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<source>
  <publisher>Regeneron Pharmaceuticals Inc.</publisher>
  <publisherUrl>https://www.regeneron.com/</publisherUrl>
  <lastBuildDate>Wed, 17 Jun 2026 21:58:41 GMT</lastBuildDate>
  <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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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, Device Development & Secondary Packaging]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45549]]></requisitionid>
    <referencenumber><![CDATA[R45549]]></referencenumber>
    <apijobid><![CDATA[r45549]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45549/manager-device-development-secondary-packaging/]]></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 Manager, Combination Product Development, to join our Process Sciences—Drug Product Engineering team. In this role, you will lead the device product development group with a focus on secondary packaging, driving the development and advancement of drug delivery devices that address emerging needs across Regeneron’s product pipeline. </p><p>As a Manager, Combination Product Development a typical day might include the following: </p><ul><li>Own technical performance for a team delivering off the shelf and custom secondary packaging solutions for regulatory and commercial needs. </li></ul><ul><li>Ensure technically robust packaging via engineering analyses, reliability, and performance assessments. </li></ul><ul><li>Define design inputs and rationales; translate requirements into clear technical specifications. </li></ul><ul><li>Collaborate with suppliers to develop and qualify packaging design outputs. </li></ul><ul><li>Oversee product characterization and Design Verification testing connected to packaging. </li></ul><ul><li>Author protocols and technical reports to support development milestones. </li></ul><ul><li>Define essential performance requirements and traceability to design outputs. </li></ul><ul><li>Establish development control strategies, including statistically based, risk driven sampling plans. </li></ul><ul><li>Support regulatory filings (IND, BLA, MAA) for drug products. </li></ul><ul><li>Lead and develop a cross functional engineering team; recruit, coach, and grow talent. </li></ul><ul><li>Manage multiple projects to deliver on time, in scope, and within budget. </li></ul><ul><li>Partner with peer managers to ensure program success; escalate and resolve technical risks quickly. </li></ul><ul><li>Build strong interfaces with internal design, QA, external manufacturing, and broader engineering teams. </li></ul><ul><li>Champion design controls and technical excellence across IOPS. </li></ul><ul><li>Build organizational standards and systems to scale development for a growing product portfolio. </li></ul><ul><li>Define and integrate standard design and development procedures with Regeneron business and quality systems. </li></ul><ul><li>Identify and implement improvements to streamline device product development and cross team interfaces. </li></ul><ul><li>Represent the combination product device development group at industry forums. </li></ul><ul><li>Monitor evolving regulations, standards, and best practices. </li></ul><ul><li>Develop and maintain relationships with vendors, partners, and key opinion leaders. </li></ul><p>This role might be for you if you: </p><ul><li>Possess strong technical writing and oral communication skills. </li></ul><ul><li>Have experience with secondary packaging product design including cartons, carton inserts, blister trays and Tyvek lids, product and package labeling. </li></ul><ul><li>Enjoy developing, mentoring and coaching a team. </li></ul><ul><li>Have experience with different common secondary manufacturing technologies for secondary packaging and labeling. </li></ul><ul><li>Have experience with tolerance and mechanical stack analysis and other engineering analysis tasks. </li></ul><ul><li>Have knowledge and experience utilizing design of experiments or other problem-solving methodologies during product development. </li></ul><p>To be considered for the Manager, Combination Product Development you must be willing and able to work Monday- Friday, 8am-4:30pm and travel occasionally. You must have a B.S in Biomedical Engineering, Mechanical Engineering, Chemical Engineering or related field. For various levels you must have the following: </p><ul><li>Associate Manager Combination Product Development: 6+ years of relevant experience </li></ul><ul><li>Manager Combination Product Development: 7+ years of relevant experience </li></ul><p>Previous experience within packaging & combination product development is preferred. Previous people leadership/ supervisory 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>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Sr Manager QA (Visual Inspection, Packaging& Labeling)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46659]]></requisitionid>
    <referencenumber><![CDATA[R46659]]></referencenumber>
    <apijobid><![CDATA[r46659]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46659/sr-manager-qa-visual-inspection-packaging-labeling/]]></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 the quality floor oversight of the finish (i.e. visual inspection, assembly, labeling, and packaging) operations and visual inspection qualification program for SA13.</p><p>As a Sr. Manager QA, a typical day might include the following:</p><ul><li><p>Provide leadership to multiple teams under your supervision, including being responsible for:</p><ul><li><p>AQL of inspection, assembly, and packaging activities</p></li><li><p>Quality Oversight of all finish operations</p></li><li><p>Qualification of all visual inspection operators (including manufacturing, quality, and QC)</p></li></ul></li><li><p>Responsible for programs that support the department, for example: in-process reject management</p></li><li><p>Support development and growth of team, including your people leaders</p></li><li><p>Leadership point of contact for escalation of events, process updates, etc.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Proven leadership in cGMP environments, including experience speaking and preparing for regulatory inspections and audits</p></li><li><p>Strong collaboration and communication cross-functionally</p></li><li><p>Ability to think critically, and continuously improve processes</p></li><li><p>Ability to lead a department through a fast-paced and dynamic environment</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 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[産業オペレーションと製品供給]]></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 - North Central]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46775]]></requisitionid>
    <referencenumber><![CDATA[R46775]]></referencenumber>
    <apijobid><![CDATA[r46775]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46775/associate-director-thought-leader-liaison-north-central/]]></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 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[コマーシャル]]></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 (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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Site Office Manager]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46900]]></requisitionid>
    <referencenumber><![CDATA[R46900]]></referencenumber>
    <apijobid><![CDATA[r46900]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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>When & where:</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>Good level of English in addition to the local country language.</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>Equivalent experience may be substituted for education.</p></li><li><p>Further education.</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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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 Clinical Data Reporting]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47783]]></requisitionid>
    <referencenumber><![CDATA[R47783]]></referencenumber>
    <apijobid><![CDATA[r47783]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Clinical Data Management Tech Solutions]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47777]]></requisitionid>
    <referencenumber><![CDATA[R47777]]></referencenumber>
    <apijobid><![CDATA[r47777]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47777/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>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, AI Agents and Workflow, you will play a hands-on role in building and deploying LLM-powered automation solutions that transform clinical data operations. You will work closely with cross-functional teams to deliver reliable, scalable AI-driven workflows that improve efficiency, reduce manual effort, and enhance data quality across the clinical trial lifecycle.</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>Designing and developing AI agent-based automation solutions across Clinical Data Management operations</p></li><li><p>Building and deploying LLM-powered agents to automate workflows in data ingestion, quality management, reporting, and study operations</p></li><li><p>Developing and maintaining automation solutions for complex clinical processes such as query generation, reconciliation, deviation detection, and data review workflows</p></li><li><p>Supporting regulatory and inspection readiness by automating documentation, audit trails, and data validation processes</p></li><li><p>Building scalable data ingestion and transformation pipelines to process data from EDC systems and external vendors</p></li><li><p>Developing machine learning models for anomaly detection, predictive analytics, and data quality monitoring</p></li><li><p>Implementing data reconciliation and validation frameworks across multiple clinical data sources</p></li><li><p>Working closely with IT and platform teams to integrate AI solutions into existing clinical systems and data platforms</p></li><li><p>Supporting AI governance activities including validation, auditability, and compliance with regulatory standards</p></li><li><p>Contributing to team enablement by sharing knowledge, supporting AI adoption, and developing best practices</p></li></ul><p><strong>This job may be for you if you have:</strong></p><ul><li><p>Strong hands-on experience in AI/ML, large language models (LLMs), and workflow automation</p></li><li><p>Experience working with LLM tools, APIs, or agent frameworks such as OpenAI, Anthropic, or similar technologies</p></li><li><p>Good understanding of clinical data management, EDC systems, and clinical trial workflows</p></li><li><p>Familiarity with CDISC standards (SDTM, CDASH) and regulatory requirements in a GxP environment</p></li><li><p>Strong programming skills in Python and SQL, with experience in data pipelines and automation</p></li><li><p>Experience with machine learning concepts such as anomaly detection and predictive modeling</p></li><li><p>Strong problem-solving, collaboration, and communication skills</p></li><li><p>Ability to work in a cross-functional environment and support technical delivery</p></li></ul><p><strong>To be considered for this role, you must have:</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>7–9+ years of experience in AI/ML, data science, or related domains</p></li><li><p>Experience building or deploying AI or LLM-based solutions (preferably in a regulated environment)</p></li><li><p>Exposure to clinical data, healthcare, or life sciences domain is 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[グローバル展開]]></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 Compliance]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コーポレートファンクション]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Associate Scientist - Protein Expression Science]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47298]]></requisitionid>
    <referencenumber><![CDATA[R47298]]></referencenumber>
    <apijobid><![CDATA[r47298]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47298/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>We are looking for an <strong>Associate Scientist</strong> to join the B cell Isolation Group in the Protein Expression Sciences department. You will be primarily responsible for the preparation and immunofluorescence staining of mouse splenocytes for the isolation of antibody expressing cells through <strong>fluorescence activated cell sorting</strong> (FACS). You will be working in the B Cell Isolation group, which is key to the Regeneron therapeutic pipeline. Through this platform, you will get exposure to different targets, giving you the opportunity to see a wide range of therapeutic focus areas. This is a lab-based role, with great opportunity to perform cutting-edge research, and great potential for growth.</p><p><strong>Responsibilities during a typical day might include the following:</strong></p><ul><li>Laboratory animal handling (mice) – splenectomy, lymphadenectomy, hind limb removal, post-mortem bleed collection</li><li>Single cell suspension preparation from organs (mouse spleen, lymph nodes, bone marrow)</li><li>Immunofluorescence cell staining</li><li>Analyzing flow cytometry data from stained samples</li><li>Isolating target cells through fluorescence activated cell sorting (FACS)</li><li>Immunofluorescence beads based binding affinity assay</li><li>Documentation of experimental procedures and results</li><li>Recording and organizing data in electronic notebook/database, Powerpoint and LIMS</li><li>Analyze data using tools such as <strong>FlowJo, Omiq, Microsoft Office, MacOS, and GraphPad Prism</strong></li><li>Periodic data presentation</li><li>Lab preparation, organization and resource acquisition</li><li>Collaborating and coordinating workflow intra and interdepartmentally to keep antibody discovery pipeline on track</li></ul><p><strong>This role may be for you, if you: </strong></p><ul><li>Enjoy working in a collaborative and fast paced environment</li><li>Have a strong desire to develop your skills</li><li>Excel at maintaining experimental documentation, exhibit meticulous attention to detail</li><li>Have great oral and written communication skills, organizational skills, as well as good interpersonal skills</li><li>Are comfortable working in a dynamic environment where priorities can change from day to day</li><li>Self-starter with an ability to follow protocols, ask scientific questions, and adapt to evolving methods</li><li>Have an eye for detail and pride yourself on the quality of your work</li><li>Work on current problems while thinking of future solutions</li></ul><p>To be considered for this role, you must have a minimum of B.S. in Molecular Biology, Cellular Biology or related field with 2+ years of laboratory experience. We would like someone with cellular biology lab experience, and <strong>basic laboratory animal handling experiences (mice</strong>). Experiences with immunofluorescence-based techniques, immunofluorescence cell staining, and knowledge of immunology are preferred. Experience with flow cytometry 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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Regional Tumor Lead Marketing Oncology Lung]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48209]]></requisitionid>
    <referencenumber><![CDATA[R48209]]></referencenumber>
    <apijobid><![CDATA[r48209]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48209/regional-tumor-lead-marketing-oncology-lung/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Lung to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><p><br><strong>A Typical Day:</strong><br> </p><p>Leading country insight collection and prioritization to inform global brand strategy<br><br>Ensuring alignment of local priorities with global strategic direction<br><br>Developing the regional tactical plan, including budget alignment<br><br>Facilitating regional tumor marketing meetings to drive execution against plan<br><br>Reviewing country brand plans and sharing insights to improve execution quality<br><br>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes<br><br>Driving regional launch planning and optimization, supporting excellence in country</p><p><br><strong>This Role May Be For You, if you are:</strong></p><p><br>Energized by working with, leveraging and developing talents in countries<br><br>Enjoy connecting global strategy with local market realities<br><br>Comfortable prioritizing across countries and balancing trade-offs<br><br>Energized by guiding brand planning and execution at regional level<br><br>Enjoys shaping content strategies across multiple markets<br><br>Confident leading discussions and aligning diverse stakeholders<br><br>Motivated by improving execution through insights and performance data<br><br>Open to regular travel and engaging with teams across geographies<br><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>84,675 € - 167,125 €</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 05:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Oncology Lung]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48210]]></requisitionid>
