resolution of project-related issues with tact, diplomacy, and composure.</p></li><li><p>Resiliency and flexibility in the face of challenges and adversarial situations.</p></li><li><p>Ability to understand and listen to team members and stakeholders while fostering a productive team environment toward one common project objective.</p></li><li><p>Confidence and a high emotional IQ.</p></li><li><p>Knowledge of industry practices and regulations (e.g., GxP, ISO, ICH, etc.).</p></li><li><p>Technical expertise that contributes to the development of new concepts, techniques, and standards.</p></li><li><p>Proficiency in advanced techniques with relevant software: MS Project, Excel, PowerPoint, Word, etc., in addition to experience working within shared work environments.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in any physical or biological science and the following amount of industry related experience, including prior pharmaceutical industry experience for each level:</p><ul><li><p>Associate Project Manager: 8 years</p></li><li><p>Project Manager: 10 years</p></li></ul><p> May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist - RGM Chemistry]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47688]]></requisitionid>
    <referencenumber><![CDATA[R47688]]></referencenumber>
    <apijobid><![CDATA[r47688]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47688/principal-scientist-rgm-chemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a visionary Principal Scientist – RGM Chemistry to lead the discovery, development, and optimization of antibody-oligonucleotide conjugation technologies that power next-generation targeted therapeutics. Sitting at the intersection of bioconjugation chemistry, RNA science, and process innovation, you will set scientific strategy, guide a multidisciplinary team, and translate ground breaking concepts into scalable solutions that advance our therapeutic pipeline. Your deep expertise, collaborative attitude, and passion for mentoring will drive breakthrough medicines from bench to preclinical validation and beyond.</p><p><strong>In this role, a typical day might include the following: </strong><br>- Designing and completing experiments to refine linker chemistry, payload stability, and delivery efficiency for antibody-oligo conjugates <br>- Analyzing conjugates with HPLC, LC-MS, and bioassays to ensure purity, identity, and functional potency <br>- Leading project stand-ups, mentoring scientists and research associates, and troubleshooting technical challenges in real time <br>- Partnering with Process Development and Manufacturing to scale promising conjugation methods for preclinical supply <br>- Scouting and evaluating emerging bioconjugation or RNA delivery technologies, then proposing data-driven innovation projects <br>- Presenting program updates and strategic recommendations to senior R&D leadership and cross-functional partners </p><p><strong>This job might be for you if you: </strong><br>- Thrive on pushing the boundaries of antibody and oligonucleotide conjugation science <br>- Enjoy mentoring and developing talent in a collaborative, fast-paced research environment <br>- Translate sophisticated data into clear, actionable insights and strategic plans<br>- Demonstrate a strong record of innovation, publications, and/or patents in bioconjugation or RNA therapeutics <br>- Excel at balancing deep scientific rigor with pragmatic process development and scale-up considerations <br>- Are motivated by cross-functional collaboration that accelerates breakthrough medicines to the clinic </p><p><strong>In order to be considered for this role, you must have: </strong><br>- A Ph. D. in Chemistry, Biochemistry, Molecular Biology, or related field with 5+ years of postdoctoral or industry experience in antibody/oligonucleotide conjugation <br>- Validated expertise in bioconjugation, oligonucleotide therapeutics, and advanced analytical techniques (HPLC, LC-MS, bioassays) <br>- Proven leadership of multidisciplinary teams and successful track record in advancing therapeutic candidates toward preclinical or clinical development</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[IT Product Manager – HCM & ERP (Japan)]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R39293]]></requisitionid>
    <referencenumber><![CDATA[R39293]]></referencenumber>
    <apijobid><![CDATA[r39293]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r39293/it-product-manager-hcm-erp-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong> Tokyo, Japan</p><p><br><strong>About the Role</strong><br>We are Regeneron, a global leader in biotechnology, dedicated to transforming lives through innovation. We are seeking an experienced IT Product Manager to join our dynamic General & Administrative IT team in Tokyo, Japan. This pivotal role focuses on supporting and enhancing our global Human Capital Management (HCM) systems and Enterprise Resource Planning (ERP) systems. As part of our team, you will collaborate with global and regional stakeholders to deliver innovative solutions that drive seamless integration and continuous improvement across technology platforms.</p><p>This is your opportunity to contribute to impactful projects, ensure efficient delivery processes, and make a meaningful difference in how technology supports our business goals.</p><p><strong>A Typical Day:</strong></p><ul><li>Act as the functional subject matter expert for Workday HCM and/or Oracle ERP systems, including modules such as Time and Absence, Finance, Compensation, and Procurement.</li><li>Collaborate with business partners to gather, document, and refine requirements that effectively address business processes and capabilities.</li><li>Lead project delivery for the Japan team, ensuring timely updates to global project managers and tracking risks and issues.</li><li>Oversee the full delivery lifecycle, from solution design and build oversight to quality assurance, testing, go-live, and post-production support.</li><li>Manage software/service contracts and vendor relationships, ensuring compliance with best practices and standards.</li><li>Troubleshoot and resolve post go-live issues with delivery teams, applying critical thinking under pressure.</li><li>Build and maintain strong relationships with Japan-based business stakeholders and global IT teams.</li><li>Translate technical concepts into practical business terms for diverse audiences, fostering collaboration and mutual understanding.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You have 6+ years of proven experience as a technical lead or systems analyst, specializing in HCM or ERP systems.</li><li>You possess hands-on expertise in Workday HCM modules (e.g., Core HCM, Compensation, Time and Absence) or Oracle ERP (e.g., Finance, OTC, Procurement).</li><li>You are skilled in facilitating requirements traceability during testing phases such as SIT and UAT.</li><li>You thrive in fast-paced environments, managing multiple high-priority tasks with a “get-it-done” attitude.</li><li>You excel in both independent work and cross-functional team collaborations, leveraging an agile mindset to drive efficient use of technology.</li><li>You are well-organized, with the ability to prioritize tasks and deliver high-quality solutions on time.</li><li>You possess strong business-level English communication skills (written and spoken).</li></ul><p><strong>To Be Considered:</strong><br>Candidates must hold a Bachelor’s Degree in Computer Science, Information Systems, Business, or a related field. Certifications in cloud technology applications such as Workday or Oracle are advantageous. Experience with Jira, ServiceNow, or other cloud-based service management applications is a plus.</p><p>Join us in Tokyo and be part of a team that values innovation, collaboration, and the transformative power of technology. Apply now to make an impact with Regeneron!</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Portfolio Governance]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48028]]></requisitionid>
    <referencenumber><![CDATA[R48028]]></referencenumber>
    <apijobid><![CDATA[r48028]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48028/director-portfolio-governance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Director, Portfolio Governance</strong> is a strategic leadership role accountable for designing, enabling, and continuously improving the Development governance framework that drives high-quality, timely decision-making across the development portfolio. This role embeds decision excellence, clarity of decision rights, and disciplined execution across the governance forums.<br>This leader ensures decisions are made at the right level, with the right information, at the right time—enabling portfolio tradeoff decisions, reducing cycle time, and improving decision quality and durability.</p><p>This role is a hands-on contributor and people manager responsible to build relationships at all levels of the organization in order to solicit and action stakeholder input regarding the governance framework. This role will navigate the fast-paced and agile environment of Regeneron in a collaborative and innovative manner.</p><p><em>***Please note this role is an onsite opportunity and is not eligible remote.</em></p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Own and continuously evolve the governance framework to enable effective, scalable decision-making across the portfolio.</li><li>Establish and enforce decision quality and readiness standards, including clear articulation of options, trade-offs, risks, and recommendations.</li><li>Where required, facilitate governance forums to ensure structured, decision-focused discussions and clear, actionable outcomes.</li><li>Define and manage governance performance metrics (e.g., decision cycle time, right-first-time decisions, deferrals, forum utilization) to assess effectiveness.</li><li>Translate governance metrics and feedback into actionable insights, driving a closed-loop continuous improvement model.</li><li>Synthesize governance outputs into portfolio-level insights, identifying cross-program risks, recurring issues, and systemic bottlenecks.</li><li>Establish and maintain centralized decision documentation and knowledge management practices to ensure transparency and traceability.</li><li>Oversee governance intake, prioritization, and scheduling to ensure alignment to strategic importance, while advancing efficient, scalable processes and leveraging technology to streamline execution.</li><li>Drive cross-forum integration to streamline escalation pathways, eliminate duplication, and improve decision flow.</li><li>Partner closely with senior leaders, governance chairs, and stakeholders to align priorities and reinforce governance expectations.</li><li>Implement governance quality and experience measurement, incorporating multi-directional feedback from teams, executives, and chairs to improve effectiveness.</li><li>Coach and develop team members ensuring that the organizational strategy delivers the skills, capabilities and processes that enable portfolio delivery are present in his/her team</li></ul><p><strong>This role may be for you if you have: </strong></p><ul><li>Deep understanding of drug development lifecycle and portfolio management.</li><li>Proven experience designing governance frameworks, operating models, or decision-making processes.</li><li>Strong analytical skills with ability to translate data into insights and actions.</li><li>Experience with process improvement methodologies (Lean, Six Sigma) preferred.</li><li>Exceptional executive communication and facilitation skills.</li><li>Demonstrated ability to influence senior leadership and drive change in matrixed environments.</li><li>Strong stakeholder management and cross-functional leadership capabilities.</li><li>Demonstrate experience leading and developing high-performance teams, including direct people management.</li><li>Experience leveraging technology and digital solutions to enable scalable processes, improve efficiency and enhance decision-making (e.g. dashboards, workflow tools, analytics platforms).</li><li>Ability to travel (<10%).</li></ul><p><br><strong>In order to be considered qualified for the this role</strong> a minimum of a Bachelor's degree and Minimum 12+ years of experience in biotechnology, pharmaceutical development, or consulting.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison  - Neurology (Great Lakes)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48119]]></requisitionid>
    <referencenumber><![CDATA[R48119]]></referencenumber>
    <apijobid><![CDATA[r48119]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48119/associate-director-thought-leader-liaison-neurology-great-lakes/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Illinois]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Neurology Marketing team. It will be focused on enhancing and improving interactions with key external US Neurology thought leaders at academic centers and leading community practices for our neurology product.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Neurology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><p><strong>The typical day may include the following:</strong></p><ul><li>The Neurology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You possess a strong science background with deep knowledge of rare neurology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p><strong>To be considered for this opportunity, you will possess the following:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10years of relevant work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in Neurology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry. Launch experience preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li><li>Must have a valid driver’s license</li><li>Must be able to travel 60%-80% of time </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - General Medicine]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44952]]></requisitionid>
    <referencenumber><![CDATA[R44952]]></referencenumber>
    <apijobid><![CDATA[r44952]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44952/director-global-patient-safety-sciences-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director </strong>to join our <strong>Patient Safety</strong> team.</p><p>The Global Patient Safety (GPS) Lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s)/asset(s) assigned within a given therapeutic area (TA), and is the GPS representative on the cross functional strategic program team (SPT) for the compound. The GPS Lead leads the safety strategy and ensures the optimal support from within GPS and works collaboratively with stakeholders to deliver the safety strategy. This position requires the ability to work with and influence colleagues in a matrix environment within and external to GPS including senior management. The GPS Director joins Regeneron’s industry leading scientific organization, and has a direct impact on drug development, operations, and commercialization in all relevant global territories.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.)</p></li><li><p>Leads cross-functional Safety Monitoring Team (SMT) activities</p></li><li><p>Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs)</p></li><li><p>Proactively identify and develop safety strategies and planning for non-compound specific Global Patient Safety activities (mechanism of action etc.)</p></li><li><p>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds</p></li><li><p>Actively participate in the development and maintenance of relevant SOPs, working practices and guides </p></li><li><p>Actively participates in continuous improvement activities within both the TA and the GPS organization, including cultivating cross functional relationships and mentoring junior safety scientists</p></li><li><p>Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.</p></li><li><p>Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest.</p></li><li><p>A proven ability to lead and develop a diverse team of Safety Professionals in a constructive, goal-oriented environment.</p></li><li><p>An ability to work across organizational levels, effectively communicating safety viewpoints and findings as required, and recommended risk management and minimization activities.</p></li><li><p>Ability to utilize GPS safety database for purposes of medical case review and simple queries. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum 10+ years of total relevant experience in PV and/or relevant medical field or equivalent of industry experience in drug safety including significant experience with PSURs/ DSURs/(d) RMPS; or in clinical development with demonstrated achievements in safety (ex. supporting an ISS; responsible for CSR content). </p></li><li><p>5+ years of total relevant experience in PV and/or relevant medical field with PharmD / PhD / MD degree required.</p></li><li><p>Clinical experience and/or industry experience in Oncology is a plus</p></li></ul><p>#MDJOBSPS #GDPSJobs</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-New York Metro]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47569]]></requisitionid>
    <referencenumber><![CDATA[R47569]]></referencenumber>
    <apijobid><![CDATA[r47569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47569/regional-director-neurology-new-york-metro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the [INSERT] Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: New York Metro</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><ul><li></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 20:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Gastro)-Miami, FL]]></title>
    <date><![CDATA[Tue, 02 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48147]]></requisitionid>
    <referencenumber><![CDATA[R48147]]></referencenumber>
    <apijobid><![CDATA[r48147]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48147/medical-specialist-i-gastro-miami-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Miami]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Gastroenterology (MS) will report to the District Manager, Gastroenterology, and be responsible for engaging Gastroenterologists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies, and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US. </p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Gastroenterology therapeutic area to generate product utilization. The MS will develop strong working relationships with experts and all Gastroenterologists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p><strong>When & where:</strong></p><ul><li><p>Field role</p></li><li><p>Location: <strong>Miami, FL</strong></p></li></ul><p><strong>Discover your role:</strong></p><p>A core responsibility of the MS will be to collaborate with their district colleagues, alliance counterparts, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Proven success navigating and demonstrating positive impact with large groups, institutional settings, and Ambulatory Surgery Centers</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Gastroenterology market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 02 Jun 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists - Hematology - Minnesota]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46705]]></requisitionid>
    <referencenumber><![CDATA[R46705]]></referencenumber>
    <apijobid><![CDATA[r46705]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46705/medical-account-specialists-hematology-minnesota/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Minnesota]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Hematology Oncology Account Specialist, is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat R/R Multiple Myeloma, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if: </strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually)</strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - RICHMOND, VA]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48017]]></requisitionid>
    <referencenumber><![CDATA[R48017]]></referencenumber>
    <apijobid><![CDATA[r48017]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48017/medical-account-specialist-ii-neurology-richmond-va/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Richmond]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Richmond (Metro), VA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Drug Production, Associate Manufacturing Specialist (Overnights)]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46370]]></requisitionid>
    <referencenumber><![CDATA[R46370]]></referencenumber>
    <apijobid><![CDATA[r46370]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46370/drug-production-associate-manufacturing-specialist-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Biotech Production Specialist to join our Global Manufacturing team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment.</p><p>When & where:</p><ul><li><p>3rd shift, 10pm-8:30am with the potential for 1-2 weekend days</p></li><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Occasional flexibility may be requested for on-call schedule/weekend work</p></li></ul><p>What you'll do:</p><ul><li><p>Covering all facets of drug production in a clean room including cell culture and purification of monoclonal antibodies</p></li><li><p>Completing and reviewing batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)</p></li><li><p>Performing in-process sampling and analysis of buffer solutions, cell culture, and drug substance</p></li><li><p>Operating automated equipment such as bioreactors, chromatography columns, and filtration skids</p></li><li><p>Supporting equipment start-up, troubleshooting, and validation</p></li><li><p>Partnering with R&D teams to implement new drug manufacturing processes and technologies</p></li><li><p>Enjoy working in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients</p></li><li><p>Are highly organized, detail oriented and perform work accurately the first time</p></li><li><p>Work well in both small and large teams to accomplish tasks adhering to a schedule</p></li><li><p>Can operate in a highly regulated environment strive to continuously improve processes and maintain compliance to manufacture safe and effective medicines for patients</p></li><li><p>Are able to learn and use computerized systems for daily performance of tasks</p></li><li><p>Are a good communicator and can give and receive feedback constructively</p></li></ul><br><p>The environment and physical rhythms of the role:</p><ul><li><p>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><br><p>Let's find out if we're a fit:</p><ul><li><p>HS diploma + 4 years of relevant work experience is required</p></li><li><p>Or AS, BS or BA in Life Sciences or related field</p></li><li><p>Level will be determined based on experience</p></li></ul><p>Thrive today. Grow Tomorrow.</p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family care benefits</p></li><li><p>Relocation assistance</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.78 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 18 Jun 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Coordinator]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47633]]></requisitionid>
    <referencenumber><![CDATA[R47633]]></referencenumber>
    <apijobid><![CDATA[r47633]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47633/calibration-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Calibration Coordinator</strong> to join our <strong>Technical Operations </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Shift Requirements: Monday - Friday 08.00am - 4.30pm</p></li><li><p>Location: Rensselaer, New York</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Coordinating with equipment owners across departments to obtain and send out instruments to be calibrated by external service providers</p></li><li><p>Managing shipment and logistics for all instruments and standards sent off-site for calibration and/or repair. Follows up with vendors to ensure timely return of equipment once it has been serviced </p></li><li><p>Providing oversight for contractors performing calibration and preventive maintenance work on site, including escorting contractors into various manufacturing and quality control areas to facilitate servicing of equipment</p></li><li><p>Ensuring contractors abide by Regeneron procedures and policies, including gowning requirements and good documentation practices </p></li><li><p>Reviewing calibration worksheets and certificates provided by external service providers for completeness and accuracy, and documents work electronically within the Blue Mountain Regulatory Asset Manager (BMRAM) System</p></li><li><p>Collaborating with the Materials Management Group to ensure that Calibration Technicians have the required supplies and standards necessary to perform their work (e.g. pH Buffers, Conductivity Standards, Fyrite and UV Solutions, 0.2 micron Filters, etc.). Ensuring all standards are suitable for use, including the verification of Temperature Standards </p></li><li><p>Reporting Out of Tolerance (OOT) events to Calibration Management and the Facilities Compliance Group for vendor-performed calibration work. Ensuring OOT events are reported in a timely manner and that all vital documentation is available to facilitate closure of the associated deviation investigations</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Demonstrate basic problem-solving skills</p></li><li><p>Ability to learn and follow routine procedures independently as well as part of a team</p></li><li><p>Comfortable and have the flexibility to work in a changing environment</p></li><li><p>Seek to build and maintain positive working relationships with the business</p></li><li><p>Possess strong written and verbal communication skills</p></li><li><p>Maintain effective time management skills to allow deadlines to be met in a timely manner</p></li><li><p>Must be able to lift, push and/or pull at least 50lbs</p></li><li><p>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</p></li><li><p>Full gowning required when entering and working on production floor</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Applicants ideally should have an AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum amounts of experience for each level:</p></li></ul><p>Calibration Coordinator II: 2+ years of related experience</p><p>Calibration Coordinator III: 4+ years of related experience</p><p>Calibration Coordinator IV: 6+ years of related experience</p><p>Equivalent combination of education and experience may be considered. Level will be determined based on qualifications relevant to the role.</p><p>Prior experience in the maintenance and operation of large-scale utilities plant preferred and ISA CCST Certification is strongly preferred but not required.</p><p>#REGENTOSK </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.49 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 07:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Therapeutic Protein]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48041]]></requisitionid>
    <referencenumber><![CDATA[R48041]]></referencenumber>
    <apijobid><![CDATA[r48041]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48041/associate-scientist-therapeutic-protein/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Scientist to join our Therapeutic Protein department to support ongoing programs by purifying and biochemically characterizing protein reagents and antibodies. You will work in a fast-paced, collaborative lab environment, ensuring high-quality outputs and clear, timely communication of results.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location- Tarrytown, 5 days on-site</p><p><strong>Discover your role:</strong></p><ul><li>Purify protein reagents and antibodies using standard chromatography platforms and automated systems</li><li>Perform purification and analytical chromatography, including affinity, ion-exchange (IEX), hydrophobic interaction (HIC), and size-exclusion (SEC)</li><li>Characterize proteins using Western blotting, SDS-PAGE, SEC, and UV/Vis spectrophotometry</li><li>Enter, analyze, and document data in Benchling; prepare presentations and summaries for team review</li><li>Communicate findings clearly and concisely to managers and cross-functional partners</li></ul><p><strong>This Role May Be for You If You Have Experience:</strong></p><ul><li>Detail-oriented with strong documentation practices</li><li>Productive and proactive in a fast-paced, collaborative environment</li><li>Problem-solver with a continuous improvement mindset</li><li>Strong time management with the ability to handle multiple priorities</li></ul><p><strong>The role requires: </strong></p><ul><li>BS or MS in biology, molecular biology, protein chemistry, chemical engineering, chemistry, or a related field</li><li>1–3 years of relevant laboratory experience (industry or academic)</li><li>Hands-on experience with PCR and sequencing</li><li>Proficiency in protein characterization techniques (e.g., Western blot, SDS-PAGE, SEC, spectrophotometry)</li><li>Strong foundation in protein chemistry</li><li>Excellent organizational, verbal, and written communication skills</li></ul><p><strong>Preferred Qualifications: </strong></p><ul><li>Experience operating ÄKTA or comparable chromatography systems and associated software</li><li>Familiarity with method development and troubleshooting across affinity, IEX, HIC, and SEC workflows</li><li>Proficiency with Benchling and data analysis/visualization tools (e.g., Excel, GraphPad Prism)</li><li>Experience preparing technical presentations and contributing to cross-functional project discussions</li></ul><p><strong>Tools & Technologies (a plus):</strong></p><ul><li>ÄKTA/Unicorn or similar chromatography platforms</li><li>Benchling and ELN systems</li><li>UV/Vis spectrophotometers, SEC systems, gel imaging platforms</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47243]]></requisitionid>
    <referencenumber><![CDATA[R47243]]></referencenumber>
    <apijobid><![CDATA[r47243]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47243/senior-manager-field-medical-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron Japan, we are expanding our Field Medical Affairs team to bring innovative solutions in oncology and hematology oncology to the forefront. As a Senior Manager, Field Medical Affairs, you will play a pivotal role in advancing scientific exchange, collaborating with therapeutic area experts, and supporting clinical development initiatives. Join us in shaping the future of healthcare while contributing to meaningful, impactful work in a dynamic and collaborative environment.</p><p><strong>A Typical Day:</strong><br>As part of your role, you will:</p><ul><li><p>Identify and maintain relationships with medical and therapeutic area experts, investigators, and other stakeholders.</p></li><li><p>Respond to scientific and clinical inquiries in compliance with industry regulations.</p></li><li><p>Perform disease management and therapeutic area education for practitioners, payers, and researchers.</p></li><li><p>Attend medical conferences to gather and report scientific, clinical, and competitive intelligence.</p></li><li><p>Collaborate with investigators and internal medical affairs teams to support investigator-initiated studies (IIS).</p></li><li><p>Assist in the development and communication of clinical data through abstracts, posters, presentations, and manuscripts.</p></li><li><p>Support site initiation and enrollment activities for clinical trials.</p></li><li><p>Ensure adherence to company policies, procedures, and compliance standards.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You are passionate about oncology and have deep knowledge in lung cancer, solid tumors, or hematology oncology.</p></li><li><p>You thrive in a collaborative, matrix organization and enjoy building relationships in academic and clinical practice settings.</p></li><li><p>You have excellent communication skills and are fluent in both Japanese and English.</p></li><li><p>You are experienced in immuno-oncology and clinical trials, and possess a strong commitment to compliance.</p></li><li><p>You are comfortable traveling 30–50% of the time to engage with stakeholders and attend conferences.</p></li></ul><p><strong>To Be Considered:</strong><br>We’re looking for healthcare or scientific professionals with:</p><ul><li><p>A PhD, PharmD, or MD preferred, though a Master’s Degree with extensive oncology experience may be considered.</p></li><li><p>At least 6 years of relevant experience in pharmaceutical industry or clinical settings, such as drug information or disease management programs.</p></li><li><p>Proven expertise in oncology, particularly lung cancer, solid tumors, or hematology oncology.</p></li><li><p>Immuno-oncology experience is preferred.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Pharmaceutical Sales Specialist Immunology - Alsace]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47580]]></requisitionid>
    <referencenumber><![CDATA[R47580]]></referencenumber>
    <apijobid><![CDATA[r47580]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47580/pharmaceutical-sales-specialist-immunology-alsace/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Chez Regeneron, nous croyons que lorsque la bonne idée trouve la bonne équipe, un réel changement est possible. Alors que nous travaillons activement à travers notre réseau pour inventer, développer et commercialiser des médicaments transformant la vie des personnes atteintes de maladies graves, nous établissons de nouvelles façons de penser la science, la fabrication et la commercialisation. </p></div><div><p>En tant que <strong>Délégué(e) Hospitalier(e) Immunologie</strong>, vous jouerez un rôle central dans la réalisation de nos objectifs et encouragerez une culture de haute performance. </p></div><div><p>De nature curieuse et proactive, vous serez responsable de la gestion du <strong>secteur Alsace (Strasbourg – Mulhouse - Colmar)</strong>, en assurant une planification et une gestion professionnelles des différents interlocuteurs/rices clés dans le domaine de l’Immunologie sur votre secteur, comprendre le fonctionnement des établissements hospitaliers et développer la croissance de Regeneron dans le respect du bon usage du médicament. </p></div><div></div><div><p><strong>En tant que Délégué(e) Hospitalier(e), une journée typique pourrait inclure les activités suivantes</strong> : </p></div><div><p>- Établir des interactions de haute qualité avec les Professionnels de Santé (PDS) en maintenant continuellement à jour les connaissances scientifiques autour du produit, de l'indication et des messages tout en mettant en œuvre de manière optimale le plan de vente et de marketing. </p></div><div><p>- Délivrer constamment la proposition de valeur de la marque à travers la communication des messages clés aux PDS. </p></div><div><p>- Travailler en alignement avec le plan de marque, développer et mettre en œuvre un plan stratégique local basé sur des sources de données clés et des insights du marché local. </p></div><div><p>- Collaborer étroitement avec les équipes médicales pour mettre en œuvre des programmes régionaux et des activités pertinentes pour soutenir les besoins des PDS. </p></div><div><p>- Optimisez tous les canaux de communication, y compris les canaux numériques, en collaboration avec d'autres fonctions, pour obtenir la meilleure part de voix possible sur le marché. </p></div><div><p>- Développer et mettre en œuvre, en ligne avec la stratégie de l’alliance Regeneron, un plan sectoriel reposant sur des données clés et le développement d’une connaissance assidue du marché local. </p></div><div><p><strong>Ce rôle pourrait être pour vous si</strong> : </p></div><div><p>- Vous êtes passionné(e) par le fait de garantir que les objectifs de l'actif sont atteints en communiquant les messages clés aux PDS, conformément aux bonnes pratiques. </p></div><div><p>- Vous êtes engagé(e) à travailler en collaboration et à développer d'excellents partenariats en interne et en externe, une expérience préalable dans une alliance est utile. </p></div><div><p>- Vous êtes enthousiaste à l'idée de gérer plusieurs canaux pour optimiser l'engagement des clients (par exemple, en face à face, appels à distance, e-mails approuvés, plateformes de communication numérique, etc.). </p></div><div><p>- Vous pouvez opérer efficacement dans un environnement naissant au sein d’une équipe collaborative, performante et ambitieuse. </p></div><div></div><div><p>Pour être considéré(e) pour cette opportunité, vous devez détenir un Diplôme de la Visite Médicale avec un minimum de 5+ années d'expérience professionnelles en vente pharmaceutique dans le domaine de l'Immunologie, idéalement en Pneumologie. Vous êtes mobile géographiquement et possédez un permis de conduire valide. L'anglais conversationnel serait souhaitable, mais non requis. </p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€47,550.00 - €79,250.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology (f/m/d) - Trier - Saarbrücken - Kaiserslautern - Ludwigshafen]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48471]]></requisitionid>
    <referencenumber><![CDATA[R48471]]></referencenumber>
    <apijobid><![CDATA[r48471]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48471/sales-specialist-immunology-fmd-trier-saarbruecken-kaiserslautern-ludwigshafen/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>As a Sales Specialist Immunology (f/m/d), you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our Dermatology division at key meetings. You will identify the key people in Dermatology, understand the account context and tailor calls based on individual and account requirements and build KOL support for our portfolio.</p><br><p><strong>Where:</strong></p><br><p>Field based in the territory: <strong>Trier - Saarbrücken - Kaiserslautern - Ludwigshafen</strong></p><p><br><br></p><p><strong>Discover your role:</strong></p><br><ul><li>Competent advice and support for relevant Healthcare Professionals (HCP) and, where applicable, customers in the hospital segment</li><li>Building and maintaining intensive and sustainable customer relationships - in person and using digital channels</li><li>Target-oriented, substantive dialogue focused on the benefits for customers and added value for patients</li><li>Independent regional management including account analyses, route planning and documentation of your activities in the CRM system</li><li>Participation in trade fairs and congresses as well as independent planning, coordination and realization of training events and specialist presentations</li><li>Regular reporting to the sales management</li></ul><p><br><br></p><p><strong>This role requires:</strong></p><br><ul><li>Deep understanding of the local healthcare economy, with the ability to identify key players in Dermatology</li><li>“Patient first” value system</li><li>Bachelor’s degree or equivalent experience and a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</li><li>5+ years of sales experience within the biotech/pharmaceutical sector</li><li>Dermatology experience is preferred</li><li>Proficiency in German as well as conversational English </li><li>Readiness for very frequent travel and a driver's license cl. 3/B.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>64.125,00 € - 106.875,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Biostatistics - Genetic Medicine]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46282]]></requisitionid>
    <referencenumber><![CDATA[R46282]]></referencenumber>
    <apijobid><![CDATA[r46282]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46282/associate-director-biostatistics-genetic-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This position is for a qualified statistician/biostatistician to support Clinical Biostatistics with Global Development. </p><p><strong>In this role, a typical day might include:</strong> ​</p><p>The incumbent will lead efforts of the Biostatistics department with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. The incumbent will represent statistical issues in regulatory agency meetings. The incumbent will lead the development and delivery of training to non-statistical colleagues, lead the development of new infrastructure and processes, and be active in representing the company in professional associations, conferences, and publications. As an Associate Director, the incumbent will be responsible for mentoring and overseeing less experienced statisticians, with the potential to manage full-time staff. </p><p><strong>This role might be for you if can:</strong> ​</p><ul><li><p>Represent Biostatistics at Global Clinical sub-teams. </p></li><li><p>Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.</p></li><li><p>Lead contributions to the preparation of material to be used in regulatory interactions, including drafting analysis plan and reviewing TFLs to be used in regulatory meetings, slides for advisory committee meetings, etc.</p></li><li><p>Lead and contributes to process improvement and technical working groups and sets timelines and expectations for the deliverables. Authors new/revised SOPs and contributes to cross-functional EPIC workstreams. </p></li><li><p>Evaluate appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.</p></li><li><p>Prepare presentations and written reports to effectively communicate results to the project team, management, and regulatory agencies. Co-presents findings to management. </p></li><li><p>Is involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to non-statisticians. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>PhD or equivalent degree in statistics/biostatistics with >6 years of experience in the pharmaceutical industry OR MS degree in statistics/biostatistics with >11 years of experience</p></li><li><p>Preferred: Hematology, IO, non-oncology, Multiple Myeloma experience or similar Therapeutic Area.</p></li><li><p>Time to Event (TTE) experience.</p></li><li><p>Knowledge of drug discovery and development and ability to integrate statistical concepts into drug discovery and development strategies.</p></li><li><p>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </p></li><li><p>Must be able to work productively in a fast-paced collaborative environment, with demonstrated critical thinking skills, time management skills, and effective communication skills.</p></li><li><p>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</p></li><li><p>Expertise in statistical software</p></li></ul><p>#GDBDMJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Clinical Data Reporting Specialist]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48291]]></requisitionid>
    <referencenumber><![CDATA[R48291]]></referencenumber>
    <apijobid><![CDATA[r48291]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48291/senior-clinical-data-reporting-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a Senior Clinical Data Reporting Specialist to join our Data Management team, supporting clinical studies in a hybrid model. In this role, you will develop high-quality clinical data reporting outputs that enable efficient data review and operational oversight while collaborating with clinical data management, technology partners and cross-functional teams. This position offers the opportunity to strengthen reporting consistency, improve data visibility and support reliable study-level delivery.</p><p><strong>When & where:</strong></p><p>Hyderabad, India (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Develop clinical data reports, listings and review outputs.</li><li>Translate study requirements into clear reporting specifications.</li><li>Validate exception reports, reconciliation outputs and performance reports.</li><li>Monitor data pipelines and troubleshoot reporting quality issues.</li><li>Support inspection readiness through traceable reporting documentation.</li><li>Identify automation opportunities that improve reporting efficiency.</li><li>You collaborate across functions to clarify reporting needs.</li><li>You share knowledge and support continuous improvement.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s or Master’s degree in Data Science, Computer Science, Life Sciences or a related field.</li><li>4+ years of experience in clinical data, data visualisation or related disciplines.</li><li>Proficiency in electronic data capture systems and reporting tools, including SAS, R, Python, JReview, elluminate, Tableau, Power BI or Spotfire.</li><li>Strong understanding of clinical trial processes, clinical data standards and regulated data lifecycle management.</li><li>Knowledge of Good Clinical Practice, GDPR, HIPAA and related regulatory requirements.</li><li>Experience with data lakes, data pipelines, data integration, automation, reporting and analytics in clinical research.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Payroll Service Delivery Analyst]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47443]]></requisitionid>
    <referencenumber><![CDATA[R47443]]></referencenumber>
    <apijobid><![CDATA[r47443]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47443/senior-payroll-service-delivery-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a<strong> </strong>Senior Payroll Service Delivery Analyst to join our Global Payroll team within our Global Capability Center in a hybrid role. In this position, you will support the accurate and timely processing of payroll across multiple countries by validating employee payroll data, coordinating with payroll vendors, supporting compliance activities, and maintaining payroll documentation. You will collaborate closely with Global Payroll, Human Resources, and Finance teams to ensure payroll excellence while contributing to process improvements and standardization initiatives. This role offers an excellent opportunity to build expertise in global payroll operations within a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Support payroll processing activities for assigned international countries by collecting, validating, and entering employee payroll data.</p></li><li><p>Perform routine payroll audits, reconciliations, and data reviews to ensure accuracy, completeness, and compliance.</p></li><li><p>Maintain payroll calendars, processing schedules, checklists, and supporting documentation.</p></li><li><p>Partner with Global Payroll, Human Resources, and Finance teams to ensure employee data integrity and timely payroll input submissions.</p></li><li><p>Coordinate with external payroll vendors to provide required data, monitor deliverables, and resolve routine payroll-related inquiries.</p></li><li><p>Support the implementation of statutory and regulatory payroll updates across assigned countries.</p></li><li><p>Generate payroll reports and assist with month-end payroll and accounting activities.</p></li><li><p>Participate in payroll process improvement initiatives, system enhancements, and GCC standardization projects.</p></li><li><p>Ensure adherence to internal controls, company policies, confidentiality requirements, and compliance standards.</p></li><li><p>Build effective working relationships with cross-functional stakeholders while delivering a high level of customer service and operational support.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Business, Human Resources, Accounting, Finance, or a related field; equivalent experience may be considered.</p></li><li><p>5+ years of experience in payroll operations, HR shared services, accounting, finance operations, or a related field.</p></li><li><p>Strong attention to detail with the ability to work accurately with large volumes of data.</p></li><li><p>Proficiency in Microsoft Excel and the ability to learn and navigate new systems quickly.</p></li><li><p>Strong communication, organizational, and time-management skills.</p></li><li><p>Ability to work effectively in a fast-paced, deadline-driven environment.</p></li><li><p>Experience working with HRIS or payroll systems such as Workday, SAP, ADP, or equivalent platforms is preferred.</p></li><li><p>Exposure to global payroll operations or shared services environments is preferred.</p></li><li><p>Experience working across multiple countries, cultures, or time zones is preferred.</p></li><li><p>Strong analytical, problem-solving, and customer service skills.</p></li><li><p>Ability to maintain confidentiality and demonstrate integrity when handling sensitive employee information.</p></li><li><p>Learning agility with a continuous improvement mindset and the ability to collaborate effectively within a global team environment</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Compliance Specialist (Quality Risk Management)]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46551]]></requisitionid>
    <referencenumber><![CDATA[R46551]]></referencenumber>
    <apijobid><![CDATA[r46551]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46551/quality-compliance-specialist-quality-risk-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Quality Compliance Specialist (Quality Risk Management) position. This position is responsible for supporting Regeneron’s Internal Drug Product Manufacturing operations through the use of quality risk management (QRM). Job functions will primarily consist of the broad application of patient centered QRM across a full spectrum of processes vital to the operations. Specifically, the active facilitation of quality risk assessments, risk reviews and other quality risk-based programs supporting the Quality System (e.g., change control, deviation management, etc.). The person in this role will be consistently challenged with assignments, touching almost every phase of our process.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Providing technical expertise in quality risk management to a broad base of customers throughout the organization, including Quality Assurance, Quality Control, Manufacturing, Medical Device and Facilities</p></li><li><p>Facilitating data driven risk assessments and risk reviews using appropriate methodologies (e.g., FMEA, RBIA, REM and HACCP)</p></li><li><p>Partnering with Risk Assessment Owners to define scope, acceptance criteria, and evaluation scales</p></li><li><p>Guiding teams through risk identification, analysis, control/mitigation, and residual risk evaluation</p></li><li><p>Preparing and revising QRM documents</p></li><li><p>Developing and improving the quality risk management program</p></li><li><p>Contributing to contamination control strategy (CCS) and aseptic processing risk assessments for fill/finish operations; interface with EM, utilities, and equipment owners.</p></li><li><p>Preparing for and supporting regulatory, customer, and internal audits/inspections</p></li><li><p>Coaching colleagues on QRM principles and driving consistency in application</p></li><li><p>Tracking metrics (e.g., on-time risk reviews, cycle time) and identifying opportunities for continuous improvement.</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Excel in a quality driven organization</p></li><li><p>Have excellent collaboration, influence, and communication skills</p></li><li><p>Are effective at facilitating cross-functional discussions</p></li><li><p>Proficient digital literacy in Microsoft (MS) Word, Excel and PowerPoint required. Experience with Veeva heavily preferred.</p></li><li><p>Have an understanding of QRM principles</p></li><li><p>Are able to interpret complex technical and systems information and make sound risk-based decisions.</p></li><li><p>Are organized and have an attention to detail</p></li><li><p>Can prioritize multiple assignments and changing priorities</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Biological Sciences, Chemistry, Biochemistry, Engineering or related field and the following amount of relevant work experience for each level:</p><ul><li><p>Specialist - 2+ years</p></li><li><p>Sr Specialist - 5+ years</p></li></ul><p>May substitute proven experience for education requirement. Level to be determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Pulmonology-Hartford CT/RI]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48655]]></requisitionid>
    <referencenumber><![CDATA[R48655]]></referencenumber>
    <apijobid><![CDATA[r48655]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48655/medical-specialist-i-pulmonology-hartford-ctri/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hartford]]></city>
    <state><![CDATA[Connecticut]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field Role</p></li><li><p>Location: <strong>Hartford, CT/RI - representative must reside within or close to the territory.</strong></p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups. </p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Columbus, OH]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48363]]></requisitionid>
    <referencenumber><![CDATA[R48363]]></referencenumber>
    <apijobid><![CDATA[r48363]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48363/medical-specialist-i-allergyent-columbus-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbus]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Our Medical Specialists are at the forefront of engaging Allergists and Immunologists as well as other key customers. We need someone who is highly proficient in presenting clinically focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, result-oriented, customer-focused team if you are up for the challenge.</p><p><strong>When & where: </strong></p><ul><li><p>Field Role</p></li><li><p>Location: Columbus, OH</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings, and medical conferences.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience.</p></li><li><p>Having a minimum of 2 years’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology experience preferred.</p></li><li><p>We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments.</p></li><li><p>This role requires the ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Corporate Counsel Transactions]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48785]]></requisitionid>
    <referencenumber><![CDATA[R48785]]></referencenumber>
    <apijobid><![CDATA[r48785]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48785/director-corporate-counsel-transactions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>As part of the Law Department, this attorney will serve as counsel for the company in connection with licensing, business development, strategic transactions, research collaborations and services arrangements. The role is responsible for drafting, reviewing, and negotiating agreements; advising senior management on proposed transactions; and ensuring compliance with existing contractual obligations, company policy, and applicable law. The successful candidate will have proven experience in biotech, pharmaceuticals, technology or similar transactions, including structuring complex deals, advising on intellectual property matters, and managing risk across regulatory and corporate legal matters. The ideal candidate will have a history of progressive in-house or firm experience and will thrive in a highly collaborative culture.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Partner with senior management and the business development team on major corporate initiatives, including collaborations, partnerships, and licensing agreements.</p></li><li><p>Negotiate and draft sophisticated licensing, collaboration, services and other agreements, including novel structures where no precedents exist.</p></li><li><p>Support critical collaborations with the alliance management team and provide legal counsel as issues arise.</p></li><li><p>Work closely with the intellectual property department to ensure accurate protection and management of IP assets.</p></li><li><p>Advise on regulatory and legal matters affecting existing or proposed arrangements, including privacy, antitrust, securities, and corporate law.</p></li><li><p>Manage outside counsel relationships on relevant legal matters, including strategy, workstreams, and budget oversight.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>JD with strong academic credentials; BA/BS required.</p></li><li><p>Minimum 8 years of relevant experience negotiating and drafting complex agreements in the biotech, pharmaceutical, or life sciences sector.</p></li><li><p>In-house experience preferred; biotech experience strongly preferred.</p></li><li><p>Licensed to practice law in New York, or eligible for licensure as registered in-house counsel.</p></li><li><p>Please include a representative deal sheet with your application.</p></li><li><p>Deep expertise in contracts law, including drafting, negotiation, and risk analysis.</p></li><li><p>Ability to manage a high volume of client requests and competing priorities effectively.</p></li><li><p>Strong track record in business development, strategic alliances, partnerships, and collaborations.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 21:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Sourcing Specialist Global Procurement]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46412]]></requisitionid>
    <referencenumber><![CDATA[R46412]]></referencenumber>
    <apijobid><![CDATA[r46412]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46412/sr-sourcing-specialist-global-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking for a Sr Sourcing Specialist Global Procurement. In this role, you will be responsible for end-to-end management of assigned categories, including the category strategy development, category sourcing plan execution, and projects to optimize value. You will also support the planning and execution of strategic sourcing initiatives. This person will develop sourcing specifications, requirements and related scope of work, conducting data gathering, support spend analytics, assist in delivering measurable cost savings, and monitor savings against contracts.</p><p>In this role, a typical day may include the following:</p><p> Strive towards continuous vendor improvement and effectively manage relationships with key category vendors and business stakeholders.</p><p>· Develop and sustain vendor and customer relationships as well as assist in ensuring accountability exists within the managed category and performance is tracked.</p><p>· Align with stakeholders and business leaders on their needs and provide Project Management and support for multiple projects within budget and on time</p><p>· Responsible for continuous quality and service from suppliers to support efficient business operations</p><p>· Accountable for category spend savings targets and objectives</p><p>This role may be a fit for you if you:</p><p>· Are responsible for sound contract management and drive continuous value out of the contract</p><p>· Are accountable for contract agreements and addendums and ensure valid contracts are in place</p><p>Can lead category supplier relationships and sourcing opportunities, including RFPs, negotiations, etc.</p><p>To be considered for this role you must possess a Bachelor’s degree in a relevant field of study with at least 5 years of relevant experience. Pharmaceutical industry experience preferred. Will substitute relevant experience for education requirement.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 08:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Contract Operations Analyst]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46474]]></requisitionid>
    <referencenumber><![CDATA[R46474]]></referencenumber>
    <apijobid><![CDATA[r46474]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46474/contract-operations-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's US Contract & Pricing Operations team is seeking a highly organized and analytical <strong>Contract Operations Analyst</strong> to support our ever-evolving Group Purchasing Organization (GPO) contracting space. This role is critical in managing the daily operations and contract performance of accounts and ensuring compliance with our pricing agreements in both the Oncology and Ophthalmology franchises. The Contract Operations Analyst will successfully partner with functional market access, strategy, sales, finance, legal, and government pricing teams.</p><h3>A typical day may include:</h3><ul><li>Creating and testing program components in the Model N contracting and rebate platforms based on set program strategies.</li><li>Updating customer membership details in Model N.</li><li>Timely and accurate processing of all GPO and similar rebate claims.</li><li>Staying up to date with pricing programs for the different brands.</li><li>Reviewing all new customers entering Regeneron’s ecosystem of databases and effectively communicate with internal and external customers and vendors (Specialty Distributors, 3PL, GPOs, HCPs) to ensure that accurate pricing and discounts are being extended, providing resolution of customer issues in a timely manner.</li><li>Monitoring contract requirements to ensure customer and Regeneron remain in compliance with contract terms and conditions as well as any government regulations.</li><li>Maintaining contract parameters in partnership with our 3PL, including customer membership/affiliations, product, prices, performance tiers, date ranges, and incentive percentages.</li><li>Communicating changes in any pricing program activities to customers and vendors.</li><li>Resolving all chargebacks issues in an accurate and timely manner. Proactively review, analyze, and establish claim processing standard operating procedures as needed to ensure claims are processed according to company policies and contractual obligations.</li><li>Developing reports and analysis to support metric tracking statistics to departmental management as requested in order to advise as to the status, volume, and potential accrual needs of future rebates, fees, and other payments.</li><li>Responding to internal and independent audit requests related to our rebate and system processes.</li><li>Producing departmental materials to document work activity and processes.</li><li>Developing and maintain appropriate policies and procedures related to pricing strategies.</li></ul><h3>This role may be for you if:</h3><ul><li>Demonstrates attention to detail, strong time management, and takes a hands-on approach to contract-related activities.</li><li>Can work in a fast-paced environment with several concurrent priorities.</li><li>Has a strong knowledge of Excel.</li></ul><p>To be considered for this role you must have a bachelor's degree. We would prefer you to have 2 years of experience in the pharmaceutical industry. Lastly, you will need to be onsite for 4 days a week in the Sleepy Hollow, NY office.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 11:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Corporate Counsel]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48766]]></requisitionid>
    <referencenumber><![CDATA[R48766]]></referencenumber>
    <apijobid><![CDATA[r48766]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48766/senior-director-corporate-counsel/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build Our Future Together</strong></p></div><p>The Senior Director, Assistant General Counsel – Market Access Legal will provide proactive, efficient, strategic, and collaborative legal support to Regeneron’s Market Access Commercial Business Unit. More specifically, this person will advise a wide range of internal Market Access and other clients, including Market Access Strategy; National and Regional Payer Account Teams; the Government Pricing, Contract Strategy, Pricing, and Operation Team; as well as Commercial; Marketing; Sales; Public Policy and Government Affairs; Regulatory; and Corporate Compliance. The level of counseling requires a deep understanding of market access principles, market access strategy, payers, pharmacy benefit managers (“PBM”), payer and PBM contracts, pharmaceutical distribution channels, contract operations, government pricing, regulatory and compliance issues, the False Claims Act, the Anti-Kickback Statute, and OIG guidance, and other applicable state and federal healthcare laws. </p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Providing proactive, efficient, strategic, and collaborative legal advice and support on market access, market access strategy, payer and PBM contracts, payer and PBM strategies, government pricing, and other Commercial-related matters in a fast-paced environment</p></li><li><p>Providing legal guidance on various issues, tactics, and activities, including market access strategy development, creation of market access materials, contract drafting and negotiation, government pricing reporting, and interactions with healthcare providers, distributors, pharmacies, payers, PBMs, and GPOs</p></li><li><p>Drafting and negotiating a wide variety of commercial contracts including payer and PBM agreements, GPO agreements, distribution agreements, pharmacy agreements, rebate agreements, service agreements, and other corporate agreements</p></li><li><p>Provide support to various Commercial teams and Product Attorneys on product-specific Market Access issues</p></li><li><p>Provide support to Corporate Compliance on Market Access issues</p></li><li><p>Maintain an independent and objective perspective while developing and maintaining a strong partnership with the client organizations</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>JD with 10+ years relevant legal experience</p></li><li><p>Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel</p></li><li><p>Prior in-house healthcare/pharmaceutical and/or biotech experience required</p></li><li><p>Significant knowledge of life sciences regulatory enforcement trends, market access, market access strategy, payer and PBM-related issues, payer and PBM contracts, other market access contracts, contract operations, government pricing requirements (ideally for both medical and pharmacy benefit products), regulatory and compliance issues, the FDCA, the False Claims Act, federal and state fraud and abuse laws, and antitrust laws</p></li><li><p>Excellent interpersonal and conflict resolution skills, and ability to work in highly collaborative, team-oriented environment</p></li><li><p>Excellent understanding of healthcare laws and proven experience in applying them to complex business situations</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 11:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Toxicology Operations - Remote]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47614]]></requisitionid>
    <referencenumber><![CDATA[R47614]]></referencenumber>
    <apijobid><![CDATA[r47614]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47614/manager-toxicology-operations-remote/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Toxicology Operations Manager to join our Toxicology team, leading scientific, technical, and operational tasks as assigned to support toxicology program representatives and toxicology department leadership. In this role, you will independently manage and be responsible for the contracting, drug supply, protocol development, and conduct of non-GLP and GLP Toxicology studies through remote and on-site CRO monitoring. The individual will also contribute to the review and evaluation of study data providing program toxicologists with data summaries to enable alignment on study results. The individual will also contribute outside of the Toxicology department presenting study results to preclinical subteams and global project teams as required.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p><strong>Location </strong>– Full Time - Remote position with occasional International and Domestic travel.</p><p><strong>Discover your role:</strong></p><p><strong>This role might be a fit for you,</strong></p><ul><li>Serves in a principal operational role for the Toxicology department, ensuring assigned department and project goals are achieved as assigned</li><li>Assists in defining standard departmental practices (including SOPs) for the conduct and reporting of Toxicology studies</li><li>Serves as the lead study monitor or sponsor representative with administrative oversight related to the conduct of Toxicology studies conducted at CRO</li><li>Collaborates with lead scientists providing direct input and suggestions on study designs and protocols</li><li>Responsible for independent coordination of study outsourcing (RFP, contracting, protocol development, monitoring, and reporting)</li><li>Provides detailed evaluation of experimental data from Toxicology studies and aligns with program toxicologists to interpret, report and present results</li><li>Assists/Directs the collection and evaluation of metrics associated with the conduct of Toxicology studies</li><li>Provides toxicology leadership assistance in regulatory inspection readiness activities</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s or Master’s degree in biological sciences with more than 7 years of post-degree experience within a pharmaceutical/drug development environment.</li><li>Significant experience in the design, monitoring and interpretation of regulated nonclinical safety studies.</li><li>Knowledge of communicating Toxicology study results up to the level of global project teams.</li><li>Ability to trouble-shoot challenges arising during the conduct of Toxicology studies</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - OKLAHOMA CITY, OK]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48929]]></requisitionid>
    <referencenumber><![CDATA[R48929]]></referencenumber>
    <apijobid><![CDATA[r48929]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48929/medical-account-specialist-ii-hematology-oklahoma-city-ok/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Oklahoma]]></city>
    <state><![CDATA[Oklahoma]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Oklahoma City, OK</strong></p><ul><li><strong>Geography: </strong><strong>Oklahoma City, Tulsa, Albuquerque, Amarillo</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY- WASHINGTON, DC]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48926]]></requisitionid>
    <referencenumber><![CDATA[R48926]]></referencenumber>
    <apijobid><![CDATA[r48926]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48926/medical-account-specialist-ii-hematology-washington-dc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Washington DC</strong></p><ul><li><strong>Geography: </strong><strong>Washington DC, Arlington, Cumberland, Alexandria</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  ORLANDO, FL]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48921]]></requisitionid>
    <referencenumber><![CDATA[R48921]]></referencenumber>
    <apijobid><![CDATA[r48921]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48921/medical-account-specialist-ii-hematology-orlando-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Orlando</strong></p><ul><li><strong>Geography: </strong><strong>Orlando, Lakeland, Port Saint Lucie</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Great Lakes)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48127]]></requisitionid>
    <referencenumber><![CDATA[R48127]]></referencenumber>
    <apijobid><![CDATA[r48127]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48127/field-reimbursement-manager-neurology-great-lakes/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Chicago (Metro) IL</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vice President, Research (Neuroscience)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42013]]></requisitionid>
    <referencenumber><![CDATA[R42013]]></referencenumber>
    <apijobid><![CDATA[r42013]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42013/vice-president-research-neuroscience/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Seeking experienced, rigorous, and innovative leader to direct Regeneron’s Neuroscience research team, consisting of approximately 50 dynamic researchers currently focusing on development of therapeutics against neurodegenerative diseases, motor neuron disease, chronic pain, and neuropsychiatric disorders, utilizing biologics and genetic medicines. Successful candidate would direct and inspire Neuroscience’s preclinical team by using their deep and broad expertise to set strategic vision, suggest novel technological approaches, and critically evaluate data and projects. Candidate would be expected to participate in translational activities, progressing drug targets along the pipeline from early research through clinical development. Candidate would also participate in Regeneron’s broader scientific community, participating actively in cross-functional meetings and representing Regeneron’s Neuroscience vision to Senior Leadership and external collaborators. </p><p><strong>As a Vice President of Neuroscience Research a typical day might look like: </strong></p><ul><li>Directly supervise Regeneron’s senior Neuroscience leadership team and manage the broader group, providing vision, inspiration, and both short-term and long-term goals. Communicate priorities, policies, and goals of Regeneron Senior Leadership to the broader Neuroscience group.</li><li>Identify new strategies or technologies, including genetic medicines, for pursuing novel targets and approaches.</li><li>Set priorities and ensure progression of, or go/no-go decisions for, targets and projects. Be familiar with processes and procedures for moving targets from preclinical research through the development pipeline.</li><li>Actively participate in departmental, cross-functional, senior leadership, and external meetings to contribute neuroscience expertise and to represent the goals and vision of the Neuroscience group.</li><li>Interact broadly and collaboratively with other therapeutic focus areas and technology groups within the company, forging relationships and active collaborations, as well as leveraging technologies to advance neuroscience research as a systems-level endeavor.</li><li>Identify and mentor the Neuroscience group, providing opportunities, visibility, and challenge in order to develop all group members to their maximum scientific and professional potential.</li><li>Conduct or oversee review of neuroscience-related documents, including regulatory submissions, manuscripts, contracts, etc. </li></ul><p><strong>This role might be for you if: </strong></p><ul><li>Both deep and broad expertise in the field of Neuroscience essential.</li><li>Familiarity with cutting edge technology, including genetics medicines, and proven experience applying technology to neuroscience-related questions essential.</li><li>Strong written and oral communication skills with the ability to communicate both science and vision essential.</li><li>Strong leadership skills with managerial and mentorship experience and excellence essential.</li><li>Experience with administratively directing a group (managing budget and organization, etc.) essential.</li><li>Exposure to drug development or similar regulated activities highly desirable.</li><li>Broad network of colleagues and collaborators, strong publication record, and national/international reputation desirable.</li><li>At least 10 years experience after PhD; 20+ years desirable; a minimum of 5 years in an industry or translational setting.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, QA Validation Oversight]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43170]]></requisitionid>
    <referencenumber><![CDATA[R43170]]></referencenumber>
    <apijobid><![CDATA[r43170]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43170/manager-qa-validation-oversight/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div><div><p>Regeneron is hiring a Manager, QA Validation Oversight to lead a team dedicated to ensuring the integrity of our process validation processes. This role is integral in supporting process validation activities, ensuring global consistency, addressing recurring themes in process documentation, and playing a pivotal role in regulatory inspections and compliance. </p></div><div></div><div><p>In this role, a typical day might include the following: </p></div><div><ul><li><p>Ensuring alignment between validation activities and Process Sciences initiatives to support successful transition of processes from development to manufacturing. </p></li></ul></div><div><ul><li><p>Collaborate closely with internal Process Sciences team to provide technical expertise and ensure consistency in Process Validation strategies. </p></li></ul></div><div><ul><li><p>Presenting/defending validation strategies, documentation, and processes to FDA and other regulatory agencies. </p></li></ul></div><div><ul><li><p>Reviewing and approving process validation documents, procedures, and protocols, proposing modifications and corrections where necessary to meet regulatory requirements and expectations. </p></li></ul></div><div><ul><li><p>Overseeing all aspects of QA Validation including review and approval of failure investigations, change controls, SOPs, Validation protocols and summary reports, and validation master plans. </p></li></ul></div><div><ul><li><p>Conduct one-on-one discussions with team members to review their performance feedback and set development goals, fostering professional growth within the team. </p></li></ul></div><div></div><div><p>This role might be a for you if you: </p></div><div><ul><li><p>Bring hands-on validation experience in a GMP-regulated environment. </p></li></ul></div><div><ul><li><p>Possess deep understanding and expertise in Process Validation. </p></li></ul></div><div><ul><li><p>Enjoy building strong, collaborative relationships across global internal teams. </p></li></ul></div><div><ul><li><p>Have a continuous improvement mindset. </p></li></ul></div><div><ul><li><p>Are an experienced leader who inspires and guides a multi-tiered team. </p></li></ul></div><div></div><div><p>To be considered for this role, you must hold a Bachelor’s degree in Engineering, Chemistry, or Life Sciences degree and the following minimum years of experience for each level: </p></div><div><ul><li><p>Associate Manager: 6+ years </p></li></ul></div></div><div><div><ul><li><p>Manager: 7+ years </p></li></ul></div><div></div><div><p>May substitute relevant experience in lieu of education requirement. Level is determined on qualifications relevant to the role. </p></div><div></div><div><p>#REGNQA </p></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$90,800.00 - $173,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Quality Technical Operations]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45585]]></requisitionid>
    <referencenumber><![CDATA[R45585]]></referencenumber>
    <apijobid><![CDATA[r45585]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45585/director-quality-technical-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is hiring! As the Director of Quality Technical Operations you will lead a high-impact Quality function spanning QA MES, QA Validation Oversight, and QA Tech Transfer. You’ll define and implement cGMP best practices, set quality standards and metrics, and ensure clinical and commercial manufacturing operations meet and exceed regulatory compliance requirements.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Define and implement quality standards, systems, and metrics across clinical and commercial manufacturing operations.</p></li><li><p>Provide quality oversight to activities related to validation and ensure that they are effectively administered and comply with regulatory requirements.</p></li><li><p>Oversee QA tasks related to electronic manufacturing record management and tech transfer.</p></li><li><p>Compile, organize, and present quality metrics and trends to senior leadership.</p></li><li><p>Plan and allocate QA resources to meet program goals, timelines, and priorities.</p></li><li><p>Coordinate prioritization of activities with area management to optimize execution.</p></li><li><p>Prepare for regulatory and customer audits; ensure observations are addressed effectively and on schedule.</p></li><li><p>Maintain safety and operational standards and approve documents related to QA functions.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Proven leadership in cGMP environments with hands-on experience in QA systems and metrics.</p></li><li><p>A track record of successful audit readiness, execution, and response management.</p></li><li><p>Strong collaboration, communication, and stakeholder engagement skills.</p></li><li><p>An understanding of bulk API biologics manufacturing operations.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Life Sciences or related field and the following amount of relevant pharmaceutical manufacturing experience for each level:</p><ul><li><p>Director – 12+ years</p></li><li><p>Sr Director – 15+ years</p></li></ul><p>Level to be determined based on qualifications relevant to the role. May substitute proven experience for education requirement.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician, Tuesday-Saturday 3rd Shift]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45542]]></requisitionid>
    <referencenumber><![CDATA[R45542]]></referencenumber>
    <apijobid><![CDATA[r45542]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45542/calibration-technician-tuesday-saturday-3rd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a Calibration Technician to our growing team, working a Tuesday-Saturday 10:00pm – 8:30am shift. Our Calibration Technicians support our manufacturing by performing mechanical, electrical, calibration, electronic, or utility related tasks.</p><p><strong>Please note training will take place Monday-Friday 8:00am-4:30pm for approximately 6 months. Working hours thereafter will be Tuesday-Saturday 10:00pm-8:30am. </strong><strong>Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a Calibration Technician, a typical day might include the following:</p><ul><li>Calibrating various types of instrumentation including temperature, pressure, level, flow and analytical instruments</li><li>Performing loop check, tune, troubleshoot, and start-up of instrumentation</li><li>Working with medium and low voltages</li><li>Performing basic plumbing and tube bending jobs</li><li>Assisting the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</li><li>Performing daily Work Orders (WO) and Preventative Maintenance (PM) and efficiently coordinate the workflow and documentation of PMs and WOs</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Following current Good Manufacturing Practices (cGMPs)</li><li>Occasionally working on other facility related work tasks/issues that are outside the calibration department’s normal work duties</li><li>May include planning and scheduling outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, and quality standards</li><li>Participation in compliance investigations if and when necessary</li><li>Full gowning required when entering and working on production floor</li><li>Participating in rotation on-call schedule</li></ul><h3>This role might be for you if you:</h3><ul><li>Demonstrate basic problem-solving skills</li><li>Are able to learn and follow routine procedures independently as well as part of a team</li><li>Are comfortable and have the flexibility to work in a changing environment</li><li>Can lift, push, and pull at least 50lbs</li><li>Seek to build and maintain positive working relationships with the business</li><li>Possess strong written and verbal communication skills</li><li>Maintain effective time management skills to allow deadlines to be met in a timely manner</li><li>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><p>To be considered for the Calibration Technician position you must be willing and able to work a Tuesday-Saturday 10:00pm – 8:30am schedule. Applicants ideally should have an AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum amounts of experience for each level:</p><ul><li>Calibration Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</li><li>Calibration Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</li><li>Calibration Technician IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>Prior experience in the maintenance and operation of large-scale utilities plant preferred and ISA CCST Certification is strongly preferred but not required.</p><p>#REGENTOSK </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$28.46 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician, Wednesday - Saturday 2nd Shift]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45540]]></requisitionid>
    <referencenumber><![CDATA[R45540]]></referencenumber>
    <apijobid><![CDATA[r45540]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45540/calibration-technician-wednesday-saturday-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>We are currently looking to add a Calibration Technician to our growing team, working a Wednesday - Saturday 2pm – 12:30am shift. Our Calibration Technicians support our manufacturing by performing mechanical, electrical, calibration, electronic, or utility related tasks.</div></div><div><div><div><div><div><div><div><div><div><p><strong>Please note training will take place Monday-Friday 8:00am-4:30pm for approximately 6 months. Working hours thereafter will be Wednesday-Saturday 2pm-12:30am. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a Calibration Technician, a typical day might include the following:</p><ul><li><p>Calibrating various types of instrumentation including temperature, pressure, level, flow and analytical instruments</p></li><li><p>Performing loop check, tune, troubleshoot, and start-up of instrumentation</p></li><li><p>Working with medium and low voltages</p></li><li><p>Performing basic plumbing and tube bending jobs</p></li><li><p>Assisting the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</p></li><li><p>Performing daily Work Orders (WO) and Preventative Maintenance (PM) and efficiently coordinate the workflow and documentation of PMs and WOs</p></li><li><p>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</p></li><li><p>Following current Good Manufacturing Practices (cGMPs)</p></li><li><p>Occasionally working on other facility related work tasks/issues that are outside the calibration department’s normal work duties</p></li><li><p>May include planning and scheduling outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, and quality standards</p></li><li><p>Participation in compliance investigations if and when necessary</p></li><li><p>Full gowning required when entering and working on production floor</p></li><li><p>Participating in rotation on-call schedule</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Demonstrate basic problem-solving skills</p></li><li><p>Are able to learn and follow routine procedures independently as well as part of a team</p></li><li><p>Are comfortable and have the flexibility to work in a changing environment</p></li><li><p>Can lift, push, and pull at least 50lbs</p></li><li><p>Seek to build and maintain positive working relationships with the business</p></li><li><p>Possess strong written and verbal communication skills</p></li><li><p>Maintain effective time management skills to allow deadlines to be met in a timely manner</p></li><li><p>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</p></li></ul><p>To be considered for the Calibration Technician position you must be willing and able to work a Wednesday - Saturday 2pm-12:30am schedule. Applicants ideally should have an AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum amounts of experience for each level:</p><ul><li><p>Calibration Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li><li><p>Calibration Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p></li><li><p>Calibration Technician IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</p></li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>Prior experience in the maintenance and operation of large-scale utilities plant preferred and ISA CCST Certification is strongly preferred but not required.</p><p>#REGENTOSK </p></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.49 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Scientist, Hematology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46313]]></requisitionid>
    <referencenumber><![CDATA[R46313]]></referencenumber>
    <apijobid><![CDATA[r46313]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46313/manager-clinical-scientist-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Clinical Sciences, Hematology leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Senior Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p>As a Manager, a typical day may include the following:</p><ul><li><p>Member of the Clinical Study Team and Global Clinical sub-team</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Develops/maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late-stage assets</p></li><li><p>Assists with development of the Expanded Synopsis and may author clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may authors/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Contributes to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority). Presents data and information to external investigators (SIV) and internal collaborators</p></li></ul><p>This role may be for you if:</p><ul><li><p>Possess demonstrated knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrate solid medical writing skills</p></li><li><p>Proven ability to influence within team and may influence across functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li></ul><p>To be considered for this position, you must have a minimum of Bachelor’s Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). We are seeking ≥ a minimum of 3 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. You have a basic knowledge of oncology or hematology therapeutic areas as well as a proven track in clinical trial process improvements. We need an individual with demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Resolves novel problems requiring creative application of advanced skill, training, and education.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Hematology ( TN, AL, MS, AR)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46458]]></requisitionid>
    <referencenumber><![CDATA[R46458]]></referencenumber>
    <apijobid><![CDATA[r46458]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46458/associate-director-field-medical-affairs-hematology-tn-al-ms-ar/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. We are expected to demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><p><strong>Territory:</strong> Tennessee, Alabama, Mississippi and Arkansas (residency in the territory is required with a preference of TN and AL. </p><p><strong>A typical day may include the following:</strong> <br>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.<br>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies<br>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.<br>• Participates in the development and management of company sponsored clinical trials including.<br>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy<br>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.<br>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally</p><p><strong>This may be for you if you:</strong><br>• Want to be a part of a pre-launch stage team potentially for multiple launches.<br>• Are skilled in the art of strategic conversation along with a proven ability to assess issues adapting appropriately.<br>• Can demonstrate an understanding of “know your audience” and ability to tailor information appropriately.<br>• Have demonstrated the ability to anticipate, organize, plan and handle multiple priorities, while adapting to the needs of the company.</p><p>To be considered a terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required. 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. </p><p><strong>Additional requirements: </strong><br>• Residency in the assigned territory <br>• Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.<br>• Possesses and maintains a valid driver’s license and clean driving record.</p><p><strong>Preferred experiences include: </strong><br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies<br>• Drug launch experience. <br> </p><p><strong> </strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Project Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47032]]></requisitionid>
    <referencenumber><![CDATA[R47032]]></referencenumber>
    <apijobid><![CDATA[r47032]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47032/principal-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an experienced Engineer to join our growing Project Engineering team. Our team designs, specifies and commissions new and renovated biopharmaceutical process and clean utility equipment. We provide engineering support and lead deviation investigations for existing equipment and manufacturing processes to support the production of our life-changing medications.</p><p>As a Principal Project Engineer, a typical day might include the following:</p><ul><li>Designing and specifying cGMP process equipment, piping, and/or controls including development and review of engineering documentation</li><li>Managing mid-to-large sized projects related to process equipment and clean utilities including start-up and commissioning</li><li>Leading the design review, site acceptance and installation of equipment</li><li>Preparing piping and instrumentation diagrams and other related drawings</li><li>Developing Process Flow Diagrams for manufacturing processes</li><li>Supporting QA/Validation department by preparing design documents and assisting in protocol execution</li><li>Assisting in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations and test plans for executing modification change control documentation</li><li>Supervising mechanical, electrical, and automation and engineering contractors</li><li>Traveling up to 10% of the time, both domestically and internationally</li></ul><p>This position might be for you if you:</p><ul><li><p>Are interested in having a broad scope with a variety of tasks, seeing the entire process, not just specific equipment or processes</p></li><li>Enjoy solving puzzles and challenges, supporting investigations across the business</li><li>Have a desire to contribute to elements of design work by helping to specify and translating customer needs into equipment</li><li>Want to do more than just project management or troubleshooting, balancing your technical and project management skills</li><li>Have a solid understanding of process control systems and automation</li><li>Are skilled at planning and tracking project activities and schedules</li><li>Are thoroughly knowledgeable with engineering documentation required for cGMP process equipment as well as sanitary equipment design requirements</li><li>Have working knowledge of biopharmaceutical equipment</li><li>Have demonstrated strengths with strong interpersonal, cross-cultural communication</li><li>Are adept at building and maintaining relationships and leading without direct authority</li><li>Show resiliency and flexibility in the face of challenging situations</li></ul><p>Qualified candidates must have a Bachelor's degree Chemical Engineering or Biochemical Engineering (or another relevant Engineering discipline) and the following minimum years of experience in project/process engineering or an equivalent combination of education and experience. Direct experience with biopharmaceutical process equipment is preferred.</p><ul><li>Senior Project Engineer: 5+ years</li><li>Principal Project Engineer: 8+ years</li></ul><p>Level will be determined based on qualifications relevant to the role. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Corporate Counsel - Privacy/ Transactions]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47353]]></requisitionid>
    <referencenumber><![CDATA[R47353]]></referencenumber>
    <apijobid><![CDATA[r47353]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47353/senior-director-corporate-counsel-privacy-transactions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Regeneron Pharmaceuticals is seeking a highly experienced transactions attorney for a pivotal role to serve as a transactional attorney and liaison to the Regeneron Data Privacy Office. This position will act as a privacy expert within the Transactions & Contracts team offering guidance to colleagues on privacy law and ensuring that privacy provisions are seamlessly integrated into our contracts. The position also involves drafting, reviewing, negotiating, and providing strategic counsel on a diverse portfolio of significant agreements across our innovative business units, overseeing the operations of Regeneron’s contract lifecycle management system, including managing the group’s Associate Director, Contracts and Systems Operations.</p></div><div><div><div><div><div><div><div><div><div><p>Your expertise will be instrumental in advising the Transactions Team on complex privacy issues, requiring a deep understanding of life sciences, business transactions, and data privacy. We are looking for a candidate with exceptional drafting and negotiation skills, life sciences law expertise, leadership capabilities and a proven track record of progressive experience in contract law and data privacy. The ideal candidate thrives in collaborative settings, working alongside multiple stakeholders to provide comprehensive legal solutions that drive Regeneron's success.</p><p><em><strong>The role will be based onsite at our offices in Cambridge, MA or Sleepy Hollow, NY. This is not open to fully remote-based work arrangements. If eligible, we can offer relocation benefits. </strong></em></p><p><br><strong>A typical day might include the following:</strong></p><ul><li><p>Providing legal support for a particular area of business transactions, which may include research collaboration agreements, master services agreements, consulting services agreements, license agreements, data use agreements, laboratory services agreements and confidentiality agreements, among others.</p></li><li><p>Maintaining subject matter expertise in data privacy laws and the Regeneron privacy policies and advising Transaction Law colleagues and clients on developments of importance.</p></li><li><p>Providing ongoing one-on-one support to members of the Transaction Law team and coordinating with internal teams and external resources to negotiate and finalize data privacy language in third-party agreements.</p></li><li><p>Responding to U.S. and ex-U.S. contracting questions.</p></li><li><p>Managing updates to the group’s data privacy contracting playbook.</p></li><li><p>Creating data privacy contracting tools and training materials.</p></li><li><p>Managing office hours with internal business partners.</p></li><li><p>Developing and training on privacy contracting tools and requirements.</p></li><li><p>Acting as liaison for the Transactions Law Group with the Data Privacy Office on data privacy policy questions and approaches.</p></li><li><p>Providing strategic direction and oversight for Regeneron’s contract lifecycle management system, including serving as the manager of the team’s Associate Director, Contracts Systems and Operations.</p></li><li><p>Providing contract law support for the Regeneron Cell Medicines team in Cambridge.</p></li></ul><p><br><strong>This role might be for you if:</strong></p><ul><li><p>You have the ability to work independently, while meeting aggressive deadlines and juggling multiple matters.</p></li><li><p>You are able to maintain an objective perspective while developing and maintaining strong partnerships with key stakeholder / client organizations and protecting Regeneron’s interests.</p></li><li><p>You are an effective leader and can work effectively and professionally with colleagues and clients at all levels of the organization and in a collaborative, team-oriented environment.</p></li><li><p>You have the ability to effectively convey to, and respond to questions from, colleagues and key stakeholders, on data privacy law and other general legal concepts. </p></li></ul><p><br><strong>To be considered for this position</strong> you must possess a JD with excellent law school credentials. Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel is preferred. At least 15 years of legal experience at a law firm and/or in-house, with biotech/pharmaceutical and/or health care experience. Solid understanding of contracts and related law. Experience with contracts involving data privacy and intellectual property. Experience in strategic leadership of contract management systems or similar role is preferred. You should also have a high level of business acumen, excellent contract drafting and negotiation proficiency, exceptional oral and written communication skills and interpersonal and conflict resolution capability.</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Allergy (western states)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47512]]></requisitionid>
    <referencenumber><![CDATA[R47512]]></referencenumber>
    <apijobid><![CDATA[r47512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47512/associate-director-field-medical-affairs-allergy-western-states/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p> This is a pre-launch opportunity to join a newly formed field medical team. As an Associate Director, Field Medical Affairs, you will serve as the primary scientific presence in your territory, engaging in meaningful exchange of clinical data and medical information with KOLs, HCPs, clinical research investigators, pharmacists, and other decision makers. You will build investigator relationships, site infrastructure, and medical intelligence that shape our program’s clinical and medical trajectory. We will align field activities with strategic medical plans, gather actionable insights on the evolving treatment landscape, and support research and development that advances both the pipeline and patient outcomes.</p><p>Territory: western states</p><p><strong>A Typical Day May Include:</strong><br>• Collaborate with Clinical Development to identify, qualify, and establish clinical research sites in your territory<br>• Cultivating investigator relationships ahead of study activation to build scientific credibility and organizational trust<br>• Mapping the KOL and investigator landscape in allergy/immunology to inform clinical and medical strategy<br>• Gathering early field insights into treatment patterns, unmet needs, and emerging science to shape the medical plan<br>• Supporting development of medical affairs infrastructure, including educational materials and scientific exchange tools, prior to launch<br>• Acting as a primary clinical/scientific resource to HCPs for disease-state and product information to ensure awareness and understanding<br>• Establishing, fostering, and maintaining peer relationships with KOLs in allergy/immunology<br>• Identifying and reporting medical insights<br>• Identifying research gaps and educational needs to inform medical strategy.<br>• Responding to requests for information related to study indications, disease states, and the therapeutic area, and discussing scientific and clinical data with appropriate audiences in a compliant manner.<br>• Ensuring company policies, procedures, principles, and financial controls are upheld with integrity and professionalism.</p><p>T<strong>his may be for you if you:</strong><br>• Thrive working independently making a meaningful impact on the company’s mission.<br>• Are passionate about developing expertise in and sharing clinical and scientific data. <br>• Enjoy building collaborative relationships across academic and clinical practice settings.<br>• Can balance multiple initiatives, prioritize amid ambiguity, and implement independently while keeping partners engaged and informed.<br>• Are energized by pre-launch work and motivated by the opportunity to build investigator networks and scientific infrastructure from the ground up.</p><p>To be considered a Clinical or scientific doctorate: MD, PharmD, PhD, DNP, or DVM is required. 8 years of experience in a relevant scientific, clinical, or pharmaceutical role, including 4+ years as a Medical Science Liaison in the pharmaceutical industry is required. Experience in allergy/immunology is required. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharmaceutical compliance, and OIG guidelines. Ability to travel frequently (approximately 50%), including air travel, overnight stays, and occasional weekend travel. Prior experience in a pre-launch or launch phase MSL role is preferred. Experience supporting clinical trial site identification, feasibility assessment, or investigator engagement would be helpful. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists  - Hematology - Richmond, VA]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47832]]></requisitionid>
    <referencenumber><![CDATA[R47832]]></referencenumber>
    <apijobid><![CDATA[r47832]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47832/medical-account-specialists-hematology-richmond-va/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Richmond]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Richmond, VA, Norfolk, VA, Virginia Beach, VA, Charleston, WV, Morgantown, WV</strong></p><p>The Hematology Oncology Account Specialist, is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Hematology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of two bispecific agents to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Engineer]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47522]]></requisitionid>
    <referencenumber><![CDATA[R47522]]></referencenumber>
    <apijobid><![CDATA[r47522]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47522/senior-automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Our Automation Engineers keep our cutting-edge process controls and process monitoring systems running at peak efficiency. We provide unsurpassed expertise in designing, developing, implementing, and optimizing Regeneron’s sophisticated biopharmaceutical manufacturing processes.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Monday-Friday 8:00am-4:30pm</li><li>East Greenbush, NY</li></ul><br><h3>Discover your role:</h3><ul><li>Provide advanced level of technical automation support and troubleshooting to Manufacturing, Quality Control, and Facilities according to established SOPs and departmental practices.</li><li>Lead and perform investigations relating to manufacturing deviations and anomalies associated with automation systems and control system software.</li><li>Develop and edit engineering design documents, technical evaluations, and test plans for cGMP process equipment and follow GAMP 5 guidelines.</li><li>Lead engineering and validation projects as well as provide support to manufacturing activities with process control and process monitoring equipment software design, commissioning, protocol review, and testing to meet end user requirements.</li><li>Update or author system specifications, user requirements, functional requirements, and system design specifications.</li><li>Generate and execute necessary testing and qualification protocols as related to the overall design and performance of automated process and monitoring equipment.</li><li>Lead multiple small to medium sized manufacturing process control projects related to corrective action, equipment performance improvement, and new equipment.</li><li>Design, develop, and implement software/hardware improvements to automated process control and process monitoring equipment according to change control procedures.</li><li>Develop and execute test plans for software/hardware improvements to automated process control and process monitoring equipment according to change control procedures.</li><li>Participate in the rotation for automation support.</li></ul><br><h3>This role requires:</h3><ul><li>BS in Engineering or a related field and 5+ years of relevant experience. Equivalent combination of education and experience with process control systems and/or data acquisition systems may be considered.</li><li>Experience in the design and maintenance of process control systems and/or data acquisition systems.</li><li>Some experience in a regulated manufacturing environment is preferred.</li><li>We use primarily Rockwell Automation control system products; specific knowledge with these products is ideal.</li><li>An appreciation for a meticulous process of change control, investigations and corrective actions.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II NEUROLOGY- LOUISVILLE, KY]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48053]]></requisitionid>
    <referencenumber><![CDATA[R48053]]></referencenumber>
    <apijobid><![CDATA[r48053]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48053/medical-account-specialist-ii-neurology-louisville-ky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Louisville-Jefferson County5]]></city>
    <state><![CDATA[Kentucky]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Louisville (Metro), Kentucky </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - Northeast]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48149]]></requisitionid>
    <referencenumber><![CDATA[R48149]]></referencenumber>
    <apijobid><![CDATA[r48149]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48149/neurology-account-director-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: Northeast (New York, Pennsylvania, Massachusetts, Vermont, New Hampshire, Maine)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist,  Obesity Muscle & Metabolism]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47942]]></requisitionid>
    <referencenumber><![CDATA[R47942]]></referencenumber>
    <apijobid><![CDATA[r47942]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47942/senior-associate-scientist-obesity-muscle-metabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Obesity, Muscle and Metabolism group is seeking an enthusiastic Associate Scientist to advance our exciting discovery and translational programs focused on metabolic disease, skeletal muscle biology, and energy balance. The successful candidate will drive hands-on experimental work in cellular and in vivo systems, develop robust assays, and collaborate across biology, chemistry, pharmacology, and data science to generate decision-making data for pipeline programs. This is a lab-focused role suited for an experienced bench scientist with a strong foundation in metabolic biology. Depending on level, you will independently execute studies, contribute to study design, and influence project strategy. You will work across adipose and muscle biology, insulin signaling, mitochondrial function, and physiological readouts pertinent to obesity and related metabolic disorders.</p><p><strong>As a Sr Associate Scientist, a typical day may include: </strong></p><ul><li><p>Support or lead <em>in vivo</em> studies in rodent models of obesity, insulin resistance, and muscle dysfunction including compound dosing, tissue collection, and metabolic phenotyping</p></li><li><p>Conduct follow-up analysis of metabolic tissues from <em>in vivo</em> studies using qPCR, western blotting, immunohistochemistry and RNAScope</p></li><li><p>Design, execute, and troubleshoot in vitro experiments in primary and immortalized cell models of adipocytes and myotubes including differentiation, stimulation, and compound testing.</p></li><li><p>Analyze and interpret data using appropriate statistical methods and clearly communicate findings in written reports and presentations</p></li><li><p>Maintain meticulous electronic lab notebooks, SOPs, and assay documentation to ensure data integrity and reproducibility</p></li></ul><p><strong>This role may be for you if: </strong></p><ul><li><p>You enjoy working in a fast-paced environment</p></li><li><p>You are a fast learner and have desire to expand your skill set and learn new techniques</p></li><li><p>You are detail oriented, well-organized and can multi-task</p></li><li><p>You are a team player</p></li><li><p>You have strong communication skills</p></li></ul><p>To be considered, you must have: In Vivo experience. BS or MS in Cell Biology, Physiology, Molecular Biology, Pharmacology, or related discipline. Minimum of 3+ years of laboratory experience, preferably working with mouse models. Experience designing and executing metabolic studies in rodent models of obesity including indirect calorimetry, glucose and insulin tolerance testing, assessing food intake and body composition Competence with data analysis and visualization tools such as Excel, Prism, R, or Python and sound understanding of experimental design and statistics. Excellent presentation, time management, and collaborative skills. Preferred Additional Qualifications- Tissue culture, western blotting, ELISA and flow cytometry experience in various cell lines.Histologic experience with metabolic tissues including liver, skeletal muscle, pancreas and brain.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Patient & Consumer Marketing (Neuro)]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48102]]></requisitionid>
    <referencenumber><![CDATA[R48102]]></referencenumber>