    <referencenumber><![CDATA[R48210]]></referencenumber>
    <apijobid><![CDATA[r48210]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48210/regional-tumor-lead-marketing-oncology-lung/]]></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 Regional Tumor Lead Marketing Lung to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><p><br><strong>A Typical Day:</strong><br> </p><p>Leading country insight collection and prioritization to inform global brand strategy<br><br>Ensuring alignment of local priorities with global strategic direction<br><br>Developing the regional tactical plan, including budget alignment<br><br>Facilitating regional tumor marketing meetings to drive execution against plan<br><br>Reviewing country brand plans and sharing insights to improve execution quality<br><br>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes<br><br>Driving regional launch planning and optimization, supporting excellence in country</p><p><br><strong>This Role May Be For You, if you are:</strong></p><p><br>Energized by working with, leveraging and developing talents in countries<br><br>Enjoy connecting global strategy with local market realities<br><br>Comfortable prioritizing across countries and balancing trade-offs<br><br>Energized by guiding brand planning and execution at regional level<br><br>Enjoys shaping content strategies across multiple markets<br><br>Confident leading discussions and aligning diverse stakeholders<br><br>Motivated by improving execution through insights and performance data<br><br>Open to regular travel and engaging with teams across geographies<br><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>106,875 € - 208,750 €</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 05:26:09 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Senior Clinical Pharmacologist]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47549]]></requisitionid>
    <referencenumber><![CDATA[R47549]]></referencenumber>
    <apijobid><![CDATA[r47549]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47549/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>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>A day in the life may look like:</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>Works (or collaborates with Research Specialist or Programming team) to prepare TFLs to support IND/CTA, PK WSs, Tox WS, Pharm WS, CSRs, DSURs, IB and other documents.</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, QC 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 may be the right role for you if you:</strong></p><ul><li><p>Are able to serve independently as study CP/QP/PPKPD lead for moderately complex</p></li><li><p>Studies or support study CP/QP/PPKPD lead for more complex studies, and to contribute to or lead non-project objectives.</p></li><li><p>Are 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><li><p>Beginning to establish own research areas within development sciences.</p></li></ul><p><strong>To be considered for this role you must have:</strong></p><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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 20:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Oncology Skin]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48206]]></requisitionid>
    <referencenumber><![CDATA[R48206]]></referencenumber>
    <apijobid><![CDATA[r48206]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48206/regional-tumor-lead-marketing-oncology-skin/]]></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 Regional Tumor Lead Marketing Skin to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br><strong>A Typical Day:</strong></p><ul><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><br><strong>This Role May Be For You, if you are:</strong></p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</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[Mon, 15 Jun 2026 04:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Hematology]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48215]]></requisitionid>
    <referencenumber><![CDATA[R48215]]></referencenumber>
    <apijobid><![CDATA[r48215]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48215/regional-tumor-lead-marketing-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Hematology to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br><strong>A Typical Day:</strong></p><ul><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><br><br><strong>This Role May Be For You, if you are:</strong></p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in hematology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</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[Mon, 15 Jun 2026 04:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician, Monday-Friday 1st Shift]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47634]]></requisitionid>
    <referencenumber><![CDATA[R47634]]></referencenumber>
    <apijobid><![CDATA[r47634]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47634/calibration-technician-monday-friday-1st-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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Calibration Technician</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>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></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>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><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 Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p><p>Calibration Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p><p>Calibration Technician IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</p><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><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><br><p><strong>Salary Range (hourly)</strong></p>$21.49 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp QC Analyst - Biochemistry (Gels/Separations)]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48429]]></requisitionid>
    <referencenumber><![CDATA[R48429]]></referencenumber>
    <apijobid><![CDATA[r48429]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48429/temp-qc-analyst-biochemistry-gelsseparations/]]></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 perform a wide variety of bioanalytical processes to support bulk drug substance manufacture in a cGMP regulatory environment.</div><div></div><div></div><div>This is 12 month contract position.</div><div></div></div><div><div><div><div><div><div><div><div><div><p><strong>As a QC Analyst - Biochemistry (Gels/Separations), a typical day might include, but is not limited to, the following:</strong> </p><ul><li><p>Ensuring that all work carried out is in compliance with current GMP, the required regulatory standards, conforms to company policies and standard operating procedures (SOPs)</p></li><li><p>Reviewing data from other analysts for accuracy and completeness</p></li><li><p>Performing review of test data on LIMS and Empower</p></li><li><p>Performing gels/separations assays (CE-SDS, iCIEF, PICO MCE) in compliance with cGMP practises</p></li><li><p>Performing data processing using Empower</p></li><li><p>Maintaining laboratory reagents and supplies</p></li><li><p>Preparing of reagent aliquots and buffers for use in assays</p></li><li><p>Maintaining of equipment in the laboratory</p></li><li><p>Conducting laboratory investigations and generates reports in response to invalid assays, Deviations, OOS/OOT</p></li><li><p>Initiating and completing CAPAs in accordance with site procedures</p></li><li><p>Writing new and updates current SOPs as needed</p></li><li><p>Presenting bioanalytical data reports clearly and concisely to management</p></li><li><p>Performing any other duties relevant to the QC laboratory position as required</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have excellent verbal and written communication skills</p></li><li><p>You have experience with electronic and systems such as Empower and LIMS</p></li><li><p>You have experience with performing and reviewing separations assays</p></li><li><p>You are adaptable and flexible individual, willing to travel when needed</p></li></ul><p>To be considered for this opportunity you should have a third level qualification (BSc degree or higher) in biology or related field or 2+ years relevant hands-on work experience working in a laboratory to cGMP regulatory guidelines within the biopharmaceutical industry.</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[産業オペレーションと製品供給]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Diagnostics]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45732]]></requisitionid>
    <referencenumber><![CDATA[R45732]]></referencenumber>
    <apijobid><![CDATA[r45732]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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>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>A typical day might include</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><li><p>Drive risk management and mitigation plans across technical, regulatory, operational, and commercial domains.</p></li><li><p>Partner with commercial and medical affairs to shape CDx launch readiness (access, coverage, distribution, training, KOL engagement).</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><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><li><p>Strong knowledge of global regulations (FDA CDRH, EU IVDR, PMDA) and pathways for CDx approval and labeling.</p></li><li><p>Excellent communication, leadership, and stakeholder management skills.</p></li><li><p>Strategic thinking with the ability to translate scientific and clinical needs into executable diagnostic solutions.</p></li><li><p>Program leadership, planning, and risk management across multiple, fast-paced workstreams.</p></li></ul><p><strong>To be considered for this position, you must have:</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></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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 19:26:08 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[R48082]]></requisitionid>
    <referencenumber><![CDATA[R48082]]></referencenumber>
    <apijobid><![CDATA[r48082]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 07:56:09 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Manager, Artificial Intelligence Data Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44147]]></requisitionid>
    <referencenumber><![CDATA[R44147]]></referencenumber>
    <apijobid><![CDATA[r44147]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44637]]></requisitionid>
    <referencenumber><![CDATA[R44637]]></referencenumber>
    <apijobid><![CDATA[r44637]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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>(1 of 2)</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[グローバル展開]]></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 Market Access DACH (f/m/d)]]></title>
    <date><![CDATA[Mon, 08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Supervisor, Vivarium Operations - Cage Wash]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45952]]></requisitionid>
    <referencenumber><![CDATA[R45952]]></referencenumber>
    <apijobid><![CDATA[r45952]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45952/supervisor-vivarium-operations-cage-wash/]]></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 Velocigene team is seeking a <strong>Cage Wash Supervisor </strong>to join their innovative and collaborative group. This position reports directly to the Cage Wash Manager. As Cage Wash Supervisor you will assist management in the daily operation of the Regeneron Vivarium’s cage wash and loading dock operations. Ensuring all caging and equipment are sanitized and processed according to regulatory standards and internal SOPs. This position is also responsible for the basic oversight and support of waste streams, supply receipt, inventory maintenance and multiple areas associate with dirty-side operations.</p><p>You will act as a liaison with animal care staff, management, EHS and Facilities to provide support and ensure all areas of the cage wash and loading dock are properly maintained and running smoothly.</p><p><strong>A Typical Day in the Role Might Look Like: </strong></p><ul><li>Oversee daily operations, including the processing of caging materials, autoclaving supplies, routine maintenance of machines and staff oversight.</li><li>Schedule, train, mentor, and evaluate cage wash personnel.</li><li>Perform daily quality assurance checks and document results. Able to address or report all deviations in a timely manner.</li><li>Assist management in creating weekly schedules and filling service requests. </li><li>Ensure adequate staffing and coverage for all shifts and assist when needed.</li><li>Understand and follow all policies and procedures to ensure compliance with state, local and federal agencies, including adherence to the “Guide for the Care and Use of Laboratory Animals”. </li><li>Working with internal Facilities Operations group to maintain facility, equipment and troubleshoot equipment malfunctions and alarms. </li><li>Monitor and maintain rack washers, robotic cage washing systems, bulk autoclaves, tabletop autoclaves, dump stations, water flush systems, chemical dispensing systems and other associated operational equipment.</li><li>Adherence to internal EHS guidelines and ability to readjust operations as guidelines evolve. </li><li>Order, receive and maintain inventory of supplies such as bedding, chemicals, PPE, caging, caging components, feed and enrichment.</li><li>Manage daily workflow of reusable PPE stocking, collection and laundry pickup. </li><li>Coordinate equipment repairs, including coordination with vendors. </li><li>Maintain areas as “inspection ready” at all times.</li><li>Operate under and enforces strict adherence to safety protocols, biosecurity measures, proper use of PPE and institutional SOPs to ensure safe a working environment at all times.</li><li>Maintain support areas such as, feed rooms, necropsy rooms, animal receiving rooms, chemical storage and supply storage rooms.</li></ul><p><strong>This Job Might Be for You If You: </strong></p><ul><li>Have an interest in science and enjoy hands-on work.</li><li>Thrive in a team environment, can collaborate effectively, and work independently when needed. </li><li>Have excellent verbal, written, time management, organizational and communication skills. </li><li>Have a strong attention to detail and can follow procedures accurately. </li><li>Are comfortable asking questions, providing feedback, and taking initiative. </li></ul><p>A High School Diploma or equivalent technical certification is required. Two or more years of experience operating in a lead role in a cage wash environment. AALAS certification at the ALAT level, or equivalent years of working experience. Strong understand of sanitation procedures and the use of traditional cleaning chemicals typically used in a cage wash setting. Strong leadership, communication and problem-solving abilities. Basic ability to use Outlook, email, PowerPoint, Excel, Microsoft Word, and internal IT applications. The ability to stand for long periods of time, perform repetitive motions, work around chemicals and operate in an environment that may get wet, have elevated temperature and mechanical noise. Perform physical duties such as breaking down pallets, disassembling caging and equipment, processing bulk supplies and moving large drums of chemicals. Operation of a forklift, electric pallet jack, bulk bedding hoist and other associated equipment necessary to maintain operations.</p><p><strong>Work Environment: </strong></p><p>This position involves physical demands, including but not limited to:</p><ul><li>Lifting up to 50 lbs., bending, pushing, pulling, and moving supplies and equipment.</li><li>Extended periods of walking and standing.</li><li>Use of Personal Protective Equipment (PPE).</li><li>Working in environments with potential noise, increased temperature, wet surfaces and allergens.</li></ul><p>Reasonable accommodations will be made for individuals with disabilities to perform essential job functions.</p><p><strong>Weekend and Holiday Requirements:</strong></p><p>This role is classified as essential personnel, meaning weekend and holiday work may be 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>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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[Scientist,  CRISPR Screening & Target Identification]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46074]]></requisitionid>