    <apijobid><![CDATA[r48102]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48102/senior-director-patient-consumer-marketing-neuro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a dynamic and results-driven Senior Director of Consumer/Patient Marketing to lead cross-portfolio initiatives within our Neurology Commercial Business Unit. This pivotal role requires a leader who can develop and execute innovative marketing strategies while implementing robust data-driven frameworks to measure and optimize the impact of those initiatives. The ideal candidate will possess a strong ability to leverage analytics and insights to refine marketing plans and provide a compelling rationale for their evolution. Additionally, the candidate will excel at executing targeted marketing initiatives, fostering patient advocacy through ambassador programs, collaborating with patient support services, and addressing access challenges through reimbursement analysis. If you are passionate about driving meaningful results through strategic marketing and data integration, we invite you to join our team and make a difference in the lives of patients</p><p>The Director, Consumer Marketing will report into the Executive Director, Neurology Marketing. The ideal candidate will understand the unique challenges involved in Neurology consumer marketing, with the ability to effectively manage budgets and prioritize marketing tactics through data-driven insight gathering. This requires the consumer marketer to embody an analytical mindset with experience in developing and executing successful omnichannel consumer marketing campaigns in the rare disease market.</p><p><strong>A typical day may include the following:</strong></p><ul><li>Lead the development and execution of consumer marketing strategies and tactical plans for rare disease portfolio assets across their respective product lifecycles (i.e., pre-launch, launch, and post-launch periods)</li><li>Build business cases for patient-oriented programs that contribute to sustainable brand growth</li><li>Develop innovative patient and caregiver focused tools and programs (e.g., disease education information and materials provided to patient, branded patient support tools/programs to improve HCP and patient communication, branded patient education information and materials provided to patient)</li><li>Develop and implement geotargeted digital marketing campaigns to effectively reach rare disease and cardiometabolic patient populations, prioritizing precision over scale in all strategies</li><li>Partner closely with the patient support services team to ensure alignment in patient communication and engagement strategies, including facilitating access to sponsored genetic testing programs</li><li>Lead the evolution, development and execution of comprehensive marketing strategies for our Patient Ambassador Program</li><li>Manage the recruitment, certification, and mentorship of new ambassadors, ensuring alignment with strategic objectives</li><li>Work with cross-functional teams to analyze reimbursement trends and barriers, ensuring marketing strategies are aligned with patient access and affordability challenges</li><li>Utilize data analytics to identify patient needs and preferences, tailoring marketing content and strategies to improve patient engagement and support outcomes</li><li>Understand and leverage trends in the marketplace impacting Consumer Marketing and competitive benchmarking to data driven strategic insights to inform of all patient/consumer marketing programs and tactics</li><li>Work with cross functional teams to enhance the patient portion of the brand website</li><li>Ensures cross-functional communication, alignment, and collaboration with Field Sales, Field Medical, Access and Reimbursement, Marketing, Legal, and Compliance</li><li>Work closely with Patient Advocacy to understand and develop patient organization & advocacy strategy</li><li>Partner with Corporate Communications to develop and integrate public relations patient strategies and programs</li><li>Work closely with HCP and scientific marketing teams to ensure consistency of branding and complimentary tactics</li><li>Work closely with the rare disease Insights & Analytics team to structure a proactive approach to data collection and analysis</li><li>Manage budgets and closely monitor performance, ensuring cost effective delivery of all programs while tracking and monitoring KPI’s</li><li>Provide support to the development of the overall brand strategy, functional plans, and budget and ensure that patient-focused strategies and tactics are incorporated within their respective annual brand plans</li><li>Attend industry conferences and networking events to promote the brand and establish connections</li></ul><p><strong>To be considered, you must possess:</strong></p><ul><li>14 years of biopharmaceutical marketing experience with at least 5 years in consumer marketing</li><li>Neurology / Rare disease experience preferred</li><li>Minimum of bachelor's degree is required, advanced degree (MBA, PhD, MD) preferred</li><li>Proven track record with developing and implementing omnichannel consumer marketing plans that align with company goals and mitigate unique rare disease market challenges</li><li>Must demonstrate ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate</li><li>Demonstrated competency in managing a consumer marketing effort for a new product launch</li><li>Effective communication, both written and oral; experience in delivering complex messages to various internal and external customers with a track record of effective and influential presentations</li><li>Demonstrated initiative, creativity, strategic capabilities, and ability to work effectively in complex, rapidly changing environments</li><li>Strong project and process management skills, along with the ability to work on multiple tasks, and to effectively prioritize</li><li>Proven team player with ability to navigate cross functionally.</li><li>Strong analytical skills both quantitative and qualitative</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation System Administrator]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43984]]></requisitionid>
    <referencenumber><![CDATA[R43984]]></referencenumber>
    <apijobid><![CDATA[r43984]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43984/automation-system-administrator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Automation System Administrator, you will be embedded in a tight-knit team responsible for administration of automated/computerized system software and firmware to meet cGMP and policy requirements. In this critical role our team specifies and maintains software configuration for biopharmaceutical process, monitoring, and testing systems. This involves evaluation of new software for functional equivalence, validation activities to demonstrate suitability of software/process and maintaining the qualified state of systems throughout their lifecycle through change control.</p><p>In this role, a typical day might include:</p><ul><li>Administering system applications including user control access; adding, modifying, and removing users; defining user types, user groups and security settings.</li><li>Monitoring data backup or archival to ensure systems can meet defined RTO (Recovery Time Objective) and RPO (Recovery Point Objective).</li><li>Utilizing configuration management and recipe/method management.</li><li>Authoring documents such as impact statements, Configuration Specifications, risk assessments, Standard Operating Procedures, Work Instructions, Policies, and corrective/prevention action plans.</li><li>Supporting system SAT (Site Acceptance Testing) / FAT (Factory Acceptance Testing), validation and qualification efforts.</li><li>Conducting system integration with existing systems (e.g. LIMS, Historian).</li><li>Ensuring systems remain in a compliant state by processing change control requests for system configuration, including requirement and/or design specifications, test plans, technical evaluation, and quality risk assessments.</li><li>Providing end-user support including system functionality training, solving problems at the application level and hardware troubleshooting (includes working with vendors to resolve issues).</li><li>Participating in, leading, or authoring investigations and root cause analysis for issues of non-compliance.</li><li>Leading aspects of the work for contractors and providing guidance as applicable.</li></ul><p>This role might be for you if you:</p><ul><li>Have experience with a combination of the following: Ignition, MQTT brokers, HiveMQ, HighByte, or other similar platforms.</li><li>Have interest in manufacturing process within a regulated technical environment.</li><li>Have a solid understanding of System Design Lifecycle and Quality Risk Management.</li><li>Enjoy designing and implementing sustainable technical\procedural solutions in a complex environment.</li><li>Understand process control systems and product release testing systems.</li><li>Are familiar with regulatory and quality policies, procedures, documentation methods.</li><li>Enjoy working independently as part of a broader team with a proven focus on customer service and maintaining compliance.</li><li>Enjoy project management and have strong organizational skills.</li><li>Are motivated to participate in continuous process improvement.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Science, Engineering or related field and 2 years of experience. Equivalent combination of education and experience may be considered.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$67,400.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Inspection Management (GCP)]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48179]]></requisitionid>
    <referencenumber><![CDATA[R48179]]></referencenumber>
    <apijobid><![CDATA[r48179]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48179/associate-director-inspection-management-gcp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>The Associate Director, Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is responsible for the effective management of GCP, GVP and GLP inspections. The GDQIM IML will engage with key stakeholders, build strategic partnerships working and liaising with Clinical Study teams, relevant functions and other GDQ functions to support teams with inspection preparation activities on all Regeneron-sponsored clinical trials.</div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include the following:</strong></p><p>Ensuring and managing the notification of all relevant internal and external stakeholders of upcoming and/or anticipated regulatory inspections.<br>• Ensuring the preparation, management and integration of inspection management processes and training activities into the clinical development programs and all relevant stakeholders.<br>• Providing effective guidance, consultancy, and support to the Clinical Study Teams (and any other key stakeholders) in advance of an impending inspection.<br>• Assisting with the identification of opportunities to conduct mock inspections and/or Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.<br>• Identifying and discussing with the Clinical Study Teams potential issues and/or gaps, in advance of an impending inspection, that may require strategies to mitigate risk and/or provide additional clarification to an inspector.<br>• Ensuring the preparation, management and conduct of inspection preparation sessions which include mock inspections, trainings, and clinical site preparation visits working with GDQA team to identify and mitigate risks to clinical programs.<br>• Serving as the back room lead/co-lead or front room co-lead, responsible for explaining, managing,and ensuring the execution of all activities, including managing the tracking of requests and inquiries, and coordinating requests for responses from relevant personnel during any regulatory inspection conducted worldwide.<br>• Responsible for managing the preparation and provision of timely inspection updates and daily/end of inspection summaries to GD Executive and Senior Management, in addition to any other key relevant internal and external stakeholders.<br>• Responsible for managing inspection response development, and Corrective Actions/Preventive Actions (CAPA) follow-up activities alongside other GDQIM colleagues, cross-functional stakeholders, and process owners.<br>• Ensuring and managing the development, collection, reporting and analysis of inspection-related quality data, trends, and metrics.</p><h3><strong>This role may be for you if have:</strong></h3><p>• Advanced knowledge, understanding and application of GCP, and/or GVP <br>guidelines including the management of significant/complex quality issues <br>and compliance activities.<br>• Extensive experience with participating in, and supporting, Regulatory <br>Agency Inspections of Investigator Sites, Sponsors and Clinical Research <br>Organizations (CROs) in a GxP environment, including inspection <br>preparation, facilitation, and follow-up.<br>• Effective management of interpersonal relationships, stakeholder <br>engagement, and collaborations.<br>• Demonstrated ability to interface and collaborate effectively with other <br>Managers and Directors within, and external to, the organization.<br>• Extensive experience in providing training and presenting information on <br>key quality and regulatory compliance information.</p><p><strong>To be considered for this opportunity we are looking for:</strong></p><p>Bachelor's degree with a minimum of 10 years of relevant <br>healthcare/pharmaceutical industry experience.<br>• Experience working in either a quality/compliance role (e.g., Quality <br>Management, Quality Assurance etc.), or in a Clinical Development role <br>with expertise and/or transferable skills related to Good Clinical Practice <br>(GCP), and/or Good Pharmacovigilance Practice (GVP).<br>• Experience in training, supervising, line management, mentoring and <br>development of staff, and leading a small team</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€101,500.00 - €165,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48463]]></requisitionid>
    <referencenumber><![CDATA[R48463]]></referencenumber>
    <apijobid><![CDATA[r48463]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48463/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Dublin, Ireland</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€172,500.00 - €288,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 03:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47182]]></requisitionid>
    <referencenumber><![CDATA[R47182]]></referencenumber>
    <apijobid><![CDATA[r47182]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47182/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions</p></li><li><p>Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution</p></li><li><p>Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials</p></li><li><p>Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work</p></li><li><p>Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies</p></li><li><p>Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics</p></li><li><p>Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and have at least six years of relevant industry experience</p></li><li><p>Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience</p></li><li><p>Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC</p></li><li><p>Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 18 Jun 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Study Lead, Internal Medicine]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47928]]></requisitionid>
    <referencenumber><![CDATA[R47928]]></referencenumber>
    <apijobid><![CDATA[r47928]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47928/senior-manager-clinical-study-lead-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Clinical Study Lead to join our Clinical Trial Management team, supporting our Inflammation & Immunology therapeutic area. The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. You will be accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</p></li><li><p>Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.</p></li><li><p>Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.</p></li><li><p>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors</p></li><li><p>Provides input into baseline budget development and management; Provides input into baseline timeline development and management</p></li><li><p>Leads risk assessment and identifies risk mitigation strategies at the study level; Leads the feasibility assessment to select relevant regions and countries for the study</p></li><li><p>Monitors progress for site activation and monitoring visits and acts on any deviations from plan</p></li><li><p>Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan; Monitors data entry and query resolution and acts on any deviations from agreed metrics</p></li><li><p>Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation</p></li><li><p>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</p></li><li><p>Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li><li><p>Responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience</p></li><li><p>We are seeking experience with line management as well as exceptional interpersonal and leadership skills</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization; Ability to influence and negotiate across a wide range of stakeholders</p></li><li><p>Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC</p></li><li><p>We are seeking extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents</p></li><li><p>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 18 Jun 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, R&D Chemistry, Peptidomimetics]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48138]]></requisitionid>
    <referencenumber><![CDATA[R48138]]></referencenumber>
    <apijobid><![CDATA[r48138]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48138/associate-director-rd-chemistry-peptidomimetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Associate Director (Peptidomimetics), R&D Chemistry</strong></p><p>We are currently seeking an established leader and drug hunter for the R&D (Research & Development) Chemistry group. In this position, they will play a key role in expanding the Regeneron peptidomimetic antibody-conjugate drug discovery capabilities, while providing innovation and leadership to seamlessly combine with the company’s existing expertise in biologics and novel genetic medicines. The candidate will drive the discovery of peptidomimetic antibody conjugate drug therapeutics across diverse research areas. Cultural fit with the Regeneron cross-functional teams will be a key driver for success. </p><p>The R&D Chemistry team is primarily composed of synthetic organic, medicinal chemistry and bioconjugation scientists that work in a highly collaborative environment with other technology, biology and therapeutic area groups. Successful candidates will have a peptidomimetic/synthetic organic/medicinal chemistry background and will require peptidomimetic synthesis, discovery and SAR (structure-activity relationship) optimization expertise as well as linker-payload synthesis experience. A firm understanding and grasp of chemical biology strategies and the importance of applying both chemical and biological solutions to solve problems in drug discovery will be key. Small molecule synthesis and drug discovery/SAR experience as well as knowledge in the latest and most advanced bioconjugation techniques, platforms, and strategies is desired. </p><p>We expect they will act as an inspiring and motivating leader, effective communicator and manager, and strong collaborator to lead and drive project teams to develop novel antibody-conjugated peptidomimetic therapeutics. The successful candidate will also address challenges related to synthesis, medicinal chemistry, bioconjugation and optimal <em>in vitro</em> and <em>in vivo</em> properties leading to development candidates.</p><p><strong> </strong></p><p><strong>Build our future together: </strong></p><ul><li>Directly supervise and manage the day-to-day activities of the R&D Chemistry Peptidomimetic group, providing vision, inspiration, and both short-term and long-term goals. Communicate priorities, policies, and goals of Regeneron Senior Leaders to the group.</li><li>Perform medicinal chemistry inspired and SAR-driven generation of novel peptidomimetic drug modalities, using synthetically feasible and simplistically designed linkers to provide overall optimal <em>in vitro</em> and <em>in vivo</em> properties of antibody-conjugated therapeutics</li><li>Troubleshoot and optimize peptide potency and stability using standard peptide-based principles (e.g., Ala scans), non-natural amino acid incorporation, alpha-Me/N-Me peptide backbone modifications, and other medicinal chemistry strategies that are guided by <em>in vitro</em> assays, plasma/serum stability, and met ID data.</li><li>Champion and lead the R&D Chemistry Peptidomimetic efforts on internal/external project teams, and demonstrate the ability to multi-task and parallel process to add to our continuous pipeline of Regeneron development candidates</li><li>Identify new strategies and technologies (e.g., linker and payload design) to improve on existing Regeneron platforms for pursuing novel synthesis and bioconjugation of peptidomimetic drug modalities</li><li>Actively participate in departmental, cross-functional, leadership, and external meetings to contribute expertise and to represent the vision of the R&D Chemistry Peptidomimetic group.</li><li>Interact broadly and collaboratively with other Regeneron groups, forging relationships and active collaborations.</li></ul><p><strong> </strong></p><p><strong>When & Where:</strong></p><ul><li><h3>This is an on-site position located in our Hawthorne, NY facility</h3></li><li>Occasional travel to our nearby Tarrytown facility may be required</li></ul><p><strong>Discover your role:</strong></p><ul><li>You are passionate and enthusiastic about the promise of peptidomimetic conjugated, antibody-targeted therapeutics and appreciate the challenges and opportunities of drug delivery and molecular targeting.</li><li>You enjoy applying and combining traditional methods and novel technologies to develop solutions for synthesis, bioconjugation and drug discovery.</li><li>You are comfortable working in a cross-functional role and excel as part of a diverse team where egos are checked at the door.</li><li>You want to provide meaningful contributions to the development of an organizational culture that supports growth and development of its people and capabilities to drive forward the Regeneron pipeline.</li><li>You prefer to work in an organization that is modality agnostic, letting the data determine the best course forward.</li></ul><p><strong> </strong></p><p><strong>In order to be considered qualified for the role, you must have:</strong></p><ul><li>Ph.D. in peptide and/or synthetic organic chemistry or a related field.</li><li>Minimum of 10 years of professional industry experience.</li><li>Extensive drug discovery experience with antibody-targeted peptidomimetic drug modalities, experience with the synthesis and manufacturing of peptidomimetic payloads and linkers, expertise in modern methods in medicinal chemistry structure-activity relationships, and a deep understanding of biological MOAs (extracellular/intracellular target evaluation, ADME/PK, PD/efficacy, toxicological evaluation). </li><li>A track record of success in the field of either peptidomimetics, small molecules or antibody targeted therapeutics (i.e., advancement of molecules into the clinic) with experience building and leading teams is required.<em> </em></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Study Lead (Clinical Experimental Sciences)]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44465]]></requisitionid>
    <referencenumber><![CDATA[R44465]]></referencenumber>
    <apijobid><![CDATA[r44465]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44465/senior-manager-clinical-study-lead-clinical-experimental-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>This role is not eligible remote, and must be onsite in one of our US office locations.</em></p><p>The <strong>Senior Clinical Study Lead (CSL) – Clinical Experimental Sciences Operations (CES Ops)</strong> is accountable for the execution of assigned clinical studies/research collaborations from study design, through execution, to study close out. Additionally, there are responsibilities for initiation, oversight and completion of CES Ops continuous improvement and Strategic Imperatives workstreams. The Sr. CSL is accountable for oversight of the contract and budget execution, study timelines, study budget management, and ensuring study conduct is in accordance with, Regeneron Standard Operating Procedures (SOPs), CES Ops Business Practice Tool processes and ICH/GCP, as applicable. The CES Ops portfolio is dynamic in nature; study types include, but are not limited to, less complex data transfer agreements, retrospective sample/data acquisition studies to more complex prospective studies including sample/data acquisition, biomarker/technology/method validation, genotypic/phenotypic call back studies, and challenge/screening studies. This role will interface heavily with Basic Research/Discovery as well as with clinical site staff, predominately at academic institutions. In rare instances the more complex studies may require out-sourcing to Clinical Research Organizations (CROs); the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives. This role may be responsible for direct line management.</p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Leads the cross-functional study team responsible for clinical study/research collaboration delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</li><li>Provides operational input into research plan and/or study protocol development</li><li>Ensures development of study specific documentation such as samples management plans and data management plans are completed on time and in accordance with the study protocol.</li><li>Oversees set-up and maintenance of study systems which may include Clinical Trial Management System (CTMS), Trial Master File (TMF), study SharePoint etc.</li><li>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors, if appropriate</li><li>Provides input into baseline timeline development and management</li><li>Provides input into baseline budget development and management, facilitates internal review of the study budget for assessment of Fair Market Value</li><li>Ensures accurate budget management and scope changes for internal and external studies</li><li>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</li><li>Oversees the execution of the clinical study against planned timelines, deliverables and budget</li><li>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the</li><li>scope of work</li><li>Manages and oversees study close-out activities</li><li>Ensures End of Study Summary is delivered and properly archived</li><li>Facilitates and contributes to study level lessons learned</li><li>Assigns tasks to Clinical Study Management staff and supports their deliverables</li><li>Recommends and participates in cross-functional and departmental process improvement initiatives</li><li>Responsible for identification of innovative approaches to clinical study execution including global considerations and continuous improvement departmental processes and procedures</li><li>Works with Therapeutic Focus Area groups within Basic Research/Discovery</li><li>Works closely with clinical site staff, predominantly at academic institutions</li><li>Expected to maintain higher volume and/or greater complexity studies</li><li>Expected to communicate learnings, best practices and relevant information to other study leads at all levels, ensures consistency and internal alignment across staff</li><li>May be responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelor's degree and8+ years of relevant clinical experience is required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 22 Jun 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PHILADELPHIA SOUTH, PA]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48014]]></requisitionid>
    <referencenumber><![CDATA[R48014]]></referencenumber>
    <apijobid><![CDATA[r48014]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48014/medical-account-specialist-ii-neurology-philadelphia-south-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Philadelphia]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Philadelphia South (Metro), PA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 02:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -  WHITE PLAINS, NY]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48009]]></requisitionid>
    <referencenumber><![CDATA[R48009]]></referencenumber>
    <apijobid><![CDATA[r48009]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48009/medical-account-specialist-ii-neurology-white-plains-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[White Plains]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: White Plains (Metro), NY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 03:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - Oncology - Richmond, VA]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48470]]></requisitionid>
    <referencenumber><![CDATA[R48470]]></referencenumber>
    <apijobid><![CDATA[r48470]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48470/medical-account-specialist-ii-oncology-richmond-va/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Richmond]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you must have a Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred). We are also seeking Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 28 Jun 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Diagnostics CDx (Precision Medicine)]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48167]]></requisitionid>
    <referencenumber><![CDATA[R48167]]></referencenumber>
    <apijobid><![CDATA[r48167]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48167/senior-manager-clinical-diagnostics-cdx-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As Senior Manager, Clinical Diagnostics, you will support end-to-end CDx strategy and execution to enable therapeutics across indications. Partnering with biomarker, clinical, regulatory, commercial, and IVD collaborators, you will translate scientific needs into fit-for-purpose assays for global decisions. You will own programs from feasibility through analytical/clinical validation, registration, launch, and post-market sustainment, ensuring timelines, quality, and budgets aligned to drug milestones. This role combines hands-on leadership, vendor management, and cross-functional orchestration under quality and regulatory frameworks. You will serve as a governance interface and refine CDx strategy.</p><p><strong>As a Senior Manager, a typical day may include: </strong></p><ul><li><p>Execute end-to-end CDx strategy, aligning diagnostic milestones with therapeutic clinical development and regulatory timelines for seamless program delivery.</p></li><li><p>Lead cross-functional teams; integrate workstreams, clear obstacles, and provide transparent, regular status reporting to governance bodies and senior leadership.</p></li><li><p>Manage IVD partners—negotiate scope, timelines, budgets, and quality; oversee co-development, Joint Steering Committees, and performance.</p></li><li><p>Define assay intent and contribute to target product profiles (TPP) for CDx platforms (e.g., NGS, PCR, IHC, Immunoassays); drive analytical validation (accuracy, precision, sensitivity, specificity, LoD, reproducibility) and clinical validation linking performance to benefit–risk.</p></li><li><p>Embed CDx assays in trials with clinical teams—screening/stratification, sampling, site readiness, and lab operations for reliable execution.</p></li><li><p>Partner with IVD Regulatory on global submissions—FDA PMA/supplements, 510(k) as applicable, EU IVDR, PMDA; support pre-subs, labeling, and responses.</p></li><li><p>Ensure compliance with ISO 13485/14971, CLSI, IVDR, and GCP; maintain documentation, audit readiness, and proactive, integrated risk management.</p></li><li><p>Oversee design transfer, manufacturing readiness, and supply; support launch readiness with Commercial/Medical teams.</p></li></ul><p><strong>This role may be for you if: </strong></p><ul><li><p>You thrive in a fast-paced environment</p></li><li><p>You are detail oriented, well-organized and can multi-task</p></li><li><p>You are a team player</p></li><li><p>You have strong communication skills</p></li></ul><p><strong>To be considered for this role, you must have</strong></p><ul><li><p>Advanced degree in molecular biology, pathology, biomedical engineering, or equivalent experience.</p></li><li><p>4+ years in diagnostics development; 2+ years leading CDx/IVD in pharma or diagnostics organizations.</p></li><li><p>Proven delivery of CDx aligned to drug approvals; successful validation and regulatory submissions.</p></li><li><p>Expertise in NGS, PCR, IHC, immunoassays; validation standards and robust quality systems.</p></li><li><p>Strategic thinking with the ability to translate scientific and clinical needs into executable diagnostic solutions.</p></li><li><p>Strong grasp of global FDA CDRH, EU IVDR, PMDA pathways for CDx labeling.</p></li><li><p>Excellent communication, leadership, and stakeholder management; clear, concise updates to executive audiences.</p></li><li><p>Strategic translation of scientific and clinical needs into executable diagnostics under QMS/GxP.</p></li></ul><p><strong>Travel:</strong></p><p>Travel up to 5-10% for partner meetings, clinical site visits, and regulatory interactions</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 28 Jun 2026 04:26:24 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Reimbursement Business Manager - Dermatology (Nashville N, TN)]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48615]]></requisitionid>
    <referencenumber><![CDATA[R48615]]></referencenumber>
    <apijobid><![CDATA[r48615]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48615/reimbursement-business-manager-dermatology-nashville-n-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Tennessee]]></city>
    <state><![CDATA[Tennessee]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Reimbursement Business Manager (RBM) is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. We are seeking someone to support HCP offices in acquiring appropriate access to Regeneron products for patients. Ensuring efficient access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron Alliance product portfolio. You will drive and support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate and across multiple internal stakeholders, sales teams, Payer teams, and Alliance partners.</p><p><strong>A typical day may include the following:</strong></p><ul><li>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</li><li>Build and execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</li><li>Provide appropriate process, payer and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products (Dupixent).</li><li>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</li><li>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that aligns with Regeneron policies, processes, and standard operating procedures</li><li>Ensure individual training and knowledge is maintained to the level required to guarantee that personnel are seen as the most knowledgeable team in the industry as it pertains to access and reimbursement across Alliance therapeutic areas as well as future product markets</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</li><li>You are an ethical, standout colleague and have can grow in a cross-functional team environment - contributing creative ideas and positive energy to the group.</li><li>You possess excellent organizational, project management, and communication skills.</li></ul><p>To be considered for this opportunity, you will possess the following:</p><ul><li>A bachelors' degree and Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience.</li><li>Experience working with products delivered through a Specialty Pharmacy network is essential.</li><li>Collaboration and proactive communication skills required.</li><li>Background in leadership and effective cross functional partnership a plus.</li><li>Established ability to work within an Account Management based structure.</li><li>Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors.</li><li>Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Third Party Risk Management]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47797]]></requisitionid>
    <referencenumber><![CDATA[R47797]]></referencenumber>
    <apijobid><![CDATA[r47797]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47797/director-third-party-risk-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Director of Third Party Risk Management within our team. In this role you will be responsible for regional oversight and execution of the enterprise third party risk management (TPRM) program. This role ensures that third-party risks across suppliers, service providers, and external partners within the assigned region are identified, assessed, mitigated, and escalated in alignment with the global TPRM framework. The Director will report to the Executive Director of TPRM and support the global TPRM strategy through strong regional execution, consistent application of risk processes, and effective engagement with business and functional stakeholders.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Execution of the global TPRM vision, framework, and operating model</p></li><li><p>Ensuring consistent, risk-based application of third-party risk processes</p></li><li><p>Providing regional oversight for supplier risk activities and serve as the escalation point for material or emerging risks.</p></li><li><p>Supporting global governance bodies, through regional insights and reporting.</p></li></ul><ul><li><p>Maintaining regional alignment with regulatory and industry standards applicable to third-party risk management.</p></li><li><p>Partnering with Compliance and Risk domain owners to support supplier assessments, issue remediation, and corrective action plans.</p></li><li><p>Overseeing the end-to-end lifecycle of third-party risk management: onboarding, due diligence, ongoing monitoring, issue management, and offboarding.</p></li></ul><ul><li><p>Supporting the effective use of TPRM technology platforms, ensuring accuracy, completeness, and consistency of risk data. </p></li></ul><ul><li><p>In partnership with leadership, drive the adoption of automation, AI, analytics, and data-driven tools to improve efficiency and scalability of TPRM processes.</p></li></ul><p>This role may be a fit for you if you:</p><ul><li><p>Have the ability to leverage AI-enabled capabilities within approved platforms to assist with activities such as risk screening, monitoring, analysis, and reporting.</p></li><li><p>Can partner with Procurement Technology and risk teams to identify opportunities to streamline workflows and enhance risk insight while remaining aligned with governance and compliance requirements.</p></li><li><p>Are able to partner with Procurement, Legal, Compliance, IP, Information Security, and other risk domain owners to manage third-party risks holistically.</p></li><li><p>Act as a trusted regional advisor to business stakeholders on supplier risk matters.</p></li><li><p>Bachelor’s degree in a relevant field required; advanced degree or certifications preferred.</p></li></ul><p>To be considered for this role you must hold a Bachelor's degree in a relevant field of study plus 12+ years of progressive experience in Third Party Risk Management, preferably within pharmaceutical, biotech, or other regulated industries. Previous people management experience is required.</p><p>Experience working with TPRM technologies and risk monitoring platforms, including application of automation and AI-enabled tools within risk or compliance processes strongly preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 24 Jun 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QA Investigation Specialist]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43465]]></requisitionid>
    <referencenumber><![CDATA[R43465]]></referencenumber>
    <apijobid><![CDATA[r43465]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43465/qa-investigation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a QA Investigation Specialist position with our Bulk Drug Substance Manufacturing Quality Assurance team. This position performs all compliance related tasks vital to complete investigations and implementation of robust corrective actions for supporting manufacturing operations.<br><br>In this role, a typical day might include the following:</p><ul><li><p>Independently investigating non conformances and preventing reoccurrences in support of manufacturing operations</p></li><li><p>Preparing investigation reports that include recommendations on investigation findings for medium/high severity non conformances</p></li><li><p>Analyzing and evaluating information captured through investigations, summarizes information and trends in investigation reports</p></li><li><p>Communicating findings and recommendations at group meetings</p></li><li><p>Reviewing completed batch records and logbooks in accordance with cGMP standards in support of investigations</p></li><li><p>Reviewing, editing, and revising controlled documents (batch records, logbooks, SOPs, etc.) in accordance with cGMP standards to ensure compliance with written procedures</p></li><li><p>Monitoring production processes to acquire vital data in support of investigations and track efficiency of changes</p></li><li><p>Participating in and/or leading cross-functional study teams to get results, support and or author investigations</p></li><li><p>Gathering, trending, and analyzing process related data to drive consistency and timeliness</p></li><li><p>Documenting all training</p></li><li><p>Training new employees on investigative processes and techniques</p></li><li><p>Coordinating and/or leading cross-functional meetings with multiple departments</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Excel in a quality driven organization</p></li><li><p>Have an understanding of biologics manufacturing operations</p></li><li><p>Are organized and have an attention to detail</p></li><li><p>Can prioritize multiple assignments and changing priorities</p></li><li><p>Are able to learn and utilize computerized systems for daily performance of tasks</p></li></ul><p>Gowning and Environment:</p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Life Sciences, Engineering, or related field and the following minimum amounts of relevant experience for each level:</p><ul><li><p>Associate Specialist – 0-2 years</p></li><li><p>Specialist – 2+ years</p></li><li><p>Senior Specialist – 5+ years</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$66,400.00 - $108,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 15:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Bethesda, MD]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48431]]></requisitionid>
    <referencenumber><![CDATA[R48431]]></referencenumber>
    <apijobid><![CDATA[r48431]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48431/medical-specialist-i-pulmonology-bethesda-md/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: <strong>Bethesda, MD - representative must reside within the territory.</strong></p></li></ul><p><strong>​</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups.</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p>​<strong>This role requires:</strong></p><ul><li><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 26 Jun 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44611]]></requisitionid>
    <referencenumber><![CDATA[R44611]]></referencenumber>
    <apijobid><![CDATA[r44611]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44611/principal-statistical-programmer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>***Please note this is an onsite opportunity and is NOT eligible remote. </em></p><p>A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies.</p><p><strong>In this role, a typical day might include:</strong> ​</p><p>As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent assists in providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.</p><p><strong>This role might be for you if can:</strong> ​</p><ul><li>Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones. </li><li>Integration of data across studies in support of CSS/CSE. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. </li><li>Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).</li><li>Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.</li><li>Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations.</li><li>Participate in department working groups; provide input in development of tools and improvement of processes.</li></ul><p><br><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li>Masters Degree</li><li>SAS, (Base, Stat, Macro, graph). </li><li>3 + Years experience</li></ul><p>#statprogramming </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Biostatistics - Medical Affairs]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47321]]></requisitionid>
    <referencenumber><![CDATA[R47321]]></referencenumber>
    <apijobid><![CDATA[r47321]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47321/manager-biostatistics-medical-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Manager, Biostatistics to join our team! This individual will be responsible for statistical support for oncology compounds within Medical Affairs.</p><p><strong> </strong></p><p><strong>In this role, a typical day may include:</strong></p><p>As part of a collaborative medical affairs team, you will implement the statistical function’s role in the oncology compounds’ medical impact plans. Together with medical directors, HEOR, medical writing, market access, and other colleagues within medical affairs, you will plan and execute evidence generation efforts, such as post-hoc analysis with innovative analytical approaches, respond to payer and reimbursement needs, review investigator initiated studies, and design and execute Phase IV studies as the study biostatistician, and ensure statistical rigor in all these duties. You will also work with fellow clinical development biostatisticians and programmers to deep dive into the clinical trial data for comprehensive understanding. You will be responsible for following departmental guidelines of collaboration, innovation, and intrinsic motivation. Working in a dynamic team with a wide range of interfaces, the role requires both strategic and operational skills combining innovative statistical thinking with a strong sense of business acumen, and excellent communication and interpersonal skills. Your manager will work with you to manage stakeholders, learn about oncology and the company’s compounds, develop Regeneron cultural understanding, and general industry knowledge.</p><p><strong> </strong></p><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Strong interest and motivation in exploring existing clinical trial data for post-hoc analysis and innovative idea investigations</p></li><li><p>Experience with clinical trial design, including observational studies</p></li><li><p>Exposure to oncology study endpoints and analysis techniques</p></li><li><p>Strong communication skills to interpret, explain, and discuss results of complex statistical concepts and analyses to both technical and non-technical audiences.</p></li><li><p>Desire to present and share results with internal and external stakeholders.</p></li><li><p>Comfort with providing scientific/statistical input into study design, formulating novel methods to problem solving, and independently developing the statistical analysis plan to implement those solutions.</p></li><li><p>Authored Statistical Analysis Plans (SAP) and Protocols</p></li><li><p>Generated tables, listings, and figures for external communication use in publications/presentations and for internal purposes.</p></li><li><p>Ability translate and apply relevant innovative statistical methodology to everyday work.</p></li><li><p>Educate and disseminate knowledge throughout the organization for areas within the expertise of medical affairs.</p></li></ul><p><strong> </strong></p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>PhD / DrPH in statistics/biostatistics or related disciplines with >2 years experience in the pharmaceutical/biotech industry or MS degree in statistics/biostatistics with >7 years’ experience in the pharmaceutical industry as a statistician. </p></li><li><p>Knowledge of drug discovery/development/life cycle management(LCM) and ability to integrate statistical concepts into drug discovery/development/LCM strategies</p></li><li><p>Prior experience or knowledge of oncology is strongly preferred</p></li><li><p>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </p></li><li><p>Demonstrated critical thinking skills, time management skills, and effective communication skills.</p></li><li><p>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</p></li><li><p>Ability to write code in at least one common statistical software is required (i.e. SAS, R, Python). Ability to read SAS code is required</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager QA Auditor GCP Strategy]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48943]]></requisitionid>
    <referencenumber><![CDATA[R48943]]></referencenumber>
    <apijobid><![CDATA[r48943]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48943/senior-manager-qa-auditor-gcp-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div><div><div><div><div><div><div><p><strong>Build our future together: </strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, GCP Audit Strategy, Global Development to join our Global Development Quality Assurance (GDQA), supporting our Global Development organization in a remote work mode. In this role, you will lead risk-based audit strategy programs and oversee compliance across therapeutic areas, studies, and audit activities while collaborating with Global Development teams, auditors, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p><p><strong>When & where: </strong></p><p>UK Remote - Ireland Remote </p><p><strong>Discover your role: </strong></p><ul><li><p>Lead risk-based audit planning across therapeutic areas and studies </p></li><li><p>Drive strategic audit programs using risk indicators from study teams </p></li><li><p>Ensure audits align with approved programs and scheduled timelines </p></li><li><p>Manage audit outcomes to identify trends and communicate risks </p></li><li><p>Represent quality assurance on complex cross-functional initiatives </p></li><li><p>Deliver reports and metrics to Global Development leadership </p></li><li><p>You collaborate effectively with stakeholders across global functions </p></li><li><p>You navigate ambiguity while prioritizing multiple complex activities </p></li><li><p>10-20% travel might be required</p></li></ul><p>This role requires: </p><ul><li><p>Bachelor’s degree with 8+ years of relevant industry experience </p></li></ul><ul><li><p>5+ years of GCP audit strategy or audit experience </p></li></ul><ul><li><p>Knowledge of FDA, EU, and ICH GCP regulations and guidance </p></li></ul><ul><li><p>Experience supporting or participating in regulatory inspections </p></li></ul><ul><li><p>Strong project management and stakeholder management capabilities </p></li></ul><ul><li><p>Excellent written and verbal communication skills with senior audiences </p></li></ul></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - LEXINGTON, KY]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48021]]></requisitionid>
    <referencenumber><![CDATA[R48021]]></referencenumber>
    <apijobid><![CDATA[r48021]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48021/medical-account-specialist-ii-neurology-lexington-ky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Lexington-Fayette]]></city>
    <state><![CDATA[Kentucky]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Lexington (Metro), KY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 28 Jun 2026 05:26:23 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Commercial Finance]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46819]]></requisitionid>
    <referencenumber><![CDATA[R46819]]></referencenumber>
    <apijobid><![CDATA[r46819]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46819/senior-manager-commercial-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This role leads Commercial Financial Planning & Analysis (FP&A) consolidation activities for monthly close and quarterly forecasts, ensuring a single source of truth across brands, functions, and geographies. In addition to core consolidation responsibilities, the role will help drive standardization and automation across commercial finance. The Senior Manager sets cadence, standards, and systems discipline to deliver accurate, timely, and insight-driven outputs for decision-making.</p><p><strong>A day in the life may look like:</strong></p><p>• Own end-to-end consolidation of monthly actuals and forecast updates for the Commercial organization</p><p>• Govern calendars, milestones, templates, and submission protocols to drive accountability and on-time deliverables</p><p>• Standardize definitions and mappings for revenue, GTN components, OpEx categories, and headcount across brands and geographies</p><p>• Review, challenge, and synthesize brand and functional submissions; ensure alignment with corporate guidance and macro assumptions</p><p>• Deliver executive-ready materials: bridges, variance analyses, trend diagnostics, and scenario views</p><p>• Partner with Corporate FP&A and Accounting on close deliverables, accrual processes, and policy alignment</p><p>• Lead rapid-turnaround ad hoc analyses for Finance and Commercial leadership, translating ambiguous asks into structured scenarios that quantify revenue and P&L impacts across GTN, pricing and contracting strategies, channel inventory dynamics, and forecast sensitivities</p><p>• Deliver concise, executive-ready options with assumptions, risks, and recommendations</p><p><strong>This may be the right role for you if you:</strong></p><p>• Drive automation of recurring reporting, dashboards, and forecast quality checks; partner with IT on enhancements and UAT</p><p>• Define model structures, hierarchies, and master data standards that enable efficient consolidation and flexible scenario planning</p><p>• Identify and implement improvements that shorten cycle time, reduce errors, and improve insights</p><p><strong>To be considered for this role</strong>, <strong>you must have:</strong></p><ul><li>7+ years of experience, preferably in a pharmaceutical/biotech environment with a US-listed public company or exposure through Big 4 service engagements</li><li>Bachelor degree required in Business, Finance, Accounting, or a similar field</li><li>MBA, CPA, CFA are all nice to have</li><li>Knowledge of generally accepted accounting principles, financial reporting and analysis, and compliance</li><li>Extensive knowledge of ERP/Planning tools is required; Oracle/Hyperion a plus</li><li>Hands-on experience with BI tools in Finance is highly preferred (MS Power BI, Tableau, etc.)</li><li>Experience with driving standardization and automation in finance is highly preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Finance Operations & Technology]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46449]]></requisitionid>
    <referencenumber><![CDATA[R46449]]></referencenumber>
    <apijobid><![CDATA[r46449]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46449/director-global-finance-operations-technology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The <strong>Director, Global Finance Operations & Technology</strong> is a leader who combines strong operational execution with strategic leadership to advance Regeneron’s global finance transformation agenda. This role sits between tactical delivery and enterprise strategy—owning critical finance technology initiatives, leading global process modernization, and shaping a scalable, data‑driven finance ecosystem.</p><p>The Director is expected to be hands‑on where needed, while also setting direction, influencing stakeholders, and leading cross‑functional teams across regions. This role plays a key part in translating finance strategy into executable solutions that improve efficiency, compliance, and insight generation.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Lead and deliver major global finance technology initiatives, including Oracle Fusion, automation, and advanced analytics programs.</p></li><li><p>Design and implement standardized global finance operations frameworks that balance enterprise consistency with regional requirements.</p></li><li><p>Provide operational leadership across core finance processes, ensuring accuracy, compliance, and continuous improvement.</p></li><li><p>Drive adoption of cloud platforms, AI, and automation by partnering closely with Finance, IT, HR, and other business functions.</p></li><li><p>Serve as a key liaison between business stakeholders and technology teams to translate requirements into scalable solutions.</p></li><li><p>Own finance data enablement efforts, including master data governance, metadata management, and data quality improvements.</p></li><li><p>Develop actionable insights from operational and financial data to support senior leadership decision‑making.</p></li><li><p>Identify process gaps, risks, and control issues; implement remediation plans to strengthen governance and compliance.</p></li><li><p>ERP & Cloud Platforms: Hands‑on experience with modern ERP solutions (e.g., Oracle Fusion, Workday) and cloud‑native technologies.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Finance, Accounting, Information Systems, or related field; MBA preferred</p></li><li><p>10+ years of progressive experience in finance operations, finance technology, or large‑scale transformation initiatives.</p></li><li><p>Demonstrated success delivering global ERP implementations, automation programs, or finance modernization efforts.</p></li><li><p>Strong understanding of end‑to‑end finance processes, shared services models, and regulatory/compliance frameworks.</p></li><li><p>Proven ability to lead cross‑functional, multinational teams in complex environments.</p></li><li><p>Excellent communication, stakeholder management, and change leadership skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Accounting Operations]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47280]]></requisitionid>
    <referencenumber><![CDATA[R47280]]></referencenumber>