    <referencenumber><![CDATA[R46074]]></referencenumber>
    <apijobid><![CDATA[r46074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46074/scientist-crispr-screening-target-identification/]]></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 qualified scientist to join the Oncology & Immuno‑Oncology group. The successful candidate will support the identification and validation of novel tumor drug targets using in vitro and in vivo approaches. The ideal applicant is motivated, organized, detail‑oriented, and effective in a fast‑paced, team‑driven environment. Strong communication skills are essential. Experience with murine tumor models, mammalian cell culture, and molecular or cell‑based assays is highly desirable. Familiarity with CRISPR screening is a plus.</p><h3>As a Scientist, CRISPR, a typical day may include:</h3><ul><li><p>Perform vivo tumor experiments in mice, including injection, blood and tissue collection</p></li><li><p>Perform vitro cell culture and molecular biology experiments</p></li><li><p>Analyze and document data, and communicate results clearly and concisely to supervisor and peers</p></li><li><p>Organize and compile results into a finished format for presentation</p></li><li><p>Maintain precise lab notebooks</p></li><li><p>Daily lab maintenance (e.g., ordering reagents and supplies)</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><li></li></ul><p><strong>To be considered for this role, you must meet the following:</strong></p><ul><li><p>BS or MS with at least 3 years work experience.</p></li><li><p>Experience with mouse tumor models (e.g., subcutaneous implantation, drug dosing, measuring tumors and tumor harvest)</p></li><li><p>Experience with mammalian cell culture</p></li><li><p>Experience with basic molecular biology and biochemistry techniques (e.g., preparation of cell/tissue lysates for DNA/RNA protein analysis, western blots, transfection, PCR, and cloning)</p></li><li><p>Experience designing FACS panels, performing multi-color FACS analysis preferred but not required</p></li><li><p>Experience with CRISPR screens preferred but not required</p></li><li><p>Strong organization and communication skills</p></li><li><p>Strong ability to learn new techniques</p></li><li><p>Ability to work well in a team</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[研究と前臨床開発]]></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, Biostatistics - Immunology & Inflammation]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46192]]></requisitionid>
    <referencenumber><![CDATA[R46192]]></referencenumber>
    <apijobid><![CDATA[r46192]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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, Medical Information]]></title>
    <date><![CDATA[Mon, 08 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Specialist I - Pulmonology - Cincinnati, OH]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46417]]></requisitionid>
    <referencenumber><![CDATA[R46417]]></referencenumber>
    <apijobid><![CDATA[r46417]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46417/medical-specialist-i-pulmonology-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>Geography: Cincinnati, OH (Hillsboro, Chillicothe, Jackson)</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).<br> </p></li></ul><p><strong>This Position Might Be For You If</strong><br> </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<br> </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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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 - Clinical Bioanalysis]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47363]]></requisitionid>
    <referencenumber><![CDATA[R47363]]></referencenumber>
    <apijobid><![CDATA[r47363]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47363/senior-scientist-clinical-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>Regeneron's Bioanalysis group, located in Tarrytown NY, is seeking a Sr Scientist (Principal Investigator.)</p><p><strong>In this role a typical day might include the following:</strong></p><ul><li>Serves as PI for multiple clinical and/or nonclinical programs. Responsible for the oversight of all study-related activities, including protocol review, approval of the bioanalytical data, assessing the impact of any incurred deviations, accurate reporting of data in reports and submitting documentation for archival, as appropriate.</li><li>Responsible for coordinating run planning and resource allocation for multiple concurrent studies/programs. Provides scientific guidance to laboratory staff and makes scientific decisions regarding the data. Leads initiatives to troubleshoot assay performance and oversees investigations to evaluate the validity of results, as needed. Ensures the scientific quality of the data and regulatory compliance, as appropriate. Prepares data summaries, draws appropriate conclusions, and presents data in a logical manner to cross-functional Management</li><li>Communicate with internal and external collaborators, as needed. Ensures the timely delivery of bioanalytical data and reports to support internal milestones and regulatory filings (Pre-IPA, INDs, BLAs, etc.).</li><li>Actively participates in and presents work at sub-team/group meetings. Presents data at department meetings. Contributes to posters or manuscripts. Presents posters internally and may present posters at external conferences.</li><li>Ensure compliance, as appropriate, for all laboratory work and documentation in accordance with working practices, company SOPs, bioanalytical method procedures (BMPs), and regulations (e.g., GLP and GCP). Corresponds with the Quality Assurance Unit (QAU) regarding internal audits pertinent to the study.</li><li>May train on and execute bioanalytical methods to perform bioanalysis for clinical and nonclinical studies, as needed, for studies where they are not the assigned PI.</li><li>Provides cross-functional support to other teams or groups, as needed. Coordinates and performs method validation/qualification activities.</li><li>Ensures compliance, as appropriate, for all laboratory work and documentation in accordance with working practices, company SOPs, bioanalytical method procedures (BMPs), and regulations (e.g., GLP and GCP). Corresponds with the Quality Assurance Unit (QAU) regarding internal audits pertinent to the study.</li></ul><p><strong>This Role Might Be for You if You:</strong> </p><ul><li>Possess significant experience in ensuring the quality of documentation and data.</li><li>Are knowledgeable about immunology and have experience with bioanalysis assays such as ELISAs or MSD chemiluminescent assays.</li><li>Are a strong collaborator and communicator that can work cross-functionally to achieve group and departmental objectives.</li><li>Have experience working in a high performing team, and are capable of providing higher-level oversight, guidance, and leadership.</li><li>Anticipates and adapts to changing priorities and deliverables and initiates action with the appropriate parties, as needed.</li></ul><p><strong>To be considered for this position</strong>, you must have a BS or MS degree with 8+ years of relevant post-degree experience or a PhD with 0-3 years of relevant post-degree 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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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 Scientist - Genetic Medicines, In Vivo]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47944]]></requisitionid>
    <referencenumber><![CDATA[R47944]]></referencenumber>
    <apijobid><![CDATA[r47944]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47944/associate-scientist-genetic-medicines-in-vivo/]]></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 curious and motivated <strong>Associate Scientist </strong>to join our Regeneron Genetic Medicines group. You will be working on in vivo experiments to support groundbreaking pre-clinical gene therapy programs. </p><p><strong>As an Associate Scientist, a typical day might include:</strong></p><ul><li><p>Supporting in vivo experiments including injecting viral vectors and other compounds in mice, performing blood draws, and necropsies.</p></li><li><p>Processing various samples for downstream analysis.</p></li><li><p>Developing and optimizing in vivo techniques and translational assays to assess bio-distribution and efficacy of viral vectors in mice.</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You enjoy working with animals and are enthusiastic about translating research discoveries into therapeutic candidates. </p></li><li><p>You are meticulous, take excellent notes, and are comfortable communicating professionally with both junior and senior colleagues.</p></li><li><p>You enjoy working in a fast-paced, team environment, collaborating with others, and are comfortable with quickly shifting priorities.</p></li><li><p>You are looking for an opportunity to grow your career in the gene therapy space and be exposed to multiple technologies in discovery phase through to clinical development.</p></li></ul><p><strong>In order to be considered for this role, you must have:</strong></p><ul><li><p>A Bachelor Degree in a related field.</p></li><li><p>1+ of relevant work experience. Experience should include mouse handling, familiarity with various rodent injection and blood collection techniques, and experience with collection and preparation of multiple rodent tissue types for histological analysis.</p></li><li><p>Comfort asking questions, taking notes, and summarizing high-level takeaways is an advantage.</p></li><li><p>The ability to work on multiple projects at once.</p></li><li><p>Experience developing and optimizing protocols, assays, or SOPs is a distinct advantage.</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[研究と前臨床開発]]></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 - Bioinformatics]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47854]]></requisitionid>
    <referencenumber><![CDATA[R47854]]></referencenumber>
    <apijobid><![CDATA[r47854]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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, Ophthalmology Marketing]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48100]]></requisitionid>
    <referencenumber><![CDATA[R48100]]></referencenumber>
    <apijobid><![CDATA[r48100]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48100/manager-ophthalmology-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[<h3>Build our future together:</h3><p>The Marketing team is looking for a skilled marketing manager to help support the Ophthalmology portfolio. This role will be a key member of the Ophthalmology marketing team and will report to the Senior Director, Scientific Marketing.</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>When & where:</h3><p>Based in Sleepy Hollow, NY 4 days a week and travel approximately 10–15% domestically, including attendance at major ophthalmology congresses, regional speaker programs, and periodic field engagements with the sales team.</p><h3>Discover your role:</h3><ul><li>Implement tactical marketing campaigns and promotional programs for ophthalmology products, managing day-to-day project workflows from creative briefing, including Needs Assessment Forms (NAF), through medical, legal, regulatory (MLR) approval to final deployment across field and digital channels.</li><li>Develop, update, and manage field-facing promotional materials including speaker program presentations and training material and messaging guides, ensuring all content is aligned with the current approved brand narrative.</li><li>Coordinate the end-to-end MLR review process for all assigned promotional materials, serving as the primary point of contact with Medical Affairs, Legal, and Compliance reviewers to facilitate timely approvals and resolve feedback efficiently.</li><li>Support the planning and on-site logistics for customer engagement activities including regional speaker programs, educational events, and congress-related activations at meetings such as AAO and ASRS.</li><li>Manage day-to-day agency and vendor workflows, including briefing creative teams on project requirements, tracking deliverables against timelines, reviewing work product for quality, and reconciling project-level budgets.</li><li>Collaborate with the marketing team (HCP & Customer Engagement) to ensure all promotional material is aligned, optimized, and works in harmony with complimentary material.</li><li>Ensure compliance with federal, state, and local laws, industry regulations, and company guidelines within all areas of responsibility at all times.</li></ul><h3>This role requires:</h3><ul><li>A bachelor’s degree in Marketing, Business Administration, Life Sciences, Communications, or a related field; an MBA or advanced scientific degree is a plus but not required.</li><li>A minimum of 3–5 years of commercial marketing experience within the pharmaceutical, biotechnology, or medical device industry, with at least 2 years focused on HCP marketing for a specialty or biologic brand.</li><li>Experience in ophthalmology, retina, or a related specialty injectable therapeutic area is preferred; familiarity with anti-VEGF therapies and the retinal disease treatment landscape is a distinct advantage.</li><li>Proven ability to develop promotional materials from concept through MLR approval, including a working understanding of pharmaceutical regulatory requirements and promotional compliance guidelines.</li><li>Strong written and verbal communication skills, with the ability to distill complex clinical information into clear, persuasive marketing messages for both internal and external audiences.</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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Senior Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47333]]></requisitionid>
    <referencenumber><![CDATA[R47333]]></referencenumber>
    <apijobid><![CDATA[r47333]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47333/senior-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>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, Uxbridge, UK</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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Pulmonology - Grand Rapids, MI]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46983]]></requisitionid>
    <referencenumber><![CDATA[R46983]]></referencenumber>
    <apijobid><![CDATA[r46983]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46983/medical-specialist-i-pulmonology-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[<p><strong>Geography: Grand Rapids, MI</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).<br> </p></li></ul><p><strong>This Position Might Be For You If</strong><br> </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<br> </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[コマーシャル]]></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[Senior Specialist – Data Lake Operations]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48284]]></requisitionid>
    <referencenumber><![CDATA[R48284]]></referencenumber>
    <apijobid><![CDATA[r48284]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 06:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 28 May 2026 23:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Medical Account Specialist II -  NEUROLOGY - BIRMINGHAM, AL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48045]]></requisitionid>
    <referencenumber><![CDATA[R48045]]></referencenumber>
    <apijobid><![CDATA[r48045]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48045/medical-account-specialist-ii-neurology-birmingham-al/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Birmingham]]></city>
    <state><![CDATA[Alabama]]></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: Birmingham (Metro), AL</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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[Manager, Development Program Management]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44512]]></requisitionid>
    <referencenumber><![CDATA[R44512]]></referencenumber>