    <apijobid><![CDATA[r47280]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47280/manager-accounting-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This role leads Accounting Operations systems and process optimization for biopharmaceutical manufacturing, ensuring a single source of truth across modules, plants, and functions. In addition to core responsibilities, the Manager drives standardization and automation across accounting and ERP workflows. The Manager sets cadence, standards, and systems discipline to deliver accurate, timely, and data-driven outputs that support monthly close, compliance, and operational decision-making.</p><p><strong>A day in the life may look like:</strong></p><ul><li><p>Own end-to-end configuration, maintenance, and governance of accounting’s Oracle applications across OPM, Order Management, Inventory, and Financials</p></li><li><p>Govern close calendars, achievements, templates, and submission protocols to drive accountability and timely, accurate financial results</p></li><li><p>Liaise with Accounting and IT to diagnose and resolve functional setup issues and sophisticated system problems impacting close and financial reporting</p></li><li><p>Engage with process owners to identify automation opportunities, assess feasibility, prioritize implementation, and measure realized efficiency gains</p></li><li><p>Translate business requirements into clear deliverables: functional design specifications, use cases, and workflow/process diagrams</p></li><li><p>Conduct end-to-end testing cycles for application improvements, ERP upgrades, and project implementations, with rigorous impact analysis and UAT sign-off</p></li><li><p>Partner with Manufacturing, Supply Chain, and Corporate Finance to align master data, mappings, and policies across modules for smooth close and reporting</p></li><li><p>Deliver executive-ready outputs: reconciliations, variance analyses, issue logs with root-cause and corrective actions, KPI dashboards, and control health check</p></li></ul><p><strong>This may be the right role for you if you:</strong></p><ul><li><p>Drive automation of recurring close reporting, reconciliations, exception dashboards, and data quality checks</p></li><li><p>Partner with IT on improvements and UAT</p></li><li><p>Define model structures, hierarchies, and master data standards that enable efficient consolidation, consistent mappings, and flexible scenario analysis.</p></li><li><p>Standardize accounting definitions and cross-module controls for GL, AR, AP, FA, Inventory, and Order Management to reduce manual work and errors</p></li><li><p>Identify and implement improvements that shorten cycle time, strengthen controls, and improve insights for stakeholders across Finance and Operations</p></li><li><p>Translate ambiguous asks into structured solution options with assumptions, risks, effort estimates, and recommendations</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><p>BS/BA in Accounting, Information Systems, or a related field; 7+ years experience</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Payroll Service Delivery]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47441]]></requisitionid>
    <referencenumber><![CDATA[R47441]]></referencenumber>
    <apijobid><![CDATA[r47441]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47441/associate-manager-payroll-service-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. We continue to strengthen our global payroll and finance capabilities to support accuracy, compliance, and consistent employee experience.</p><p>As an Associate Manager – Payroll Service Delivery, you will support accurate, compliant, and timely payroll delivery across multiple countries within Regeneron’s Global Capability Center. You will work closely with Payroll, HR, Finance, and external vendors to support end‑to‑end payroll operations, maintain strong controls, and contribute to process standardization and service improvement.</p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li><p>Support day‑to‑day international payroll operations across assigned countries</p></li><li><p>Review payroll inputs, validations, audit checks, reconciliations, and approval workflows</p></li><li><p>Coordinate with external payroll vendors to support timely delivery and issue resolution</p></li><li><p>Partner with HR and Finance teams to ensure payroll data accuracy and completeness</p></li><li><p>Monitor payroll variances and highlight observations for follow‑up</p></li><li><p>Support payroll accounting activities and alignment with month‑end close processes</p></li><li><p>Ensure adherence to payroll controls, governance standards, and regulatory requirements</p></li><li><p>Track regulatory or statutory changes and coordinate updates with internal teams and vendors</p></li><li><p>Prepare documentation, reports, and data to support internal and external audits</p></li><li><p>Maintain and update payroll standard operating procedures and process documentation</p></li><li><p>Support process improvement, standardization, and system optimization initiatives</p></li><li><p>Guide and support payroll operations analysts in day‑to‑day execution.</p></li></ul><p><strong>This Job May Be for You If You Have:</strong></p><ul><li><p>Experience supporting payroll operations or payroll service delivery in a shared services environment</p></li><li><p>Working knowledge of payroll compliance, statutory requirements, and internal controls</p></li><li><p>Experience working with global payroll vendors and payroll or HR systems</p></li><li><p>Ability to review payroll data, identify issues, and support resolution</p></li><li><p>A structured, detail‑oriented approach to managing operational activities</p></li><li><p>Clear written and verbal communication skills</p></li><li><p>Comfort working with global stakeholders across time zone<strong>s.</strong></p></li></ul><p><strong>To be considered for this role:</strong></p><ul><li><p>Bachelor’s degree in Accounting, Finance, Business Administration, HR, or a related field</p></li><li><p> Typically 6–8+ years of experience in payroll operations, including exposure to multi‑country or international payroll</p></li><li><p> Experience working in a Shared Services Center or Global Capability Center is preferred</p></li><li><p> Payroll or professional certifications are an advantage</p></li><li><p> Proficiency in English and experience supporting global teams and stakeholders</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47270]]></requisitionid>
    <referencenumber><![CDATA[R47270]]></referencenumber>
    <apijobid><![CDATA[r47270]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47270/associate-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a highly motivated <strong>Flow Cytometry Associate</strong> to join Regeneron’s Protein Expression Sciences team. In this role, you will operate and maintain high-speed cell sorters and analyzers supporting a busy departmental core facility. You will perform cell sorting and data acquisition for scientific staff and assist in developing flow cytometry protocols.</p><p><strong>Responsibilities during a typical day might include the following:</strong></p><ul><li>Independently operate multi-laser, high-speed cell sorter and analyzers.</li><li>Perform routine maintenance, alignment, calibration, and troubleshooting to meet experimental requirements.</li><li>Provide data acquisition, analysis, and interpretation of flow cytometry experiments.</li><li>Partner with field engineers and technical support; stay current with emerging technologies to maintain a high level of expertise within the core facility.</li><li>Analyze data using flow cytometry software.</li><li>Follow and maintain standard operating procedures (SOPs), as needed.</li><li>Train users to operate analyzers, as needed.</li><li>Maintain inventory of laboratory supplies and reagents.</li></ul><p><strong>This role may be for you, if you: </strong></p><ul><li>Knowledge of flow cytometry principles and hands-on technical experience.</li><li>Exposure to a multi-laser, high-speed and spectral cell sorter and analyzer (preferred but not required).</li><li>Interest in learning and contributing to instrument troubleshooting and continuous improvement.</li><li>Flexibility and willingness to perform flow cytometry duties that support scientific staff goals and objectives.</li><li>Bachelor’s degree or relevant experience.</li><li>Ability to work independently and collaboratively in a team environment.</li><li>Ability to multitask, prioritize work, and maintain confidentiality.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - MEMPHIS, TN]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48923]]></requisitionid>
    <referencenumber><![CDATA[R48923]]></referencenumber>
    <apijobid><![CDATA[r48923]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48923/medical-account-specialist-ii-hematology-memphis-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Memphis</strong></p><ul><li><strong>Geography: </strong><strong>Memphis, Jackson, MS, Jonesboro, AR</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (South Central)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48129]]></requisitionid>
    <referencenumber><![CDATA[R48129]]></referencenumber>
    <apijobid><![CDATA[r48129]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48129/field-reimbursement-manager-neurology-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Houston]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Dallas/Houston, (Metro) TX</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Mountain West)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48130]]></requisitionid>
    <referencenumber><![CDATA[R48130]]></referencenumber>
    <apijobid><![CDATA[r48130]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48130/field-reimbursement-manager-neurology-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Phoenix]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong> Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: San Francisco (Metro), CA, Seattle (Metro), WA, Oakland, (Metro), CA, Las Vegas (Metro), NV, Thousand Oaks (Metro), CA Los Angeles (Metro) CA, Riverside (Metro) CA, San Diego, (Metro), CA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Associate Scientist, Neuroscience]]></title>
    <date><![CDATA[Sun, 05 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48792]]></requisitionid>
    <referencenumber><![CDATA[R48792]]></referencenumber>
    <apijobid><![CDATA[r48792]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48792/sr-associate-scientist-neuroscience/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an Sr. Associate Scientist to join our Neurotherapeutics research team. This role will support our R&D efforts to generate novel therapeutics for the treatment of neurodegenerative diseases, including Alzheimer's Disease.</p><p><strong>As an Sr. Associate Scientist, a typical day may include:</strong></p><p>Conducting lab experiments and research studies to validate therapeutic targets, establish new models of neurodegenerative diseases, screen preclinical therapeutic candidates, and advance technologies to more effectively deliver therapeutics to the central nervous system.</p><p><strong>This role may be for you if: </strong></p><ul><li><p>You enjoy working in a fast-paced environment</p></li><li><p>You are a fast learner and have desire to expand your skill set and learn new techniques</p></li><li><p>You are detail oriented, well-organized and can multi-task</p></li><li><p>You are a team player</p></li><li><p>You have strong communication skills</p></li></ul><p><strong>​To be considered for this role, you must have the following:</strong></p><p>Minimum BS -3-6 years, MS 2–5, with laboratory research experience. Knowledge of </p><p>Alzheimer's biology and a genuine passion for scientific research is a plus. </p><p>Relevant technical skills:</p><ul><li><p>Experience with in vivo experiments including stereotaxic surgeries and brain injections, systemic injections (e.g. subcutaneous and intravenous), mouse handling, blood and tissue collection</p></li><li><p>Experience with biochemical and immunoassays such as immunohistochemistry, immunofluorescence, Western blotting, ELISAs, tissue lysis and processing</p></li><li><p>Experience with data analysis software including HALO, PRISM, and Excel</p></li></ul><p>We hope you are excited to join our team!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 05 Jul 2026 11:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Procurement - Commercial]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43833]]></requisitionid>
    <referencenumber><![CDATA[R43833]]></referencenumber>
    <apijobid><![CDATA[r43833]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43833/executive-director-global-procurement-commercial/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Executive Director, Global Procurement – Commercial Procurement will provide strategic leadership and direction with a focus on Commercial Communications Procurement. The role focuses on a very exciting part of Commercial Procurement which includes Advertising, Media, Corporate Affairs/Public Relations, and Promotional Medical Communications. This role will be critical to driving performance across the Commercial Communications categories including alignment with stakeholder goals, driving towards competitive advantages (strategic and financial), optimizing supplier relationships, including small and diverse suppliers. This role works in close collaboration with Commercial Stakeholders to enable company revenue targets and the new product pipeline.<br><br>This individual will report to the Vice President of Commercial Procurement and serve as a member of the Global Procurement Extended Leadership Team, contributing to a continual path towards excellence in Procurement. The role will be accountable for managing direct reports to drive short-term priorities and the long-term vision to support stakeholder and Global Procurement priorities. They will lead the development, retention, and recruiting of talent to enable the company’s Commercial Procurement team. This includes collaborating with the VP of Commercial Procurement on performance goals, coaching and mentoring, and fostering a collaborative and inclusive work environment that encourages innovation and continuous learning.<br><br><strong><em>The role is based at our HQ campus in Sleepy Hollow, NY and is hybrid / onsite 4 days per week - it is not eligible for remote work. </em></strong></p><p><strong>A Typical Day May Include</strong></p><ul><li>Lead the composition, development and execution of category strategies in Commercial Communications;</li><li>Translate category strategies into achievable and meaningful sourcing projects that deliver value to Regeneron and its patients;</li><li>Partner with Commercial Procurement Leadership colleagues to ensure strategies evolve as Regeneron and its pipeline evolves;</li><li>Implement category strategies to meet objectives, including meeting our ESG objectives (sustainability, supplier diversity);</li><li>Collaborate with other parts of Global Procurement to best manage cross-category suppliers;</li><li>Anticipate needs and plan strategies to optimize achievement of corporate goals;</li><li>Collaborate and execute a best in class partner management program;</li><li>Implement and manage technology solutions to drive value via efficiency and effectiveness</li><li>Build and manage a team that provides all Commercial Communications Procurement support globally;</li><li>Continually enhance capability and capacity through ongoing talent development; establishing/communicating criteria for evaluating staff performance; managing direct reports, implementation of consistent work processes; and</li><li>Drive process excellence with a focus on stakeholder experience</li></ul><p><strong>This Role May Be For You If You </strong></p><ul><li>Believe that value can be driven through strategic partnerships and efficient ways of working.</li><li>Embrace challenging the status quo.</li><li>Are curious about how to deliver value to Commercial Communications stakeholders in a changing biopharma landscape.</li><li>Enjoy tracking global v local trends.</li><li>Can tap into strong in-depth knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of a Global Procurement organization.</li><li>Enjoy successfully leading global categories or global teams, processes, and suppliers within a multi-national organization.</li><li>Serve as role-model leader consistently exhibiting behaviors across an organization of direct reports to create clarity, provide a clear and understandable vision with transparency and trust both within and outside of the organization.</li><li>Operate with integrity, focus, clarity, and sound judgement in an environment of ambiguity.</li><li>Can influence and partner with senior executives and peer functions to drive strategic change and efficiency.</li></ul><p><strong>To Be Considered For This Position You Should Possess </strong></p><ul><li>Experience managing Associate Director+ level professionals required with previous success driving results within a multi-national Global Procurement team.</li><li>~15 years or more experience in relevant functions or industries, demonstrating growth in experience, scale, and development throughout.</li><li>In-depth knowledge of marketing and sales procurement categories including but not limited to media, content, production, and medical communications.</li><li>Ability to identify root causes and develop solutions to address complex problems.</li><li>Problem solving, risk management, program rollouts, and ability to put together forecasts for volume and savings.</li><li>Negotiation and contract management skills.</li><li>Ability to adapt in fast paces and ever-evolving space.<br> </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Dir Health Economics & Outcomes Research, Solid Tumors]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45357]]></requisitionid>
    <referencenumber><![CDATA[R45357]]></referencenumber>
    <apijobid><![CDATA[r45357]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45357/assoc-dir-health-economics-outcomes-research-solid-tumors/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director you will develop HEOR strategies and plans, conduct HEOR and RWE studies and develop publications and deliverables. We work closely with Market Access, Medical Affairs, Clinical Development, Commercial, Regulatory and other groups to ensure evidence needs are identified and addressed to demonstrate the value with a focus on solid tumors.</p><p><br>This position is at our Sleepy Hollow, NY location and will require you to be onsite 4 days/week. We cannot offer a remote option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong><br>• Develop and implement global HEOR strategies and programs for our portfolio throughout the product’s lifecycle, to inform and support clinical development and regulatory needs during early pipeline phase and ensuring optimal market access.<br>• Collaborate with business partners to develop and support compelling product value propositions with aim to optimize future patient access. <br>• Identify HEOR evidence requirements and gaps, and design, conduct, and deliver studies and tools to support relative value demonstration and product differentiation.<br>• Leverage RWD analytic tools and collaborate with HEOR RWDnA and Epidemiology teams generating insights to inform development programs and key business questions.<br>• Co-lead conduct of regulatory-grade real world evidence studies and provide education on emerging opportunities for employing RWE across the solid tumor portfolio.<br>• Collaborate on conduct and communication of epidemiology and pharmacoepidemiology analyses and studies. <br>• Provide relevant input into selection of patient population, comparators and endpoints within clinical trials to enable demonstration of robust incremental value over standard of care that can facilitate optimal future patient access.<br>• Develop and implement Clinical Outcomes Assessment (COA) measurement strategies and plans in support of product labeling, patient access and product differentiation. <br>• Develop and validate COA endpoints for integration in clinical studies. Produce COA evidence dossiers for regulatory submissions. <br>• Evaluate relevant payer and health technology assessment (HTA) decisions, collect feedback in advisory meetings and apply key learnings to pipeline products.<br>• Maintain an up-to-date awareness of regulatory (e.g. FDA, EMA) and payer/HTA considerations that may impact planning for and implementation of HEOR programs.<br>• Report, publish and disseminate HEOR data and study results in compliance with company, industry and regulatory requirements.</p><p><strong>This may be for you if you:</strong><br>• Want to have an impact on patient lives<br>• Enjoy working in a ‘rapid response’ environment<br>• Would like an opportunity to present to senior leaders<br>• Want to be part of a growing high performing team</p><p>To be considered it is required to have an Advanced graduate degree (Ph.D., MS, or MD, PharmD., B.Pharm with Master’s degree) in HEOR-related field (e.g. pharmacoepidemiology, epidemiology, healthcare/data analytics, health economics, health services research, public health). 4+ years with PhD or 6+ years with MS in HEOR; at least 3 years of life science company or healthcare consulting experience is a plus. Strong technical expertise required in design and conduct of HEOR studies and models. Solid understanding of regulatory (e.g. FDA, EMA) and HTA considerations. Experience in design and implementation of patient experience data in clinical trials, including experience in instrument selection, analysis and reporting of data. Experience with Oncology is preferred. <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology -  Naples, Miami, Ft. Myers]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45442]]></requisitionid>
    <referencenumber><![CDATA[R45442]]></referencenumber>
    <apijobid><![CDATA[r45442]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45442/medical-specialist-ii-ophthalmology-naples-miami-ft-myers/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Fort Myers]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Territory: South Florida</strong> (Miami, West Palm Beach, Ft Lauderdale, Naples, Ft Myers, Sarasota, and other surrounding cities)</p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets several medicines, including for eye diseases, and has product candidates in development in other areas of high unmet medical need.</p><p><strong>A typical day might include the following:</strong><br>The Medical Specialist II will report to the Regional Director and will be responsible for daily development and management of relationships with Retina Specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The primary focus on this role will be the approved indications suffered by patients as it relates to conditions of the eye. The Medical Specialist II will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you:</strong><br>• Have experience in biologics and buy and bill products<br>• Can demonstrate history of high sales performance<br>• Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Ophthalmology and/or Buy & Bill with relevant retina experience is preferred. Residency in the territory is required. Overnight travel may be necessary.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Marketing - HCP+DTC (Dermatology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45693]]></requisitionid>
    <referencenumber><![CDATA[R45693]]></referencenumber>
    <apijobid><![CDATA[r45693]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45693/director-marketing-hcpplusdtc-dermatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director of Marketing (DTC + HCP), US Dermatology is responsible for leading, developing and completing comprehensive US digital marketing strategies to reach, educate, and activate consumers and HCPs across the omnichannel ecosystem, including web, social media, influencer, paid media, and CRM, carried out in collaboration with the Dermatology alliance team. The Director formulates and fosters innovation to provide optimal patient and customer experience. This role requires a strategic and creative problem solver with a deep understanding of bio/pharmaceutical brand marketing, digital and omnichannel marketing trends, and online consumer/HCP behavior. This role will report to the Senior Director of Dermatology Consumer Marketing.</p><h3><strong>A Typical Day Might Look Like this:</strong></h3><ul><li>Lead the development of the Dermatology Omnichannel Marketing strategy (DTC and HCP) within the overall brand strategy across all current and future Dermatology indications</li><li>Plan, develop, and help execute branded, unbranded, and multi-cultural digital consumer and NPP marketing initiatives across various online channels, including but not limited to web, social media, display, SEM, CRM, email. Includes supporting and sponsoring materials through joint medical, regulatory, and legal review committees </li><li>Own end-to-end social media strategy and activation for DTC, architecting a first-in-class influencer model and scaling integrated paid and owned programs to accelerate patient demand and optimize ROI</li><li>Lead and mentor consumer and HCP digital marketing/NPP professional(s), fostering a collaborative and innovative work environment</li><li>Demonstrated leadership experience managing direct report(s), fostering a collaborative working environment</li><li>Partner with alliance media to develop efficient and effective media mix strategies</li></ul><h3><strong>This Position Might Be for You if:</strong></h3><ul><li>You bring Strategic, scientific, and analytical competence focused on delivering results</li><li>You can demonstrate leadership and experience managing direct report(s).</li><li>You bring brand marketing experience, with expertise in DTC/HCP media and ROI analysis </li><li>You can demonstrate competency and tenured experience in social media marketing channels (influencer activation a plus)</li><li>You can focus on execution and manage multiple projects in a fast-paced environment.</li><li>You have organizational agility and the capability to reprioritize based on external or internal changes.</li><li>You can manage external partners like agencies.</li></ul><p>To be considered you must have a bachelor’s degree is required; an MBA is a plus. 12+ years of “progressive” industry/relevant professional experience in strategic roles. 8+ years of experience in pharmaceutical/biotech marketing or a related industry, including consumer/HCP brand marketing/franchise management and omnichannel strategy, with strong understanding of digital marketing trends and innovations. Experience navigating and managing alliance partnerships is preferred. Must be willing to travel 20% of the time, including weekend travel as needed. Willingness to work in a hybrid environment with a minimum of 4 days on-site at Sleepy Hollow, NY</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Endocrinology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46016]]></requisitionid>
    <referencenumber><![CDATA[R46016]]></referencenumber>
    <apijobid><![CDATA[r46016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46016/medical-director-clinical-development-endocrinology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Director, Clinical Development, Endocrinology </strong></p><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Endocrinology team supporting our Clinical Development Unit. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>4 days a week on-site in Tarrytown, NY, Washington, D.C., or Cambridge, Massachusetts</p><p><strong>Discover your role:</strong></p><ul><li>You guide the Global Clinical Study Team to deliver high-quality trials on time.</li></ul><ul><li>You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance</li><li>You lead clinical study and protocol development and present to internal and external stakeholders.</li><li>You provide clinical and scientific leadership for data review, study reports, and publications.</li><li>You work closely with cross-functional partners to advance program goals and key deliverables.</li><li>You collaborate with discovery teams to help shape future targets and development opportunities in the field.</li></ul><p><strong>This role requires:</strong></p><ul><li>An M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable.</li><li>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</li><li>Experience in rare disease drug development strongly preferred</li><li>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</li></ul><p>#MDJobsCD, #MDJobs, #GDTherapeuticJobs, #Obesity</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director of IT Operations (Infrastructure Architecture)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45562]]></requisitionid>
    <referencenumber><![CDATA[R45562]]></referencenumber>
    <apijobid><![CDATA[r45562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45562/associate-director-of-it-operations-infrastructure-architecture/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of IT Operations (Infrastructure Architecture) ensures the reliable operation, delivery, and management of IT/Operational Technology (IT/OT) infrastructure and services, with a focus on supporting a highly regulated GxP environment. This role provides strategic direction, operational management, and administrative oversight for the daily IT operational activities, including hardware, communications & WiFi infrastructure, and service delivery. The position also ensures integration and alignment with corporate IT systems and infrastructure while maintaining robust compliance, security, and service standards.</p><p>As an Associate Director of IT Operations (Infrastructure Architecture), a typical day might include the following:</p><ul><li>Ensure the reliable operation of IT/OT infrastructure, including but not limited to servers, hardware, communications and desktop support, plus oversight of daily operational activities.</li><li>Define, implement, and lead IT/OT infrastructure architecture, with a focus on hyper-converged systems, advanced networking, and wireless technologies, to ensure robust connectivity and security.</li><li>Build scalable and secure wireless networks to support industrial and enterprise needs.</li><li>Provide operational management for data centre operations, network services, telecom, asset management, and security plus ensure systems and procedures are in place for effective monitoring and reporting.</li><li>Maintain compliance with industry standards, including experience with automation systems such as DeltaV/Emerson and Rockwell/Allen-Bradley.</li><li>Manage service providers to ensure high-quality service delivery and alignment to service level agreements (SLAs) and act as the escalation point for major incidents.</li><li>Ensure compliance with relevant regulations and standards, including GxP, FDA and other global regulatory requirements.</li><li>Maintain robust security measures to protect IT/OT infrastructure, including data integrity and disaster recovery planning.</li><li>Lead and mentor a diverse technical team and run recruitment, training, performance evaluations, and target setting for the IT Operations team.</li><li>Collaborate with partners to ensure seamless integration between IT and OT systems.</li><li>Provide regular management reporting on service performance and IT operations.</li></ul><p>​​​</p><p>This role may be for you if you:</p><ul><li>Have management and delivery experience including management of a diverse technical team, including Helpdesk, Desktop, Server and Network staff, with experience managing vendors and managed services.</li><li>Have experience in developing and deploying SLAs, Metrics and other best practices, as well as having successfully implemented ITIL practices into an organisation.</li><li>Have experience with Business Continuity and Disaster Recovery planning.</li><li>Have a strong background in Microsoft OS, in particular Server and GPO elements.</li><li>Have a strong understanding of Data Integrity and associated tools.</li><li>Possess hands-on experience designing and documenting infrastructure architecture across networking, compute, and security domains.</li><li>Have demonstrated experience with security frameworks (NIST CSF, IEC 62443, or ISO 27001) and applying them within regulated environments.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field along with</p><ul><li>Senior Manager: 8+ years of progressively more responsible experience, including 8+ years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment.</li><li>Associate Director: 10 years of progressively more responsible experience, including 10 years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Preferred knowledge of understanding of IT compliance guidelines, including PICS, CFR21 Part 11, Annex 11, and GAMP.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Resource Management]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46443]]></requisitionid>
    <referencenumber><![CDATA[R46443]]></referencenumber>
    <apijobid><![CDATA[r46443]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46443/director-resource-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Resource Management (DRM) is a key liaison across multiple functions in Research and Preclinical Development (RpD) providing comprehensive resource management and strategic resource planning for RpD functions with respect to current programs as well as planning for the future development portfolio. The DRM will supervise and coach two resource managers on the team. To be successful, the DRM will need to have an in-depth understanding of pharmaceutical discovery, pre-clinical development, research and early development functional roles, responsibilities and work effort. The DRM will be an expert in industry standard resource management tools and respective reporting tools to provide key insights regarding capacity, resource planning and forecasting. The DRM will be confident in the design of effective insight driven dashboards and collaborate closely with the IT function to enable development, implementation, and support. The DRM will promote the adherence to RM best practices, processes and the delivery of high-quality resource planning, capacity management, tracking, and forecasting of functional resources.</p><h3><strong>As a Director, a typical day may include the following:</strong></h3><ul><li><p>Serves as the key interface and point of contact with R&pD for the review and assessment of functional resource strategies including the assessment of available resources against requirements and confirmation of resource plans with functional leadership</p></li><li><p>Works with partners to ensure that Target, Project, and Program assumptions are current and resource utilization is optimized</p></li><li><p>Partners with applicable functions to design, develop, implement, and update algorithms in the RM tool used in resource demand forecasts</p></li><li><p>Directs other RMs assigned to additional functional areas to ensure cross-functional consistency for resource and headcount management</p></li><li><p>Assists partner functions with capacity management providing support for annual headcount planning and ensuring data quality for the quarterly budget reforecast activities</p></li><li><p>Deliver regular and ad-hoc resource reports, including forecasted resource demand, capacity, gap analyses, and FTE planned vs. actuals that provide clear insights needed for decision making</p></li><li><p>Is viewed as Subject Matter Expert (SME) in Resource Management for targets, assets, programs, and studies</p></li><li><p>Provides leadership and operational support for resource management processes including active resource management, capacity planning, and strategic workforce planning</p></li><li><p>Liaises with the Data Analytics (DA) team to design reports to help identify trends and develop metrics and analytics around resourcing and to develop functional and portfolio resourcing benchmarks and metrics</p></li><li><p>Conducts portfolio and program level scenario analyses. Models impact of changes in assumptions on resource estimates</p></li><li><p>Proactively identifies and communicates resource-related gaps, issues and risks to partner functions based on analysis of resource data. Supports review and discussion to resolve resource and/or capacity conflicts</p></li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li><p>Adept at managing a limited supply of resources against constantly changing portfolio</p></li><li><p>Excellent analytical, budgeting, and resource balancing skills</p></li><li><p>Problem solving abilities, troubleshooting, conflict resolution, and resourcefulness</p></li><li><p>Effective communication (clear and concise written and verbal skills), influencing, negotiating, and selling</p></li><li><p>Excellent interpersonal and leadership skills, ability to build relationships internally and externally (e.g. with supervisors, peers, partners and stakeholders)</p></li><li><p>Detail oriented and capable of working independently in ambiguous situations</p></li><li><p>Ability to manage multiple tasks and tight deadlines with confidence</p></li><li><p>Ability to prioritize and organize workload across multiple groups</p></li><li><p>Experience with supervising, coaching, and mentoring direct reports</p></li><li><p>Proficiency in Microsoft Office Suite</p></li></ul><p>To be considered for this role, you must have a Bachelor’s Degree required and 12+ years’ experience in Biotech/Pharmaceutical/CRO, including, but not limited to, Research, Early and Late Development functional areas. Master’s Degree (MS/MBA) and 10+ years of relevant experience may be considered. A solid understanding of the drug discovery and development process with particular emphasis on preclinical development, translational medicine, and early development for biological molecules. Expert with Planisware for project planning and resource forecasting including the design, development, and implementation of algorithms. We are seeking extensive experience with reporting for business facing resource management in research and development. This opportunity requires the ability to travel up to 20%.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Validation Specialist (Fill Finish)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46783]]></requisitionid>
    <referencenumber><![CDATA[R46783]]></referencenumber>
    <apijobid><![CDATA[r46783]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46783/principal-qa-validation-specialist-fill-finish/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently seeking a Principal QA Validation Specialist to join our Quality Assurance department. They will lead the utilities and EMPQ team for fill finish facility, overseeing qualification of utilities, cleanrooms, and filling lines critical to commercial production; ensure regulatory compliance, strengthen the contamination control strategy, and drive key licensure activities.</p><p>As a Principal QA Validation Specialist, a typical day might include the following:</p><ul><li>Lead validation and serve as SME for utilities and environmental qualification; assess change controls, review CAPAs/NOEs, approve documents, and lead audits</li><li>Plan and execute cleanroom qualifications and requalification; oversee EMPQ for filling line clean air equipment</li><li>Drive QRM deliverables including HACCP assessments and continuous trending/reporting</li><li>Lead investigations of contamination events associated with environmental monitoring in cleanrooms and clean air equipment</li><li>Qualify critical utilities: WFI (Water for Injection), pharmaceutical air, AHUs, clean steam generators, and nitrogen distribution systems</li><li>Manage and develop a specialist and a team of consultants to meet project milestones and deliver qualification/documentation deliverables</li><li>Establish processes that ensure compliance with regulatory requirements, including participation in Annex 1 gap assessments</li><li>Influence the creation and revision of local/global policies, standards, procedures, and business processes to align with industry best practices</li></ul><p>This role might be for you if you:</p><ul><li>Demonstrated experience in a cGMP-regulated environment, including validation, inspection and audit readiness</li><li>Possesses strong cross-functional collaboration and communication skills</li><li>Have proven ability to lead teams in a fast-paced, dynamic environment</li><li>Are able to gown and work in manufacturing areas as required</li></ul><p>Gowning and Environment </p><ul><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </li></ul><p>To be considered for the Principal QA Validation Specialist you must be willing and able to work Monday-Friday, 8am-4:30pm. You must hold a BS/BA in Engineering, Chemistry, or Life Sciences and 8+ years of relevant experience. Experience in utility and facility qualification/validation is required. Level is determined based on qualifications relevant to the role. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. MSAT Specialist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47490]]></requisitionid>
    <referencenumber><![CDATA[R47490]]></referencenumber>
    <apijobid><![CDATA[r47490]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47490/sr-msat-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Sr. Manufacturing Sciences & Technology (MSAT) Specialist to join our Process Sciences Drug Product Engineering department. This role will provide key technical support for internal and external technology transfer of drug substance manufacturing processes for small molecules, oligonucleotides, peptides, and antibody conjugates.</p><p>As a Sr. MSAT Specialist a typical day might include the following:</p><ul><li>Leads assessments of manufacturing requirements and capabilities prior to the transfer of new processes into the manufacturing facilities; generates facility fit assessments and high-level gap assessments</li><li>Coordinate the creation, management, and maintenance during the lifecycle of a transfer</li><li>Accountable for generating and reviewing documentation supporting technology transfer (e.g., master plans and reports, process descriptions, memos, detailed gap assessments etc.)</li><li>Leads projects and initiatives associated with improving technical support tools for technology transfers</li><li>Collaborates with managers to continuously assess and adjust technical support activities and functions</li><li>Performs sophisticated, in-depth reviews of technical document content, including FMEAs, PAR reports, regulatory submissions, etc</li><li>Leads study teams and investigations during transfers, as applicable</li><li>Generates options to resolve technical challenges and present them for endorsement</li><li>As a person in plant, provides technical support and training of manufacturing personnel to improve understanding of synthesis, purification, and other related operations across the sites</li><li>Captures, trends, and analyzes process generated data; summarizes findings in memos, reports, and presentations</li><li>Performs review of manufacturing documentation generated by the receiving unit (manufacturing records, batch sheets, changeover protocols, SOPs, etc.)</li><li>Helps to build process knowledge base, controls for technology transfer and knowledge management and lessons learned database; identifies continuous improvement activities to improve performance</li></ul><p>This role might be for you if you:</p><ul><li>Work optimally and efficiently in a team-oriented environment to ensure maximum and high-quality output</li><li>Have experience interacting with Contract Manufacturing Organizations</li><li>You continuously seek to improve processes for improved performance</li><li>Are willing to travel 10-15% annually</li><li>Can serve as a mentor for lower-level specialists</li></ul><p>To be considered for the Sr. MSAT Specialist, you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS/BA in Life Sciences or Engineering; PhD is preferred and 5+ years of relevant experience. Experience with small molecule, oligonucleotide, peptide manufacturing process development, or process engineering experience is preferred. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-(Gastro)-Omaha, NE]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47495]]></requisitionid>
    <referencenumber><![CDATA[R47495]]></referencenumber>
    <apijobid><![CDATA[r47495]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47495/medical-specialist-i-gastro-omaha-ne/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Omaha]]></city>
    <state><![CDATA[Nebraska]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Specialist, Gastroenterology (MS) - Omaha, NE</strong></p><p>The Medical Specialist (Sales Representative), Gastroenterology (MS) will report to the District Manager, Gastroenterology, and be responsible for engaging Gastroenterologists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies, and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US. </p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Gastroenterology therapeutic area to generate product utilization. The MS will develop strong working relationships with experts and all Gastroenterologists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p><strong>A typical day may include the following:</strong></p><p>A core responsibility of the MS will be to collaborate with their district colleagues, alliance counterparts, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>This role may be for you if:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Proven success navigating and demonstrating positive impact with large groups, institutional settings, and Ambulatory Surgery Centers</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p>To be considered you must possess a Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Gastroenterology market and/or a similar subcutaneous self-injectable biologic specialty market. Ability to travel and cover large geographic territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Facilities Maintenance Scheduler & Planner]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47525]]></requisitionid>
    <referencenumber><![CDATA[R47525]]></referencenumber>
    <apijobid><![CDATA[r47525]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47525/senior-facilities-maintenance-scheduler-planner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is looking for an outstanding Maintenance Planner & Scheduler, to prioritize, coordinate, and optimize preventive, predictive, and corrective maintenance for MEP, HVAC, refrigeration, and other critical facility systems across a multi-building research campus. Their efforts will safeguard asset reliability, ensure regulatory compliance, and minimize operational disruptions in laboratory and research environments. Reporting to Facilities Operations/Engineering leadership, they will turn service requests into fully scoped computerised maintenance management system (CMMS) work orders, develop standardized job plans, and align weekly schedules with technician availability and facility windows.</p><p>This position collaborates with technicians, engineers, contractors, and materials management teams to secure parts, allocate labor, and communicate priorities. Using their strong planning approach and knowledge of maintenance standard processes, they will drive efficient execution, equipment uptime, and continuous improvement in maintenance processes.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Reviewing new service requests and converting them into detailed CMMS work orders with clear scope, labor hours, and safety requirements</p></li><li><p>Developing and publishing weekly/daily schedules that align with technician availability and research-critical maintenance windows</p></li><li><p>Crafting or updating standardized job plans, task lists, and PM templates to ensure consistent execution across all buildings</p></li><li><p>Coordinating materials, spare parts, and contractor services to ensure everything is staged before work begins</p></li><li><p>Supervising work order progress, adjusting schedules for emergent priorities, and closing out completed jobs with accurate documentation</p></li><li><p>Communicating status, constraints, and upcoming activities to Facilities Operations, Engineering, and lab stakeholders</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Thrive on organizing complex information into clear, actionable plans</p></li><li><p>Enjoy collaborating with technicians, engineers, and vendors to solve maintenance challenges</p></li><li><p>Have a strong grasp of HVAC, refrigeration, boiler, chilled-water, and electrical distribution systems</p></li><li><p>Are comfortable balancing multiple priorities in regulated or mission-critical environments</p></li><li><p>Excel at using CMMS platforms (e.g., TRIRIGA, Maximo, SAP PM) and Microsoft Office tools</p></li><li><p>Communicate clearly, anticipate issues, and keep projects on track with minimal direction</p></li></ul><p><strong>In order to be considered for this role, you must have:</strong></p><ul><li><p>Associate Degree in Electrical/HVAC/Mechanical Engineering</p></li><li><p>5+ years of maintenance planning, industrial maintenance, or utilities operations experience (10+ years accepted in lieu of degree)</p></li><li><p>Proven expertise with commercial/industrial MEP systems and CMMS software</p></li><li><p>CMRP or equivalent planning/scheduling certification preferred</p></li><li><p>Valid New York State driver’s license</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$30.24 - $47.36]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Mountain West]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47571]]></requisitionid>
    <referencenumber><![CDATA[R47571]]></referencenumber>
    <apijobid><![CDATA[r47571]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47571/regional-director-neurology-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Minnesota]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the Mountain West Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Mountain West (Minnesota, Iowa, Missouri, Kansas, Idaho, Colorado, New Mexico and Arizona)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Manager Corporate Communications]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47986]]></requisitionid>
    <referencenumber><![CDATA[R47986]]></referencenumber>
    <apijobid><![CDATA[r47986]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47986/sr-manager-corporate-communications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>BUILD OUR FUTURE TOGETHER:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Corporate Communication to join our Product and Pipeline Communications team within Corporate Affairs, supporting our U.S. and international oncology business in a hybrid role. In this role, you will lead communications for our blood cancer portfolio and pipeline and support solid tumour programmes while collaborating with Commercial, Clinical, Medical Affairs, Legal, Regulatory, and in-country Corporate Affairs teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>WHEN & WHERE: </strong>Sleepy Hollow, NY. Hybrid, minimum four days on-site per week.</p><p><br><strong>DISCOVER YOUR ROLE:</strong><br>- Lead U.S. and Global communications for our blood cancer portfolio and pipeline</p><p>- Partner with Commercial, Clinical, Legal, and Regulatory teams as a trusted strategist and media coach</p><p>- Manage media relations, congress support, regulatory milestones, and stakeholder engagement</p><p>- You translate complex science into compelling narratives for diverse external audiences</p><p>- Identify and assess communications risks, recommending response strategies</p><p>- Collaborate with in-country Corporate Affairs teams to extend global strategies locally</p><p>- Oversee agency partners, resources, and budget to deliver cohesive outcomes</p><p>- You build consensus and foster trusted relationships across functions and levels</p><p><br><strong>THIS ROLE REQUIRES:</strong><br>- Bachelor's degree with 8–10+ years of relevant experience, including 5+ years in product or pipeline communications (in-house or agency)</p><p>- Strong writing, editing, and content design skills with ability to translate complex clinical data for external audiences</p><p>- Knowledge of the regulatory, commercial, and legal landscape governing pre-approval and post-approval pharmaceutical communications</p><p>- Proven experience with social media and digital communications strategies</p><p>- Experience managing agency partners and vendor workstreams</p><p>- Background in biotechnology or pharmaceutical communications in oncology (preferred)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison  - Neurology (West)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48120]]></requisitionid>
    <referencenumber><![CDATA[R48120]]></referencenumber>
    <apijobid><![CDATA[r48120]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48120/associate-director-thought-leader-liaison-neurology-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - California]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Neurology Marketing team. It will be focused on enhancing and improving interactions with key external US Neurology thought leaders at academic centers and leading community practices for our neurology product.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Neurology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><p><strong>The typical day may include the following:</strong></p><ul><li>The Neurology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You possess a strong science background with deep knowledge of rare neurology</li><li>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</li><li>You can successfully collaborate with and provide input/feedback to all functions within the project team</li><li>You can balance/lead multiple projects simultaneously</li><li>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</li></ul><p><strong>To be considered for this opportunity, you will possess the following:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10years of relevant work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in Neurology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry. Launch experience preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li><li>Must have a valid driver’s license</li><li>Must be able to travel 60%-80% of time </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Fill/Finish Associate (Internal Fill/Finish MFG)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46367]]></requisitionid>
    <referencenumber><![CDATA[R46367]]></referencenumber>
    <apijobid><![CDATA[r46367]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46367/fillfinish-associate-internal-fillfinish-mfg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Fill/Finish Associate. The Fill/Finish Associate performs all duties related to the production and support of drug product manufacturing. Works individually, and as part of a team, to support and perform operations to maintain formulation, filling, assembly, labeling and cartoning/packing equipment for parenteral biological products. Seeks to understand and develops proficiency in processes or procedures of increasing complexity.<br><br>As a Fill/Finish Associate, a typical day might include the following:</p><ul><li><p>Produces life-saving therapeutics for various indications developed from a dynamic internal pipeline</p></li><li><p>Works with a team that is accountable for production activities ranging from formulation of drug product to packaging of final drug product, which may include the following process-related responsibilities:</p></li><li><p>Operates highly automated equipment to fill drug product into vials or syringes within isolators or other aseptic environments</p></li><li><p>Assembles filled drug product into syringes and autoinjectors</p></li><li><p>Operates state of the art packaging lines to place assembled and labeled drug product into packaging configurations for distribution</p></li><li><p>Monitors production line for proper operation through process controls including pneumatics, robotics, manual and PLC feedback loop systems</p></li><li><p>Cleans, handles, and installs interchangeable parts for various systems and equipment</p></li><li><p>Collaborates to create and maintain operating procedures to perform routine activities that adhere to regulatory expectations</p></li><li><p>Ensures working spaces and equipment are clean, safe, and ready for processing activities</p></li><li><p>Maintains gowning qualification and adheres to clean room behaviors wherever required</p></li><li><p>Performs environmental sampling using various methods where applicable</p></li><li><p>Records GMP data that is accurate, legible, attributable, and contemporaneous and completes review on those records</p></li><li><p>Maintains and ensures proper documentation of all training</p></li><li><p>Navigates and utilizes electronic systems to support manufacturing operations</p></li><li><p>Travel (domestic and international) may be required.</p></li><li><p>Ensures compliance with applicable procedures while executing activities and escalates any non-conformities during operations</p></li><li><p>Performs reconciliation of product and controlled materials where applicable</p></li></ul><p>This role might be for you if:</p><ul><li><p>Ability to perform basic algebra and geometry</p></li><li><p>Reading/writing skills</p></li><li><p>Must be able to stand for extended periods of time and lift, push and pull at least 50lbs.</p></li><li><p>Knowledge of cGMP and FDA regulated (preferred) manufacturing environment and familiarity with cGMP filling, assembly or packaging processes preferred.</p></li><li><p>Necessary to have keen attention to detail and demonstrate from previous work experiences.</p></li><li><p>Preferred experience with aseptic technique and operating filling equipment or with assembly or packaging of parenteral products in vials, syringes and cartridges using both manual and automated equipment preferred.</p></li><li><p>Basic understanding of Microsoft Office Suite.</p></li><li><p>Demonstrates strong interpersonal, cross-cultural, communication, negotiation and has a high emotional IQ.</p></li><li><p>Exhibits confidence and strong problem-solving skills and demonstrates ingenuity, creativity and resourcefulness.</p></li><li><p>Gains understanding from provided instructions and works towards established goals.</p></li><li><p>Understands and listens to team members and stakeholders’ needs while supporting a positive team environment.</p></li><li><p>Possess a strong and effective communication style among peers and with management team</p></li><li><p>Values and acts with integrity</p></li></ul><p>Shift Requirements: Physical</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours):</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p>Gowning and Environment</p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li></ul><p><br>To be considered for the Fill/Finish Associate you must have a GED/High School diploma and previous work experience.</p><p><em>Level is figured out based on qualifications relevant to the role. </em></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$16.44 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Submission Project Management (RSPM)]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44752]]></requisitionid>
    <referencenumber><![CDATA[R44752]]></referencenumber>
    <apijobid><![CDATA[r44752]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44752/manager-regulatory-submission-project-management-rspm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an experienced and detail-oriented Manager, Regulatory Submission Project Management (RSPM) to join our dynamic team. This pivotal role offers the opportunity to lead the planning, execution, and review of regulatory operations activities, ensuring the successful submission of regulatory documents and data to health authorities. If you thrive in a collaborative environment and are passionate about driving regulatory milestones, this position could be your next career step.</p><p><strong>A Typical Day:</strong></p><ul><li>Collaborating with cross-functional teams to create submission timelines and responsibility matrices.</li><li>Guiding teams and resolving issues related to submission documents to maintain quality and timelines.</li><li>Managing submission deliverables and coordinating with Regulatory Publishing and vendors on document status.</li><li>Reviewing submission content plans and validating documents for compliance with health authority guidelines.</li><li>Supporting PMDA consultations, Clinical Trial Notifications, PCAs, MCNs, and NDAs through operational excellence.</li><li>Maintaining submission templates and obtaining literature references to support submissions.</li><li>Ensuring consistency and standardization across regulatory submissions.</li><li>Tracking and managing metadata within the electronic data management system (EDMS).</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You have a strong knowledge of Regulatory Agency regulations, guidelines, and specifications (e.g., PMDA, FDA, EMA, and ICH).</li><li>You excel in project management and timeline management for regulatory submissions.</li><li>You enjoy working with submission processes and systems such as Veeva Vault RIM or docuBridge.</li><li>You are adept at eCTD preparation and validation processes.</li><li>You thrive in fast-paced environments and can adapt quickly to changing priorities.</li><li>You have strong proficiency with MS Office applications and Adobe Acrobat.</li><li>You value collaboration and have exceptional attention to detail.</li><li>You are driven by the opportunity to make meaningful contributions to regulatory milestones.</li></ul><p><strong>To Be Considered:</strong><br>To excel in this role, you must have a Bachelor's Degree and at least six years of pharmaceutical industry or relevant experience. Strong knowledge of submission processes, eCTD guidelines, and regulatory tools is essential. Proficiency with systems like Veeva Vault RIM and docuBridge is highly desirable. Native level fluency in Japanese and business level English is required.</p><p>This is your chance to be part of a team that drives impactful regulatory submissions while fostering innovation and collaboration. Apply now to make a difference in regulatory excellence!</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Site Office Manager]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47684]]></requisitionid>
    <referencenumber><![CDATA[R47684]]></referencenumber>
    <apijobid><![CDATA[r47684]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47684/site-office-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. As we continue to scale globally, enabling an efficient, safe, and well-managed workplace is critical to supporting our people and operations.</p><p>As an Office Manager, you will play a key role in ensuring smooth day-to-day office operations and maintaining a productive work environment. You will partner with cross-functional teams to support facilities management, vendor coordination, workplace services, and employee experience initiatives.</p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li><p>Coordinate and manage day-to-day office operations to ensure a safe and efficient work environment</p></li><li><p>Partner with Facilities, HR, IT, Finance, and other functions to support workplace needs</p></li><li><p>Manage vendor relationships, including onboarding, contracts, and service delivery</p></li><li><p>Raise and track purchase requisitions and support invoice processing in collaboration with procurement</p></li><li><p>Oversee office facilities including maintenance, repairs, layout planning, and workspace readiness</p></li><li><p>Manage office supplies, inventory, and procurement of equipment and consumables</p></li><li><p>Act as a point of contact for office communication, including calls, emails, visitors, and mail handling</p></li><li><p>Coordinate workplace services such as housekeeping, security, and courier management</p></li><li><p>Support onboarding and offboarding activities, including workspace setup and asset coordination</p></li><li><p>Partner with IT for site-level coordination of equipment and basic support needs</p></li><li><p>Ensure compliance with health, safety, and environmental standards in collaboration with EHS</p></li><li><p>Support emergency preparedness and response activities, including safety drills and communication</p></li><li><p>Coordinate site meetings, document minutes, and track action items where required</p></li><li><p>Support internal communications and employee engagement activities, events, and initiatives</p></li><li><p>Manage office expenses, including PC ard usage and expense tracking</p></li><li><p>Collaborate with Office Managers across locations to drive standard processes and best practices.</p></li></ul><p><strong>This Job May Be for You If You Have:</strong></p><ul><li><p>Experience in office administration, facilities coordination, or workplace operations</p></li><li><p>Understanding of vendor management and office services delivery</p></li><li><p>Ability to coordinate with multiple stakeholders across functions</p></li><li><p>Strong organizational skills with the ability to manage multiple priorities</p></li><li><p>Ability to identify issues and implement practical solutions</p></li><li><p>Strong communication and stakeholder management skills</p></li><li><p>Ability to work independently and in a dynamic environment</p></li><li><p>Attention to detail and a structured approach to tasks.</p></li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li><p>3–6+ years of experience in Office Administration, Facilities, or Workplace Operations</p></li><li><p>Bachelor’s degree in any discipline (preferred)</p></li><li><p>Experience working in a corporate or multinational environment is an advantage</p></li><li><p>Exposure to procurement systems or office tools is preferred</p></li><li><p>Proficiency in Microsoft Office tools (Outlook, Excel, Word, PowerPoint, Teams)</p></li><li><p>Fluency in English; knowledge of local language(s) is an advantage</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Accounts Payable Service Delivery]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48255]]></requisitionid>
    <referencenumber><![CDATA[R48255]]></referencenumber>
    <apijobid><![CDATA[r48255]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48255/supervisor-accounts-payable-service-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that improve lives for people with serious diseases. As we continue to expand globally, strong financial operations and governance frameworks are critical to supporting sustainable growth and operational excellence.</p><p>As a Supervisor – Accounts Payable (AP Delivery, you will play a key role in managing day-to-day AP operations, ensuring accurate and timely processing of invoices and payments while maintaining strong internal controls and compliance standards. You will partner with cross-functional teams, drive operational efficiency, and support continuous improvement initiatives within the Procure-to-Pay (P2P) function.</p><p>This position is office-based in Hyderabad</p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li><p>Oversee end-to-end Accounts Payable operations, including invoice processing, payment cycles, and issue resolution</p></li><li><p>Manage AP inquiries and requests from vendors and internal stakeholders, ensuring timely and effective resolution</p></li><li><p>Monitor AP shared inbox, prioritize requests, and maintain high service delivery standards</p></li><li><p>Ensure compliance with internal policies, procedures, and SOX requirements</p></li><li><p>Review and validate payment disbursements prior to processing</p></li><li><p>Track and manage aging and held invoices to ensure timely closure</p></li><li><p>Analyse AP reports and metrics to ensure timely payments and identify process gaps</p></li><li><p>Collaborate with Accounting, Procurement, Tax, and other teams to resolve discrepancies and improve processes</p></li><li><p>Maintain and review logs and dashboards to monitor team productivity and SLAs</p></li><li><p>Identify system or process issues and drive resolution and improvement initiatives</p></li><li><p>Prepare and present operational reports and insights to management</p></li><li><p>Participate in and support process improvement initiatives and special projects</p></li><li><p>Build strong working relationships with internal stakeholders and external vendors</p></li></ul><p><strong>This Job May Be for You If You Have:</strong></p><ul><li><p>Strong understanding of Accounts Payable and Procure-to-Pay processes</p></li><li><p>Experience working with internal controls and compliance requirements (SOX)</p></li><li><p>Ability to manage high-volume transactions in a fast-paced environment</p></li><li><p>Strong analytical and problem-solving skills</p></li><li><p>Effective communication and stakeholder management capabilities</p></li><li><p>Ability to identify inefficiencies and drive process improvements</p></li><li><p>Experience working with ERP systems and invoice workflow tools</p></li><li><p>Strong attention to detail and focus on accuracy</p></li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li><p>5–8+ years of experience in Accounts Payable or P2P operations</p></li><li><p>Prior experience in a shared services or global delivery environment preferred</p></li><li><p>Bachelor’s degree in commerce, Finance, or related field required</p></li><li><p>Experience with ERP systems (Oracle preferred)</p></li><li><p>Proficiency in Microsoft Office tools, especially Excel</p></li><li><p>Familiarity with invoice processing and workflow tools preferred</p></li><li><p>Experience working in a global or matrixed environment is an advantage</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Los Angeles North, CA (San Fernando Valley, Santa Barbara, Santa Maria)]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47241]]></requisitionid>
    <referencenumber><![CDATA[R47241]]></referencenumber>
    <apijobid><![CDATA[r47241]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47241/medical-specialist-i-dermatology-los-angeles-north-ca-san-fernando-valley-santa-barbara-santa-maria/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Los Angeles]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Los Angeles North, CA (San Fernando Valley, Santa Barbara, Santa Maria)</strong></p><p>Our Medical Specialists are at the forefront of engaging Dermatologists and other key customers. We need someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</p></li><li><p>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. Having a minimum of 2 years selling in the Immunology market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role, dermatology experience preferred. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Northeast]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47570]]></requisitionid>
    <referencenumber><![CDATA[R47570]]></referencenumber>
    <apijobid><![CDATA[r47570]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47570/regional-director-neurology-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the Northeast Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Northeast (New York, Pennsylvania, Massachusetts, Vermont)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 18:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Finance]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47681]]></requisitionid>
    <referencenumber><![CDATA[R47681]]></referencenumber>
    <apijobid><![CDATA[r47681]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47681/senior-manager-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization focuses on inventing, developing, and commercializing medicines that help people with serious diseases. As we continue to expand globally, our finance organization plays a critical role in supporting business decision-making through analysis, insights, and strong financial planning.</p><p>As a Senior Manager – Finance, you will support global financial planning, analysis, and forecasting activities. You will partner with cross-functional teams across geographies to provide insights into financial performance, support business decisions, and drive planning processes. This role focuses on financial analysis and business partnering and does not involve direct accounting entries or transaction processing.</p><p><strong>A Typical Day May Include the Following</strong></p><ul><li>Support preparation of budgets and forecasts across international markets</li><li>Perform analysis of actual financial results and provide insights against plan</li><li>Partner with global Commercial, Medical Affairs, and other functions to support decision-making</li><li>Support consolidated international P&L analysis, particularly for Oncology business</li><li>Maintain product and brand-level P&L models</li><li>Work closely with country finance teams to:<ul><li>Track revenue across markets (units, local currency, USD)</li><li>Monitor operating expenses across functions</li><li>Prepare dashboards and performance reports</li></ul></li><li>Prepare materials for monthly business reviews and leadership reporting</li><li>Support preparation of monthly sales reports and performance summaries</li><li>Calculate accruals and prepayments and share inputs with Accounting teams</li><li>Support Gross-to-Net analysis across markets</li><li>Perform constant currency analysis for financial comparisons</li><li>Support financial modelling for rebates, claw-backs, and pricing agreements</li><li>Provide analysis for tenders and pricing/volume decisions</li><li>Prepare FTE cost and rate calculations</li><li>Support regulatory reporting such as HCP spend tracking</li><li>Load and manage data in budgeting and forecasting systems</li><li>Coordinate quarterly revenue landing and forecast updates</li><li>Deliver ad-hoc analysis and respond to business queries</li></ul><p><strong>This Job May Be for You If You Have</strong></p><ul><li>Strong experience in financial planning & analysis (FP&A) or commercial finance</li><li>Expertise in P&L management, forecasting, and financial modelling</li><li>Ability to interpret financial data and translate it into business insights</li><li>Experience working with global teams and cross-functional stakeholders</li><li>Strong analytical thinking and problem-solving skills</li><li>Ability to work in ambiguous and evolving business environments</li><li>Good communication skills with the ability to explain complex financial concepts</li><li>High attention to detail with a structured approach to analysis</li></ul><p><strong>To Be Considered for This Role</strong></p><ul><li>6+ years of relevant post-qualification experience in Finance or FP&A</li><li>Bachelor’s degree in Finance, Accounting, or related field; MBA or equivalent preferred</li><li>Professional qualifications such as ACA, ACCA, CMA, CIMA, CPA, or similar</li><li>Experience in biotech/pharma industry or Shared Services environment is an advantage</li><li>Fluent in English; additional language skills are beneficial</li><li>Experience supporting international or multi-country finance environments</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Solutions Architect - Back End Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46204]]></requisitionid>
    <referencenumber><![CDATA[R46204]]></referencenumber>
    <apijobid><![CDATA[r46204]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46204/senior-solutions-architect-back-end-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an outstanding Senior Solutions Architect - Back End Engineer, to own the technical evolution of our digital transformation platform. This role combines deep backend engineering expertise with strategic solution architecture responsibilities, focusing on building scalable, secure, and compliant systems for healthcare data management.</p><p>As the lead Backend Developer, you will be the primary technical owner of our backend systems, driving the architecture and implementation of a robust multi-tenant platform capable of handling critical PII/PHI data in compliance with healthcare regulations.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p><strong>Solution Architecture</strong>: Define and implement the technical architecture for our platform’s hosting, ensuring scalability, security, and compliance</p></li><li><p><strong>Multi-Tenant Architecture Migration</strong>: Build and implement the migration from single-tenant to multi-tenant architecture, enabling efficient resource utilization and client isolation</p></li><li><p><strong>Technical Strategy</strong>: Collaborate with product and engineering leadership to align technical solutions with business requirements and long-term platform vision</p></li><li><p><strong>Data Layer Development</strong>: Design and implement a comprehensive data abstraction layer to support multiple database technologies and optimize data access patterns</p></li><li><p><strong>Backend API Development</strong>: Build and maintain robust, scalable RESTful APIs and serverless functions to support platform functionality</p></li><li><p><strong>Hosting</strong>: Serve as the primary technical lead for hosting infrastructure</p></li><li><p><strong>PII/PHI Data Handling</strong>: Develop and implement secure data handling practices for Protected Health Information (PHI) and Personally Identifiable Information (PII)</p></li><li><p><strong>Security Best Practices</strong>: Implement authentication, authorization, encryption, and audit logging mechanisms to protect critical data</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p><strong>8+ years</strong> of professional software development experience with strong backend focus</p></li><li><p><strong>Hosting production applications </strong>in regulated domains (healthcare, life science, genetics research platforms) with experience in data-intensive patient engagement platforms</p></li><li><p><strong>Expert-level proficiency</strong> JavaScript/TypeScript, Node.js, and AWS serverless architecture (Lambda, API Gateway, DynamoDB, S3)</p></li><li><p><strong>Strong knowledge</strong> of relational databases (PostgreSQL, MySQL) and NoSQL databases (DynamoDB, MongoDB) with validated experience Designing RESTful APIs at scale</p></li><li><p><strong>Solid understanding</strong> of microservices architecture and distributed systems patterns</p></li><li><p><strong>Required</strong>: Experience handling PII/PHI data, with Strong understanding of healthcare compliance requirements (HIPAA, HITRUST)</p></li><li><p><strong>Knowledge of security guidelines </strong>including OWASP Top 10, encryption, authentication/authorization, audit logging, data encryption at rest and in transit</p></li><li><p><strong>Deep AWS expertise</strong> required (EC2, RDS, Lambda, CloudFront, VPC, IAM, etc.) and proficiency with Infrastructure as Code tools</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><ul><li><p><strong>Bachelor’s degree</strong> in Computer Science, Software Engineering, or related field (or 8+ years equivalent work experience)</p></li><li><p><strong>Minimum 5+ years</strong> of professional software development experience</p></li><li><p><strong>Minimum 2+ years</strong> in a senior or lead engineering role</p></li><li><p>Proven track record of delivering sophisticated, production-grade systems</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Supply Analyst - Kinaxis Maestro]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43446]]></requisitionid>
    <referencenumber><![CDATA[R43446]]></referencenumber>
    <apijobid><![CDATA[r43446]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43446/principal-supply-analyst-kinaxis-maestro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal Supply Analyst - Kinaxis Maestro will drive innovation in supply chain planning and execution. In this role, you’ll design, implement, and optimize solutions using the Kinaxis Maestro platform, helping deliver life-saving products to patients worldwide.</p><div><p>As a Principal Supply Analyst, a typical day might include the following:</p><ul><li>Design and configure Maestro solutions for campaign management, lifecycle planning, and inventory optimization.</li><li>Develop worksheets, dashboards, and analytics to support planning and execution.</li><li>Build custom templates, algorithms, and scripts to enhance functionality. Integrate Maestro with ERP systems (e.g., Oracle, SAP) and life sciences platforms.</li><li>Ensure compliance with FDA, EMA, GMP, and other regulatory standards.</li><li>Train end-users on Maestro functionalities and best practices.</li><li>Maintain detailed documentation for workflows and configurations.</li><li>Monitor system performance and identify improvement opportunities.</li><li>Resolve issues related to data integrity and system integrations.</li><li>Work cross-functionally with operations, logistics, planning, manufacturing, and finance teams.</li></ul></div><p>This role may be for you if you have:</p><ul><li>Strong understanding of demand planning, clinical trial supply chains, SIOP and regulatory compliance.</li><li>Experience integrating ERP and life sciences-specific software, preferably Oracle.</li><li>Good understanding of Kinaxis Maestro data model, control table, and data management.</li><li>Excellent problem-solving and communication abilities.</li><li>Proficiency in Agile methodologies (e.g., Scrum) and programming skills (Python, SQL) are a plus.</li></ul><p>In order to be considered for this position, you must hold a Bachelor’s degree in supply chain management, Computer Science, Engineering, or related field and</p><ul><li>Senior Supply Analyst: 5+ in Supply Chain Planning solutions, 3+ years Hands-on experience with Kinaxis Maestro, preferably in life sciences.</li><li>Principal Supply Analyst: 8+ in Supply Chain Planning solutions, 5+ years Hands-on experience with Kinaxis Maestro, preferably in life science.</li><li>Kinaxis Maestro Author or Administrator certifications, Level 2 or higher preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -MIAMI, FL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48032]]></requisitionid>
    <referencenumber><![CDATA[R48032]]></referencenumber>
    <apijobid><![CDATA[r48032]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48032/medical-account-specialist-ii-neurology-miami-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Miami]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Miami (Metro), FL</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 18:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -  SAINT LOUIS, MO]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48055]]></requisitionid>
    <referencenumber><![CDATA[R48055]]></referencenumber>
    <apijobid><![CDATA[r48055]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48055/medical-account-specialist-ii-neurology-saint-louis-mo/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[St. Louis]]></city>
    <state><![CDATA[Missouri]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: St. Louis (Metro) MO</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager,  Research Program Management]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46243]]></requisitionid>
    <referencenumber><![CDATA[R46243]]></referencenumber>
    <apijobid><![CDATA[r46243]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46243/associate-manager-research-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Manager in Research Program Management plays a key role in executing Regeneron’s programs through the drug discovery pipeline. The Associate Manager drives projects with a moderate to high level of complexity and coordinates with cross functional groups including the Therapeutic Focus Area, Technology centers, and the broader Research team to achieve portfolio and program goals. </p><p><strong>As an Associate Manager, a typical day may include: </strong></p><ul><li><p>Executes programs with guidance; manages projects and tasks independently and with awareness of internal/external interdependencies.</p></li><li><p>Can identify and may champion resolution of critical gaps, risks, or issues, as related to assigned programs, projects, and tasks.</p></li><li><p>May be aware of strategic goals related to programs and projects. </p></li><li><p>With guidance, can prioritize projects and programs and allocate team resources. Manager's input is needed to align with organizational strategic objectives. </p></li></ul><p><strong>Communication and Team Management </strong></p><ul><li><p>With minimal guidance, drives and contributes to decision making amongst cross functional program teams. </p></li><li><p>With minimal guidance, distills complex information and identifies the most pertinent key information; effectively captures rationale for decision-making.</p></li><li><p>With minimal guidance, facilitates collaboration between functional areas to ensure effective, accurate, and timely scientific / technical and program-related communication. </p></li><li><p>With minimal guidance, can tailor communications based on audience.</p></li><li><p>Has strong relationships with project leaders, managers and individuals within each project team and key cross-functional partners.</p></li></ul><p><strong>This role might be for you if you: </strong></p><ul><li><p>Identifies and collates key data and functions needed to drive discussion and decision making for moving projects/programs through discovery and drug development process.</p></li><li><p>May provide technical and/or operational guidance to project teams and/or other RPM members for their assigned programs. </p></li></ul><ul><li><p>Has technical expertise in existing processes that relate to and support projects and programs.</p></li><li><p>Independently analyzes and identifies areas of minimal complexity for process improvement.</p></li><li><p>Contributes to process improvement initiatives</p></li><li><p>Creates new processes as needed with guidance, leads the development and gains alignment on process improvement solutions, informed by knowledge of technical/scientific challenges faced by the project teams.</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Minimum of BS/MS/PHD. </p></li><li><p>Knowledge of molecular biology, protein structure-function, and assay development concepts is required</p></li><li><p>Prior experience in drug development is required</p></li><li><p>Regularly utilizes strategic thinking around complex scientific principles</p></li><li><p>Ability to organize complicated workflows/operations</p></li><li><p>Prior project/program management experience is desirable</p></li><li><p>Excels in team building and communication</p></li><li><p>Excellent written, verbal, organizational, and interpersonal communication skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology - Alberta]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47980]]></requisitionid>
    <referencenumber><![CDATA[R47980]]></referencenumber>
    <apijobid><![CDATA[r47980]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47980/sales-specialist-immunology-alberta/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a S<strong>pecialty Representative, Immunology in Alberta </strong>to join our International Immunology team, supporting our Canada in a hybrid work mode. In this role, you will drive sales growth and deliver impactful customer engagement while collaborating with regional teams, business partners, and management. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Alberta, Canada</li><li>Field based</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Establish and lead high quality HCP interactions by continuously keeping scientific knowledge around the product, indication and brand sales messaging up to date and optimally implementing sales & marketing plan.</li><li>Consistently deliver on the value proposition for the brand through key message communication to HCPs.</li><li>Work in alignment with the Brand Plan, develop and implement a local account plan based on key data sources and local market insights.</li><li>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs.</li><li>Leverage all communication channels including digital channels, in collaboration with other functions, to achieve the best possible share of voice in the market.</li><li>Report results and developments proactively and clearly to the Immunology leadership team</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree</li><li>Minimum 5 years’ experience as a Specialty Pharmaceutical Representative</li><li>Experience working within a commercial alliance environment is desirable</li><li>Proven track record to run accounts and meet performance objectives</li><li>Experience engaging healthcare professionals using multiple communication channel</li><li>Ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</li><li>Working in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</li><li>Balancing multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</li><li>You can operate optimally in a “start-up” model as this is a completely new team.</li><li>Regular travel and have a valid driver's license. Proficiency in English is required.</li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 05:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Patient Advocacy]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48219]]></requisitionid>
    <referencenumber><![CDATA[R48219]]></referencenumber>
    <apijobid><![CDATA[r48219]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48219/senior-manager-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Role Summary:</strong><br>The Senior Manager, Patient Advocacy is a strategic and execution-focused role responsible for building trusted relationships with patient advocacy organizations, elevating the patient voice, and delivering compliant, high-impact programs that advance disease education, access, and outcomes. This role partners closely with Medical Affairs, Clinical Development, Market Access, Corporate/External Affairs, and Commercial to ensure patient insights inform decisions from early development through commercialization, and represents the company at patient events, advisory boards, and key congresses.</p><br><p><strong>Location and Work Model:</strong><br>This role is based in Sleep Hollow, NY, on-site 4 days/week. Travel approximately 25–50% for patient engagements, conferences, and advocacy meetings; some evenings/weekends may be required based on community schedules </p><br><p><strong>Impact and Scope:</strong></p><ul><li>With Patient Advocacy leadership, lead execution of therapeutically aligned patient advocacy strategy in assigned therapeutic areas.</li><li>Apply and adapt standard methodologies and governance frameworks for engagement with advocacy and professional societies. Identify opportunities to enhance processes and ensure alignment with evolving business needs</li><li>Collaborate with cross-functional partners in Medical, Commercial, Market Access, Policy, and Clinical Development to support established advocacy strategy</li><li>Accountable for delivering measurable improvements in disease awareness, time to diagnosis, clinical trial awareness, access, and patient experience</li></ul><br><p><strong>Roles and Responsibilities</strong></p><br><p><strong>Advocacy Strategy and Execution</strong></p><ul><li>Assess shifting company priorities and external dynamics to inform strategic decisions, recommending strategic choices and trade-offs with clear implications for patients and the business</li><li>Continuously evolve therapeutic area advocacy strategies and operating plans, including educational programs, disease awareness, advisory boards, patient speaker engagement, clinical trial awareness, and coordination on relevant policy initiatives</li><li>With Patient Advocacy leadership, lead the development and execution of advocacy campaigns; ensure external partner plans align to Regeneron’s goals and compliance standards</li><li>Coordinate and design patient advisory boards and insight-generation activities, ensuring strategic alignment, high-quality outputs, and effective dissemination of insights to inform decision-making. Ensure materials developed for ad boards are accurate, inclusive, and compliant.</li></ul><br><p><strong>Executive Engagement and Influence</strong></p><ul><li>Serve as a trusted advisor to leaders; create materials/presentations that articulate patient impact, risks, and demonstrate Patient Advocacy’s role in supporting Regeneron’s business objectives</li><li>Represent the company at advocacy meetings, conferences, and coalition activities; identify collaboration opportunities and areas of mutual interest </li><li>Monitor policy and access topics impacting patient communities and partner with internal stakeholders on advocacy positions and engagement plans </li></ul><br><p><strong>Relationship Management</strong></p><ul><li>Build and maintain long-term, trust-based partnerships with patient advocacy and professional societies at national and regional levels; serve as a responsive, empathetic point of contact </li><li>Ensure Regeneron’s leadership position is evident through presence at priority events; synthesize and disseminate insights to internal stakeholders</li></ul><br><p><strong>Cross-Functional Collaboration and Alignment</strong></p><ul><li>Build strong, collaborative relationships with Medical, Commercial/Brand, Market Access, Government Affairs, Health Policy, Clinical Development, and Legal/Compliance</li><li>Drive cross-functional alignment and execution of advocacy initiatives; co-create plans with Alliance partners where applicable</li><li>Contribute to therapeutically aligned assigned strategy and annual planning and budgeting.</li></ul><br><p> <strong>Patient Voice and Insights</strong></p><ul><li>Lead initiatives that elevate patient voice, such as advisory boards, listening sessions, and patient storytelling, ensuring insights inform clinical development and commercialization plans </li><li> Champion a patient-centric mindset and provide the patient perspectives to inform clinical trial design, evidence generation, disease education, patient services, and access strategies</li></ul><br><p><strong>Financial and Business Acumen</strong></p><ul><li>Track engagement metrics, manage budgets, and report outcomes to leadership </li></ul><br><p><strong>Grants and Governance </strong></p><ul><li>Strategically fund programs that advance patient engagement and disease education aligned to therapeutic priorities Act as a grant reviewer as part of a compliant grant review process; manage budgets and financial stewardship effectively and in a timely manner Ensure all interactions adhere to legal, regulatory, and compliance standards; maintain high transparency and trust with stakeholders </li></ul><br><p><strong>Qualifications Required</strong></p><ul><li>Bachelor’s degree required; advanced degree a plus (e.g., MPH, MS, MA in Communications/Health Policy). </li><li>8+ years of industry experience, patient advocacy, community engagement, or related roles within biopharma/biotech or patient organizations </li><li>Experience building high-trust partnerships with diverse stakeholders, stakeholder management; proven ability to translate insights into action </li><li>Strong project management skills with experience executing multi-stakeholder programs and events on time and within budget. </li><li>Excellent communication skills (written, verbal, and presentation) with executive presence. </li><li>Working knowledge of clinical development, real-world evidence, market access, and the compliance environment for patient interactions (e.g., sponsorships, fair market value, privacy, AE reporting).</li><li>Comfortable operating in a matrixed, fast-paced environment with shifting priorities.<strong> </strong></li></ul><br><p><strong>Preferred</strong></p><ul><li>Experience in rare diseases, oncology, hematology, and/or cardio-metabolic<strong> </strong></li></ul><br><p><strong>Reporting and Collaboration </strong></p><p><strong>Reporting Line:</strong></p><ul><li>Reports to Director, Patient Advocacy</li></ul><br><p><strong>Key Internal Partnerships:</strong></p><ul><li>Medical, Commercial, Market Access, Government Affairs, and Health Policy.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 19 Jun 2026 07:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist, R&D Chemistry, Peptidomimetic Synthesis]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48139]]></requisitionid>
    <referencenumber><![CDATA[R48139]]></referencenumber>
    <apijobid><![CDATA[r48139]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48139/scientist-rd-chemistry-peptidomimetic-synthesis/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Scientist (Peptidomimetic Synthesis), R&D Chemistry</strong></p><p>We are currently seeking a lab-centric peptide chemist to join the R&D (Research & Development) Chemistry group. In this position, they will play a key role in Regeneron’s peptidomimetic antibody-conjugate drug discovery capabilities to enable seamless combination with the company’s existing expertise in biologics and novel genetic medicines. The candidate will drive the synthesis and discovery of peptidomimetic payloads and linker payloads for antibody conjugate drug therapeutics across diverse research areas. Cultural fit with the Regeneron cross-functional teams will be a key driver for success. The R&D Chemistry team is primarily composed of synthetic organic, medicinal chemistry and bioconjugation scientists that work in a highly collaborative environment with other technology, biology and therapeutic area groups. Successful candidates will have a peptidomimetic/synthetic organic/medicinal chemistry background and will require peptidomimetic synthesis, discovery and SAR (structure-activity relationship) optimization expertise as well as linker-payload synthesis experience. A firm understanding and grasp of chemical biology strategies and the importance of applying both chemical and biological solutions to solve problems in drug discovery will be key. Small molecule synthesis and drug discovery/SAR experience as well as knowledge in the latest and most advanced peptide synthesis techniques, platforms, and strategies is desired. We expect they will act as an inspiring and motivating colleague, effective communicator, and strong project team collaborator to help develop novel antibody-conjugated peptidomimetic therapeutics. The successful candidate will also participate in problem solving related to synthesis, medicinal chemistry, bioconjugation and optimal <em>in vitro</em> and <em>in vivo</em> properties leading to development candidates.</p><p><strong> </strong></p><p><strong>Build our future together:</strong></p><ul><li>Actively participate and collaborate in the day-to-day activities of the R&D Chemistry Peptidomimetic group.</li><li>Perform medicinal chemistry inspired and SAR-driven synthesis of novel peptidomimetic drug modality payloads/linker payloads, using modern peptide synthesizer, isolation, and characterization instrumentation and techniques</li><li>Troubleshoot and optimize peptide potency and stability using standard peptide-based principles (e.g., Ala scans), non-natural amino acid incorporation, alpha-Me/N-Me peptide backbone modifications, and other medicinal chemistry strategies that are guided by <em>in vitro</em> assays, plasma/serum stability, and met ID data.</li><li>Participate in the R&D Chemistry Peptidomimetic efforts on internal/external project teams, and demonstrate the ability to multi-task and parallel process to add to our continuous pipeline of Regeneron peptidomimetic conjugates.</li><li>Identify new strategies and technologies (e.g., peptidomimetic synthesis and design) to improve on existing Regeneron platforms for pursuing novel synthesis of peptidomimetic drug modality conjugates</li><li>Actively participate in departmental, cross-functional, leadership, and external meetings to contribute expertise and to represent the vision of the R&D Chemistry Peptidomimetic group.</li><li>Interact broadly and collaboratively with other Regeneron groups, forging relationships and active collaborations.</li></ul><p><strong> </strong></p><p><strong>Discover your role:</strong></p><ul><li>You are passionate and enthusiastic about the promise of peptidomimetic conjugated, antibody-targeted therapeutics and appreciate the challenges and opportunities of drug delivery and molecular targeting.</li><li>You enjoy applying and combining traditional methods and novel technologies to develop solutions for synthesis, bioconjugation and drug discovery.</li><li>You are comfortable working in a cross-functional role and excel as part of a diverse team where egos are checked at the door.</li><li>You want to provide meaningful contributions to the development of an organizational culture that supports growth and development of its people and capabilities to drive forward the Regeneron pipeline.</li><li>You prefer to work in an organization that is modality agnostic, letting the data determine the best course forward.</li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required, Master’s degree preferred in peptide/peptidomimetic and/or synthetic organic chemistry (or related)</li><li>Extensive hands-on experience of the synthesis and reaction troubleshooting of peptidomimetics, extensive experience running modern synthesis/isolation/characterization equipment and instrumentation</li><li>Expertise in modern methods of peptidomimetic synthesis and analytical characterization, and a minimum of 5-10 years of industry experience. A track record of success in the field of either peptidomimetics or small molecules is required. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 18 Jun 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PHILADELPHIA NORTH, PA]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48013]]></requisitionid>
    <referencenumber><![CDATA[R48013]]></referencenumber>
    <apijobid><![CDATA[r48013]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48013/medical-account-specialist-ii-neurology-philadelphia-north-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Philadelphia]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Philadelphia North (Metro), PA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director , Quantitative Pharmacology]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47970]]></requisitionid>
    <referencenumber><![CDATA[R47970]]></referencenumber>
    <apijobid><![CDATA[r47970]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47970/senior-director-quantitative-pharmacology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build Our Future Together</strong></p></div><p>In this capacity the <strong>Senior Director</strong> is accountable for the successful and timely completion of Quantitative Pharmacology related activities, encompassing a broad array of deliverables in support of Drug Safety and Pharmacometrics. The successful applicant will support a range of assets from Early Clinical Development through submission and beyond.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Warren, NJ and Cambridge, MA</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Providing technical guidance and mentoring of colleagues within the function and across the organization.</p></li><li><p>Performance management and assessment of staff and providing guidance and training to enable their success.</p></li><li><p>Utilizing a mastery level of PK/PD knowledge and strategic leadership skills, effectively developing and implementing strategic analyses in support of research and development projects.</p></li><li><p>Taking accountability for the PK/PD evaluation of a portfolio of products or projects, and/or highly complex projects that are wide in scope.</p></li><li><p>Identifying opportunity for process and procedural improvements, product or service improvements.</p></li><li><p>Solving unique and complex problems that have a broad impact on the business.</p></li><li><p>Want the ability to make a significant impact on the organization and external groups, and can influence and effect change.</p></li><li><p>Enjoy making contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.</p></li><li><p>Understand long-term career opportunities and can guide other QP staff on potential directions.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD degree (PharmD or MD degree) with 10+ years of industry experience focusing on modeling and simulation, PK/PD (pharmacokinetics/pharmacodynamics), systems pharmacology, and quantitative drug development strategies.</p></li><li><p>Hands on usage of a broad range of quantitative tools and systems is required, as is a strong publication record in the field.</p></li><li><p>A proven ability to display excellent interpersonal and communication skills both written and oral and ability to communicate complex information succinctly.</p></li><li><p>Strong collaborative skills and effective at building alliances across functions, as well as the ability to effectively influence colleagues and multi-disciplinary project teams.</p></li><li><p>The ability to handle all types of projects and leverage higher level staff for technical input and brainstorming to implement solutions for complex projects.</p></li><li><p>Proven experience interacting with regulatory agencies without supervision, and within the company to develop regulatory strategy.</p></li></ul><p>#pmx</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 23 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead Warehouse Associate | Days]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48758]]></requisitionid>
    <referencenumber><![CDATA[R48758]]></referencenumber>
    <apijobid><![CDATA[r48758]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48758/lead-warehouse-associate-days/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p></div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Warehouse & Inventory Team Lead to join our plant operations team, supporting materials management and logistics in an on-site, floor-based role. In this role, you will provide hands-on leadership to a team responsible for the receipt, documentation, and movement of inventory within the plant and from outside sources, while collaborating with Quality Assurance, Manufacturing, and Supply Chain teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>East Greenbush, New York <strong>| Work Model: </strong> 1st | Mon-Fri | 08:00a-04:30p<strong> </strong> <strong> | Travel: </strong>0%</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead and support a warehouse team on the floor, overseeing receipt, documentation, labeling, and movement of inventory and non-inventory items throughout the plant</p></li><li><p>Unload trucks, inspect incoming goods against purchase orders and packing slips, and transfer materials to QA Release, storage, or process areas</p></li><li><p>Maintain accurate paper and electronic records of received goods, inventory transfers, and material disbursements to production</p></li><li><p>Generate and apply labels to received inventory; schedule deliveries of incoming raw materials and coordinate outbound shipments per SOPs</p></li><li><p>Examine, stock, and distribute materials to manufacturing; fill requisitions manually and electronically for production workers</p></li><li><p>Support shipping and receipt of finished products in coordination with fillers, labelers, and distribution partners</p></li><li><p>Ensure the warehouse environment is clean, organized, and compliant with cGMP safety practices and established SOPs</p></li><li><p>Monitor employee training completion and timesheets; conduct monthly performance feedback meetings and escalate issues to management or HR as needed</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Lead Warehouse Associate I: High school diploma or GED and 0 – 2 years of experience</p></li><li><p>Lead Warehouse Associate II: High school diploma or GED and 2+ years of experience</p></li><li><p>Lead Warehouse Associate III: High school diploma or GED and 4+ years of experience</p></li><li><p>Lead Warehouse Associate IV: High school diploma or GED and 6+ years of experience</p></li><li><p>Associate’s degree and/or dedicated warehouse experience in a cGMP environment preferred</p></li><li><p>Ability to perform physical tasks including unloading trucks, lifting heavy items, and operating a forklift</p></li><li><p>Forklift certification, handheld scanner experience, and/or CDL a plus</p></li><li><p>Shift Requirements (Schedule): 1st | Mon-Fri | 08:00a-04:30p<strong> </strong></p></li><li><p>Shift Requirements (Physical): Role involves regular lifting of heavy items, standing, and operating material handling equipment</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.49 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Analytical & Bioanalytical Mass Spectrometry (ABMS)]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46354]]></requisitionid>
    <referencenumber><![CDATA[R46354]]></referencenumber>
    <apijobid><![CDATA[r46354]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46354/associate-scientist-analytical-bioanalytical-mass-spectrometry-abms/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Pharmaceutical's Analytical and Biological Mass Spectrometry Group (ABMS), located in Tarrytown, NY is seeking a motivated <strong>Associate Scientist</strong> to join our fast-paced and interdisciplinary team working on analytical and bioanalytical development on novel siRNA/oligonucleotide-based modalities in a diverse genetic medicine pipeline.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li>Develop and optimize liquid chromatography coupled to mass spectrometry (LC-MS) related methods for the enrichment, detection, quantification, and structural characterization of siRNAs, oligonucleotides, novel siRNA conjugates and monoclonal antibodies (mAbs)</li><li>Perform analytical testing and sample preparation of siRNA/oligonucleotides with a focus on chromatographic fractionation, LC, LC-MS, solid phase extraction (SPE), hybridization-capture, and other mass spectrometry related methods</li><li>Independently conduct sample preparation and LC-MS analyses in compliance with SOPs or drafted protocols, and document experimental procedures and results in electronic laboratory notebook (ELN)</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You are mentally flexible and adapt quickly to changing priorities in a fast-paced environment.</li><li>You are an excellent team player who can follow directions while also bringing your own insights to problem-solving.</li><li>You have a growth mindset and eagerly embrace new challenges and learning opportunities.</li><li>You are interested in learning about genetic medicines and development for impactful RNA-based therapies.</li></ul><p>This role requires a BS or MS degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field with 0–3 years of relevant hands‑on laboratory experience in analytical chemistry or bioanalytical sciences. Strong hands-on experience with liquid chromatography (such as reversed-phase, size-exclusion, ion exchange chromatography) is essential, particularly HPLC or UPLC techniques. Hands-on experience with various types of biological matrices is a plus. Hands-on experience with fractionation, solid phase extraction and/or hybridization techniques would be particularly valuable.</p><p>While mass spectrometry experience is beneficial, we prioritize candidates with excellent chromatography skills and the ability to optimize separation methods. You should be comfortable working independently after initial guidance and be able to communicate effectively about technical challenges and results.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 22 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Product and  Pipeline Communications Manager]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48510]]></requisitionid>
    <referencenumber><![CDATA[R48510]]></referencenumber>
    <apijobid><![CDATA[r48510]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48510/product-and-pipeline-communications-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Product and Pipeline Communications, Europe and Canada to join our Product and Pipeline Communications International team, supporting our Europe and Canada. In this role, you will strengthen and protect Regeneron’s reputation through science-driven, patient-centered communications while collaborating with in-country cross-functional teams, Commercial, Clinical, Medical Affairs, and Global Corporate Affairs. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Munich , Paris , Madrid</p><p>Hybrid model</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead in-country communications priorities, strategies, and processes.</p></li><li><p>Develop country-level strategies for stakeholder communications programs.</p></li><li><p>Partner with Commercial, Clinical, and Medical Affairs teams.</p></li><li><p>Manage media relations, medical congress support, and milestone communications.</p></li><li><p>Identify communications risks and recommend appropriate response strategies.</p></li><li><p>Shape Corporate Affairs strategies with regional insights and local updates.</p></li><li><p>You advise cross-functional partners with sound judgement and clarity.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree, or equivalent, with 7–9+ years’ relevant experience.</p></li><li><p>3+ years’ product and/or pipeline communications experience.</p></li><li><p>Global, regional, and in-country communications expertise within Europe.</p></li><li><p>Understanding of EU regulatory, commercial, and legal pharmaceutical communications.</p></li><li><p>Fluent in English as well as German , French or Spanish</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€58,200.00 - €97,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 05:26:18 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43877]]></requisitionid>
    <referencenumber><![CDATA[R43877]]></referencenumber>
    <apijobid><![CDATA[r43877]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43877/senior-manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>***Please note this is an onsite position and NOT eligible remote.</em></p><p>A <strong>Senior Manager Statistical Programming</strong> provides timely support to the project team on all programming matters according to the project strategies within a therapeutic area. As an integral part of a project team, the incumbent provides project leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified according to a Statistical Analysis Plan, programming specifications or user requirements/design documents using internal standards and guidelines. The incumbent is responsible for leading the programming aspect of the project, both internally or CROs, for all programming deliverables and participates in the identification and development of programming standards and macro development to facilitate the creation of statistical deliverables from a single study through to regulatory approval, product launch, and annual reports. May be asked to oversee special projects / work with clinical task force. Meets statistical adhoc requests of senior management.</p><p><br><strong>As a Senior Manager, A typical day may include:</strong></p><ul><li>Independently coordinate and oversee the preparation, execution, reporting and documentation of project analysis programming within a therapeutic area using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Manage and coordinate programming and QC of analysis datasets and TFLs following Regeneron standard data models and/o integration of data across studies in support of CSS/CSE and esub deliverables.</li><li>Implement and mentor others on the use of department standardization tools or therapeutic area standard analysis when programming clinical data or system application deliverables.</li><li>Contribute to programming development and quality control of the programming deliverables utilizing Regeneron tools and methodologies.</li><li>Programming representative within a therapeutic area in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, programming representative for an application development to the user audience.</li><li>Develop data models, programming standards and code, and training end users in the use of project standards to support programming deliverables that follow regulatory submission requirements.</li><li>Mentor junior level staff in therapeutic area requirements. Develop collaborative work environment and be a positive role model.</li><li>Advises all relevant employees about the procedures surrounding retention of data, records, and information for employees in their group.</li></ul><p><strong>To be considered for this role, you must meet the following requirements</strong>:</p><ul><li>Masters Degree and 8-10 years of relevant experience</li><li>SAS Certification desirable.</li></ul><p>#statprogramming</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Clinical Data Management]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45840]]></requisitionid>