    <apijobid><![CDATA[r44512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r44512/manager-development-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>With guidance, this role M<strong>anager, Development Program Management </strong>uses program management knowledge and experience in the drug development industry to provide operational leadership and manage components of development program(s). This individual contributes to the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and track the execution of these plans from preclinical through commercialization/lifecycle management. </p><p><em>***Note this role is expected to be onsite 4 days per week with 1 day from home either to be based in Warren, NJ or Tarrytown, NY and is not eligible remote. </em></p><p><strong>As a Manager, a typical day may include: </strong></p><ul><li><strong>Development Teams: </strong>Under the direction of their manager or DPM Lead, supports select subteam and/or functional area meetings. May lead functional area and/or working group meetings. Participates in development of risk management plans. Tracks deliverables, risks, and issues.</li><li><strong>Business Acumen: </strong> Under direction of their manager or DPM Lead, Identifies stakeholders across organization to facilitate cross functional reviews/alignments of key documents. Manages project management planning systems (MS Project, SharePoint) for assigned programs/projects. Uses systems and tools to move the program and business forward. </li><li><strong>Communication: </strong>Facilitates collaboration on selected assignments between functional areas to ensure effective, accurate, and timely scientific/technical and program-related communication. Keeps manager and other stakeholders informed to ensure alignment of key decisions/actions items of the assigned projects. Escalates issues/risks to appropriate stakeholders in a timely manner. </li><li><strong>Problem Solving: </strong>Supports the team and lead DPM in gathering information relevant to issues and formulating solutions to issues encountered during project implementation. With direction, supports development of processes and tools to document issues and their resolution. Escalates complex problems or issues to lead DPM in a timely and appropriate manner </li><li><strong>Leadership:</strong> Influences within workstream and/or sub-sets of project team. Builds relationships and effectively collaborates with department and cross-functional colleagues. Seeks out support for resolution of conflicts.</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Are action oriented and organized</li><li>Intellectually curious</li><li>Comfortable dealing with ambiguity</li><li>Demonstrate good judgement</li><li>Think critically</li><li>Communicate and collaborate well</li><li>Are a team player </li><li>Regularly demonstrate professional maturity, and take setbacks and constructive criticism well.</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelor's degree is required and 5+ years of relevant project management experience, preferably in the drug development/pharmaceutical industry.</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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 12:26:09 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Regional Tumor Lead Marketing Oncology Lung]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48208]]></requisitionid>
    <referencenumber><![CDATA[R48208]]></referencenumber>
    <apijobid><![CDATA[r48208]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48208/regional-tumor-lead-marketing-oncology-lung/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Lung to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><p><br><strong>A Typical Day:</strong><br> </p><p>Leading country insight collection and prioritization to inform global brand strategy<br><br>Ensuring alignment of local priorities with global strategic direction<br><br>Developing the regional tactical plan, including budget alignment<br><br>Facilitating regional tumor marketing meetings to drive execution against plan<br><br>Reviewing country brand plans and sharing insights to improve execution quality<br><br>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes<br><br>Driving regional launch planning and optimization, supporting excellence in country</p><p><br><strong>This Role May Be For You, if you are:</strong></p><p><br>Energized by working with, leveraging and developing talents in countries<br><br>Enjoy connecting global strategy with local market realities<br><br>Comfortable prioritizing across countries and balancing trade-offs<br><br>Energized by guiding brand planning and execution at regional level<br><br>Enjoys shaping content strategies across multiple markets<br><br>Confident leading discussions and aligning diverse stakeholders<br><br>Motivated by improving execution through insights and performance data<br><br>Open to regular travel and engaging with teams across geographies<br><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>79,800 € - 156,375 €</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 05:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Hematology]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48213]]></requisitionid>
    <referencenumber><![CDATA[R48213]]></referencenumber>
    <apijobid><![CDATA[r48213]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48213/regional-tumor-lead-marketing-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Hematology to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br>A Typical Day:</p><ul><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><br><br>This Role May Be For You, if you are:</p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in hematology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</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[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 04:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Warehouse Associate]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45739]]></requisitionid>
    <referencenumber><![CDATA[R45739]]></referencenumber>
    <apijobid><![CDATA[r45739]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 LCoE Training Operations]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47647]]></requisitionid>
    <referencenumber><![CDATA[R47647]]></referencenumber>
    <apijobid><![CDATA[r47647]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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 Director, Global Data Protection & AI Security]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47426]]></requisitionid>
    <referencenumber><![CDATA[R47426]]></referencenumber>
    <apijobid><![CDATA[r47426]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47426/senior-director-global-data-protection-ai-security/]]></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 are building a dedicated Data Protection function to safeguard the intellectual property, patient data, genomic assets, and proprietary information that underpin our $15B+ revenue pipeline and increasingly global operations. As Regeneron has expanded its commercial, research, and manufacturing presence across Europe, the Asia-Pacific region, and beyond, the regulatory surface for data storage, use, and movement has grown materially. Concurrent growth in data sovereignty requirements, insider risk exposure, and AI-driven data workflows has created an inflection point that demands a dedicated, strategically led function.</p><p>The Sr. Director of Global Data Protection and AI Security serves as the Global Data Protection Lead and is accountable for the strategy, architecture, and execution of Regeneron’s enterprise data protection program. This leader drives concepts, techniques, and standards across Data Security Posture Management (DSPM), Data Loss Prevention, Insider Risk, and data classification, working without appreciable direction to identify and evaluate fundamental issues and provide strategy and direction for this major functional area. This role reports directly to the VP & CISO and serves as the principal spokesperson for data protection on highly significant matters, interacting internally and externally with senior management and functional heads.</p><p>This is an on-site position 4 days/week primarily based at our Sleepy Hollow, NY or Warren, NJ office. If eligible, we can offer relocation benefits; we cannot offer a fully remote option.</p><p><strong>A typical day in this role looks like: </strong></p><ul><li>Determine organizational structures and allocate subordinate management responsibilities across the Global Data Protection function, including DS Consulting, Auto-Classification, Application and API Data Protection, Trusted Share/Data Mover, and DLP Monitoring sub-functions.</li><li>Develop and execute a multi-year data protection strategy aligned to Regeneron’s business strategies and the company’s goals, including a phased roadmap for DSPM coverage expansion, DLP maturity, and insider risk program buildout.</li><li>Serve as a member of, or key advisor to, the Enterprise Data & AI governance council on matters of data protection, privacy security, and AI data risk.</li><li>Develop objectives for the function and monitor performance against goals across all sub-functions, ensuring schedules and performance requirements are met.</li><li>Own the enterprise Data Security Posture Management (DSPM) strategy and program, overseeing the discovery, classification, and risk assessment of Regeneron’s 112+ PB data estate across on-premises, cloud (AWS, Snowflake, Databricks/Unity Catalog), and SaaS environments.</li><li>Direct the phased expansion of Varonis coverage from current M365/O365 scope to Isilon NAS, cloud/IaaS, and additional SaaS platforms in alignment with the Secure Enterprise Data Fabric program roadmap.</li><li>Provide strategy and direction for the full lifecycle of data protection controls spanning data in motion, data at rest, and data in use, across endpoint, cloud, email, and network channels.</li><li>Oversee the development, deployment, and continuous tuning of DLP policies leveraging Microsoft Purview, Zscaler, Varonis, and complementary CASB/SASE capabilities.</li><li>Own the enterprise Insider Risk program strategy, establishing a cross-functional program structure that integrates Human Resources, Legal, Corporate Security, and Security Operations capabilities under a unified operating model.</li><li>Develop and mature the behavioral analytics and detection capability for intentional and accidental data misuse, leveraging Splunk UBA and DLP telemetry to identify anomalous data access, movement, and exfiltration patterns.</li><li>Establish case management, investigation, and escalation protocols for insider risk incidents, ensuring appropriate coordination with HR, Legal, and Corporate Security while preserving investigative integrity and chain of custody.</li><li>Interact regularly with senior management across functional areas to align data protection priorities with business strategies, including IOPS, Research, Commercial, and GCC India leadership.</li><li>Develop and maintain audit-ready documentation, operational metrics, and program reporting for the CISO, Audit Committee, and external regulators.</li><li>Engage external partners, managed security service providers, and industry peers to benchmark program maturity and import current-state threat intelligence relevant to pharmaceutical data protection.</li></ul><p><strong>This role might be for you if: </strong></p><ul><li>Hands-on experience auditing AI/ML systems, Leads data protection-by-design across AI and agentic AI systems — covering model training data governance, input/output monitoring, data residency enforcement, and access controls in multi-agent environments.</li><li>Experience in pharmaceutical, biotechnology, or life sciences environments with direct exposure to GxP data integrity requirements, clinical trial data protection, or manufacturing IP security.</li><li>Familiarity with Databricks Unity Catalog, Snowflake, or AWS data lake security architectures as they relate to DSPM and access governance.</li><li>Experience operating or advising on AI data security considerations, including LLM training data governance, model output handling, and AI-specific insider risk vectors.</li><li>Working knowledge of data catalog and metadata governance platforms (Collibra, Privacera) and their role in enforcing data protection policies.</li><li>Relevant certifications: CISSP, CIPP/E, CIPP/US, CDPSE, CIPM, CISM, or equivalent.</li></ul><p><strong>This role requires</strong></p><ul><li>Bachelor’s degree in Information Technology, Computer Science, Cybersecurity, Information Management, or a related field required. An advanced degree (MS, MBA, or equivalent) is preferred. </li><li>15+ years of progressive experience in information security or data protection, with demonstrated depth in DSPM, DLP, and insider risk disciplines.</li><li>5+ years in a leadership role with responsibility for a recognized security or data protection function, including people management at the Director or Senior Manager level.</li><li>3+ years of hands-on experience with enterprise DSPM or DLP platforms in a complex, multi-cloud environment.</li><li>Demonstrated experience leading cross-functional programs involving HR, Legal, Privacy, and Security stakeholders.</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[コーポレートファンクション]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 I - Analytics Automation Development]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47917]]></requisitionid>
    <referencenumber><![CDATA[R47917]]></referencenumber>
    <apijobid><![CDATA[r47917]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47917/process-development-engineer-i-analytics-automation-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 and Process Development (PMPD) department is seeking an energetic Process Development Engineer I, supporting research and development efforts. In this exciting role, you will be executing experiments with minimal supervision and have a good understanding of core laboratory techniques (e.g., pipetting). Responsibilities include developing and validating automated methods for platform analytical assays, routine sample characterization, as well as planning, programming, and maintaining automated systems in a fast-paced, collaborative environment, with opportunities to contribute to additive manufacturing and data automation initiatives.</p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li>Develop, implement, and troubleshoot automated workflows on automated systems including Hamilton Robotics, Biosero, and HighRes.</li><li>Increase efficiency and throughput while improving data quality through process and tooling innovations.</li><li>Provide hands-on support for operation, troubleshooting, and maintenance of automated systems and peripheral devices.</li><li>Evaluate and recommend new technologies; assess their impact on existing workflows.</li><li>Contribute to programming projects that support automated data initiatives.</li><li>Ensure GLP-compliant work and documentation for automated assay verification; maintain a clean, safe, and compliant laboratory.</li><li>Self-starter that is highly organized and a good problem solver with technical, detail-oriented mindset.</li><li>Strong analytical and written/oral communication skills. Team-oriented and experienced in working in a diverse and multicultural environment.</li></ul><h3><strong>This Role Might Be For You If You Are:</strong></h3><ul><li>A self-starter, highly organized and problem solver with technical,</li><li>Possess a detail-oriented mindset.</li><li>Strong in analytical and written/oral communication skills.</li><li>Team-oriented and experienced in working in a diverse and multicultural environment.</li></ul><p>This role requires a BS in Engineering discipline with 3+ years of experience or a MS with 0-3 years. A successful candidate has strong lab automation experience, including programming liquid handlers (e.g., Hamilton) and integrating work cells with scheduling software (e.g., Green Button Go, Cellario). Experience with developing and validating automated methods for platform analytical assays, routine sample characterization, as well as planning, programming, and maintaining automated systems is highly 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>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Medical Specialist I (Gastro)- Long Island, Brooklyn, Queens, and Staten Island]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48134]]></requisitionid>
    <referencenumber><![CDATA[R48134]]></referencenumber>