    <referencenumber><![CDATA[R45840]]></referencenumber>
    <apijobid><![CDATA[r45840]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45840/senior-director-clinical-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Job title</strong></p><p>Senior Director, Clinical Data Management, India</p><p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Clinical Data Management, India to join our Clinical Data Management Leadership Team, supporting our clinical pipeline in an on-site role. In this role, you will shape the global operational vision and strategy for Data Management, building a high-performing regional organisation while collaborating with Clinical Data Operations, Central Services, External Data Acquisition, and external partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>This position is office-based and will be on site at <strong>Regeneron’s Hyderabad office.</strong></p><p><strong>Discover your role:</strong></p><ul><li>Build and lead a regional Clinical Data Management organisation spanning reporting, review, coding, lab data processing, and database operations.</li><li>Define functional metrics and quality indicators to drive compliance, quality, and timely delivery across the portfolio.</li><li>Provide oversight of functional service providers and external data vendors, managing performance and risk.</li><li>You build trusted partnerships across functions and levels, influencing senior collaborators to drive alignment.</li><li>Lead cross-functional initiatives that strengthen operations, improve efficiency, and support inspection readiness.</li><li>Advance the adoption of automation and AI solutions to reduce manual effort and accelerate data access.</li><li>Shape organisation design, evaluate resource needs, and hire and develop talent across the team.</li><li>You stay current on emerging trends and technologies, bringing fresh thinking to data management practice,</li></ul><p><strong>This role requires:</strong></p><ul><li>15+ years of clinical data management experience in pharmaceutical or biotech, including 10+ years of functional leadership and 8+ years of people management.</li><li>Experience leading teams of 50-150 supporting global data management functions.</li><li>Strong knowledge of clinical data management regulations and standards including 21 CFR Part 11, ICH-GCP, GxP, and GDPR.</li><li>Expertise in clinical data management systems such as EDC, eSource, eCOA, IRT, and medical coding platforms.</li><li>Willingness to travel up to 25%.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Specialist, EDC Administration]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47959]]></requisitionid>
    <referencenumber><![CDATA[R47959]]></referencenumber>
    <apijobid><![CDATA[r47959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47959/senior-specialist-edc-administration/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div></div><div><div><div><div><div><div><div><div><div><p><strong>About Regeneron</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p></div></div></div></div></div></div></div></div></div><p>As a <strong>Senior Specialist, EDC Administration</strong>, you will support and lead EDC system administration activities across Regeneron’s clinical trial portfolio. You will serve as a key operational resource responsible for Medidata Rave administration, user access management, study environment setup, and ongoing platform support while collaborating with CRO partners and cross-functional stakeholders to ensure compliant and efficient clinical data operations.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong></p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Administer Medidata Rave user management activities including user account setup, role assignments, access provisioning, modifications, and deactivations</p></li><li><p>Configure and maintain study environments and handle production participant access within Medidata Cloud Administration</p></li><li><p>Serve as the main point of contact for EDC access-related queries from internal teams and CRO partners</p></li><li><p>Maintain and update user access records, reports, dashboards, and operational metrics across the study portfolio</p></li><li><p>Perform study archiving activities and handle database access workflows across EDC, SharePoint, and other clinical data systems</p></li><li><p>Coordinate EDC administration timelines, breakthroughs, environment setup deadlines, and release readiness activities</p></li><li><p>Provide operational support for inspection readiness activities, audit trails, and compliance documentation related to EDC administration</p></li><li><p>Partner with Clinical Data Management teams and CROs to support database development operational meetings and issue resolution</p></li><li><p>Deliver training and mentorship on EDC administration standards, Medidata platform capabilities, and access management workflows</p></li><li><p>Contribute to process improvements, SOP development, platform upgrades, migrations, and system integration projects</p></li></ul><p><strong>This job may be for you if you have:</strong></p><ul><li><p>Strong expertise in Medidata Rave administration including Cloud Administration, User Management, environment configuration, and PDF Generator</p></li><li><p>Knowledge of clinical data management processes and EDC platform administration standards</p></li><li><p>Understanding of 21 CFR Part 11, ICH-GCP Guidelines, and CDISC standards in regulated clinical environments</p></li><li><p>Solid understanding of access controls, audit trail requirements, and compliance documentation</p></li><li><p>Excellent interpersonal skills with the ability to handle high-volume operational tasks accurately and efficiently</p></li><li><p>Good communication, problem-solving, and stakeholder management skills</p></li><li><p>Ability to work effectively in cross-functional and virtual team environments</p></li><li><p>Experience developing and improving operational workflows and standard processes</p></li><li><p>Strong time management skills with the ability to manage multiple concurrent studies and priorities</p></li><li><p>Proficiency with SharePoint, Microsoft Office Suite, and collaboration tools</p></li></ul><p><strong>To be considered for this role</strong>, you must have a minimum of 4+ years of experience in the biotechnology, pharmaceutical, or healthcare industry, including at least 2 years of direct EDC administration or clinical systems administration experience. Experience with Medidata Rave platform administration is required. A bachelor’s degree in mathematics, science, information systems, or a related field is preferred.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Specialist–Full Stack Developer- Clinical Data Operation]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48286]]></requisitionid>
    <referencenumber><![CDATA[R48286]]></referencenumber>
    <apijobid><![CDATA[r48286]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48286/senior-specialist-full-stack-developer-clinical-data-operation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist, Data Quality & Insights to join our Data Management team, supporting our clinical data operations in India in a hybrid work model. In this role, you will perform end-to-end reconciliation, validation, and quality oversight of external clinical data while collaborating with Data Management, Pharmacometrics, Imaging, Precision Medicine, Biomarker Sciences, GD-IT, and Data Acquisition teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad, India(Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Perform reconciliation across external clinical data and EDC systems</p></li><li><p>Develop Python and SQL reconciliation scripts and ETL pipelines</p></li><li><p>Investigate data discrepancies and coordinate vendor issue resolution</p></li><li><p>Execute protocol-aligned data quality timelines and validation checkpoints</p></li><li><p>Build automated reporting pipelines and operational quality dashboards</p></li><li><p>Generate vendor KPIs and present findings in operational meetings</p></li><li><p>You collaborate effectively across global cross-functional stakeholder teams</p></li><li><p>You apply analytical thinking to improve data quality processes continuously</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s or Master’s degree in Life Sciences, Data Science, Computer Science, Bioinformatics, or a related field</p></li><li><p>4–6 years of experience in clinical data management or external data reconciliation within the pharmaceutical or biotechnology industry</p></li><li><p>Strong expertise in external clinical data domains including Central Lab, Imaging, PK/PD, Cytokines, eCOA, and Biomarkers</p></li><li><p>Proficiency in SQL, Python, SAS, and cloud-based data lake platforms</p></li><li><p>Hands-on experience building automated reconciliation scripts, ETL pipelines, and data quality checks</p></li><li><p>Experience working with EDC systems such as Medidata Rave</p></li><li><p>Knowledge of Clinical Data Acquisition Standards Harmonization (CDASH) standards and protocol schedule management</p></li><li><p>Experience collaborating with global teams across multiple external data modalities</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Commercial Insights & Analytics - Ophthalmology]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48440]]></requisitionid>
    <referencenumber><![CDATA[R48440]]></referencenumber>
    <apijobid><![CDATA[r48440]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48440/executive-director-commercial-insights-analytics-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director </strong>to lead our <strong>Commercial</strong><strong> Insights and Analytics Ophthalmology</strong> team. The Executive Director, Commercial Insights and Analytics (I&A), Ophthalmology, will report directly into the Vice President, Commercial Strategy and Insights & Analytics (CSI&A) within the CSI&A department. This role will lead the I&A team responsible for the Ophthalmology Commercial Business Unit (CBU) to drive deeper insights that inform business decisions across some of Regeneron’s leading brands. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong> </strong></p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><p><em>Lead</em></p><p>1) Lead and mentor the CSI&A Ophthalmology team in providing business analytics, customer insights and competitive intelligence to deliver rich insights to solve key business problems</p><p>2) Set the strategic I&A direction that aligns with CBU priorities and helps drive launch excellence</p><p>3) Serve as a member of the Ophthalmology CBU Leadership Team, providing I&A expertise</p><p>4) Serve as a member of the CSI&A leadership team to drive cross-commercial innovation and best-in-class delivery</p><p><em>Develop</em></p><p>5) Translate complex analyses into compelling insights and recommendations that will be used to inform business decision-making for senior Regeneron teams, including the CBU, Chief Commercial Officer, Chief Executive Officer and Board of Directors</p><p>6) Develop people from both a functional skills and leadership perspective, with the goal of growing internal talent</p><p>7) Assess and implement novel methodologies and frameworks to <strong>a)</strong> garner meaningful insights to inform brand differentiation, market growth and business impact; and <strong>b)</strong> consider business potential for pipeline products</p><p><em>Partnership and collaboration</em></p><p>8) Collaborate with the Ophthalmology CBU and other members of senior leadership to contribute to ongoing brand strategies and decisions, including long-term data, analytics and insights roadmap</p><p>9) Develop and maintain a mutually beneficial partnership with CBU stakeholders; ensure insight generation and feedback are embraced; strike a balance between project rigor, timelines and ability to influence decisions</p><p>10) Lead efforts to identify and crystalize insights that inform strategic plans for the Ophthalmology CBU </p><p>11) Work with other CSI&A leads to develop standardized adoption of capabilities such as marketing mix, promotional optimization, data science, market structure analyses, patient/treatment flow modeling, analog modeling and ML/AI methodologies across I&A</p><p><em>Execute</em></p><p>12) Proactively communicate with the Ophthalmology CBU and provide strategic recommendations and insights as well as anticipated future needs</p><p>13) Construct and deliver integrated business reviews, I&A summary overviews with the Ophthalmology CBU and with CSI&A leadership</p><p>14) Manage third-party vendor relationships</p><p><strong>This role requires:</strong></p><ul><li><p>20+ years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with buy-and-bill brands in highly competitive markets is required</p></li><li><p>Minimum Bachelor’s degree in data science, public health, statistics, engineering, or a related field (MBA, MPH, MS preferred)</p></li><li><p>Functional expertise in business analytics, customer insights, analog forecast development, market access, and competitive intelligence</p></li><li><p>Prior experience managing I&A groups with responsibility for analytics, customer insights, market access analytics, and competitive intelligence</p></li><li><p>Demonstrated knowledge of the legal and regulatory environment, as it relates to commercialization in the pharmaceutical/biotechnology industry</p></li><li><p>Knowledge of data industry standards</p></li><li><p>Proven ability to influence, communicate and negotiate with all levels of management across functional and business unit boundaries</p></li><li><p>Extensive experience with managing numerous projects concurrently against stringent deadlines</p></li><li><p>Prior experience working with I&A projects and initiatives where a balance between project rigor and timeliness was needed</p></li><li><p>Ability to think strategy to execution with hands on experience in implementing large initiatives with cross-functional stakeholders</p></li><li><p>Expertise in data visualization and data storytelling</p></li><li><p>Strong interpersonal, facilitation and communication skills, with the ability to resolve conflict, drive consensus and work across multiple departments</p></li><li><p>Strong organizational, project management, influencing and change management skills </p></li><li><p>Proven ability to manage multiple project and priorities concurrently, while meeting stringent deadlines</p></li><li><p>Ophthalmology disease category experience is strongly desired</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Data Management]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44832]]></requisitionid>
    <referencenumber><![CDATA[R44832]]></referencenumber>
    <apijobid><![CDATA[r44832]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44832/senior-manager-clinical-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[[Unknown]]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Data Management to join our Data Management [team/function], supporting our [region/business area]. In this role, you will oversee clinical data management studies and ensure high-quality, timely delivery of data management outputs while collaborating with clinical study teams, CROs, and external data vendors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Remote US</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead data management activities across studies from start-up to archiving</p></li><li><p>Serve as primary contact for study teams, CROs, vendors</p></li><li><p>Oversee data quality review, acceptance, and database lock processes</p></li><li><p>Manage data transfers, coding, and reconciliation across systems</p></li><li><p>Review and approve study documentation including data plans and specifications</p></li><li><p>Ensure inspection readiness and maintain compliant documentation in eTMF</p></li><li><p>You collaborate effectively across cross-functional and external teams</p></li><li><p>You prioritize multiple activities while maintaining strong attention to detail</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Mathematics, Science, or related field</p></li><li><p>Minimum 8+ years of clinical data management experience in relevant industry</p></li><li><p>Demonstrated knowledge of regulations including 21 CFR Part 11 and ICH-GCP</p></li><li><p>Proven experience leading studies and data management teams</p></li><li><p>Strong understanding of data management processes and industry standards</p></li><li><p>Certified Clinical Data Manager (CCDM) certification</p></li><li><p>Experience with people management and team development</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs - Neurology]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48689]]></requisitionid>
    <referencenumber><![CDATA[R48689]]></referencenumber>
    <apijobid><![CDATA[r48689]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48689/medical-director-medical-affairs-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Neurology / Myasthenia Gravis Medical Affairs team, supporting our European medical affairs activities in a hybrid work mode. In this role, you will co-develop medical strategy, plan and execute medical affairs activities, and serve as a key scientific and medical resource, while collaborating with the Global Medical Team, cross-functional matrix partners, and external collaborators including healthcare practitioners, key opinion leaders, and payers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Munich, Germany (Hybrid - 3 days a week on-site)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Co-develop medical strategy for Myasthenia Gravis (MG) as an integral member of the cross-functional Global Medical Team.</p></li><li><p>Serve as the primary medical and scientific liaison for Neurology / MG community engagements across the assigned region (Europe / Germany).</p></li><li><p>Lead and contribute to data generation, analysis, and interpretation, safety monitoring, and post-marketing study reports for Phase 4 interventional and observational research.</p></li><li><p>Provide scientific input and medical support for publications, communications, and integrated real-world evidence generation planning and execution.</p></li><li><p>Develop and present medical content at congresses, symposia, and advisory boards.</p></li><li><p>Deliver medical training to internal staff on investigational and approved products, disease state, and unmet needs.</p></li><li><p>Maintain deep scientific and medical knowledge of Neurology / MG, the treatment landscape, and clinical decision making.</p></li><li><p>You bring the patient and physician voice into cross-functional teams to enable effective, impactful decision making.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>PhD, or MD (preferred).</p></li><li><p>10+ years of professional experience, including 5+ years in the pharmaceutical or biotechnology industry.</p></li><li><p>Product launch experience preferred.</p></li><li><p>Direct experience in Myasthenia Gravis and/or Neurology rare disease strongly preferred.</p></li><li><p>Thorough understanding of the Neurology and Myasthenia Gravis healthcare environment and key partners.</p></li><li><p>Deep understanding of all medical affairs accountabilities.</p></li><li><p>Proven ability to work in a dynamic, matrix environment with excellent collaboration and communication skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€125,250.00 - €208,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Commercial Training - Ophthalmology Market Access]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47809]]></requisitionid>
    <referencenumber><![CDATA[R47809]]></referencenumber>
    <apijobid><![CDATA[r47809]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47809/senior-manager-commercial-training-ophthalmology-market-access/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Ophthalmology Market Access Training is responsible for supporting all areas of Ophthalmology commercialization including reimbursement, marketing, market access strategy, patient services, and sales in a buy-and-bill market. This position reports to the Director, Commercial Training – Ophthalmology. Focus areas include product and competitive readiness training, market access, customer interaction skills, and national field meeting preparation including workshop development for the field reimbursement teams.</p><p>Additional areas of responsibility may include logistical support and coordination of the training of colleagues, as needed, in international markets. Training support includes all areas of commercialization including sales, marketing, and reimbursement.</p><p><strong>A typical day may include the following:</strong></p><p>Develop</p><ul><li>Design and development of product training for pre-launch, post launch, POA and advanced training including conducting needs assessment with relevant stakeholders</li><li>Creates and facilitates workshops for POA and other training meetings, using best-in-class means of training delivery including eLearning, self-study, computer-based training, audio/video, classroom, and experiential learning to ensure the relevant teams are trained to effectively and compliantly deliver the access and acquisition related attributes of our products and services</li><li>Develops content for and facilitates new hire, Phase II, and advanced training</li><li>Responsible for developing training activities, including backgrounders and FAQs on payer landscape and pull through associated with promoting and executing brand strategies and tactics</li></ul><p>Operate</p><ul><li>Assists in the development of Regeneron Field trainers</li><li>Partner with leadership and department of Learning and Development (OD & T) to determine performance models and identify gaps in order to provide recommendations on appropriate representative, market access and management training to enhance performance and business results</li><li>Collaborates and aligns with field force effectiveness, medical, commercial operations, market access, and brand marketing to develop high-impact training</li><li>Provides courses in such a way to stimulate and motivate attendees, utilizing a variety of media</li><li>Monitors the effectiveness of training programs through testing and metrics platforms, leveraging data to enhance the development and execution of (Brand) market access training</li></ul><p>Execute</p><ul><li>Ensures all training is provided in accordance with company policies and procedures and are conducted in strict compliance with all applicable laws and regulations</li><li>Ensure the field force is educated and effectively trained to comply with all legal and regulatory requirements, including HIPPA, PhRMA Code, OIG Compliance, PDMA, etc. This requires coordination of key internal functions for training materials and workshop development as well as certification of sales and other commercial personnel</li><li>Ensures all developed materials are appropriately approved through the Medical/Legal/Regulatory process.</li><li>Remain abreast of the industry, life sciences, and training related topics. Maintain familiarity with competitive products.</li><li>Conducts field visits with Reimbursement Business Managers to keep abreast of current trends, to identify training opportunities</li></ul><p><strong>To be considered, you must possess:</strong></p><ul><li>Bachelor’s degree required</li><li>8+ years of experience, preferably within the pharmaceutical/ biotech industry with 4-5 years of demonstrated success in Reimbursement, Reimbursement Leadership, Commercial or Reimbursement Training & Development.</li><li>2+ years training or regional training experience preferred</li><li>Strong interpersonal communication skills, ability to work across multiple departments and create effective teams</li><li>Demonstrated mastery in presentation, facilitation, collaboration and influencing skills are required</li><li>Ability to manage multiple priorities, with strong organizational, planning, and project management skills are necessary</li><li>Demonstrated mastery in oral and written technical communication as well as background with instructional design</li><li>Demonstrates the Regeneron Way in the execution of all professional duties</li><li>Remote-based position; regular travel required</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison - Gastroenterology (Dallas, TX)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48773]]></requisitionid>
    <referencenumber><![CDATA[R48773]]></referencenumber>
    <apijobid><![CDATA[r48773]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48773/associate-director-thought-leader-liaison-gastroenterology-dallas-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director, Thought Leader Liaison - Gastroenterology, is a field-based, non-sales role, passionate about enhancing and improving interactions with external Gastroenterology Key Thought Leaders (KTLs). We are seeking someone who can engage, develop advocacy, capture insights, and liaise with multiple functional partners. We expect you will work cross-functionally with colleagues in Marketing, Medical Affairs, Sales, and Market Access. The attributes that are needed for success include teamwork, communication, planning, and the ability to implement initiatives. You will report to the National Director, Thought Leader Liaisons, within the Commercial organization.</p><h3>When & where:</h3><p>Territory Includes: TX, NM, OK, AR, LA. Need to have the ability to travel to meetings/trainings/programs (60-80% travel) and must live within the geographic area of the assigned territory, and hold a valid driver's license.</p><br><h3>Discover your role:</h3><ul><li>Conducting discussions related to aligned therapeutic areas, disease states, and general corporate overviews</li><li>Collaborating and communicating cross-functionally with respect to assigned Thought Leaders in order to ensure strategic and tactical cohesiveness</li><li>Plan and complete key thought leader engagements and senior executive encounters at local, regional and national conferences, POAs, in field engagements, and other venues in a complaint manner</li><li>Act as a liaison between thought leaders and home office cross-functional teams</li><li>Assisting with on-label key thought leader development, including speakers, with approved decks and materials</li><li>Facilitating certain speaker logistical and scheduling activities and working cross functionally to ensure timely communication</li><li>Providing feedback on GI Franchise and brand-related marketing strategies/materials to commercial leadership</li><li>Providing advisory board participant recommendations, and attending advisory boards where needed</li><li>Facilitate speaker bureau management, speaker recommendations and including contracting when requested</li><li>Follow and be knowledgeable of all laws, regulations and corporate policies</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree, Master’s degree or advanced education/certification a plus.</li><li>Specialty pharmaceutical/biopharmaceutical experience with a minimum of five years of work experience in one or more of the following: key thought leader management, market development, field sales, product marketing, or medical / clinical experience</li><li>including experience in the Gastroenterology and/or Allergy, market or a similar subcutaneous, self-injectable biologic specialty market.</li><li>Launch experience preferred.</li><li>Ability to lead cross-functional teams toward a shared vision of success.</li><li>Ability to present ideas effectively to individuals or groups, targeting presentation to the needs of the audience.</li><li>Proven leadership skills (past leadership experience a plus but not required). Strong organizational skills.</li><li>Strong project management experience, including superior analytical and planning skills. We seek someone with the ability to handle multiple projects simultaneously.</li><li>Ability to complete strategic and tactical plans under tight timelines.</li></ul><p>Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 11:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - MANHATTAN SOUTH, NY]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48917]]></requisitionid>
    <referencenumber><![CDATA[R48917]]></referencenumber>
    <apijobid><![CDATA[r48917]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48917/medical-account-specialist-ii-hematology-manhattan-south-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>MANHATTAN SOUTH, NEW YORK</strong></p><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  ATLANTA SOUTH, GA]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48920]]></requisitionid>
    <referencenumber><![CDATA[R48920]]></referencenumber>
    <apijobid><![CDATA[r48920]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48920/medical-account-specialist-ii-hematology-atlanta-south-ga/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Atlanta South</strong></p><ul><li><strong>Geography: </strong><strong>Augusta, Savannah, Macon, Athens</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Northeast)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48125]]></requisitionid>
    <referencenumber><![CDATA[R48125]]></referencenumber>
    <apijobid><![CDATA[r48125]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48125/field-reimbursement-manager-neurology-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Boston]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Boston, (Metro) MA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Oracle ERP Business Program Lead]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44473]]></requisitionid>
    <referencenumber><![CDATA[R44473]]></referencenumber>
    <apijobid><![CDATA[r44473]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44473/executive-director-oracle-erp-business-program-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Business Program Lead is responsible for the overall management, execution, and delivery of Regeneron’s ERP Modernization Program and reports to the Program Sponsors. This role provides strategic leadership, governance, and oversight across all workstreams, ensuring alignment with business objectives and adherence to guiding principles. The Program Lead drives oversight of program planning, execution, risk management, and stakeholder engagement, while championing business-led change and adoption. Operating in a matrix environment, this role partners with Program Managers, Global Process Owners, IT leadership, System Integrators, and functional teams to deliver measurable business outcomes.</p><div></div><p><strong>A typical day in this role might look like: </strong></p><ul><li>Accountable for the integrated program plan, scope, schedule, dependencies, budget as well as alignment to the business case.</li><li>Lead governance forums (SteerCo, Design Review Board) and enforce guiding principles and key design decision (template-first, clean core).</li><li>Accountable for the execution of program deliverables; monitor progress, risks, and issues; implement mitigation plans.</li><li>Serve as primary liaison to executive sponsors; prepare and present status updates and decision requests.</li><li>Oversee vendor and SI performance; ensure deliverables meet scope, timeline, and quality standards.</li><li>Champion change management and readiness; oversee communications, training, and adoption strategies.</li><li>Ensure compliance with SOX, GxP, and audit requirements in all program activities.</li><li>Define and track success metrics; ensure benefit realization and continuous enhancements post-go-live.</li></ul><div></div><p><strong>This role might be for you if: </strong></p><ul><li>Bachelor’s degree in Business, Finance, Engineering, or related field; MBA preferred.</li><li>15+ years of experience in large-scale ERP or business transformation programs; 10+ years in program leadership.</li><li>Proven ability to manage complex, multi-year global programs with cross-functional teams and vendors.</li><li>Strong knowledge of ERP systems (Oracle Fusion preferred) and end-to-end life science business processes.</li><li>Expertise in program governance, risk management, and change leadership.</li><li>PMP or PgMP certification preferred; Iterative methodology delivery experience a plus.</li><li>Exceptional communication, stakeholder management, and leadership skills.</li><li>Willingness to travel up to 25%.</li></ul><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist - South West England]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45109]]></requisitionid>
    <referencenumber><![CDATA[R45109]]></referencenumber>
    <apijobid><![CDATA[r45109]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45109/sales-specialist-south-west-england/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Sales Specialists at Regeneron are at the forefront of engaging key professionals and customers. We are looking for someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. We are driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p>This role is focused on the maintenance and growth of key accounts within the South West England territory.</p><p><strong>As a Sales Specialist, a typical day may include the following:</strong></p><ul><li>Developing, implementing and supervising territory account plans based on market insights. Ensure continuous and timely updates to the plan in response to changing market dynamics.</li><li>Outstanding account management and operational excellence applying key data sources to strategically develop a territory account plan. And to supervise and progress activity and sales metrics.</li><li>Working closely with alliance partners to develop innovative solutions whilst adhering to SOP’s, regulatory, legal compliance guidelines and ABPI Code</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Ability to work across multiple indications in a specialist therapeutic area.</li><li>Leading with the Science and put the patient front and centre of all we do. Ensure patient access through partnering with key customer stakeholders</li></ul><h3>This role may be for you if:</h3><ul><li>You are confident in demonstrating strong and consistent sales performance that goes above and beyond related to product goals</li><li>Innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>Have a competitive spirit and harness your “grit” to power your approach to sales, collaborating effectively with internal and external partners</li><li>Share a passion for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>Are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree and, at least, 5 years' pharmaceutical sales experience. Previous respiratory or specialist medicine experience desired but not essential. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Commercial Operations Lead]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45302]]></requisitionid>
    <referencenumber><![CDATA[R45302]]></referencenumber>
    <apijobid><![CDATA[r45302]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45302/director-commercial-operations-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Commercial Operations Lead to join our team in Munich, supporting our commercial business across the Germany<strong>.</strong> This is an impactful role focused on translating strategic commercial plans into flawless local execution. You’ll partner closely with sales, marketing, and training teams to drive operational perfection, while helping ensure alignment with regulatory standards and evolving business priorities.</p><p>You'll be joining a dynamic global team, with the opportunity to craft how we deliver commercial support to field-based teams in a fast-paced and highly collaborative environment.</p><h3><strong>A Typical Day:</strong></h3><ul><li><p>Providing strategic and operational leadership to Commercial Operations teams.</p></li><li><p>Translating global commercial strategies into locally relevant, tactical plans.</p></li><li><p>Supervising performance analytics and reporting to advise business decisions.</p></li><li><p>Handling key Sales Operations activities such as field sizing, onboarding, communications, and incentive tracking.</p></li><li><p>Partnering with Commercial Training to coordinate development for field-based staff.</p></li><li><p>Supporting the localization of promotional materials with Marketing and IT.</p></li><li><p>Collaborating with Compliance and Internal Audit teams to maintain adherence to internal policies and external regulations.</p></li><li><p>Building strong relationships with field managers to proactively identify and resolve operational issues.</p></li><li><p>Coordinating contracts and logistics for Speaker Programs and Advisory Boards.</p></li><li><p>Ensuring oncology meetings, sponsorships, and events align with business needs.</p></li></ul><h3><strong>This Role May Be For You:</strong></h3><ul><li><p>You enjoy redefining big-picture strategy into practical local execution.</p></li><li><p>You’re comfortable collaborating across departments and geographies.</p></li><li><p>You bring structure and accountability to multi-stakeholder projects.</p></li><li><p>You thrive in complex environments where priorities shift and evolve.</p></li><li><p>You value accuracy and clarity in communications, especially when supporting external teams.</p></li><li><p>You take pride in mentoring others and encouraging team growth.</p></li><li><p>You’re motivated by solving operational challenges that support patient-impacting work.</p></li></ul><p><strong>To be considered</strong></p><p>You’ll need to bring significant leadership experience in Commercial Operations within the German biopharmaceutical industry. A strong grasp of market dynamics, local laws, and reporting requirements is important. You should be confident navigating analytics, experienced with tools like PowerPoint, Excel, Veeva, and WORD, and able to communicate fluently in English. Prior experience supporting field sales in a pharma setting is desirable, along with a Bachelor’s degree and at least 7 years of industry experience, including 5 years in global commercial operations.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€125,250.00 - €208,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Lab Integration Developer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45570]]></requisitionid>
    <referencenumber><![CDATA[R45570]]></referencenumber>
    <apijobid><![CDATA[r45570]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45570/principal-it-lab-integration-developer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal IT Lab Integration Developer is responsible for designing, developing, validating, and supporting integrations between laboratory systems, analytical instruments, enterprise platforms (LIMS), and data platforms within a regulated pharmaceutical environment. This role combines application development, system integration, data management, and regulatory compliance within a GMP-regulated laboratory environment.</p><p>As a Principal IT Lab Integration Developer, a typical day might include the following:</p><ul><li>Support the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across all Laboratory instruments and middleware.</li><li>Define integration patterns (APIs, event-driven, message queues, file-based where needed).</li><li>Ensure scalability, resilience, and performance of lab integrations.</li><li>Translate QC business processes into orchestrated digital workflows.</li><li>Design and develop integrations between instruments and the Orchestration Layer.</li><li>Build and support API-based, file-based, and message-based integrations (REST, SOAP, SFTP, JSON, XML).</li><li>Provide level 2/3 support for QC Lab Systems.</li><li>Partner with QC Analysts, QA, IT infrastructure and external vendors.</li><li>Develop instrument data capture and automation workflows.</li><li>Configure and support middleware and integration platforms.</li><li>Ensure all integrations comply with GxP, 21 CFR Part 11, and data integrity (ALCOA+) requirements.</li><li>Participate in Computer System Validation (CSV/CSA) activities (IQ/OQ/PQ documentation).</li><li>Perform impact assessments and change control documentation.</li><li>Monitor and troubleshoot integration issues in production environments.</li><li>Collaborate with QC, R&D, Manufacturing, and QA teams.</li><li>Support audits and regulatory inspections.</li></ul><p>This role may be for you if you have:</p><ul><li>Skill in connecting various lab instruments (e.g., liquid handlers, analyzers) to central platforms like LIMS or ELNs to automate data capture and reduce manual transcription.</li><li>Knowledge of RESTful APIs, web services, and middleware tools used to bridge communication between the orchestration engine and disparate lab hardware.</li><li>Proficiency in languages such as Python or VBA for customizing automated workflows and data parsing.</li><li>Ability to understand data formats across different systems, ensure consistent values/naming conventions, and providing the correct data to the authorized locations.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology, Math or related field and </p><ul><li>Senior: 5 years of relevant experience or equivalent combination of education and experience.</li><li>Principal: 8 years of relevant experience or equivalent combination of education and experience.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Analytical and Biological Mass Spectrometry (ABMS)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46464]]></requisitionid>
    <referencenumber><![CDATA[R46464]]></referencenumber>
    <apijobid><![CDATA[r46464]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46464/associate-scientist-analytical-and-biological-mass-spectrometry-abms/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Pharmaceutical's Analytical and Biological Mass Spectrometry Group (ABMS), located in Tarrytown, NY is seeking a highly motivated Associate Scientist. In this role, you will work in an innovative mass spectrometry lab and execute LC-MS methods for characterizing biotherapeutic products to support all stages of drug development, from early-stage candidate selections to late-stage regulatory submissions. You will perform routine technical tasks to support a diverse R&D pipeline.</p><h3><strong>A Typical Day in This Role Looks Like:</strong></h3><p><strong> </strong></p><ul><li><p>Execute established protocols and clearly communicate analytical characterization of biotherapeutics, including monoclonal and bispecific antibodies, Fc-fusion proteins, and other modalities (adeno-associated virus, siRNA, etc.) to support drug development.</p></li><li><p>Execute characterization activities, with an emphasis on intact-mass LC-MS technique to elucidate critical quality attributes such as charge variants, size variants, and post-translational modifications.</p></li><li><p>Provide analytical support for cross-functional teams, including formulation development, upstream/downstream process development, and manufacturing to solve drug development challenges.</p></li><li><p>Independently conduct sample preparation and LC-MS analyses in compliance with SOPs and document experimental procedures and results in electronic laboratory notebook (ELN).</p></li><li><p>Use strong organization and communication to plan and prioritize work, manage and visualize data, and deliver clear, timely updates.</p></li></ul><p><strong> </strong></p><h3><strong>This Role May Be for You If:</strong></h3><p><strong> </strong></p><ul><li><p>You thrive in a fast-paced, collaborative environment and consistently deliver results with efficiency and ownership.</p></li><li><p>You quickly learn new technologies, solve complex problems, and demonstrate strong passion for science and innovation.</p></li><li><p>You are self-motivated and proactive, with the ability to prioritize effectively and drive work forward with minimal supervision.</p></li></ul><p>To be considered for this role, you must have a Bachelor’s or Master’s degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a closely related field. Familiarity with advanced mass spectrometers (Q Exactive Plus, Q Exactive UHMR, Q-TOF, etc.), liquid chromatography, liquid-handling systems and data processing software (Skyline, Protein Metrics, etc.) is desired. Exposure to automated liquid-handling systems (e.g., Bravo, KingFisher) is a plus; willingness to learn is valued.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II - Analytics]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46534]]></requisitionid>
    <referencenumber><![CDATA[R46534]]></referencenumber>
    <apijobid><![CDATA[r46534]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46534/process-development-engineer-ii-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Process Development Analytics group with PMPD (Preclinical Manufacturing Process Development) core mission is to analyze samples received by PMPD subgroups and provide quality and impurity data, and to characterize and optimize assay robustness, precision, and accuracy. Tech development and automation is also prioritized to further optimize assays and resources. The group is seeking a laboratory Scientist or Engineer interested in the analytical characterization of biopharmaceuticals. In this role, you will conduct analytical experiments that support manufacturing process development and research activities in a fast-paced, high-throughput laboratory setting.</p><h3>A Typical Day in the Role of Engineer II Might Look Like:</h3><ul><li>Conduct high throughput biophysical/biochemical analysis of samples generated during manufacturing process development and research projects.</li><li>Conduct experiments to further statistical understanding of assay performance and interpret the results in collaboration with multi-functional groups.</li><li>Deliver written or oral communications as a representative of the PMPD Analytics group at a wide variety of internal projects.</li><li>Collaborate with team members and supervisor to develop novel analytical assays and investigate new analytical technologies.</li><li>Contributes to continuous improvement efforts for increasing efficiency and throughput within the PMPD Analytics group.</li></ul><h3>This Role Might Be For You if You Have:</h3><ul><li>A working knowledge of modern methods of protein research, such as liquid chromatography, capillary electrophoresis, and immunoassays.</li><li>An interest in high throughput analytical methodologies, and their use in biopharmaceutical manufacturing process development.</li><li>An interest in joining a collaborative team with a focus on continuous improvement.</li></ul><p>This role requires a B.Sc., with 5+, or M.Sc. with 3+ years of biochemistry/ chemical/biochemical engineering or a related field. A good understanding of the principles and practice in one or more fields of analytical methodology such as size and charge variant based analysis, Reversed Phase or Mixed Mode chromatography. Knowledge of statistical analyses and statistical design of experiments is a plus.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Market Access Analytics - Neurology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46822]]></requisitionid>
    <referencenumber><![CDATA[R46822]]></referencenumber>
    <apijobid><![CDATA[r46822]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46822/associate-director-market-access-analytics-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Pharmaceuticals is seeking an Associate Director, Market Access Analytics, Neurology to join our organization supporting both launch and in-line brands.</p><p><strong>In this role, a typical day might include:</strong></p><p>This is a hands-on analytics role responsible for transforming complex data assets and advanced analytical tools into evidence-based market access decisions across Payer & Provider/GPO, Contracting, and Pricing. The Associate Director will lead the design, curation, and evaluation of market access data - translating it into strategic analytical solutions that sharpen payer and channel strategy, optimize provider and GPO contracting, and drive portfolio performance.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Lead </em></p><p>1) Shape payer and channel strategy by synthesizing market, payer, and account-level data to inform strategic positioning, coverage decisions, and channel optimization across the portfolio.</p><p>2) Drive payer segmentation and policy analytics across Commercial, Medicare Part B/D, Medicare Advantage, Managed Medicaid, FFS Medicaid, VA/DoD, and Exchange segments - integrating intelligence on Payer willingness and ability to manage drug utilization to surface actionable insight.</p><p><em>Partnership and Collaboration </em></p><p> 3) Build strong, productive relationships with cross-functional stakeholders across Market Access Strategy, Payer Account teams, GPO Account Directors, and Brand colleagues - balancing analytical rigor, timelines, and influence to drive aligned outcomes.</p><p>4) Serve as a strategic thought partner by sharpening business questions, structuring analyses, and translating complex findings into clear, compelling recommendations for senior leadership.</p><p><em>Develop </em></p><p>5) Proactively identify emerging analytics opportunities that address critical market access challenges and unlock growth across the portfolio.</p><p>6) Advance measurement frameworks to evaluate pre- and post-performance across Payer and GPO initiatives, enabling continuous strategic improvement.</p><p>7) Deliver provider and GPO analytics - including account- and segment-level opportunity assessments and pull-through analysis tied to recent payer coverage or brand-level developments.</p><p><em>Execute </em></p><p>8) Serve as the day-to-day analytics partner to Market Access Strategy, HEOR, Pricing, Trade, GPO, and Field Reimbursement teams - scoping questions, executing analyses, and delivering actionable insights on time.</p><p>9) Lead performance reporting tied to strategic imperatives and priority business questions, ensuring clarity, consistency, and alignment across stakeholders.</p><p>10) Triangulate across diverse datasets to surface and deliver actionable insights that uncover opportunities and portfolio-level strategies.</p><p>11) Manage analytics vendor workstreams from scoping through delivery - defining deliverables, maintaining rigor, and driving timely execution.</p><p>12) Apply Regeneron's proprietary Market Access semantic layer across key third-party data sources - including payer medical policy, patient-level claims, and reimbursement data - to ensure analytical consistency and depth.</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum 10 years of pharmaceutical/biotech commercial experience (or 7+ years for MBA/MS), in roles of increasing accountability; prior experience with market-leading brands is desired.</p></li><li><p>BS/BA in STEM related field, e.g., Statistics, Econometrics, Mathematics, Business Analytics; Advanced degree preferred. </p></li><li><p>Proficiency across key market access data sources — MMIT, IQVIA LAAD/DDD/Xponent, Remittance, Model N, Integrichain 852/867, and Patient HUB — with working knowledge of Payer spine bridge files and account hierarchy.</p></li><li><p>Experience coding in Python, R and/or SQL. </p></li><li><p>Experience in data visualization and commercial business intelligence tools required (e.g., Dataiku, Databricks, PowerBI, Tableau, QlikView, Oracle BI, Microstrategy, Cognos, Spotfire or similar tools). </p></li><li><p>Expertise in data visualization and data storytelling of key findings. </p></li><li><p>Advanced proficiency in Excel, and PowerPoint required. </p></li><li><p>Experience in data mining, descriptive analytics, application of statistical methods, analyses and modeling, predictive modeling, opportunity assessment and quantification. </p></li><li><p>Proven track record of managing multiple external vendors and project teams concurrently against stringent deadlines in a fast-paced, timeline-driven atmosphere. </p></li><li><p>Communication and influencing skills with demonstrated ability to succinctly and effectively present compelling reviews of analyses that integrate analytics and patient journey implications/actions to be taken. </p></li><li><p>Strong analytical skills and strategic thinking ability. </p></li><li><p>Concise and impactful written and verbal communication skills with demonstrated experience in influencing and driving decision making. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison - Northeast]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46776]]></requisitionid>
    <referencenumber><![CDATA[R46776]]></referencenumber>
    <apijobid><![CDATA[r46776]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46776/associate-director-thought-leader-liaison-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Maine]]></city>
    <state><![CDATA[Maine]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oncology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Oncology Marketing team reporting into the Senior Director, Scientific Marketing. The role is focused on enhancing and improving interactions with key external US Oncology thought leaders at academic centers and leading community practices for our Oncology Solid Tumor portfolio, particularly in the area of Non-Small Cell Lung Cancer (NSCLC).</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Oncology/Hematology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><h3>The typical day may include the following:</h3><ul><li><p>The Oncology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</p></li><li><p>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</p></li><li><p>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</p></li><li><p>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or during day-to-day business</p></li><li><p>Develop/maintain list of key thought leaders in the assigned geography</p></li><li><p>Assist with thought leader development</p></li><li><p>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</p></li><li><p>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</p></li><li><p>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</p></li><li><p>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</p></li></ul><h3>This role may be for you if:</h3><ul><li><p>You possess a strong science background with deep knowledge of Oncology</p></li><li><p>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</p></li><li><p>You can successfully collaborate with and provide input/feedback to all functions within the project team</p></li><li><p>You can balance/lead multiple projects simultaneously</p></li><li><p>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</p></li></ul><p>To be considered for this opportunity, we expect you to have a bachelor’s degree required; Master’s degree or other advanced education/certification is a plus. Along with specialty pharmaceutical/biopharmaceutical experience, with a minimum of 8 years of work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in hematology/oncology markets strongly preferred. You also have expertise in marketing strategies within the pharmaceutical industry. Ideally, you would have launch experience. You must be able to travel 60%-80% of time </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician, Wednesday-Saturday 2nd shift]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46908]]></requisitionid>
    <referencenumber><![CDATA[R46908]]></referencenumber>
    <apijobid><![CDATA[r46908]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46908/hvac-technician-wednesday-saturday-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>We are currently looking to add a HVAC Technician to our growing team, working a Wednesday-Saturday 14:00pm–12:30am shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment; troubleshooting, preventative maintenance, calibration, and repair work for all mechanical related systems.</div></div><div><div><div><div><div><div><div><div><div><p><strong>Please note training will take place Monday-Friday 7:00am-3:30pm for approximately 6 months. Working hours thereafter will be Wednesday-Saturday 14:00pm-12:30am. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a HVAC Technician, a typical day might include the following:</p><ul><li><p>Maintaining coolers and freezers including Ultra Low temperature Freezer</p></li><li><p>Maintaining Centrifugal and Reciprocating refrigeration chillers</p></li><li><p>Maintaining Chilled water systems including distribution and condenser pumps</p></li><li><p>Maintaining Air Compressors</p></li><li><p>Electrical power systems and stand-by power generation equipment</p></li><li><p>Following current good manufacturing practices (cGMPs) and good business practices (G)</p></li><li><p>Participating in rotational on-call for site emergency work</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOP's, cGMP's, GDP’s and quality standards</p></li><li><p>Becoming fully gown qualified to work within Production areas</p></li><li><p>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</p></li><li><p>May plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Demonstrate basic problem-solving skills</p></li><li><p>Are able to learn and follow routine procedures independently as well as part of a team</p></li><li><p>Are comfortable and have the flexibility to work in a changing environment</p></li><li><p>Can lift, push, and pull at least 50lbs</p></li><li><p>Seek to build and maintain positive working relationships with the business</p></li><li><p>Possess strong written and verbal communication skills</p></li><li><p>Maintain effective time management skills to allow deadlines to be met in a timely manner</p></li><li><p>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</p></li></ul><p>To be considered for the HVAC Technician position you must be willing and able to work a Wednesday-Saturday 14:00pm–12:30am schedule. Applicants ideally should have technical school training with field experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance and the following minimum amounts of experience for each level:</p><ul><li><p>HVAC Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li><li><p>HVAC III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p></li><li><p>HVAC IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</p></li></ul><p>Level will be determined based on qualifications relevant to the role. Will substitute relevant work experience in lieu of education. Electronic, PLC, mechanical and building automation systems experience in Pharmaceutical Industry preferred. EPA certified for refrigeration gases.</p></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff GMP Data Integrity Business Partner]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46942]]></requisitionid>