    <apijobid><![CDATA[r48134]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48134/medical-specialist-i-gastro-long-island-brooklyn-queens-and-staten-island/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Brooklyn]]></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 Medical Specialist (Sales Representative), Gastroenterology (MS) will report to the District Manager, Gastroenterology, and be responsible for engaging adult and pediatric 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>Long Island, Brooklyn, Queens, and Staten Island</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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Drug Production, Associate Manufacturing Specialist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46369]]></requisitionid>
    <referencenumber><![CDATA[R46369]]></referencenumber>
    <apijobid><![CDATA[r46369]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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 Drug Production, Associate Manufacturing Specialist in the Global Manufacturing department. 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>A typical day for a Drug Production, Associate Manufacturing Specialist might include:</p><ul><li><p>Performing all aspects 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></ul><p>This role might be for you if you:</p><ul><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>Value trust and transparency in everyday work</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><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>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>Shift & Physical Requirements</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>To enable a healthy work life balance we offer multiple shifts that are 4 working days (10 hours) to support 24/7 production.</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>To be considered for this role you must meet the below minimum education and experience requirements:</p><p>Drug Production, Associate Manufacturing Specialist:</p><ul><li><p>HS diploma + 4 years of relevant work experience <strong>or</strong></p></li><li><p>AS, BS or BA in Life Sciences or related field</p></li></ul><p>Regeneron offers an exciting and competitive benefits package! For details check out: <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</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[産業オペレーションと製品供給]]></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[Medical Director, Clinical Sciences]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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>Supporting the clinical components of assigned clinical development programs (CDPs) in Japan.</li><li>Providing clinical and scientific input for regulatory documents, including J-NDA/J-CTD submissions.</li><li>Contributing to the development and adaptation of clinical trial protocols and related documentation for Japan-specific needs.</li><li>Collaborating with cross-functional teams to ensure clinical feasibility and address local medical needs in global studies.</li><li>Participating in investigator meetings, site initiation visits, and vendor kick-off meetings to drive study execution.</li><li>Offering medical/scientific input to resolve issues during study conduct and execution.</li><li>Staying current on scientific advancements in therapeutic areas and representing the company at national and international conferences.</li><li>Building and maintaining relationships with key opinion leaders (KOLs) and investigator sites.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You have a strong understanding of the drug development process, clinical trial design, and good clinical practice (GCP).</li><li>You excel in both Japanese and English, with business-level proficiency in English communication.</li><li>You enjoy collaborating across cross-functional teams, bringing diplomacy and influence to your interactions.</li><li>You are detail-oriented and possess exceptional analytical and problem-solving skills.</li><li>You thrive in dynamic environments and are adept at managing regulatory interactions effectively.</li><li>You value diversity, different perspectives, and are committed to fostering inclusive teamwork.</li></ul><p><strong>To Be Considered:</strong></p><p>We are looking for candidates with the following qualifications:</p><ul><li><strong>Required:</strong> MD or MD/PhD with at least 5 years of pharmaceutical industry experience, including 3 years of clinical development experience.</li><li>Expertise in regulatory filings and clinical document preparation, particularly CTN and J-NDA/J-CTD submissions.</li><li>Proven ability in protocol design, clinical data review, and familiarity with medical monitoring activities.</li><li>Strong knowledge of Phase I–III clinical trial design and objectives.</li><li><strong>Preferred:</strong> Experience with clinical feasibility assessments and Japan-specific enrollment considerations.</li></ul><p>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[グローバル展開]]></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 Manager, Commercialization]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47655]]></requisitionid>
    <referencenumber><![CDATA[R47655]]></referencenumber>
    <apijobid><![CDATA[r47655]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47655/associate-manager-commercialization/]]></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>勤務地:</strong> 東京, 日本</h3><br><h3>私たちRegeneronは、革新を通じて人々の生活を向上させることに取り組む、世界をリードするバイオテクノロジー企業です。このたび、日本のイミュノロジー事業にてコマーシャライゼーション アソシエイトマネージャーを募集いたします。このポジションでは、皮膚科、呼吸器科、耳鼻咽喉科の治療分野におけるコマーシャライゼーション戦略の策定と実行において重要な役割を果たします。クロスファンクショナルチームや社内外の関係者と協力し、効果的な販売促進を推進いただきます。成長を続けるダイナミックな組織で、インパクトのある影響を与えるポジションとなります。</h3><br><h3><strong>1日の業務の流れ:</strong></h3><ul><li><h3>営業チームと連携し、パフォーマンス向上のためのツールや情報を提供します。</h3></li><li><h3>クロスファンクショナルチームと協力して、地域商業化戦略を実施します。</h3></li><li><h3>主要業績評価指標（KPI）のモニタリングや追跡を行い、戦術の成功を確実にします。</h3></li><li><h3>地域市場向けにカスタマイズされたマーケティングおよび販売支援資料の作成に貢献します。</h3></li><li><h3>戦術計画の実施をサポートし、地域およびグローバル戦略と整合性を持たせます。</h3></li><li><h3>イミュノロジー事業部の営業活動で必要なツールを管理します。</h3></li><li><h3>ベンダーのオンボーディング、契約の維持管理、その他の運用タスクを監督します。</h3></li><li><h3>地域市場の開発や商業活動に対して高品質なインプットを提供します。</h3></li></ul><br><h3><strong>このポジションに適している方:</strong></h3><ul><li><h3><strong>スピード感のある製品ローンチ環境</strong>で活躍し、多様なチームと協働することが好きな方。</h3></li><li><h3><strong>細部に注意を払う</strong>ことが得意で、プロジェクトやプロセスを効率的に管理できる方。</h3></li><li><h3><strong>強力なコミュニケーション能力</strong>を持ち、社内外のステークホルダーと効果的に関わることができる方。</h3></li><li><h3><strong>継続的な学びを大切にし</strong>、自己成長のための論理的な思考を持つ方。</h3></li><li><h3><strong>チームの成功に貢献すること</strong>や、生産的な職場関係を築くことを楽しめる方。</h3></li><li><h3><strong>イノベーションに情熱を持ち</strong>、製薬業界で変化をもたらしたいと考えている方。</h3></li></ul><br><h3><strong>応募資格:</strong></h3><h3>ビジネスまたはライフサイエンス分野の学位を持ち、<strong>5年以上の専門的な経験</strong>を積んだ方を求めています。</h3><h3>製薬/バイオテクノロジーのマーケティング、免疫学、バイオロジクス、またはスペシャルティケアの経験がある方は特に歓迎します。</h3><h3>また、共同プロモーションやアライアンス管理、製品ローンチの経験があればさらに有利です。</h3><h3>ビジネスレベル以上の日本語および初級レベルの英語力は必須です。</h3><br><h3><strong>日本の医療の未来を一緒に築きましょう。</strong> このエキサイティングな挑戦に挑む準備ができている方のご応募をお待ちしております。</h3><p>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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[Senior Manager, Global Development IT & Digital]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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><br><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><br><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><br><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><br><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><br><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><br><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>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コーポレートファンクション]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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 EDC Administration]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47770]]></requisitionid>
    <referencenumber><![CDATA[R47770]]></referencenumber>
    <apijobid><![CDATA[r47770]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Field Reimbursement Manager  - Neurology (Atlanta,GA)]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48131]]></requisitionid>
    <referencenumber><![CDATA[R48131]]></referencenumber>
    <apijobid><![CDATA[r48131]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48131/field-reimbursement-manager-neurology-atlanta-ga/]]></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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 13:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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 Field Medical Affairs Oncology - France]]></title>
    <date><![CDATA[Mon, 08 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lab Equipment Maintenance Technician (2nd Shift: 3:00PM-11:30PM)]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41868]]></requisitionid>
    <referencenumber><![CDATA[R41868]]></referencenumber>
    <apijobid><![CDATA[r41868]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r41868/lab-equipment-maintenance-technician-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>Regeneron is looking for an outstanding Lab Maintenance Technician to independently perform advanced preventative and corrective maintenance on critical laboratory and process utilities, including purified water, vacuum, compressed air, specialty gas, and washing systems. Acting as a senior technical resource, this role troubleshoots complex electromechanical and controls issues, drives continuous system reliability, and mentors junior technicians while upholding safety and regulatory standards.</p><p>The Lab Maintenance Technician will partner with facilities leadership, vendors, and research stakeholders to ensure uninterrupted operation of laboratory infrastructure, complete detailed work-order documentation in the CMMS, and provide rapid response to alarms and after-hours events.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Performing advanced preventative maintenance and corrective repairs on critical utilities (purified water, vacuum, compressed air, specialty gases, washers)</p></li><li><p>Independently troubleshooting electromechanical, PLC, VFD, and control-system faults using schematics, P&IDs, and technical manuals</p></li><li><p>Completing, closing, and properly documenting work orders in the CMMS while identifying recurring issues and recommending corrective actions</p></li><li><p>Being responsible for vendors and contractors during equipment installation, commissioning, and startup activities, verifying completion and compliance</p></li><li><p>Responding to BMS/environmental monitoring alarms, providing initial diagnosis, and restoring system functionality</p></li><li><p>Providing on-the-job mentorship to Technician 1/2 team members and coordinating daily priorities with Leads and Supervisors</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Enjoy solving complex technical problems and can work independently with minimal direction</p></li><li><p>Thrive in a fast-paced research environment where utility uptime is critical</p></li><li><p>Can read and interpret detailed engineering drawings, P&IDs, and control schematics with ease</p></li><li><p>Communicate clearly with scientists, vendors, and cross-functional teams, delivering excellent customer service</p></li><li><p>Take pride in maintaining meticulous documentation and promoting a strong safety culture</p></li><li><p>Are willing to participate in an on-call rotation and occasionally operate company vehicles for site support</p></li></ul><p><strong>In order to be considered for this role, you must have:</strong></p><ul><li><p>5–7 years of advanced maintenance experience in laboratory, pharmaceutical, or similar process environments. Trade school certificate is preferred</p></li><li><p>Demonstrated expertise with electromechanical systems, PLCs/VFDs, CMMS work-order management, and utility system troubleshooting</p></li><li><p>A valid driver’s license recognized by New York State</p></li></ul><div><div><div><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>$29.81 - $46.63]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コーポレートファンクション]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Manager Statistical Programming]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44717]]></requisitionid>
    <referencenumber><![CDATA[R44717]]></referencenumber>
    <apijobid><![CDATA[r44717]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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- 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 02:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Regional Tumor Lead Marketing Oncology Lung]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47470]]></requisitionid>
    <referencenumber><![CDATA[R47470]]></referencenumber>
    <apijobid><![CDATA[r47470]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47470/regional-tumor-lead-marketing-oncology-lung/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Lung to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><h3>A Typical Day:</h3><ul><li></li><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><h3>This Role May Be For You, if you are:</h3><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>101,500€ - 200,400€</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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 08:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Associate Manager, Statistical Genetics]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48436]]></requisitionid>
    <referencenumber><![CDATA[R48436]]></referencenumber>
    <apijobid><![CDATA[r48436]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48436/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 contribute to the analysis and interpretation of millions of genotyped and sequenced humans linked with rich phenotype data from around the world. You will leverage these data to gain new insights into disease mechanisms and generate new discoveries that enable Regeneron to create and deliver better medicines to patients in need. Within the broad domain of cardiovascular, metabolic disease, and skeletal diseases, you will work collaboratively with other specialists in genomic data analysis, translational genetics, functional biology, and medicine, to design, execute, and refine analyses that connect genetic variation to human health and disease. You will help develop and implement statistical and computational tools that will allow these analyses to be executed and interpreted at scale. </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 maintain and improve analytical workflows and implement analytical best practices.</p><p>· Integrate computational tools and diverse molecular data types to generate insights about human disease, interpret results, and prioritize candidate therapeutic targets.</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><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. 0-2+ years experience required; 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 modeling, 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[研究と前臨床開発]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[HCP Contract Specialist]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47844]]></requisitionid>
    <referencenumber><![CDATA[R47844]]></referencenumber>
    <apijobid><![CDATA[r47844]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47844/hcp-contract-specialist/]]></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 main responsibility of the <strong>HCP Contract Specialist</strong> is to collaborate closely with internal and external stakeholders to facilitate the efficient and timely progression of HCP consultancy agreements and providing oversight throughout lifecycle of the agreements.</p><p><strong>A typical day in this role loos like: </strong></p><ul><li>Acting as a delegate for the HCP contracting Sponsor, ensure that all business-facing and other process requirements / information is available and entered in the systems completely and in a timely manner to ensure efficient progression of all assigned HCP contracts</li><li>Diligently manage all HCP contracting tasks and activities assigned to the HCP Sponsor, ensuring their informed participation and involvement in decision-making throughout the process</li><li>Prepares Conflict of Interest (COI) Disclosure Form for distribution to each potential IDMC member, executes Confidentiality Disclosure Agreement (CDA), and facilitates review and execution of IDMC consulting agreements.</li><li>Independently manage assigned business functions, ensuring continuous and active engagement to proactively address the HCP contractual needs of Sponsor stakeholders</li><li>Cultivate and sustain strong business relationships with internal support functions engaged in the HCP contracting process to ensure contracts progress efficiently and timely to execution and ultimately through close-out (e.g., Clinical Study team, Commercial Operations HCP team, Finance, Corporate Compliance, Legal, etc.)</li><li>Identify opportunities for process improvement throughout the HCP contract lifecycle and develop effective business cases along with initial ideas for potential solutions</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelors degree and 2+ years of relevant industry related 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>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 14:56:09 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Senior Associate Scientist - Therapeutic Antibodies]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47670]]></requisitionid>