    <referencenumber><![CDATA[R46942]]></referencenumber>
    <apijobid><![CDATA[r46942]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46942/staff-gmp-data-integrity-business-partner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Staff GMP Data Integrity Business Partner role implements the data governance standards, policies, and procedures into business operations. This position serves as a site resource and subject matter authority on good data governance and integrity (DGI) practices and ensures business groups are aligned to Regeneron Manufacturing's Data Governance Program. </p><p>In this role, a typical day might include the following:</p><ul><li><p>Implementation of standards, policies, and procedures and engage with the allocated business unit on DGI priorities, action plans.</p></li><li><p>Assess business unit’s current policies and processes and be responsible for the achievement of local DGI significant metrics.</p></li><li><p>Conduct regular data audits and assessments to identify DGI issues and work to prepare for DGI auditing and inspections.</p></li><li><p>See opportunities to improve data-related processes, systems and tools within allocated business area that are aligned with the business’s evolving needs and industry standard processes.</p></li><li><p>Work in partnership with other DGI Business Partners, Technical Experts & ECM Experts to deliver on the plan and feedback themes to allow CI & evolution of the DGI approach.</p></li><li><p>Feedback themes to Data Governance Leadership team to allow CI & evolution of the data governance approach.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Stay updated on latest industry trends, regulatory changes and enforcement actions within the biopharma industry and assessing the impact of these within Regeneron.</p></li><li><p>Can foster a culture of quality & DGI within the organization.</p></li><li><p>Encourage CI by actively seeking feedback and supporting initiatives designed to enhance data quality and governance.</p></li><li><p>Have knowledge of applicable federal, state, and local regulations (e.g. GDPR), rules, policies, and procedures such as FDA Guidance on Data Integrity, EMA Data Integrity Guide, and WHO Guide to Data Integrity.</p></li><li><p>Have expert knowledge of cGMP & GDP.</p></li><li><p>Can translate complex regulatory and technical requirements into clear guidance for cross-functional teams.</p></li><li><p>Possess strong stakeholder management and influencing skills.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree and the following amount of relevant experience for each level:</p><ul><li><p>Principal: 8+ years</p></li><li><p>Staff: 10+ years</p></li><li><p>Senior Staff: 12+ years</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Automation]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47040]]></requisitionid>
    <referencenumber><![CDATA[R47040]]></referencenumber>
    <apijobid><![CDATA[r47040]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47040/manager-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Manager Automation to supervise a team responsible for cGMP automation quality systems, software change control, and automation related corrective actions. The Manager Automation develops procedures and methods for executing automation projects and support activities, while coaching and developing Automation professionals. This group ensures manufacturing systems are operating as expected and provides time-sensitive fixes to keep manufacturing running. This is a dynamic role that focuses on providing impeccable customer service, while developing direct reports to ensure their continued success and growth.</p><p>As a Manager Automation, a typical day might include the following:</p><ul><li>Managing the performance, training, development, and results of the team</li><li>Providing technical and automation support to manufacturing</li><li>Overseeing activities related to the configuration and support of manufacturing process equipment and the maintenance of cGMP software administration program</li><li>Managing periodic evaluation reports for automated systems used in commercial manufacturing</li><li>Overseeing the investigation of manufacturing deviations and anomalies related to automation and software</li><li>Managing projects related to corrective action or equipment performance improvement.</li><li>Implementing modification/change control procedures and protocols.</li><li>Supporting Validation with initial design review, software testing and protocol review</li></ul><p>This job might be for you if you:</p><ul><li><p>Have the demonstrated ability to mentor and empower a team of automation professionals to deliver results under demanding timelines and situations</p></li><li>Can organize and present technical overviews to engineering staff, multi-functional departments, and management independently while influencing desired courses of action</li><li>Possess a unique blend of business and technical savvy</li><li>Are able to communicate across all levels and capable of effectively meeting and exceeding customer expectations</li><li>Have the skills to balance changing priorities by making timely decisions and delegating tasks</li><li>Possess an understanding of bioprocessing and testing software, cGMP software quality system principles, and data integrity regulations</li><li>Consistently maintain professionalism in communication, maintaining composure in high-pressure situations</li><li>Strive for compliance with regulatory, corporate, and site-specific policies and procedures</li></ul><p>To be considered for this position, you should have a BS/BA in engineering, software programming or related field and the following experience with automated equipment used in pharmaceutical or biopharmaceutical industry:</p><ul><li>Associate Manager: 6+ years including 1+ year of leadership/supervisory experience</li><li>Manager: 7+ years including 2+ years of leadership/supervisory experience</li><li>Senior Manager: 8+ years including 3+ years of leadership/supervisory experience</li><li>1+ year of direct experience in design, installation, maintenance, and or trouble shooting of automated control systems</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$103,300.00 - $231,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Technician, Wednesday-Saturday 2nd shift]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47301]]></requisitionid>
    <referencenumber><![CDATA[R47301]]></referencenumber>
    <apijobid><![CDATA[r47301]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47301/process-technician-wednesday-saturday-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Process Technician position with a Wednesday-Saturday 2:00pm-12:30am schedule. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Process Technicians play a vital role in supporting our manufacturing operations. They provide operational, maintenance, and troubleshooting support for manufacturing process area maintenance through strict compliance with Standard Operating Procedures (SOPs) and cGMPs.</p><p><strong>Please note training will take place Monday-Friday 1st shift 6:00am-2:30pm for several weeks. Working hours thereafter will be Wednesday-Saturday 2:00pm-12:30am.</strong></p><p>As a Process Technician, a typical day might include the following:</p><ul><li><p>Performing daily operations, maintenance and repairs on utility systems, manufacturing equipment and building systems in a cGMP environment</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment</p></li><li><p>Identifying any off-nominal conditions with mechanical equipment and mechanical troubleshooting of manufacturing/utility equipment in a clean room environment</p></li><li><p>Performing daily Work Orders (WOs) and PMs and efficiently coordinating the workflow and documentation of PMs and WOs</p></li><li><p>Troubleshooting electrical equipment during off-nominal conditions; locating the source of trouble and arranging for/performing all necessary repairs</p></li><li><p>Coordinating with each impacted department and within Facilities Management when planned and unplanned work events occur</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Can interpret P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs</p></li><li><p>Have prior experience in equipment maintenance or a related position requiring mechanical skills and abilities</p></li><li><p>Are safety-minded while looking for opportunities to continuously improve</p></li><li><p>Strive for compliance with regulatory, corporate, and site-specific policies and procedures</p></li><li><p>Can fully gown as required when entering and working on production floor</p></li><li><p>Are able to support a rotational on-call schedule</p></li></ul><p>To be considered for this position you must be willing and able to work Wednesday-Saturday 2:00pm-12:30am. Applicants should have an AAS degree, preferably in an Engineering or Construction Technologies related field, and the following minimum amounts of proven experience for each level:</p><ul><li><p>Process Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li></ul><p>#REGENTOSK</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Assistant - Law Department]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47226]]></requisitionid>
    <referencenumber><![CDATA[R47226]]></referencenumber>
    <apijobid><![CDATA[r47226]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47226/executive-assistant-law-department/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we pair science with technology to accelerate the discovery and delivery of life‑changing medicines. We are searching for an Executive Assistant to support Law Department executives who oversee and interact with multiple functional teams, including Privacy, Trade Controls, and Industrial Operations Law — as well as the attorneys and professionals within those teams. This role requires advanced understanding of the Law Department and its business clients, including key relationships. We're looking for someone who brings strategic thinking, technological fluency, and genuine curiosity to the work of a fast-moving, high-impact legal team. The Executive Assistant will exercise considerable judgment and initiative, with the ability to influence stakeholders and understand key relationships.</p><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>Managing complex calendars, expenses, and time commitments for executives.</p></li><li><p>Anticipating the needs of leaders and teams before they arise; resolving scheduling conflicts with minimal direction.</p></li><li><p>Triaging incoming requests and inquiries, escalating time-sensitive or significant matters with good judgment and discretion.</p></li><li><p>Identifying, developing, and implementing process improvements, bringing new tools or approaches to the team proactively, while maintaining highly organized and efficient administrative workflows and independently executing solutions.</p></li><li><p>Leveraging AI tools (such as Microsoft CoPilot) to draft communications, summarize information, and streamline administrative workflows.</p></li><li><p>Planning, managing and executing internal and external meetings end‑to‑end, including team meetings, large offsites, live trainings, and cross-functional gatherings, with attention to gathering agendas, logistics, coordination with stakeholders, catering decisions, materials and follow up.</p></li><li><p>Building polished PowerPoint presentations by synthesizing inputs from multiple contributors into organized, executive-ready decks.</p></li><li><p>Submitting requisitions, tracking of deadlines, monitoring purchase orders and renewals.</p></li><li><p>Collaborating cross‑functionally and serving as a trusted partner to peers.</p></li><li><p>Communicating effectively across all levels while maintaining confidentiality.</p></li><li><p>Demonstrating organizational knowledge and understanding leader priorities, including support for increasingly complex responsibilities.</p></li><li><p>Handling travel arrangements and expense reports for executives including managing complex international travel (typically VP+), visas and expense reporting.</p></li><li><p>Maintaining departmental SharePoint, Teams and Intranet sites, keeping them current, organized and useful as working resources.</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Are highly collaborative and adept at coordinating across teams to develop and implement solutions and operate under minimal guidance.</p></li><li><p>Exhibit discretion, independence, and sound judgment.</p></li><li><p>Adapt well to change, ambiguity, and shifting priorities, and can embrace AI and modern productivity tools as a part of how you work.</p></li><li><p>Work comfortably with senior leaders and understand how they think and what they expect.</p></li><li><p>Possess advanced knowledge or ability to readily learn company and Law Department policies, practices, and resources and act as a point person for supported leaders and departments.</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Associate or bachelor’s degree preferred.</p></li><li><p>8 or more years of administrative experience required, with at least 4 years supporting senior leaders in a business or legal environment.</p></li><li><p>Advanced proficiency in Microsoft 365 (Outlook, PowerPoint, Excel, Word, Teams), SharePoint, Concur, and collaboration platforms; ability to troubleshoot and train others.</p></li><li><p>Proven ability to manage complex calendars, orchestrate senior‑level meetings and events, and coordinate domestic/international travel with precision.</p></li><li><p>Exceptional organization, prioritization, and follow‑through; positive, can‑do attitude and respect for colleagues at all levels.</p></li><li><p>Flexibility to support after‑hours needs tied to executive travel, global time zones, and critical events.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$38.61 - $63.03]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Cloud DevSecOps Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47382]]></requisitionid>
    <referencenumber><![CDATA[R47382]]></referencenumber>
    <apijobid><![CDATA[r47382]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47382/principal-cloud-devsecops-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Regeneron Genetics Center (RGC) IT team is looking for a passionate Principal Cloud DevSecOps Engineer with strong technical ability, communication, and collaboration skills. As the Principal Cloud DevSecOps Engineer, you will be responsible for the design and implementation of cloud infrastructure, automation, security controls, and compliance processes on AWS, supporting data, HPC, AI, and microservice platforms used by research scientists and bioinformaticians. You will work hands-on to build and implement cloud DevSecOps solutions, embed security into system design, and provide technical support and guidance to end users and internal teams. You will also provide technical mentorship for Lead and Senior DevSecOps engineers and coordinate with InfoSec, Privacy, and internal IT teams to ensure security, scalability, and reliability of the RGC cloud platform.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Design and implement infrastructure-as-code, automation scripts, and CI/CD pipelines supporting data, HPC, AI, and microservice platforms on AWS</p></li><li><p>Embed security controls into system design and implementation — including IAM policies, network segmentation, secrets management, and compliance validation pipelines</p></li><li><p>Design and implement tools to automate operational processes across RGC’s cloud and systems engineering platforms</p></li><li><p>Support all audit related activities including providing evidence and remediation of findings for RGC’s cloud platform</p></li><li><p>Develop and implement continuous delivery systems and CI/CD methodologies for RGC’s systems engineering platforms using both AWS services and GitHub Actions, ARC self-hosted runners on EKS, and SAST/DAST integration.</p></li><li><p>Recommend and deploy monitoring, metrics, and logging systems on RGC’s cloud engineering platforms</p></li><li><p>Identify and implement opportunities to build systems that are highly available, scalable, and self-healing</p></li><li><p>Develop SOPs and configure cloud services to support compliance validation</p></li><li><p>Provide technical support, training, and documentation to end users and research teams using RGC’s data, HPC, AI, and microservice platforms</p></li><li><p>Serve as a technical point of contact for user-facing issues related to cloud platform, DevOps pipelines, security services, and solving problems in collaboration with internal IT teams</p></li><li><p>Stay on top of the latest advances in cloud platforms and related security & compliance controls</p></li><li><p>Provide technical guidance and mentorship for Lead and Senior DevSecOps engineers</p></li><li><p>Interact with InfoSec and Privacy teams to define and iterate on security requirements, and implement them across the platform</p></li></ul><p><strong>This job might be for you if:</strong></p><ul><li><p>You have an eye for detail and pride yourself on the quality of your work. Operational excellence and secure-by-design thinking matter more than just finishing the tasks.</p></li><li><p>You thrive in a fast-paced environment working across data, HPC, AI, and microservice platforms, and enjoy being a technical resource for the teams that depend on them.</p></li><li><p>You work on current problems while thinking of future solutions, and take satisfaction in both building the right thing and supporting the people who use it.</p></li></ul><p><strong>To be considered for the Principal Cloud DevSecOps Engineer, you must have: </strong> </p><ul><li><p>Bachelor's Degree in Computer Science, or related field.</p></li><li><p>8+ years of in-depth AWS services experience and relevant security certifications.</p></li><li><p>Hands-on experience designing and implementing cloud infrastructure automation, CI/CD pipelines, infrastructure-as-code, and security controls. </p></li><li><p>Solid understanding of cloud security posture including IAM, network segmentation, secrets management, compliance validation, and security-by-design principles. </p></li><li><p>Experience supporting data, HPC, AI, or microservice platforms in a technical or user-facing capacity. Knowledge of core AWS services EC2, EBS, S3, ELB, RDS, EKS, and IAM. Tangible experience with Linux administration and automation of security controls and compliance validation. </p></li><li><p>Experience with monitoring tools like Splunk, Grafana, Prometheus. AWS and other related certifications are a plus.</p></li></ul><p><strong>Level commensurate on experience and qualifications.</strong> Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Public Policy - Science and FDA Policy]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47412]]></requisitionid>
    <referencenumber><![CDATA[R47412]]></referencenumber>
    <apijobid><![CDATA[r47412]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47412/director-public-policy-science-and-fda-policy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Washington]]></city>
    <state><![CDATA[District of Columbia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director of Policy & Government Affairs – Science and FDA Policy will lead Regeneron’s science and FDA policy portfolio, developing, shaping and influencing government and multinational organization policy related to the scientific research and development of biopharmaceutical medicine and cell and gene therapy across the product lifecycle. Relevant issues include but are not limited to product approval standards and pathways, scientific ethics and integrity, clinical trial activity, evidence development, manufacturing and CMC criteria, and biosimilars. Although US-focused, the position may also support the ex-US Public Policy & Government Affairs lead on key science and biotechnology medicine policy around the world as needed.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage with internal subject matter experts and leaders to understand Regeneron’s business and corporate interests, recognize policy risks and opportunities, and determine short and long-term policy objectives in order to navigate and balance competing interests and objectives</p></li><li><p>Communicate Regeneron's policy positions and initiatives to internal and external audiences through various channels;</p></li><li><p>In collaboration with relevant internal team members, organize and participate in events, conferences, and forums to promote Regeneron's policy agenda;</p></li><li><p>As needed, represent the Regeneron PP&GA team at key stakeholder meetings and engage with key external partners at meetings to identify opportunities for collaboration to advance common policy priorities.</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Engage with industry associations, advocacy groups, and other external stakeholders in collaboration with the alliance development lead to build coalitions and advance shared policy objectives</p></li><li><p>Develop and advance strategic public policy positions and initiatives that align with and advance Regeneron's business objectives;</p></li><li><p>Monitor and analyze legislative and regulatory developments at the federal, state, local, and international levels to determine the potential impact on and importance to Regeneron;</p></li><li><p>Develop and execute strategic advocacy plans, including proactively crafting and vetting legislative and regulatory proposals to advance company priorities and mitigate risks;</p></li><li><p>Provide expert advice and guidance on policy and regulatory matters to internal stakeholders</p></li></ul><p><strong>To be considered for this position, you must have:</strong></p><ul><li><p>Bachelor’s degree is required; advanced degree/s in Public Policy, Political Science, Law, or related field and science background strongly preferred.</p></li><li><p>Minimum of 12 years of relevant experience in science and regulatory policy, preferably with substantial experience at the US FDA</p></li><li><p>Proven record of successfully crafting and influencing public policy and navigating complex and highly technical issues</p></li><li><p>Strong understanding of the biopharmaceutical industry, including regulatory and legislative processes</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, MASH/Metabolism (Regeneron Genetics Medicine)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47478]]></requisitionid>
    <referencenumber><![CDATA[R47478]]></referencenumber>
    <apijobid><![CDATA[r47478]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47478/medical-director-clinical-development-mashmetabolism-regeneron-genetics-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Medical Director, Clinical Sciences, MASH/Metabolism works with their supervisor and other members of the cross-functional study team to author protocols and facilitate execution of study activities and data summarization. The Medical Director leads collaborations with discovery scientists and translational colleagues to understand current and emerging genetic targets across a variety of therapeutic areas and disease states including but not limited to MASH and metabolism, rare diseases, and others; provides input on potential disease areas/indications; and crafts clinical experiments that corroborate or inform the biology for decision-making purposes and enable clinical development programs within the Regeneron Genetics Medicine Clinical Development Unit. This Medical Director will report into the VP Therapeutic Area Lead.</p><p><strong>As a Medical Director, a typical day might include the following:</strong></p><p>• Leads the cross-functional study team to craft novel clinical development strategy for genetic medicines, including First in Human (FIH), Phase 2, and Phase 3 clinical trials</p><p>• Responsible for the relevance and accuracy of medical science underpinning of clinical study based on detailed scientific review and consultation</p><p>• Authors, reviews, and finalizes the medical and scientific portions of study strategies and clinical study protocols and amendments</p><p>• Authors, reviews, and edits documents related to trials, such as monitoring plans, SAPs, amendments, IRB/IEC submissions and regulatory submissions</p><p>• Accountable for timely clinical trial execution, reviewing adverse events, monitoring patient health, and quality of results</p><p>• Analyzes the benefits and risk aspects of an assigned therapeutic candidate</p><p>• Ensures clinical team compliance with FDA, EMEA, ICH and GCP guidelines as well as SOPs regarding safety</p><p>• Authors clinical sections of communications/documentation for regulatory agencies and may participate in meetings as needed</p><p>• Conducts detailed literature reviews and analysis of development opportunities from mechanistic, pharmacological and clinical development perspectives</p><p><strong>This role may be for you if: </strong></p><p>• You want to make an impact delivering genetic medicines for patients with serious diseases</p><p>• You have specialist postgraduate clinical training and practice, and/or scientific research training and with a track record of success</p><p>• You demonstrate critical, science-to-medicine translational thinking skills and sound decision making</p><p>• You have the ability to work productively in a fast-paced collaborative working environment</p><p>To be considered for this role, you must have an M.D. Degree (M.D./Ph.D. Degree or prior research experience preferred). Board Certification/Eligibility in a relevant therapeutic area (Hepatology, Gastroenterology, Endocrinology, or Nephrology preferred. A minimum of 2-3 years of clinical practice or industry experience is preferred. This role requires a minimum of four days on-site weekly in Tarrytown, NY.</p><p>#MDJOBS, #MDJOBSCD</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Product Management - Delivery & Operations Product Lead - Medical Affairs Domain]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47701]]></requisitionid>
    <referencenumber><![CDATA[R47701]]></referencenumber>
    <apijobid><![CDATA[r47701]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47701/senior-manager-product-management-delivery-operations-product-lead-medical-affairs-domain/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Global Development IT (GDIT) is seeking an experienced and motivated Senior Manager with deep technical and functional expertise in Veeva CRM, Veeva Medical Vault, Medical Affairs systems and AI. This role is responsible for end-to-end implementation, support and continuous improvement of technology products and data within the Medical Affairs domain. This role will also work closely with their business counterparts, Business Process Owners, Subject Matter Experts, Training, Process and Procedures and Corporate Enterprise IT. </p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Lead detailed business and technical requirements' analysis for Veeva Medical CRM, Veeva Medical Vault and Medical Affairs systems, translating Medical processes into scalable, complaint system designs.</p></li><li><p>Configure and optimize Veeva CRM components, including but not limited to: Medical Inquiry, Call Reporting, Key Medical Insights, Events, Approved email, Consent Management, Page layout, Profiles, Permission sets and Sharing Rule.</p></li><li><p>Design and configure Veeva Vault Medical Vault objects, relationships, lifecycles, workflows, user roles, document types, and metadata to support scientific content management and medical review processes.</p></li><li><p>Define and support AI-driven Medical Affairs workflows including automated medical inquiry categorization, sentiment and topic analysis of MSL interactions, and proactive identification of emerging medical insights.</p></li><li><p>Collaborate with Global Development and IT team members to extract insights from CRM and other data sources using AI and digital tools.</p></li><li><p>Define and maintain Veeva data models and data quality standards to enable AI/ML readiness, ensuring alignment across CRM and Vault platforms, including reference data, picklists, field dependencies, and master data governance.</p></li><li><p>Partner with integration teams to design and validate integrations using Veeva APIs, Vault APIs, middleware platforms, and standard connectors with systems such as MDM, ERP, data lakes, and analytics tools.</p></li><li><p>Collaborate with global stakeholders in Medical Affairs, GDIT functions, Corporate IT and other relevant functions to support multi-country deployments, localization, and regulatory requirements across FDA, EMA, and other regional compliance frameworks.</p></li></ul><p><strong> This Job might Be for you if you have:</strong></p><ul><li><p>Knowledge of Medical Affairs business processes, systems and key trends in the Industry.</p></li><li><p>Experience on Jira, Agile product management, backlog management, Scrum and Kanban boards.</p></li><li><p>Technical Experience and ability to Partner with data science and integration teams to build, validate, and operationalize AI solutions using APIs, middleware, and AI/ML platforms (e.g., NLP, large language models, predictive analytics).</p></li><li><p>Proven track record of managing competing priorities across a multitude of stakeholders, and to lead teams to deliver value-oriented, prioritized solutions. </p></li><li><p>Excellent interpersonal skills, and the ability to indirectly influence key partners and stakeholders with clear, concise, and well-formed message tailored to the audience </p></li><li><p>Experience managing technology capability identification, selection, implementation, and operations </p></li><li><p>Excellent problem-solving skills to address day-to-day challenges associated with business solutions </p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>A BS/BA Degree with 8+ years of relevant experience, or a MS Degree with 6+ years relevant experience</p></li></ul><ul><li><p>Experience partnering with technology teams and driving value in the Medical Affairs space with specific technologies like Veeva Medical CRM, Veeva Medical Vault, Salesforce</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Quantitative Pharmacology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47830]]></requisitionid>
    <referencenumber><![CDATA[R47830]]></referencenumber>
    <apijobid><![CDATA[r47830]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47830/associate-director-quantitative-pharmacology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated Associate Director to join the Quantitative Pharmacology (QP) group. The Associate Director will lead model-informed drug development strategies supporting one or more therapeutic areas across modalities including antibodies, siRNA, and gene therapies. This role combines scientific depth with cross-functional leadership to inform dose selection, trial design, and regulatory strategy from early development through submission.</p><p><strong>A day in the life of an Associate Director may look like:</strong></p><ul><li><p>Driving model-informed development (MIDD) and pharmacometrics strategies in partnership with Clinical Pharmacology, Biostatistics, Clinical and Translational teams to support regulatory and clinical decision-making.</p></li><li><p>Leading the QP evaluation of one or more assets, accountable for timely delivery of population PK/PD, exposure–response, and translational modeling analyses.</p></li><li><p>Representing QP at program and governance meetings, communicating quantitative insights clearly to non-modeling audiences.</p></li><li><p>Contributing to regulatory interactions and authoring key components of regulatory documents related to QP (e.g., IB, briefing books, etc.).</p></li><li><p>Mentoring and developing junior scientists and fostering a culture of scientific rigor and collaboration.</p></li><li><p>Identifying and implementing process improvements, new modeling approaches, and innovative quantitative tools to enhance efficiency and impact.</p></li><li><p>Ensuring analyses and documentation are of the highest scientific quality and regulatory compliance.</p></li></ul><p><strong>This may be the right role for you if you:</strong></p><ul><li><p>Want to make a visible impact on the organization by driving data-driven decisions that shape clinical and regulatory strategy.</p></li><li><p>Thrive in multi-disciplinary environments, bridging discovery, clinical, and commercial teams.</p></li><li><p>Communicate complex modeling concepts clearly and persuasively to diverse stakeholders.</p></li><li><p>Have strong collaboration and leadership skills, influencing cross-functional teams without formal authority.</p></li><li><p>Can independently design, execute, and oversee multiple modeling workstreams simultaneously.</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 6+ years of post-doctoral or industry experience; or MS with 9+ years of relevant experience.</p></li><li><p>Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R.</p></li><li><p>Proven track record of delivering analyses supporting regulatory submissions and engaging directly with agencies (e.g., FDA, EMA, PMDA).</p></li><li><p>Hands-on experience with a broad range of quantitative and computational tools and a strong publication record.</p></li><li><p>Exceptional communication and interpersonal skills, with the ability to influence and partner effectively across technical and non-technical teams.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist, Obesity, Muscle & Metabolism]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47888]]></requisitionid>
    <referencenumber><![CDATA[R47888]]></referencenumber>
    <apijobid><![CDATA[r47888]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47888/senior-scientist-obesity-muscle-metabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated and innovative Sr. Scientist to join Obesity, Metabolism and Muscle Diseases Group. The candidate will support identification and validation of novel drug targets for metabolic disorders. The successful candidate will be results-oriented individual with excellent problem-solving abilities who is flexible, team-oriented, creative and able to excel in a multi-project, fast-paced environment.</p><p><strong>As a Sr Scientist, a typical day may include: </strong></p><ul><li><p>Identify and implement novel areas, technologies and approaches for validating targets and target modalities to advance metabolic disease drug discovery</p></li><li><p>Design and conduct in vitro assays</p></li><li><p>Design and perform in vivo studies in animal models to support target validation and mechanistic understanding</p></li><li><p>Analyze data and make scientifically sound conclusions</p></li><li><p>Provide timely updates on scientific progress and communicate efficiently within the Obesity, Metabolism and Muscle Diseases Group and across different teams and functions</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You enjoy working in a fast-paced environment</p></li><li><p>You are detail oriented and well-organized</p></li><li><p>You are a fast learner and have desire to expand your areas of expertise</p></li><li><p>You can work well both independently and in a team</p></li><li><p>You are able to communicate effectively </p></li></ul><p><strong>To be considered for this role, you must have: </strong></p><ul><li><p>PhD with a minimum of three years of post-doctoral research experience</p></li><li><p>Broad expertise in biochemistry, molecular biology, in vitro assay development and in vivo techniques</p></li><li><p>Ability to independently design and perform complex in vivo studies, interpret data and summaries results</p></li><li><p>Expertise in at least one of metabolism research area, e.g diabetes, endocrinology, obesity, lipid and energy metabolism</p></li><li><p>Strong understanding of human and mouse genetics is preferred</p></li><li><p>Documented strong scientific record</p></li><li><p>Excellent communication and presentation skills</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Process Specialist - Manufacturing]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47994]]></requisitionid>
    <referencenumber><![CDATA[R47994]]></referencenumber>
    <apijobid><![CDATA[r47994]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47994/staff-process-specialist-manufacturing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Staff Process Specialist - Manufacturing position provides on the floor direction on the manufacturing process. Key member in the implementation of the manufacturing production program. </p><p>As a Staff Process Specialist - Manufacturing, a typical day might include the following:</p><ul><li>Provides technical input to resolve process problems both on and off the production suites </li><li>Coaches manufacturing personnel to increase technical knowledge of critical process steps on the floor. </li><li>Supports Manufacturing personnel on implementing improvements to the process or work systems in the suites. </li><li>Supports CAPA implementation on process related improvements. </li><li>Supports onsite educational programs to enhance technical competence of manufacturing personnel. </li><li>Supports all aspects of the manufacturing process according to approved protocols, regulation, and schedule </li><li>Supports the technology transfer of the manufacturing process </li><li>Liaises with the process science/technology transfer teams in relation to the transfer and startup of the manufacturing process. </li><li>Prepares reports by collecting, analyzing, and summarizing information and trends. Operations member reviewing trends with the Process Science Group. Present out on process trends. </li><li>Leads investigations into process variances according to site procedures. </li><li>Ensures that policies and procedures are effectively administered and that they comply with regulatory requirements. </li><li>Communicates well with supervisors on major problems regarding the process, schedules and materials. </li><li>Guides and oversees validation activities involving manufacturing equipment and processes. </li><li>Interfaces with other departments, such as Facilities, Process Development, Engineering, Process Analytical Sciences, Regulatory, Quality Assurance and Quality Control. </li><li>Works to the highest safety standards. Supports safety improvements which require technical/engineering input. </li><li>Tracks and trends relevant technical and business process metrics to ensure operations are performing effectively and efficiently. </li><li>Performs cGMP audits of production area. </li><li>Represents manufacturing during regulatory and client audits. Will also respond to some of the findings from these audits. </li><li>Writes, reviews, and/or approves Standard Operating Procedures, specifications, regulatory filing, or other controlled documents as needed. </li><li>Leads and implements continuous improvement initiatives. </li><li>Will act as system owner for defined manufacturing equipment and will be involved in the scheduling of all non-routine activities for that equipment. </li></ul><p>This role may be for you if:</p><ul><li>Knowledge of cGMP manufacturing environment and familiarity with formulation, aseptic filling, visual inspection (manual and automated), assembly, labeling, and/or packaging of liquid and lyophilized injectable products. </li><li>Demonstrated strong interpersonal, cross-cultural, communication, negotiation, and problem-solving skills. </li><li>Exhibits confidence, has a high emotional IQ, and demonstrated ingenuity, creativity and resourcefulness. </li><li>Ability to gain understanding from provided instructions and work towards established goals individually or as part of a team. </li><li>Ability to understand and listen to team members and stakeholders’ needs while supporting a positive team environment </li><li>Technology transfer and equipment / process validation experience of aseptic, parenteral fill/finish operations preferred. </li><li>Previous experience providing technical support preferred. </li><li>Experience with lyophilization is a plus. </li><li>Experience with operating and qualifying equipment with high levels of automation is a plus. </li></ul><p>In order to be considered for this position, you must hold a BS in Life Sciences or related field and</p><ul><li>Principal Process Specialist - 8 years of relevant cGMP manufacturing/engineering/scientific experience in a relevant industry or equivalent combination of education and experience.</li><li>Staff Process Specialist - 10 years of relevant cGMP manufacturing/engineering/scientific experience in a relevant industry.</li><li>Senior Staff Process Specialist - 12 years of relevant cGMP manufacturing/engineering/scientific experience in a relevant industry.</li><li>May consider experience in lieu of education OR equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - New York Metro]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48155]]></requisitionid>
    <referencenumber><![CDATA[R48155]]></referencenumber>
    <apijobid><![CDATA[r48155]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48155/neurology-account-director-new-york-metro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: New York Metro, New Jersey, Pennsylvania, Maryland, Washington DC</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Project Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45461]]></requisitionid>
    <referencenumber><![CDATA[R45461]]></referencenumber>
    <apijobid><![CDATA[r45461]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45461/associate-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking an Associate Project Engineer to join our <strong>Project Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Raheen, Limerick</li></ul><p><strong>What you’ll do:</strong></p><ul><li>Designing and specifying current Good Manufacturing Practice process equipment, piping, and/or controls</li><li>Managing small projects related to process equipment and manufacturing</li><li>Assisting in the design review, site acceptance and installation of equipment</li><li>Preparing process and instrument drawings and other related drawings</li><li>Developing Process Flow Diagrams for manufacturing processes</li><li>Supporting validation department by preparation of design documents and assists in protocol execution</li><li>Assisting in investigations of process equipment and control system anomalies</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations for and executing modification change control documentation</li><li>Supervising mechanical, electrical, and automation contractors</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>Are a self-starter with high initiative and possess a data-driven approach to problem-solving</li><li>Demonstrate strong interpersonal skills</li><li>Ability to prioritize, re-prioritize as needed and adapt to change</li><li>Strong analytical and organizational skills</li><li>Adaptability and flexibility to working in different environments, teams etc</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>To be considered for this position you should have a BEng or higher in Chemical, Process or Mechanical Engineering</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €59,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - JACKSON, MS]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48056]]></requisitionid>
    <referencenumber><![CDATA[R48056]]></referencenumber>
    <apijobid><![CDATA[r48056]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48056/medical-account-specialist-ii-neurology-jackson-ms/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Jackson]]></city>
    <state><![CDATA[Mississippi]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Jackson (Metro), MS</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - HOUSTON (NORTH), TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48060]]></requisitionid>
    <referencenumber><![CDATA[R48060]]></referencenumber>
    <apijobid><![CDATA[r48060]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48060/medical-account-specialist-ii-neurology-houston-north-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Houston]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Houston North (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - AUSTIN, TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48062]]></requisitionid>
    <referencenumber><![CDATA[R48062]]></referencenumber>
    <apijobid><![CDATA[r48062]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48062/medical-account-specialist-ii-neurology-austin-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Austin]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Austin (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div></div><div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48142]]></requisitionid>
    <referencenumber><![CDATA[R48142]]></referencenumber>
    <apijobid><![CDATA[r48142]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48142/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Warren, NJ or Cambridge, MA</p></li><li><p>Hybrid: 4 days per week onsite</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - CHICAGO North IL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48050]]></requisitionid>
    <referencenumber><![CDATA[R48050]]></referencenumber>
    <apijobid><![CDATA[r48050]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48050/medical-account-specialist-ii-neurology-chicago-north-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Chicago North (Metro), Illinois </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -LOS ANGELES, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48079]]></requisitionid>
    <referencenumber><![CDATA[R48079]]></referencenumber>
    <apijobid><![CDATA[r48079]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48079/medical-account-specialist-ii-neurology-los-angeles-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Los Angeles]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Los Angeles (Metro), CA</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 18:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48464]]></requisitionid>
    <referencenumber><![CDATA[R48464]]></referencenumber>
    <apijobid><![CDATA[r48464]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48464/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Uxbridge, UK</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Patient Advocacy]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48324]]></requisitionid>
    <referencenumber><![CDATA[R48324]]></referencenumber>
    <apijobid><![CDATA[r48324]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48324/associate-director-global-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[[Unknown]]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Global Patient Advocacy, Hematology-Oncology to cover International and US markets. In this role, you will lead the development and execution of patient advocacy strategies, building meaningful relationships with advocacy groups and professional societies to support patient needs and business objectives, while collaborating with cross-functional leaders (Medical Affairs, Market Access, Marketing, and Policy teams). This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><p>UK, Germany, Italy or Spain (Hybrid model)</p><p>Travel: 40%+</p><h3>Discover your role:</h3><ul><li><p>Lead advocacy and engagement strategy for Hematology-Oncology in Europe</p></li><li><p>Partner with senior cross-functional leaders to build advocacy strategies</p></li><li><p>Build and manage relationships with patient advocacy groups and professional societies</p></li><li><p>Oversee patient engagement initiatives, meetings, and communications</p></li><li><p>Develop frameworks to embed the patient perspective across organizational processes</p></li><li><p>Track and report outcomes of advocacy initiatives to senior leadership</p></li><li><p>You foster collaboration and consensus among diverse stakeholders</p></li><li><p>You drive a patient-centric culture and influence strategic decisions</p></li></ul><h3>This role requires:</h3><ul><li><p>Undergraduate degree required</p></li><li><p>10+ years of industry or relevant professional experience</p></li><li><p>5+ years of patient advocacy, stakeholder engagement, and issues management</p></li><li><p>European, international, or global advocacy experience and understanding of relevant regulations (e.g., EMA, HTA)</p></li><li><p>Proven leadership in developing and executing advocacy strategies</p></li><li><p>Country-level advocacy work experience preferred</p></li><li><p>Multilingual capabilities strongly preferred</p></li></ul><div><div><div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 04:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Vendor Relationship Management]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47550]]></requisitionid>
    <referencenumber><![CDATA[R47550]]></referencenumber>
    <apijobid><![CDATA[r47550]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47550/senior-manager-vendor-relationship-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Senior Manager, Vendor Management</strong>, is responsible for assessing, onboarding, and overseeing the health and performance of vendors involved in clinical trial execution. This role ensures that vendors meet the necessary qualifications and compliance standards, manage relationships, and oversee delivery to time, cost, and quality. This position is capable of leadership and oversight of vendor segments, and of the technical aspects such as quality, compliance, business continuity, and inspection readiness.</p><p>The Sr Manager may also play a critical role in advancing digital transformation and AI adoption within the vendor ecosystem, integrating emerging technologies and data-driven insights to elevate vendor governance, improve operational efficiency, and enable predictive risk management across the clinical trial portfolio.</p><p><strong>A typical day in this role looks like:</strong></p><p>This position is expected to have the ability to execute a variety of roles to meet the expectations of effective relationship management and driving compliance and high-quality delivery. </p><p>Relationship Management</p><ul><li>Oversee the performance and health of vendors within assigned segment to ensure deliver to plan – time, budget quality.</li><li>Develop/enhance vendor performance scorecards that drives identification of mitigations/contingencies against performance risks/issues</li><li>Build and maintain strong relationships with key vendors.</li><li>Act as the primary point of contact for relationship level vendor-related issues and escalations. </li><li>Assess portfolio resource demand and shortfall/mitigations for current and potential future portfolio with key vendors</li><li>Lead the integration of new vendors into Regeneron strategy and operating model(s) to create stronger probability of success with new collaborations; including alignment to Regeneron’s digital infrastructure, data standards, and AI-enabled tooling requirements as part of the onboarding process</li></ul><p>Leadership</p><ul><li>Mentor and develop team members, fostering a culture of continuous improvement.</li><li>Collaborate with cross-functional teams to ensure cohesive vendor management practices.</li><li>Engage with DSOE’s Change Mgmt function to facilitate process change, stakeholder readiness and communication strategy as required.</li><li>May have direct supervision over support staff. </li></ul><p>Quality and Compliance Oversight:</p><ul><li>Ensure vendors comply with regulatory requirements and organizational standards, including proper documentation of partnerships is developed and maintained.</li><li>Conduct regular quality and compliance assessments of vendors.</li><li>Develop and implement corrective action plans for any identified issues.</li><li>Lead relevant governance meetings on behalf of Regeneron including agendas, minutes, and timely follow-up of action items</li></ul><p>Vendor Qualification and Business Continuity:</p><ul><li>Develop and/or manage against business continuity plans involving vendors.</li><li>Conduct regular reviews and updates of business continuity plans.</li><li>Ensure minimal disruption in clinical trial operations through effective continuity planning.</li><li>Contribute to the Qualification process, with a steady focus on continuous improvement and stakeholder management</li></ul><p>Inspection Readiness and Support:</p><ul><li>Ensure vendors are prepared for regulatory inspections and applicable audits.</li><li>Coordinate and support inspection activities, including pre-inspection preparation and post-inspection follow-up.</li><li>Maintain inspection readiness documentation and records.</li></ul><p>Vendor Management Operations, and Digital/Technology Integration:</p><ul><li>Lead and facilitate the conduct of the internal governance bodies related to sourcing strategy and operating models </li><li>Accountable for continuous assessment of capacity management for external resources </li><li>Lead the integration of new processes and/or changes to process across applicable vendors, with emphasis on digital enablement, AI-assisted workflow automation, and system interoperability across the vendor ecosystem</li><li>Oversee Vendor training curriculum assignments and training compliance</li><li>Champion AI and digital transformation initiatives within the vendor management function, identifying opportunities to leverage automation, predictive analytics, and intelligent tooling to enhance oversight, decision-making, and operational efficiency</li><li>Drive technology and systems integration across vendor interfaces, ensuring alignment with Regeneron’s data governance standards, clinical technology platforms (e.g., eTMF, CTMS, EDC), and emerging AI-enabled capabilities</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Strong knowledge of GCP, FDA, EMA, and other relevant regulatory requirements.</li><li>Highly collaborative with strong written and verbal communication skills; effective customer focus; ability to interact with all levels of employees and maintain confidentiality.</li><li>High aptitude with Microsoft Office and clinical technology platforms (e.g., eTMF, CTMS, EDC);</li><li>Excellent organizational and project management skills.</li><li>Strong communication and interpersonal skills.</li><li>Ability to work independently and as part of a team.</li><li>Self starter who takes initiative, and can handle risk and uncertainty.</li><li>Ability to work in a fast-paced environment and manage multiple priorities</li><li>Able to exercise sound judgement and decision making. </li><li>May require up to 25% travel</li></ul><p><strong>In order to be considered qualified for this role, </strong>a minimum of Bachelors degree is required and 8+ years in pharma industry, specifically in operations and/or vendor management discipline.</p><ul><li>Minimum of 10 years of experience and success in a clinical project/ trial management role within biotech/pharmaceutical industry</li><li>Strong knowledge of GCP, FDA, EMA, and other relevant</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - MANHATTAN, NY]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48010]]></requisitionid>
    <referencenumber><![CDATA[R48010]]></referencenumber>
    <apijobid><![CDATA[r48010]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48010/medical-account-specialist-ii-neurology-manhattan-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Manhattan]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Manhattan (NY Metro), NY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 13:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs - Neurology (South Central)]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46423]]></requisitionid>
    <referencenumber><![CDATA[R46423]]></referencenumber>
    <apijobid><![CDATA[r46423]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46423/associate-director-field-medical-affairs-neurology-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. We expect you to demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities shaping our medical strategy. You will be considered a scientific and clinical expert on our current and future Neurology assets.</p><p>Territory: TX, AR, MS, LA</p><p><strong>A typical day may include the following: </strong></p><ul><li><p>Establish, foster, cultivate and maintain peer relationships with KOLs in Neurology</p></li><li><p>Act as a primary clinical/scientific resource to HCPs for information pertaining to disease state and our products to ensure awareness and understanding.</p></li><li><p>Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans.</p></li><li><p>Support evidence generation (company sponsored trials and investigator initiated studies) research initiatives.</p></li><li><p>Identify and report medical insights.</p></li><li><p>Identifies gaps in research and educational needs to inform medical strategy.</p></li><li><p>Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.</p></li><li><p>Performs disease management and therapeutic area education with identified practitioners, payers and researchers.</p></li><li><p>Attends conferences to collect and report relevant, scientific, clinical, & competitive intelligence.</p></li><li><p>Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p></li></ul><p>To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) with a minimum 8 years of experience, including 4+ years working as a Medical Science Liaison in the pharmaceutical industry. Experience as a Neurology MSL or Neurology is preferred. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. Demonstrated experience communicating complex data sets and the ability to be seen as a scientific peer while educating top KOLs. Established relationships with KOLs in neurology and knowledge of institutions focused on myasthenia gravis (MG) preferred as is drug launch experience. Capable of frequent business travel (approximately 70% of time), including air travel, ability to travel overnight and occasionally on weekends</p><p>#msl #medicalscienceliaison</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, CMC Regulatory Affairs (Hematology/Oncology)]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48201]]></requisitionid>
    <referencenumber><![CDATA[R48201]]></referencenumber>
    <apijobid><![CDATA[r48201]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48201/associate-director-cmc-regulatory-affairs-hematologyoncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross-functional and external partners, and serving as a key liaison in regulatory authority interactions.</p><p><strong>Where and when:</strong></p><p>This is an Uxbridge based position and would you to be on-site 3 days per week and 2 days from home. A fully remote role is not possible for this position. If eligible, we can offer relocation benefits.</p><p><strong>Discover your role:</strong></p><p>• Lead product development activities from a CMC regulatory standpoint with input from senior management.</p><p>• Represent CMC RA at program meetings and independently provide regulatory interpretation, position, and covering clinical development, initial market applications, and approval/post-approval activities.</p><p>• Identify program issues and develop appropriate regulatory strategies to mitigate risks to filings, independently find alternative solutions/work-arounds, and obtain consensus.</p><p>• Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.</p><p>• Lead and facilitate interactions with global regulatory authorities (e.g., meetings, IR responses, inspections).</p><p>• Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country-specific regulatory guidance documents;</p><p>• Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks.</p><p>• Develop and create working instructions, SOPs, and/or templates to facilitate consistent and efficient practice across the CMC RA groups.</p><p>• Identify gaps in the IOPS and global RA processes, bring up to higher management, and help to improve business efficiency.</p><p>• Support establishing, managing, and maintaining a knowledge base of current and emerging regulatory requirements and guidelines in the CMC field.</p><p>• Find opportunities to initiate operational changes and policy modifications.• Manage and coach team member(s).</p><p><strong>This role requires: </strong></p><p>To be considered a bachelor’s degree with a minimum of 10 years of pharmaceutical/biotech industry experience, including 5+ years of relevant CMC experience. An advanced degree is preferred.</p><p>Proven track record supporting biological products through development and approval is a distinct advantage.</p><p>It is required to have a good understanding of current CMC worldwide regulations and guidelines.</p><p>Experience in interacting with the US FDA and other regulatory authorities. Experience with device regulatory requirements and development processes for combination products is a plus.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 16:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Finance & Administration - Canada]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46239]]></requisitionid>
    <referencenumber><![CDATA[R46239]]></referencenumber>
    <apijobid><![CDATA[r46239]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46239/associate-director-finance-administration-canada/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are hiring an Associate Director, Finance & Administration to partner closely with country leadership and commercial teams, supporting high‑impact business decisions through financial insight, forecasting, and analysis. This role sits at the centre of the country organisation, working across Finance, Accounting, Tax, Treasury, and global CFO functions to shape commercial performance, governance, and long‑term planning.</p><p>If you enjoy combining critical thinking with hands‑on delivery—and value visible ownership at country level—this is a role where your expertise will genuinely influence outcomes.</p><h3>What You’ll Be Doing:</h3><ul><li><p>Partnering with country leadership on budgeting, forecasting, and financial planning</p></li><li><p>Preparing and presenting forecasts, including actuals versus forecast analysis</p></li><li><p>Managing resource planning, including FTE utilisation across cost centres</p></li><li><p>Supporting commercial teams with P&L ownership and profitability insights</p></li><li><p>Translating epidemiology and commercial data into financial forecasts</p></li><li><p>Coordinating with Accounting on revenue accuracy, accruals, and reporting</p></li><li><p>Acting as a local finance liaison across Tax, Treasury, and CFO functions</p></li><li><p>Ensuring compliance with internal policies and external regulations</p></li></ul><h3>This Role May Be For You If:</h3><ul><li><p>You enjoy working closely with senior collaborators to support sound decisions</p></li><li><p>You like roles that balance strategic perspective with practical execution</p></li><li><p>You are comfortable partnering across commercial, medical, and G&A teams</p></li><li><p>You value clear country ownership and accountability</p></li><li><p>You enjoy collaborating with global and local finance colleagues</p></li><li><p>You are motivated by improving processes and strengthening governance</p></li></ul><h3>To Be Considered:</h3><p>You will have a relevant undergraduate degree, along with a postgraduate qualification (such as an MBA) and/or a recognised professional finance qualification. You will bring at least five years of post‑qualification finance experience, primarily within the biotech or pharmaceutical industry, including experience supporting commercial P&Ls. Fluency in English and the local country language is required. International experience and additional language skills are an advantage.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45330]]></requisitionid>
    <referencenumber><![CDATA[R45330]]></referencenumber>
    <apijobid><![CDATA[r45330]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45330/senior-manager-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Join Us in Ensuring Patient Safety Globally!</strong></p><p>At our company, we are committed to safeguarding patient health worldwide through innovative pharmacovigilance practices. We are seeking a <strong>Senior Manager, Global Pharmacovigilance (GVP)</strong> to be based in Japan. Reporting directly to the Safety Management Officer, you will play a pivotal role in overseeing critical pharmacovigilance activities, including individual case safety reports (ICSRs), research reports (RRs), foreign safety measures (FSMTs), and aggregate reporting. If you thrive in a collaborative environment and are passionate about advancing global patient safety, this is your opportunity to make a meaningful impact.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Oversee and evaluate Japan ICSR, RR, and FSMT reports for accuracy and compliance.</p></li><li><p>Manage vendor activities related to pharmacovigilance, ensuring adherence to contracts and performance standards.</p></li><li><p>Author and update working instructions while conducting related training sessions.</p></li><li><p>Contribute to the development and implementation of Japan Risk Management Plans (J-RMPs) and ensure compliance with the associated activities.</p></li><li><p>Collaborate with cross-functional teams, including Medical Affairs, Regulatory Affairs, and external partners, to deliver key pharmacovigilance deliverables.</p></li><li><p>Support the preparation of safety sections for Japan New Drug Applications (J-NDAs) and address inquiries from the Pharmaceuticals and Medical Devices Agency (PMDA).</p></li><li><p>Lead process improvement initiatives to enhance quality and compliance in pharmacovigilance operations.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You have over seven years of experience in pharmacovigilance or drug safety within the pharmaceutical or biotech industry.</p></li><li><p>You are well-versed in PMDA/MHLW and ICH guidelines and regulations governing pharmacovigilance activities.</p></li><li><p>You excel at managing complex projects, such as safety database implementations or license succession involving data migration.</p></li><li><p>You thrive in cross-functional collaborations and have experience working with teams like Medical Affairs and Regulatory Affairs.</p></li><li><p>You have successfully supported or led regulatory inspections, including PMDA Re-examinations and GCP Reliability Inspections.</p></li><li><p>You possess strong analytical and organizational skills, enabling you to oversee multiple projects simultaneously.</p></li></ul><p><strong>To Be Considered:</strong><br>Candidates must have a Bachelor's degree or higher and at least seven years of experience in pharmacovigilance and post-marketing surveillance operations. Familiarity with contracting and managing external service providers is essential, along with prior global pharmacovigilance experience. Preferred candidates will have demonstrated success in regulatory authority inspections and cross-functional collaborations.</p><p><strong>Why Join Us?</strong><br>This is more than just a job—it’s an opportunity to contribute to a mission that directly impacts global patient safety. We offer a collaborative environment where innovation is encouraged, and your expertise will be valued and recognized.</p><p>Take the next step in your career and apply to join our dedicated team today!</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Market Access]]></title>
    <date><![CDATA[Sat, 27 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48268]]></requisitionid>
    <referencenumber><![CDATA[R48268]]></referencenumber>
    <apijobid><![CDATA[r48268]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48268/associate-manager-market-access/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Market Access Associate Manager, Rare Disease Portfolio, Japan, to join our Market Access team, supporting our Japan affiliate in a hybrid work model. In this role, you will drive launch, pricing, and reimbursement strategies for the rare disease portfolio while collaborating with commercial, marketing, HEOR (health economics and outcomes research), medical affairs, clinical, and global market access strategy teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Tokyo, Japan</p><p>Hybrid working model</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Drive pricing and reimbursement submissions to the National Health Insurance (NHI) price listing.</li><li>Prepare reimbursement dossiers and execute price negotiations aligned with product strategy.</li><li>Monitor reimbursement and policy shifts, pricing, and HTA (health technology assessment) rule changes.</li><li>Provide Japan-specific insights to shape value and evidence strategies.</li><li>Develop and maintain reimbursement tracking tools and annual tactical plans.</li><li>Build and maintain external relationships with key stakeholders, including MHLW (Ministry of Health, Labour and Welfare), HTA bodies, and key opinion leaders (KOLs).</li><li>You collaborate effectively across teams to ensure alignment with Japan-specific priorities.</li><li>You adapt to evolving challenges and provide strategic insights to inform decisions.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree required.</li><li>Native-level Japanese language proficiency.</li><li>Strong verbal and written communication skills.</li><li>In-country market access experience, including knowledge of Japan’s reimbursement environment, payer systems, and cost comparator pricing methodology.</li><li>Project and process management skills with the ability to prioritize tasks effectively.</li><li>Preferred: Experience in rare diseases, cell or gene therapy launches, and HTA negotiation in Japan.</li><li>NHI price negotiation experience with authorities in Japan.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology (f/m/d) - Heidelberg - Mainz - Trier - Saarbrücken]]></title>
    <date><![CDATA[Wed, 17 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48524]]></requisitionid>
    <referencenumber><![CDATA[R48524]]></referencenumber>
    <apijobid><![CDATA[r48524]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48524/sales-specialist-immunology-fmd-heidelberg-mainz-trier-saarbruecken/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Sales Specialist Immunology (f/m/d), you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our Respiratory division at key meetings. You will identify the key people in Pneumology, understand the account context and tailor calls based on individual and account requirements and build KOL support for our portfolio.</p><p><br></p><p><strong>Where:</strong></p><p><br></p><p>Field based in the territory: <strong>Heidelberg - Mainz - Trier - Saarbrücken</strong></p><p><br></p><p><strong>Discover your role:</strong></p><p><br></p><ul><li>Competent advice and support for relevant Healthcare Professionals (HCP) and, where applicable, customers in the hospital segment</li><li>Building and maintaining intensive and sustainable customer relationships - in person and using digital channels</li><li>Target-oriented, substantive dialogue focused on the benefits for customers and added value for patients</li><li>Independent regional management including account analyses, route planning and documentation of your activities in the CRM system</li><li>Participation in trade fairs and congresses as well as independent planning, coordination and realization of training events and specialist presentations</li><li>Regular reporting to the sales management</li></ul><p><br></p><p><strong>This role requires:</strong></p><p><br></p><ul><li>Deep understanding of the local healthcare economy, with the ability to identify key players in Pneumology</li><li>“Patient first” value system</li><li>Bachelor’s degree or equivalent experience and a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</li><li>5+ years of sales experience within the biotech/pharmaceutical sector</li><li>Respiratory experience is preferred</li><li>Proficiency in German as well as conversational English</li><li>Readiness for very frequent travel and a driver's license cl. 3/B.</li></ul><br><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>64.125,00 € - 106.875,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 27 Jun 2026 17:29:32 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, AI Engineering (Global Development)]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44760]]></requisitionid>
    <referencenumber><![CDATA[R44760]]></referencenumber>
    <apijobid><![CDATA[r44760]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44760/director-ai-engineering-global-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Our Global Development (GD) team is seeking a Director, AI Engineering to embark on a digital transformation incorporating AI, machine learning, and automation. The goal is to help us reduce cycle times, improve quality, and allow us to focus on more meaningful work. You will play a key role in developing platforms, processes and technologies across GD. </p><p><strong>A typical day may include the following: </strong><br>• Provide strategic direction and technical leadership to an eventual team of engineers to design, implement, and refine novel algorithms and scalable AI /ML solutions. These will be tailored to applications such as clinical trial design, regulatory intelligence, patient identification and stratification. Oversee the deployment of these solutions into production environments, employing hands-on technical expertise to ensure excellence in execution.<br>• Architect and refine data engineering and data architecture strategies to integrate and optimize diverse data sources. <br>• Partner with the Digital Transformation AI lead and leaders across Global Development to evaluate and implement use cases for implementing AI in the enterprise, including automating manual processes such as protocol review, monitoring, and adverse event review<br>• Provide strategic leadership to initiatives with Global Development IT and enterprise IT to building infrastructure (software and hardware) to support advanced analytics, including vendor evaluation<br>• Collaborate with senior leaders to identify high-value opportunities for AI/ML integration and lead the execution of innovative solutions that address critical business challenges.<br>• Empower colleagues to leverage AI/ML effectively by providing guidance that bridges technical expertise with strategic insights, fostering a culture of innovation and continuous learning.<br>• Establish robust validation frameworks for AI models, ensuring reliability and efficiency<br>• Stay at the forefront of AI/ML advancements, evaluating emerging technologies and methodologies for potential adoption within Regeneron.<br>• Lead initiatives to continuously improve the organization's AI capabilities, fostering a competitive edge. </p><p><strong>This may be for you if you: </strong><br>• Want to be a part of scaling AI in a growing multi-national organization. <br>• Can demonstrate managing cross functional teams. <br>• Demonstrated success bringing transformative change. <br>• Want to have an impact on patient lives</p><p>To be considered you are to have a PhD in Computer Science, Data Science, AI/ML, Engineering, or related with 10-12 years experience or a Master or Bachelor’s with 12–15+ years experience in AI?ML or software engineering. Your experience must include a deep understanding of generative AI, machine learning, natural language processing, and statistical modeling. Expertise in programming (Python, R, etc.), with a focus on applying advanced technical skills to data analysis, automation, and software development is required. Expertise in database platforms and cloud computing infrastructure. Experience managing and analyzing large-scale clinical datasets Excellent communication skills, including experience presenting to senior leadership, both technical and non-technical. Experience managing multiple projects in parallel. Experience working in and managing cross-functional teams. Have track record of model development, implementation to scale, maintenance, and evaluation in a healthcare of life sciences setting<br> May require travel up to 20%. <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director–Data Lake Operations]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47775]]></requisitionid>
    <referencenumber><![CDATA[R47775]]></referencenumber>
    <apijobid><![CDATA[r47775]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47775/associate-director-data-lake-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><div><p>As an Associate Director, Data Lake Operations, you will lead the design, implementation, and management of clinical data lake solutions supporting global clinical trial and healthcare research initiatives. You will ensure efficient data ingestion, integration, and governance while enabling advanced analytics, regulatory compliance, and informed decision-making.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><h3><strong>A typical day may include the following:</strong></h3><ul><li><p>Defining and executing the strategy and roadmap for the Clinical Data Lake aligned with business and regulatory objectives</p></li><li><p>Leading the design, development, and implementation of scalable data lake architectures across clinical data ecosystems</p></li><li><p>Building and managing data pipelines integrating diverse sources (EDC systems, lab data, biomarker data, EHR, and other healthcare datasets)</p></li><li><p>Ensuring data security, privacy, and compliance with regulatory standards such as GDPR, HIPAA, FDA, and ICH-GCP</p></li><li><p>Establishing standardized clinical data models aligned with CDISC standards (SDTM, ADaM) to enable analytics and reporting</p></li><li><p>Driving data quality, transformation, validation, and lineage tracking to ensure integrity and traceability of clinical data</p></li><li><p>Collaborating with IT, data teams, and global stakeholders to align data infrastructure with business objectives</p></li><li><p>Leading matrixed teams across data engineering, ingestion, standardization, and visualization functions</p></li><li><p>Driving innovation through adoption of new technologies and data capabilities to enhance clinical insights and decision-making</p></li></ul><h3><strong>This job may be for you if you have:</strong></h3><ul><li><p>Strong expertise in data lake architecture, data engineering, and clinical data ecosystems</p></li><li><p>Deep understanding of clinical trial processes, CDISC standards (SDTM, ADaM), and regulatory requirements</p></li><li><p>Experience working with big data platforms such as AWS, Spark, or Google Cloud</p></li><li><p>Strong proficiency in database technologies (SQL, NoSQL) and ETL tools</p></li><li><p>Proven ability to lead cross-functional teams and manage complex stakeholder environments</p></li><li><p>Strong strategic thinking, problem-solving, and communication skills</p></li><li><p>Experience integrating data from multiple sources and building scalable data solutions</p></li></ul><h3><strong>To be considered for this role, you must have:</strong></h3><ul><li><p>Bachelor’s or Master’s degree in Computer Science, Data Science, Bioinformatics, or a related field</p></li><li><p>10+ years of experience in data management, data engineering, or clinical operations</p></li><li><p>At least 5+ years of leadership experience managing teams or large-scale data initiatives</p></li><li><p>Proven experience working on large-scale data lake implementations in healthcare or clinical research domains</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, EDC User Acceptance Testing, Quality Control & Development]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48277]]></requisitionid>
    <referencenumber><![CDATA[R48277]]></referencenumber>
    <apijobid><![CDATA[r48277]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48277/specialist-edc-user-acceptance-testing-quality-control-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Specialist, EDC Development and UAT to join our Data Management team in a hybrid role. In this role, you will perform EDC database development, User Acceptance Testing, and Quality Control for assigned clinical studies, ensuring Database Development functions meet Regeneron procedures, clinical data standards, and SOPs, while collaborating with CRO Clinical Database Developers and Clinical Data Management. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Build early to late phase studies in Medidata Rave, then program edit checks, dynamics, derivations, and custom functions in Rave Architect</p></li><li><p>Configure study setup, including user administration, AE/SAE alerts, IRT accounts, and Coder registration</p></li><li><p>Run UAT end-to-end — from UAT Plan and site setup through test scripts, execution, and sign-off</p></li><li><p>Track, triage, and resolve UAT issues through to go-live</p></li><li><p>Conduct Quality Control on internal and CRO builds, covering eCRF design, edit checks, derivations, custom functions, and integrations</p></li><li><p>Document QC findings, verify corrections, and improve QC checklists, procedures, and UAT templates</p></li><li><p>Manage post-production changes through Rave Amendment Manager and support third-party integrations such as IxRS and labs</p></li><li><p>You bring a quality-focused mindset and strong attention to detail in resolving system defects</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree in mathematics, science, or a related field</p></li><li><p>2+ years of EDC development experience in biotech, pharmaceutical, or healthcare</p></li><li><p>Medidata Rave experience required</p></li><li><p>Strong understanding of UAT methodologies, test script development, and defect management</p></li><li><p>Knowledge of 21 CFR Part 11, ICH-GCP, and CDISC standards</p></li><li><p>Robust knowledge of Data Management and Database Development processes</p></li><li><p>Strong cross-functional collaboration and time management in a matrix environment</p></li><li><p>UAT coordination or execution and QC of EDC systems strongly preferred</p></li><li><p>Medidata Builder Certification, C# programming, or TrialGrid knowledge a plus</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Data Management Tech Solutions]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47796]]></requisitionid>
    <referencenumber><![CDATA[R47796]]></referencenumber>
    <apijobid><![CDATA[r47796]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47796/senior-manager-clinical-data-management-tech-solutions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a Senior Manager, Clinical Technical Solutions to join our Data Management organization. In this role, you will lead the strategy, design, and deployment of advanced automation frameworks, AI-powered solutions, and intelligent agentic workflows that transform clinical data operations across the clinical trial lifecycle. You will partner with Data Management, Clinical Sciences, Biostatistics, Safety, Precision Medicine, and Technology teams to identify high-impact opportunities, accelerate data review and cleaning processes, and improve data quality and operational efficiency across a global study portfolio.</p><p><strong>When & where:</strong></p><p>Hyderabad, India (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead the strategic roadmap and expansion of advanced automation solutions across Clinical Data Management operations.</p></li><li><p>Drive the design and implementation of AI-powered agents and intelligent workflow automation solutions that streamline clinical data processes.</p></li><li><p>Partner with Data Management, Clinical Sciences, Biostatistics, Precision Medicine, Safety, and IT teams to identify and prioritize automation opportunities.</p></li><li><p>Develop and deploy Retrieval-Augmented Generation (RAG) solutions and AI-assisted applications grounded in study-specific clinical knowledge.</p></li><li><p>Oversee intelligent data ingestion, reconciliation, anomaly detection, predictive analytics, and data quality automation initiatives.</p></li><li><p>Establish governance frameworks for AI and automation solutions, including validation, auditability, prompt management, and human-in-the-loop review processes.</p></li><li><p>Drive inspection readiness through automation of regulatory documentation, audit trail reviews, protocol deviation detection, and reconciliation workflows.</p></li><li><p>Manage and mentor a team of clinical data scientists and automation specialists while fostering a culture of innovation and automation excellence.</p></li><li><p>Evaluate emerging AI technologies and provide strategic guidance on automation investments, technology adoption, and operational transformation initiatives.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s or Master’s degree in Computer Science, Data Science, Bioinformatics, or a related field; advanced degree preferred.</p></li><li><p>8+ years of experience in data science, automation engineering, clinical informatics, or related disciplines, including at least 3 years of technical team leadership experience.</p></li><li><p>Proven experience designing and deploying advanced automation solutions within a regulated environment.</p></li><li><p>Strong expertise in generative AI technologies, including Anthropic Claude, OpenAI GPT, agentic frameworks, prompt engineering, and Retrieval-Augmented Generation (RAG) architectures.</p></li><li><p>Advanced programming skills in Python and SQL.</p></li><li><p>Strong understanding of clinical trial data structures, Electronic Data Capture (EDC) systems, and CDISC standards including CDASH and SDTM.</p></li><li><p>Knowledge of GxP, Computer System Validation (CSV), and regulatory considerations for AI-enabled solutions in clinical research.</p></li><li><p>Experience building predictive analytics, anomaly detection, and intelligent automation solutions that support clinical data operations.</p></li><li><p>Excellent leadership, stakeholder management, communication, and cross-functional collaboration skills.</p></li><li><p>Passion for leveraging AI and advanced technologies to transform clinical data management and accelerate clinical development.</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Statistical Genetics]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48469]]></requisitionid>
    <referencenumber><![CDATA[R48469]]></referencenumber>
    <apijobid><![CDATA[r48469]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48469/associate-manager-statistical-genetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a statistical geneticist to excited to build tools, workflows, and applications to analyze and interpret the genetics of nearly 3 million individuals linked with rich phenotype data from around the world. You will build and maintain a suite of tools to manage, execute, and assess genome-wide analyses leading to new discoveries and insights into disease mechanisms. Within the broad domain of cardiovascular, metabolic, and skeletal diseases, you will work collaboratively with other specialists in genomic data analysis, translational genetics, functional biology, and medicine, to enable Regeneron to create better medicines for patients in need. </p><p><strong> </strong></p><p><strong>A typical day might include the following:</strong></p><p>· Perform genome-scale analyses with genotype, imputed, and sequence data from millions of individuals across hundreds of relevant phenotypes and biomarkers. </p><p>· Work across teams to build, maintain, and improve analytical workflows that implement analytical best practices.</p><p>· Build and manage systems to execute genomic analysis on a large scale and at high throughput. This including tools for analysis tracking and post-analysis quality control.</p><p>· Employ your expertise in genetic analysis to identify and troubleshoot analyses at scale.</p><p>· Test and integrate computational tools for deployment across our collection of diverse quantitative, health outcomes, and molecular data types.</p><p>· Critically review and provide input on analysis plans, results, and summaries to ensure accuracy and reliability. Identify problems and propose solutions or analytical refinements.</p><p><strong> </strong></p><p><strong>This role might be for you if you:</strong></p><p>· Have experience in the analysis of large genetic association studies and meta-analysis, including through the analysis of UK Biobank or other biobank-scale data.</p><p>· Have experience in the management of genetic and phenotype data in human genetic studies, including familiarity manipulating sequence data (e.g., VCF files), strategies for genotype imputation, and for quality control of genetic association inputs and outputs.</p><p>· Have demonstrated coding ability in either Python, C/C++, or R. </p><p>· Enjoy working in a highly interactive environment with a diverse team of colleagues.</p><p>· Employ outstanding communication skills to summarize and present new concepts, methods, and results from human genetic studies to a variety of audiences.</p><p>· Are experienced, interested, and excited to be part of a team identifying the next generation of therapeutic targets for cardiovascular, metabolic, and skeletal diseases.</p><p><strong> </strong></p><p><strong>To be considered for this role</strong>, you must have a PhD in Human Genetics, Biostatistics, or a related field. No post-graduate experience is required, but postdoctoral training or relevant industry experience is preferred. The successful candidate should have experience and competence with approaches currently employed in the group, including genome- and exome-wide association analysis, rare variant analysis, Mendelian randomization, LD Score regression, polygenic risk score modelling, meta-analysis, and the use of functional data to prioritize variants and genes of interest. Expertise with cloud computing environments, advanced tools for genomic analyses (PLINK, REGENIE, etc.), and statistical analysis and computation (R, Python, C/C++) are necessary. Experience working in cardiovascular, metabolic, and/or musculoskeletal diseases is preferred. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Assurance Investigation Specialist]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48350]]></requisitionid>
    <referencenumber><![CDATA[R48350]]></referencenumber>
    <apijobid><![CDATA[r48350]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48350/quality-assurance-investigation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Quality Assurance (QA) Specialist to conduct investigations. In this role you will perform activities in support of dispositioning product and/or raw materials while ensuring compliance with QA policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>Monday-Friday, 8am-4:30pm</li><li>Location: Rensselaer, New York, United States</li></ul><p>What you’ll do:</p><ul><li>Represent quality assurance in support of complex deviations, change controls, corrective and preventive action etc. including active participation in investigation, evaluation, and problem resolution</li><li>Review and approve batch records</li><li>Communicate quality assurance procedures, collaborate closely with internal or external partners and stakeholders and provide input on regulatory communications</li><li>Train and/or mentor junior employees, including providing insights and education on processes and procedures</li><li>Provides consultation or advice in alignment with quality assurance policies</li><li>Perform activities associated with disposition of raw materials and product (e.g. receipt, inspection, document review, shipping, etc.). activities may be on the floor or at a desk</li><li>Review, edit, or approve Regeneron controlled documents</li><li>Review and approve investigations associated with raw materials or product</li><li>Perform status labeling of product</li></ul><p>The environment and physical rhythms of this role:</p><ul><li>Gowning: full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p>Let’s find out if we’re a fit:</p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>Assoc QA Specialist : 2+ years of experience</li><li>QA Specialist : 4 + years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p>Thrive today. Grow tomorrow.</p><ul><li>Student loan pay down program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 19 Jun 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Quality Assurance Reviewer]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48353]]></requisitionid>
    <referencenumber><![CDATA[R48353]]></referencenumber>
    <apijobid><![CDATA[r48353]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48353/principal-quality-assurance-reviewer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Quality Assurance (QA) Specialist/Reviewer to support our Fill Finish facility. In this role, you will perform all compliance related tasks necessary to review and approve investigations and provide quality oversight to the implementation of robust corrective actions for supporting manufacturing operations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>Location: Rensselaer, New York, United States</li><li>Monday-Friday, 8am-4:30pm</li></ul><p>Discover your role:</p><ul><li>Independently reviews and approves:<ul><li>Investigations into non-conformances and proposed actions to prevent reoccurrences in support of manufacturing operations</li><li>Laboratory investigations into out of specification (OOS) and out of trend ( OOT) results</li><li>Supplier corrective action requests and proposed vendor actions</li></ul></li><li>Coaches investigation team to enable preparation of investigation reports that include recommendations on investigation findings for medium/high severity non-conformances</li><li>Analyzes and evaluates information captured through investigations, summarizes information and trends in investigation reports</li><li>Presents quality considerations and recommendations at group meetings with multiple levels of management</li><li>Reviews primary data sources to assure the accuracy of investigative conclusions in accordance with cGMP standards in support of investigations</li><li>Provides quality reviews and oversight on a wide range of investigations of differing subject matter</li><li>Monitors production processes and quality systems data to acquire vital data in support of investigations and track efficiency of changes</li><li>Participates in and/or leads cross-functional study teams to get results</li><li>Captures, trends and analyzes process related data to drive consistency and timeliness</li><li>Trains employees on investigative processes and techniques</li><li>Coordinates and/or leads cross-functional meetings with multiple departments</li></ul><p>This role requires:</p><ul><li>BS/BA in Life Sciences, Engineering or related field; or equivalent combination of education and experience<ul><li>Principal QA Specialist: 8+ years of relevant experience</li><li>Staff QA Specialist: 10+ years of relevant experience</li></ul></li><li>Experience with sterile drug product manufacturing, fill finish and/or quality control testing is preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 19 Jun 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  LONG ISLAND, NY]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48915]]></requisitionid>
    <referencenumber><![CDATA[R48915]]></referencenumber>
    <apijobid><![CDATA[r48915]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48915/medical-account-specialist-ii-hematology-long-island-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>LONG ISLAND, NY</strong></p><p><strong>Geography: Long Island</strong></p><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - KENTUCKY]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48945]]></requisitionid>
    <referencenumber><![CDATA[R48945]]></referencenumber>
    <apijobid><![CDATA[r48945]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48945/medical-account-specialist-ii-hematology-kentucky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- Kentucky</strong></p><ul><li><strong>Geography: Louisville, Lexington</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director - Hematology (Mid Atlantic)]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48919]]></requisitionid>
    <referencenumber><![CDATA[R48919]]></referencenumber>
    <apijobid><![CDATA[r48919]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48919/regional-director-hematology-mid-atlantic/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong>The Regional Director (RD), Hematology will report to the National Business Director, Hematology and be responsible for hiring, leading, developing and retaining the Hematology Medical Specialist team in the Great Plains region to support our Multiple Myeloma Bispecific Antibody.</p><p>The RD is responsible for ensuring strong and consistent sales performance that meet or exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Hematology market. The RD will work closely with their cross functional partners to ensure full cooperation and transparency within the region. The RD will work closely with Training and Development to ensure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field Role</p></li><li><p><strong>Location: </strong><strong>Mid Atlantic Region- SC, NC, VA, WV, MD, DE, NJ, Eastern PA</strong></p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Build and develop a high integrity, high quality sales team and provide overall leadership to the team.</p></li><li><p>Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p></li><li><p>Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p></li><li><p>Ensure each employee is trained on, and effectively implements, customer education.</p></li><li><p>Communicate most current knowledge of the industry and competitor products to regional teams.</p></li><li><p>Ensure participation in industry related trade shows, meetings, conferences, etc.</p></li><li><p>Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p></li><li><p>Allocate and manage the region's budget and utilization of promotional resources.</p></li><li><p>Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p></li><li><p>Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Oncology, preferably Hematology.</p></li><li><p>Experience in Biologics and buy and bill products or strong relevant experience in the Oncology field required. Experience in hematology oncology a strong plus.</p></li><li><p>Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p></li><li><p>Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p></li><li><p>Strong ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel extensively with local and regional influence.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Aggregate Reporting Management]]></title>
    <date><![CDATA[Sun, 28 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48818]]></requisitionid>
    <referencenumber><![CDATA[R48818]]></referencenumber>
    <apijobid><![CDATA[r48818]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48818/senior-manager-aggregate-reporting-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Patient Safety organization is seeking a Senior Manager, Aggregate Reporting Management to join our team!</p><p><strong>In this role, a typical day might include:</strong></p><p>This position in the Global Patient Safety (GPS) Operations is responsible for management of aggregate safety reporting activities across all phases of the product lifecycle. This role supports the consistent, compliant, and scientifically robust preparation, distribution and submission of periodic and ad-hoc safety reports to health authorities, collaborators and contract research organizations worldwide.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Drives preparation, development and maintenance of Aggregate Reporting (i.e., PSURs/PBRER, PAER, DSURs, Local Periodic Reports, SUSARs) Deliverables</p></li><li><p>Leads Aggregate Report planning, production and distribution activities across GPS and other functions across US, EU, Japan and other ICH regions, as well as non-ICH regions</p></li><li><p>Provides expertise and guidance to authors and contributors of aggregate reports</p></li><li><p>Maintains compliance metrics and contributes to implementation of Quality Events and Corrective Action and Preventive Action (CAPA) for non-compliance</p></li><li><p>Implements effective structure, procedures and tools to ensure aggregate reports and other functional deliverables are completed timely and with high quality</p></li><li><p>Develops and oversees functional specifications of data requirements for aggregate deliverables from the safety and clinical databases</p></li><li><p>Collaborates with Global Patient Safety (GPS) and with other functional areas (Epidemiology, Clinical Development, Regulatory Affairs, Statistics, etc.) contributing to aggregate safety reports</p></li><li><p>Acts as subject matter expert during audits and inspection.</p></li><li><p>Provides oversight, and training as needed of CRO respective activities in support of high quality and timely aggregate reports</p></li><li><p>Acts as a functional vendor management overseeing and driving high quality outputs from our vendors</p></li><li><p>Develops and maintains aggregate report procedural package (SOPs, Work Instructions), reports’ templates, KPIs</p></li><li><p>Drives process improvement through automation and other tech initiatives.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor’s degree required (advanced degree or HCP‑focused background preferred) and 5+ years of Pharmacovigilance experience, with a demonstrated focus on Aggregate Safety Reporting.</p></li><li><p>Project management experience strongly preferred, PMP preferred</p></li><li><p>Experience with health authority inspections (PV and GCP)</p></li><li><p>Medical writing experience with regulatory documentation</p></li><li><p>Strong project management skills</p></li><li><p>Excellent strategic decision-making and analytical skills</p></li><li><p>Strong communication and writing skills</p></li><li><p>Strong understanding of Scientific content</p></li><li><p>Proven experience with technology implementations allowing for streamlined process execution.</p></li></ul><p>#GDPSJobs</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 29 Jun 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Specialist - IT]]></title>
    <date><![CDATA[Wed, 01 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46510]]></requisitionid>
    <referencenumber><![CDATA[R46510]]></referencenumber>
    <apijobid><![CDATA[r46510]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46510/principal-qa-specialist-it/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Working within the Quality Assurance organization this position is responsible for ensuring IT systems, programs and quality events are robust and compliant. The position will liaise with the IT and broader QA organizations to ensure all aspects of IT related programs are in compliance with regulatory agency expectations and internal company policies and procedures.</p><p><strong>As a Principal QA Specialist, a typical day might include the following:</strong></p><ul><li><p>Supporting IT related change controls, CAPAs, data integrity initiatives, deviations, internal and external audits and other verticals to ensure a robust, compliant state of programs</p></li><li><p>Engaging with Corporate and IOPS IT ensuring IT processes and procedures meet Regeneron’s Quality System requirements</p></li><li><p>Reviewing, editing and approving SOPs, deviation notifications, deviation investigations, and corrective actions</p></li><li><p>Responsible for compliance monitoring of area operations, including trending of failures and evaluating efficiency of corrective actions</p></li><li><p>Collaborating, investigating and troubleshooting to determine solutions or recommendations for changes and/or improvements</p></li><li><p>Participating and supporting the Quality Risk Management (QRM) principles in the formal and informal risk assessment initiatives</p></li><li><p>Supporting the development, review and approval of Quality Assurance Agreements (QAA), along with the Approved Supplier List (ASL) process</p></li><li><p>Contributing information reflecting best practices, industry trends and recommendations for strategic plans to drives changes and improvements</p></li><li><p>Communicating project and program status and metrics to Senior Management</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Demonstrate strong interpersonal skills and can collaborate effectively</p></li><li><p>Can balance changing priorities with a growing workload by communicating timely decisions</p></li><li><p>Demonstrate knowledge of 21CFR11 and Annex 11 as well MHRA, FDA and WHO data integrity guidelines</p></li><li><p>Have an understanding of the interdependencies of change management, deviation and continuous improvement</p></li><li><p>Can work in a dynamic organization where innovative solutions are required to ensure a high-level of quality is achieved with aggressive timelines</p></li></ul><p>To be considered for this position you should have a BSc/BA/BEng in IT/Automation/Analytics or related field and 5-7 years of experience or equivalent combination of education and experience. Recent experience in a data integrity role is preferred; however, it is not required. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€63,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Jul 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Writer]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48798]]></requisitionid>
    <referencenumber><![CDATA[R48798]]></referencenumber>
    <apijobid><![CDATA[r48798]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48798/senior-medical-writer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Writer to join our Medical Writing team, supporting clinical document delivery across Global Development in a remote work mode. In this role, you will author clinical study reports, protocols, consent forms, narratives, and investigator brochures while collaborating with clinical teams and biostatisticians. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>United Kingdom (remote)</p><p><strong>Discover your role:</strong></p><ul><li>Author clinical study reports (CSRs), protocols, informed consent forms (ICFs), narratives, investigator brochures, and other regulatory documents across therapeutic areas.</li><li>Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines.</li><li>Identify the right parties for content decisions and synthesise discussions into clear, accurate prose.</li><li>Review work of junior or outsourced writers and CSR-related documents like Statistical Analysis Plans and TFLs.</li><li>Write plain-language content such as ICFs and explain complex medical concepts to lay audiences.</li><li>Adhere to applicable guidelines, templates, SOPs, and internal training while contributing to process improvement across Medical Writing and Global Development.</li><li>You mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree required; advanced degree preferred.</li><li>Minimum 3 years of medical writing experience, including working knowledge of biostatistics.</li><li>Strong knowledge of the clinical research process and applicable regulations, including ICH GCP.</li><li>Clinical document reading, writing, and editing experience.</li><li>Strong knowledge of MS Word, Adobe Acrobat, PowerPoint, and electronic document management systems.</li><li>Ability to manage multiple projects with strong organisational, interpersonal, and communication skills.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 30 Jun 2026 09:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - LAS VEGAS, NV]]></title>
    <date><![CDATA[Thu, 02 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48931]]></requisitionid>
    <referencenumber><![CDATA[R48931]]></referencenumber>
    <apijobid><![CDATA[r48931]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48931/medical-account-specialist-ii-hematology-las-vegas-nv/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Nevada]]></city>
    <state><![CDATA[Nevada]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Account Specialists - Hematology- </strong><strong>Las Vegas, NV</strong></p><ul><li><strong>Geography: </strong><strong>Las Vegas, Flagstaff, AZ</strong></li></ul><p>The Hematology Oncology Account Specialist is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Nurse Educators, Key Account managers, Reimbursement and Access Specialists, and Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><ul><li>Engage Hematologists and other key Oncology customers and deliver clinically focused selling messages to support our Multiple Myeloma bispecific antibody, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Nurse Educator, Key Account Manager, Territory-based Oncology Account Specialists, and Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Jul 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Product Biochemistry]]></title>
    <date><![CDATA[Sun, 05 Jul 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48428]]></requisitionid>
    <referencenumber><![CDATA[R48428]]></referencenumber>
    <apijobid><![CDATA[r48428]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48428/associate-scientist-product-biochemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Product Biochemistry group is seeking a highly motivated Associate Scientist to support the in‑depth biochemical and biophysical characterization of biotherapeutic molecules. The successful candidate will contribute to method development, assay support, and technology innovation efforts that advance research, pre‑clinical, and clinical programs. This role involves close collaboration with cross‑functional teams and supports programs from early‑stage research to post-commercial activities. This role will primarily focus on GxP characterization and stability testing of reference standards.</p><p><strong> </strong></p><p><strong>As an Associate Scientist, a typical day may include: </strong></p><ul><li><p>Perform biochemical and biophysical characterization experiments to assess quality attributes of protein- and/or oligonucleotide‑based therapeutics using techniques such as capillary electrophoresis, size exclusion chromatography coupled to multi-angle light scattering (SEC-MALS), dynamic light scattering (DLS), fourier transform infrared spectroscopy (FT-IR), fluorescence spectroscopy, circular dichroism (CD), differential scanning fluorimetry (DSF), and general lab techniques (pH, analytical balance, sample preparation).</p></li></ul><ul><li><p>Develop, optimize, and run light scattering–based assays (e.g., SEC-MALS, DLS, and related methods) with manager guidance to support molecule characterization and method qualification.</p></li><li><p>Analyze and interpret experimental data; identify trends and communicate key findings to project teams.</p></li><li><p>Accurately document all laboratory activities, data, and analyses in electronic laboratory notebooks (ELN) in accordance with established procedures.</p></li><li><p>Oversee and maintain GxP lab equipment in adherence with quality assurance (QA) standards.</p></li><li><p>Writing SOPs, summary of analysis (SoA’s), reports and recording information in a GxP controlled environment</p></li><li><p>Prepare clear, well‑organized summaries of results (figures, tables, graphs) for presentations, reports, and regulatory‑supporting documentation.</p></li><li><p>Present experimental results at group, departmental, and cross‑functional meetings.</p></li><li><p>Maintain, troubleshoot, and operate essential laboratory instrumentation; ensure readiness of equipment and supplies.</p></li><li><p>Follow laboratory safety practices and contribute to an organized, compliant lab environment.</p></li></ul><p><strong>This role may be for you if: </strong></p><ul><li><p>You enjoy working in a fast-paced environment</p></li><li><p>You are a fast learner and have desire to expand your skill set and learn new techniques</p></li><li><p>You are detail oriented, well-organized and can multi-task</p></li><li><p>You are a team player</p></li><li><p>You have strong communication skills</p></li></ul><p><strong>To be considered, you must have the following:</strong></p><ul><li><p>Hands‑on experience with general laboratory operations and data organization, working under managerial supervision.</p></li><li><p>Fundamental technical proficiency in analytical methodologies such as:</p><ul><li><p>Size Exclusion Chromatography (SEC), UV‑Vis spectrophotometry, spectroscopic-based methods (i.e., CD and FT-IR)</p></li></ul></li><li><p>Understanding of biochemical and biophysical characterization principles for proteins and/or oligonucleotides.</p></li><li><p>Strong organizational skills with the ability to prioritize multiple tasks while keeping up with proper documentation</p></li><li><p>Clear written and verbal communication skills; ability to work both independently and collaboratively.</p></li><li><p>Scientific curiosity, attention to detail, and a willingness to learn new techniques and technologies.</p></li></ul><p><strong>Preferred Qualifications</strong></p><ul><li><p>Experience with additional analytical platforms such as HPLC/UPLC, light scattering (e.g., SEC-MALS, DLS), CD spectroscopy, fluorescence, FT-IR, and DSF.</p></li><li><p>Exposure to analytical method development and assay optimization.</p></li><li><p>Familiarity with late‑stage development, comparability, or regulatory‑supporting studies.</p></li><li><p>Experience working in a GxP lab and following SOP’s.</p></li><li><p>Experience with writing technical documents (e.g., SOP’s).</p></li></ul><p><strong>Education and Experience</strong></p><ul><li><p>Bachelor’s degree in Biochemistry, Biophysics, Chemical Engineering, Biomedical Engineering, or a related scientific discipline with approximately 0 - 5 years of post-degree laboratory experience, or</p></li><li><p>Master’s degree in Biochemistry, Biophysics, Chemical Engineering, Biomedical Engineering, or a related scientific discipline with approximately 0 - 3 years of post-degree laboratory experience.</p></li></ul><p><strong>Physical and Work Environment</strong></p><ul><li><p>Laboratory‑based roles require routine standing, sitting, handling laboratory equipment, and lifting light to moderate weights.</p></li><li>May involve exposure to common laboratory chemicals and instrumentation in a regulated research environment.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 05 Jul 2026 11:56:10 GMT]]></lastactivitydate>
  </job>
</source>