    <referencenumber><![CDATA[R47670]]></referencenumber>
    <apijobid><![CDATA[r47670]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47670/senior-associate-scientist-therapeutic-antibodies/]]></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 Late-stage ELISA Support (LES) group under the Pre-Clinical Antibody and Assay Development (PAAD) team executes potency assay development and analytical testing to support lead molecule development from Pre-IPA through BLA. The team develops fit‑for‑purpose assays, supports clinical and regulatory programs, and partners with internal drug development, manufacturing, and quality control stakeholders to enable drug substance (DS), drug product (DP) through stability and IV admixture testing, among other sample studies.</p><p><strong>Responsibilities during a typical day might include the following:</strong></p><ul><li>Perform potency testing of manufacturing, QC, and stability samples. </li><li>Design, develop, and optimize binding and blocking ELISAs to support potency testing of lead protein therapeutics across research and clinical programs.</li><li>Analyze and interpret data using GraphPad Prism and Excel; clearly summarize results for stakeholders.</li><li>Maintain accurate, thorough laboratory documentation and data records, performing internal QC checks for team members.</li><li>Prepare data summaries and presentations for internal reporting.</li><li>Communicate project status and results effectively in written and verbal formats.</li><li>Demonstrate strong attention to detail, as assays developed are used for clinical testing and regulatory documentation; prior experience in a GLP environment is a plus (role is non‑GLP).</li></ul><p><strong>This role may be for you, if you: </strong></p><ul><li>Bachelor’s or Master’s degree in a scientific discipline with typically 2+ years of relevant laboratory experience (Demonstrated expertise in ELISA‑based immunoassays is highly preferred)</li><li>Strong understanding of <strong>drug–ligand binding principles</strong>, with the ability to apply concepts to assay development and troubleshooting. This role is primarily lab-based.</li><li>Proficient in <strong>Excel and PowerPoint</strong> for data analysis and presentation; experience with <strong>GraphPad Prism</strong> preferred.</li><li>Proven ability to independently analyze, interpret, and summarize complex data with a high level of accuracy.</li><li>Exceptional <strong>attention to detail</strong>, recognizing that assays developed by our group support <strong>clinical testing and regulatory documentation</strong>.</li><li>Strong <strong>time‑management, organizational, and multitasking skills</strong>, with the ability to manage multiple projects in parallel.</li><li>Ability to work independently with minimal supervision, while contributing effectively in a <strong>collaborative, team‑oriented environment</strong>.</li><li>Strong written and verbal communication skills, including experience presenting data to cross‑functional stakeholders.</li><li>Prior experience working in a <strong>GLP or regulated laboratory environment</strong> is a plus, though the role itself is non‑GLP.</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[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Quantitative Pharmacology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45201]]></requisitionid>
    <referencenumber><![CDATA[R45201]]></referencenumber>
    <apijobid><![CDATA[r45201]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45201/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>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><p>· Manages and is accountable for the PK/PD evaluation of a small portfolio of products or projects.</p><p>· Works independently, with guidance in only the most complex situations.</p><p>· Informs PMx management of important program and regulatory developments in a timely manner.</p><p>· Ensures analyses and documentation are of the highest quality and accuracy.</p><p>· Ensures that reports and other documents have the appropriate messaging and that a meaningful “story-line” is developed.</p><p>· Ensures that study reports and other documents have an appropriate functional review and are suitable for review by senior management.</p><p>· Solves complex problems; takes a broad perspective to identify solutions.</p><p>· Has a strong publication record and actively publishes work in scientific literature</p><p>· Makes contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.</p><p>· Has excellent interpersonal and communication skills, both written and oral, and has ability to communicate complex information succinctly.</p><p><strong>This may be the right role for you if you:</strong></p><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><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><p>· Recognized as an expert in own area within the organization.</p><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><p>· Decisions are guided by policies, procedures and business plan; receives guidance from head of function.</p><p><strong>In order to be considered qualified for this role, </strong>you must have a PhD +8 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[研究と前臨床開発]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 - Allergy-ENT - Salt Lake City N, UT]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46245]]></requisitionid>
    <referencenumber><![CDATA[R46245]]></referencenumber>
    <apijobid><![CDATA[r46245]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46245/medical-specialist-i-allergy-ent-salt-lake-city-n-ut/]]></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: Salt Lake City North Allergy/ENT territory</strong></p><p>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists and Otolaryngologists 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>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology and ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/Otolaryngology 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 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 states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p><strong>Key Markets include: </strong>Bountiful, Farmington, Idaho Falls, Logan, Layton, Ogden, Park City, Pocatello, Salt Lake City, and West Valley City.</p><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 <strong>a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology and/or ENT market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. </strong>Allergy/Immunology/Otolaryngology experience preferred. We need someone with demonstrated 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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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, Autoimmune Diseases]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46984]]></requisitionid>
    <referencenumber><![CDATA[R46984]]></referencenumber>
    <apijobid><![CDATA[r46984]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46984/associate-scientist-autoimmune-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>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 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, 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>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, </strong>you should have a B.S. or M.S. degree in a relevant field with 0-2 years of experience in immunology or a related discipline. Relevant experience includes: </p><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><p>Experience in mouse handling is highly 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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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 - Bioanalytical & Biomarker Technologies]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46725]]></requisitionid>
    <referencenumber><![CDATA[R46725]]></referencenumber>
    <apijobid><![CDATA[r46725]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46725/senior-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 highly motivated bioanalytical scientist who can contribute to the development and implementation of state-of-the-art quantitative and qualitative analytical and bioanalytical methods to support biopharmaceuticals in discovery and preclinical development pipeline at Regeneron. The successful candidate need function well in a collaborative, fast-paced, multidisciplinary team environment.</p><p><strong>A Typical day in this role looks like:</strong></p><ul><li>Primarily responsible for developing LC‑MS–based bioanalytical methods in various biological matrices.</li><li>Apply these methods to quantify biotherapeutic levels, assess in vitro stability, evaluate in vivo biotransformation, and measure biomarkers (small molecules, peptides, and proteins).</li><li>Support characterization of drug candidates and critical reagents within the discovery pipeline.</li><li>Collaborate closely with chemistry, conjugation, biology, PK, and TK teams to ensure strong experimental design, accurate data interpretation, and informed decision‑making.</li><li>Contribute to advancing programs involving bioconjugates, oligonucleotides, bispecifics, and other therapeutic modalities.</li><li>Explore and evaluate innovative bioanalytical technologies and emerging platforms to support an evolving portfolio, including novel molecular modalities and therapeutic areas.</li><li>Document experiments, results, and findings in an electronic lab notebook.</li><li>Present scientific work at internal and external meetings.</li><li>Perform general lab and instrument maintenance.</li><li>Grow into the role of bioanalytical representative on cross‑functional project teams, effectively managing priorities to meet multiple project goals and timelines.</li></ul><p><strong>This role may be for you if you have experience:</strong></p><ul><li>Chemistry, Biochemistry, Pharmaceutical Science or a related discipline, B.S. with 10+ yrs, MS with 8+ yrs, or Ph.D. with 0-6 yrs postdoctoral experience.</li><li>Proven expertise and extensive experience in liquid chromatography and mass spectrometry is required, with demonstrated track record of successfully developing MS, LC-MS or LC-MS/MS method.</li><li>Hands on experience in sample preparation technique (LLE, SPE, Immunocapture, enzymatic digestion, homogenization etc.) and automation platform.</li><li>Scientific curiosity and strong capabilities in experimental design, execution, data interpretation and troubleshooting with limited supervision.</li><li>Ability to think critically and to prioritize and manage multiple projects under aggressive timeline in a fast-paced environment.</li><li>Detail-oriented, good interpersonal and effective technical writing and verbal communication skills.</li><li>Industrial experience in bioanalysis of LC-MS based small molecule, siRNA, biomarkers and biotherapeutics assay development is preferred. Job level may be adjusted based on the experience.</li><li>Previous experience in GLP lab and mass spectrometry applications in ADC analytics, metabolomics and proteomics would be advantageous.</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[研究と前臨床開発]]></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-Pulmonology-Columbus, OH]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47139]]></requisitionid>
    <referencenumber><![CDATA[R47139]]></referencenumber>
    <apijobid><![CDATA[r47139]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47139/medical-specialist-i-pulmonology-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>Geography: Columbus, OH - representative must reside within or close to the territory.</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>As a Medical Specialist, a typical day might include the following:</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 may be for you if you:</strong></p><ul><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></ul><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. Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches. 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. 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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 State Policy & Government Affairs]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47415]]></requisitionid>
    <referencenumber><![CDATA[R47415]]></referencenumber>
    <apijobid><![CDATA[r47415]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47415/director-state-policy-government-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Washington,DC]]></city>
    <state><![CDATA[District of Columbia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The State Policy & Government Affairs Director will serve as a key member of Regeneron Pharmaceutical’s Public Policy & Government Affairs (PP&GA) team, responsible for the development and execution of state-level policy strategies that advance the company’s mission to ensure patient access to innovative therapies. This individual will lead Regeneron’s engagement on critical state legislative and regulatory issues, including drug pricing, reimbursement, coverage, utilization management, data privacy, artificial intelligence and other related broader healthcare policy trends. The role requires close collaboration with internal stakeholders and external partners to shape policy outcomes and support business objectives across therapeutic areas.</p><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>Develop and execute a comprehensive state government affairs strategy aligned with Regeneron’s policy and business priorities, with a focus on patient access, affordability, and innovation.</p></li><li><p>Monitor, analyze, and influence state legislation, regulation, and policy trends impacting biopharmaceutical development, reimbursement, and access (e.g., drug pricing reforms, PBM regulation, prior authorization, step therapy, and Medicaid policies).</p></li><li><p>Lead engagement with state policymakers, including legislators, governors’ offices, Medicaid agencies, and regulatory bodies, to proactively shape policy outcomes.</p></li><li><p>Build and maintain strong relationships with key external stakeholders, including state trade associations, patient advocacy organizations, provider groups, and industry coalitions.</p></li><li><p>Represent Regeneron in state-based coalitions and industry associations, helping to shape collective advocacy strategies and advance shared policy priorities.</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Partner closely with federal policy, reimbursement, legal, compliance, and commercial teams to ensure alignment and coordination across policy strategies.</p></li><li><p>Provide strategic guidance and insights to internal leadership on state policy risks and opportunities, including emerging trends that may impact product access and commercialization.</p></li><li><p>Support the development of advocacy materials, including policy briefs, comment letters, testimony, and stakeholder communications.</p></li><li><p>Coordinate and support state-level stakeholder engagement opportunities, including legislative briefings, roundtables, and site visits.</p></li><li><p>Serve as a trusted internal advisor, bringing strategic, politically astute perspectives to advance Regeneron’s policy objectives.</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Bachelor’s degree required; advanced degree (e.g., MPP, MPH, MBA) preferred.</p></li><li><p>Minimum of 12+ years of relevant experience in state government affairs, public policy, or healthcare policy, preferably within the biopharmaceutical or healthcare sector.</p></li><li><p>Strong understanding of state healthcare policy, including Medicaid, commercial insurance markets, drug pricing, and utilization management tools.</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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Senior Manager Commercial Operations - Oncology]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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[<div><p>革新と卓越性を追求するオンコロジー事業部で活躍しませんか？ </p><p>私たちは、オンコロジー分野でのCommercial Operationsシニアマネージャーを募集しています。この重要な役割では、営業・マーケティングチームがコマーシャル戦略を効果的に実施できるサポート体制を企画・運営し、継続的なプロセス改善を推進します。コマーシャルオペレーション・アソシエイトディレクターにレポートし、早いペースで変化する環境での業務最適化の実現に重要な役割を果たします。国内海外の関係者と協働しながら、ビジネスインパクトを追求し、将来のパイプラインローンチをリードしたい方、ぜひ私たちのチームに加わってください。</p></div><p>---</p><div><p>■業務内容：</p><p>- コマーシャル業務プロセス運営をリードし、将来的なパイプライン上市にともなう組織の成長のデザインを支援し、継続的な業務クオリティの向上と拡張性を確保します。 </p><p>- プロモーション資料や製品ウェブサイトのガバナンスとコンテンツ管理を監督し、医療・法務・規制（MLR）レビューの遵守を確保します。 </p><p>- アドバイザリーボードやコンサルティング契約など、さまざまな医療関係者との協働の運営とガバナンスに関して社内外の関係者と連携します。 </p><p>- ローカルおよび市場を超えた分析チームと連携し、フィールドサイズ調整、ターゲティング、セグメンテーションを実行し、セールスチームへ展開・フォローアップをします。 </p><p>---</p><p>■この役職に向いている方：</p><p>- 協力的な環境で活躍し、ベンダーやフィールドベースの従業員を含むクロスファンクショナルチームと連携するのが得意な方。 </p><p>- 戦略的視点を持ち、複数ブランド、領域にわたるオペレーション体制作りをリードしたい方。</p><p>- 強力な実行力とプロジェクト管理スキルを持ち、複数のプロジェクトをバランスよく管理しながら成果を出せる方。 </p><p>- データの視覚化やストーリーテリングに秀でており、洞察を戦略に変える能力を持つ方。 </p><p>- Microsoft PowerPoint、Excel、Word、Veevaなどのツールに精通しており、上級レベルの英語コミュニケーションスキルを持つ方。 </p><p>- 日本のバイオ医薬品市場に関する理解があり、オンコロジー分野に強い興味関心を持つ方。 </p><p>- 急速に変化する環境で働くことを楽しみ、継続的な改善にコミットできる方。 </p><p>---</p></div><p>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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 Data Lake Operations]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47776]]></requisitionid>
    <referencenumber><![CDATA[R47776]]></referencenumber>
    <apijobid><![CDATA[r47776]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47776/manager-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>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, Data Lake Operations, you will play a critical role in delivering clinical data solutions that support end-to-end clinical data management workflows. You will be responsible for managing data ingestion, transformation, and governance within the clinical data lake, ensuring high-quality, reliable, and compliant data assets for reporting, analytics, and downstream applications.</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>Managing day-to-day operations of the clinical data lake, including monitoring pipelines, resolving data quality issues, and ensuring timely delivery of data assets</p></li><li><p>Overseeing data ingestion and onboarding of multiple data sources such as lab, eCOA, imaging, biomarker, and vendor data</p></li><li><p>Designing and maintaining a standardized clinical data model aligned with industry standards to support reporting and analytics</p></li><li><p>Building and managing data marts for downstream systems such as Safety, CTMS, and risk-based monitoring tools</p></li><li><p>Driving data governance practices including data cataloging, data quality rules, lineage tracking, and metadata management</p></li><li><p>Supporting and maintaining operational workflows such as automated data transfers, reporting pipelines, and alert systems</p></li><li><p>Developing automation frameworks using Python for data transformation, validation, and reconciliation processes</p></li><li><p>Designing SQL-based validation rules and logic for data quality checks and reconciliation across datasets</p></li><li><p>Collaborating with cross-functional teams including Biostatistics, Safety, Clinical Sciences, and IT to ensure data availability and usability</p></li><li><p>Managing and mentoring a team of data engineers and analysts to deliver high-quality data products</p></li></ul><h3><strong>This job may be for you if you have:</strong></h3><ul><li><p>Strong experience in data engineering, data pipelines, and data lake operations</p></li><li><p>Good understanding of clinical trial data, CDISC standards (SDTM, ADaM), and EDC systems</p></li><li><p>Expertise in Python, SQL, and ETL frameworks for data processing and automation</p></li><li><p>Experience working with cloud platforms such as AWS or Snowflake and data query tools</p></li><li><p>Strong understanding of data governance, data quality, and metadata management practices</p></li><li><p>Ability to work across teams and manage multiple stakeholders</p></li><li><p>Strong problem-solving, analytical, and communication skills</p></li></ul><p><strong>To be considered for this role, you must have:</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>7–9+ years of experience in data engineering, clinical data management, or related domains</p></li><li><p>At least 2+ years of team management or technical leadership experience</p></li><li><p>Experience working with clinical data systems and standards is strongly 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[グローバル展開]]></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[Senior Manager - Business Intelligence Architect]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47727]]></requisitionid>
    <referencenumber><![CDATA[R47727]]></referencenumber>
    <apijobid><![CDATA[r47727]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[Medical Specialist I: Allergy/ENT Oklahoma City, OK]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47948]]></requisitionid>
    <referencenumber><![CDATA[R47948]]></referencenumber>
    <apijobid><![CDATA[r47948]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47948/medical-specialist-i-allergyent-oklahoma-city-ok/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Oklahoma City]]></city>
    <state><![CDATA[Oklahoma]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Oklahoma City, OK</strong></p><p><strong>Build our future together: </strong> </p><p>The Medical Specialist (Sales Representative), Allergy/ENT (MS) will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists 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 allergists in the Dermatology and Respiratory therapeutic areas to generate product utilization. The MS will develop strong working relationships with experts and all 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>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>Discover your role: </strong></p><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><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 minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Dermatology or Respiratory 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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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 Staff Engineer, Synthetic and Bioconjugation Scale-Up Technologies (PMPD)]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44429]]></requisitionid>
    <referencenumber><![CDATA[R44429]]></referencenumber>
    <apijobid><![CDATA[r44429]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r44429/sr-staff-engineer-synthetic-and-bioconjugation-scale-up-technologies-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 and dynamic <strong>Sr</strong> <strong>Staff Engineer </strong>for its Synthetic and Bioconjugation Scale-up Technologies (SBST) group. In this exciting new role, you will provide scientific leadership and support for synthetic oligonucleotide process development using the principles of Quality by Design (QbD), process scale-up, and technology transfer of manufacturing-related workflows at Contract Development and Manufacturing Organizations (CDMOs) to ensure timely and reliable entrance to the clinic through product commercialization.</p><p><strong>A Typical Day in the Role of Sr Staff Engineer might include:</strong></p><ul><li>Designing and developing scalable, robust and controlled GMP-ready processes for chemical synthesis of small-molecules. This includes purification development and establishing supporting analytical characterization techniques.</li><li>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.</li><li>Ensuring a team-based evaluation of processes by working closely with several groups such as R&D chemistry, Formulations Development, Analytical Chemistry, and Protein Biochemistry to ensure integrated program success.</li><li>Generating robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</li><li>Partnering with External Manufacturing group and other key partners at Regeneron’s IOPS organization to vet CDMO’s and successfully transfer processes with immediate, first-time success.</li><li>Developing new technologies for process improvements and predictive process models, and pioneering novel at-line/in-line process analytical technologies to ensure robust processing.</li><li>Reviewing and providing domain expertise for all regulatory submissions.</li><li>Authoring publications, reports, tech transfer documents, regulatory support documents, patents.</li><li>Performing long-term planning for laboratory related personnel, supplies and equipment.</li></ul><p><strong>This role may be for you if you:</strong></p><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 Ph.D. or Master’s in organic chemistry or a related field. At least 7-8+ years of industrial experience post-PhD or a MS w/120+ years, or BS with 15+years in active pharmaceutical ingredient (API) process development is preferred. 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. Experience with solid-phase and liquid phase peptide synthesis is preferable. Proven experience in scaling-up synthetic small-molecule reactions and technology transfer to a GMP manufacturing facility is a plus. Candidate should be well-versed with International Council for Harmonization (ICH)/regulatory guidelines and their impact on process development of synthetic</p><p><strong>A typical day in the role of Staff Engineer might include:</strong></p><ul><li>Designing and developing scalable, robust and controlled cGMP-ready processes for the chemical synthesis, purification, and isolation of oligonucleotides across early and late-stage process development.</li><li>Ensuring a team-based evaluation of processes by working closely with several groups such as R&D Chemistry, Formulations Development, Analytical Chemistry, Protein Biochemistry, CDMOs, and other key stakeholders to ensure integrated program success.</li><li>Generating robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</li><li>Partnering with the External Manufacturing group and other key partners at Regeneron’s Industrial Operations and Product Supply (IOPS) organization to vet CDMOs and successfully transfer processes with immediate, first-time success.</li><li>Promote new technologies for process improvements, predictive process models, and novel at-line/in-line process analytical technologies to ensure robust processing.</li><li>Reviewing and providing domain expertise for regulatory submissions.</li><li>Authoring publications, reports, tech transfer documents, regulatory support documents, patents.</li><li>Scientifically up-to-date on advances in process chemistry and related disciplines</li><li>Requires up to 20% travel</li></ul><p><strong>This role may be for you if you:</strong></p><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 Ph.D. or Master’s in organic chemistry or a related field. At least 5 years of industrial experience post-PhD or at least 7 years of experience post-Masters in active pharmaceutical ingredient (API) process development is preferred. Experience with small-molecules in the bioconjugates space will be highly preferable. Hands-on experience with solid-phase oligonucleotide synthesis, purification, and characterization using techniques such as mass spectrometry (MS), nuclear magnetic resonance (NMR), infrared (IR) spectroscopy, and high-performance liquid chromatography (HPLC) is preferred. Proven experience in scaling-up synthetic oligonucleotide syntheses and technology transfer to a GMP manufacturing facility 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 multi-functional Chemistry, Manufacturing and Control (CMC) teams and experience in authoring publications, reports, technical transfer documents, regulatory support documents, patents is a plus.</p><p>Note: title 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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Regional Tumor Lead Marketing Hematology]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47471]]></requisitionid>
    <referencenumber><![CDATA[R47471]]></referencenumber>
    <apijobid><![CDATA[r47471]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47471/regional-tumor-lead-marketing-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Hematology to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><strong>This Role May Be For You, if you are:</strong></p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in hematology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</p><div><p><strong>Salary Range (annually)</strong></p><p>101,500€ - 200,400€</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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 08:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 08:56:07 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Temp - Quality Compliance Specialist]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47568]]></requisitionid>
    <referencenumber><![CDATA[R47568]]></referencenumber>
    <apijobid><![CDATA[r47568]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47568/temp-quality-compliance-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>In this role you will be responsible for maintaining site compliance of operations inclusive of Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities Maintenance, Materials Handling, and QA Validation adhering to mandated regulatory requirements and site expectations.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li><p>Ensuring compliance with all aspects of Quality for the Raheen site and administration of site quality systems including Deviations, CAPA Change Control, Audits, Customer Complaints, Quality Risk Management</p></li><li><p>Reviewing failure investigations, change control documents, corrective/preventative action documents, standard operating procedures</p></li><li><p>Maintaining electronic systems, procedures, policies and other instructional documents relating to quality systems to ensure compliance with company policy and local and international regulatory requirements</p></li><li><p>Monitoring and trending metrics</p></li><li><p>Participating in regulatory and customer audits and quality risk assessments</p></li><li><p>Collaborating with functional departments to resolve issues and maintain compliance</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have a quality mindset and excellent attention to detail</p></li><li><p>You demonstrate strong interpersonal skills</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 a BS/BA in a scientific discipline or related field with 2+ years of relevant work experience in pharmaceutical or related industry. Relevant experience may be substituted for education requirement.</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[産業オペレーションと製品供給]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 09:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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 Manager, Statistical Programming]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43733]]></requisitionid>
    <referencenumber><![CDATA[R43733]]></referencenumber>
    <apijobid><![CDATA[r43733]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Statistical Programming]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44857]]></requisitionid>
    <referencenumber><![CDATA[R44857]]></referencenumber>
    <apijobid><![CDATA[r44857]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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, GxP Enterprise Architecture]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44202]]></requisitionid>
    <referencenumber><![CDATA[R44202]]></referencenumber>
    <apijobid><![CDATA[r44202]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r44202/director-gxp-enterprise-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 Director, GxP Enterprise Architecture leads the IT architecture practice for manufacturing and operations (e.g., manufacturing, QA, QC, process sciences, supply chain). This role defines technology strategy and standards, governs platform decisions, and ensures solutions meet GxP and data integrity requirements while advancing business capabilities and long-term platform health.</p><p>As a Director, GxP Enterprise Architecture, a typical day might include the following:</p><ul><li>Define and evolve EA governance, standards, reference architectures, and reusable patterns across application, integration, data, and infrastructure.</li><li>Own the multi-year technology roadmap aligned to business capability priorities and lifecycle plans.</li><li>Lead architecture reviews, maintain the application portfolio, and manage technical debt and end‑of‑life risk.</li><li>Ensure alignment with enterprise-wide architecture, avoid redundant platform investments while identifying capability gaps.</li><li>Translate market trends (ERP, MES, LIMS, QMS, data, cloud, integration) into actionable guidance and adoption plans.</li><li>Manage business strategy enablement options, and trade-offs met by technology with business leaders.</li><li>Collaborate with corporate IT's Architecture team to ensure architectural standards are in place and enforced.</li><li>Ensure Architecture Standards are aligned with 21 CFR Part 11, Annex 11, data integrity, and CSV/CSA requirements.</li><li>Produce and maintain target-state architectures, capability maps, roadmaps, solution blueprints, integration diagrams, and ADRs.</li></ul><p>This role may be for you if you have knowledge in:</p><ul><li>GMP systems landscape: ERP (e.g., Oracle EBS, Oracle Fusion), MES, LIMS/ELN, QMS, WMS, EDMS; familiarity with SCADA/DCS and shop-floor integration.</li><li>Integration patterns and platforms: APIs, event-driven architecture, EDI, ETL/ELT; iPaaS/ESB (e.g., MuleSoft, Boomi), OPC UA; canonical data models.</li><li>Data and analytics: data lakehouse (e.g., Snowflake, Databricks), MDM, data governance, metadata lineage, BI platforms; ISA-95 data layers.</li><li>Cloud and infrastructure: AWS/Azure services, hybrid architectures, VPC/VNet design, containerization (Kubernetes), IaC (Terraform), CI/CD, microservices.</li><li>Security and compliance: identity and access management (Azure AD), segregation of duties, network segmentation/OT boundary patterns, NIST/ISO 27001 controls, backup/DR.</li><li>Architecture practice: TOGAF/ArchiMate, modeling tools (e.g., LeanIX, Lucidchart), solution blueprinting, ADRs, and traceability for audits.</li><li>SDLC and delivery: Agile/SAFe, DevOps in regulated environments, validation documentation (URS/FS/DS), risk-based CSA.</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>Associate Director: 10 years of experience in a relevant industry or equivalent combination of education and experience. Biotechnology/Life Sciences industry experience, preferred.</li><li>Director: 12 years of experience in a relevant industry or equivalent combination of education and experience. Biotechnology/Life Sciences industry experience, 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>$192,900.00 - $321,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Insights & Analytics - Neurology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46486]]></requisitionid>
    <referencenumber><![CDATA[R46486]]></referencenumber>
    <apijobid><![CDATA[r46486]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46486/executive-director-commercial-insights-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 is seeking an Executive Director, Commercial Insights and Analytics (I&A), Neurology to join our organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Executive Director, Commercial Insights and Analytics (I&A), Neurology, 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 Neurology Commercial Business Unit (CBU) to drive deeper insights that inform business decisions. </p><p><strong>This role might be for you if can: ​</strong></p><p><em>Lead</em></p><p>1) Lead and mentor the CSI&A Neurology 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 Neurology 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 for business decision-making</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 upcoming launch plans; and <strong>b)</strong> enhance brand differentiation and impact at launch and beyond</p><p><em>Partnership and collaboration</em></p><p>8) Collaborate with the Neurology CBU and other members of senior leadership to contribute to Commercialization roadmap, 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 Neurology 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 Neurology 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 Neurology CBU and with CSI&A leadership</p><p>14) Manage third-party vendor relationships</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>20+ years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with launch 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</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, preferably across both buy-and-bill and Rx environments</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></ul><p>Preferred skills:</p><ul><li><p>Master’s (MBA, MPH, MS) preferred</p></li><li><p>Neurology disease category experience is desired</p></li><li><p>Experience with forecasting, especially the use of launch analogs</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[コマーシャル]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Senior Clinical Pharmacologist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47532]]></requisitionid>
    <referencenumber><![CDATA[R47532]]></referencenumber>
    <apijobid><![CDATA[r47532]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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>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>A day in the life may look like:</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>Works (or collaborates with Research Specialist or Programming team) to prepare TFLs to support IND/CTA, PK WSs, Tox WS, Pharm WS, CSRs, DSURs, IB and other documents.</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, QC 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 may be the right role for you if you:</strong></p><ul><li><p>Are able to serve independently as study CP/QP/PPKPD lead for moderately complex</p></li><li><p>Studies or support study CP/QP/PPKPD lead for more complex studies, and to contribute to or lead non-project objectives.</p></li><li><p>Are 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><li><p>Beginning to establish own research areas within development sciences.</p></li></ul><p><strong>To be considered for this role you must have:</strong></p><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><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[研究と前臨床開発]]></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-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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Field Reimbursement Manager - Dermatology - Cleveland/Akron, OH]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47585]]></requisitionid>
    <referencenumber><![CDATA[R47585]]></referencenumber>
    <apijobid><![CDATA[r47585]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47585/field-reimbursement-manager-dermatology-clevelandakron-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[<h3><strong>Field Reimbursement Manager - Dermatology (Cleveland/Akron OH) </strong></h3><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><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>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</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 (Dupixent).</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 aligns with Regeneron policies, processes, and standard operating procedures</p></li><li><p>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</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</p></li><li><p>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.</p></li><li><p>You possess excellent organizational, project management, and communication skills.</p></li><li><p>Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors.</p></li><li><p>Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</p></li><li><p>Established ability to work within an Account Management based structure.</p></li></ul><p>To be considered for this opportunity, you will possess the following:</p><p>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. Experience working with products delivered through a Specialty Pharmacy network is essential. Collaboration and proactive communication skills required. Background in leadership and effective cross functional partnership 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>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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, Thought Leader Liaison (Neuro)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47711]]></requisitionid>
    <referencenumber><![CDATA[R47711]]></referencenumber>
    <apijobid><![CDATA[r47711]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47711/director-thought-leader-liaison-neuro/]]></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 Director, Thought Leader Liaison Lead for Rare Neurology is a non-sales position for someone passionate about leading a team of Thought Leader Liaisons (TLLs) across the nation. The Director will work closely with U.S Thought Leaders in Rare Neurology. We are seeking an individual who will be a key member of the Rare Neurology marketing leadership team and will collaborate with cross-functional teams to ensure alignment with the overall brand strategy and tactical execution. The TLL Director will report to the Executive Director of Rare Neurology Marketing.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Guide and define the culture, structure, and strategic direction of Regeneron’s Rare Neurology TLL Team</p></li><li><p>Build a high performing team, capable of generating quality insights with Thought Leaders</p></li><li><p>Create a compliant environment which challenges, motivates and develops team members to reach optimum performance and potential</p></li><li><p>Set clear objectives, coach/ mentor, and assess performance and skill-level to develop future leaders within Regeneron</p></li><li><p>Provide strategic customer insights to the Marketing Leadership team to assist in the further development of the Rare Neurology brand strategy</p></li><li><p>Work collaboratively with multiple matrix partners in developing and refining business plans to achieve brand objectives</p></li><li><p>Manage budget and TLL operations to ensure the TLL team is appropriately resourced</p></li><li><p>Champion and lead the TLL team in a compliant manner</p></li><li><p>Build and cultivate collaboration within alliance</p></li></ul><p><strong>This role may be for you, if you can:</strong></p><ul><li><p>Lead from the front, demonstrating visible, engaged leadership that sets the standard for performance, professionalism, and expected behaviors</p></li><li><p>Operate as a key member of the marketing leadership team, contributing strategic perspective and driving alignment across brand, field, and cross‑functional partners</p></li><li><p>Develop and inspire talent, actively coaching the team and building a strong pipeline of future leaders</p></li><li><p>Foster strong collaboration and trust, creating an inclusive, high‑performing culture aligned with company values</p></li><li><p>Drive innovation and continuous improvement, elevating the impact of field marketing insights, execution, and customer engagement</p></li><li><p>Adapt and evolve with the business, proactively recalibrating the scope, focus, and capabilities of the TLL team in response to brand needs</p></li></ul><p>To be considered, you must have a Bachelor's degree, Master’s degree or other advanced education/certification a plus. We also seek Specialty pharmaceutical/ biopharmaceutical experience with a minimum of 12 years of work experience in one or more of the following: field sales, product marketing, or medical/ clinical experience including people management experience in Rare Neurology or a similar biologic/specialty/REMS market. Lastly we expect you to have the ability to travel to congresses, meetings, programs, etc. (50-80% travel).</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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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 Force Effectiveness (Neurology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47879]]></requisitionid>
    <referencenumber><![CDATA[R47879]]></referencenumber>
    <apijobid><![CDATA[r47879]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47879/associate-director-field-force-effectiveness-neurology/]]></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 position offers the opportunity to partner and collaborate with many of the functions integral to the commercialization of our Neurology product. This individual will report to the Executive Director, Strategic Customer Engagement, Neurology CBU. This job requires working with sales leadership, the field sales teams, sales training, marketing, sales analytics, market research, HR, Legal, Compliance and other functions as required to continuously improve sales force effectiveness.</p><p><strong>A Typical Day Might Look Like This:</strong></p><ul><li>Partner with sales leadership and brand team to set operational strategy in alignment with brand strategy</li><li>Coordinate and execute tactical plans to drive the commercial success of our Neurology brand</li><li>Ensure cross-functional and cross-collaboration communication and alignment with Marketing, Field Access and Reimbursement, Trade, Medical and National Accounts</li><li>Offer lens of salesforce in internal meetings</li><li>Collaborate with the Incentive Compensation team and Regional Directors to design, implement, and track IC plans</li><li>Collaborate with Analytics and Regional Directors to develop and monitor agreed metrics for field teams and ensure regular distribution to the field leadership and the field teams</li><li>Partner with Commercial Training to develop and drive Plan of Action Meetings, Train the Trainer Meetings, Career Development, Selling Models, training curriculum, etc.</li><li>Work with Finance & brand team to ensure field force budgets are properly aligned with field initiatives and reports generated to monitor adherence to budgets</li><li>Partner with Customer Relationship Management system administrator on tools to allow the Medical Specialists and home office to gauge promotional effectiveness</li><li>Manage the overall strategic and operations calendar, interact with the Regional Directors’ direct reports, organize staff meetings and business reviews</li></ul><p><strong>This Position Might Be for You If:</strong></p><p>The Associate Director, Field Force Effectiveness must possess the expertise to interpret and draw business insights from data analysis to formulate recommendations and execute action plans. Demonstrate cross-functional coordination to execute product initiatives. Other critical success factors include:</p><ul><li>Confidence and ability to influence senior executives in support of key initiatives</li><li>Proactively and independently prioritize requests and business needs</li><li>Ability to facilitate cross-functional collaboration (e.g. Finance, Marketing, Sales Analytics, HR, Compliance, Legal, etc.)</li><li>Strong organization/coordination capabilities and excellent written and oral communication skills.</li><li>Strong business acumen & analytical skills. Proficient in excel.</li><li>Ability to develop and leverage internal network to facilitate the execution of business requirement</li></ul><p>To be considered you must possess a minimum of a Bachelor’s Degree minimum; MBA preferred. 10 or more years of progressive pharmaceutical industry experience with a strong preference for field management and home office experience. Neurology experience preferred. Product launch experience preferred. Travel as required; 25 - 30%</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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Medical Specialist I-Allergy/ENT-Tuscon, AZ]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47207]]></requisitionid>
    <referencenumber><![CDATA[R47207]]></referencenumber>
    <apijobid><![CDATA[r47207]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47207/medical-specialist-i-allergyent-tuscon-az/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tucson]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Tucson (Allergy/ENT)</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>A typical day might include the following:</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 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 states, treatment options and healthcare trends</p></li><li><p>You can 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’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology experience preferred. We need someone with demonstrated 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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[コマーシャル]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Product Manager Oncology, France (12 months CDD)]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48318]]></requisitionid>
    <referencenumber><![CDATA[R48318]]></referencenumber>
    <apijobid><![CDATA[r48318]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48318/associate-product-manager-oncology-france-12-months-cdd/]]></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><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Product Manager, Oncology Marketing, France (H/F)</strong> to join our marketing team, supporting our France affiliate. In this role, you will contribute to the implementation of the local brand strategy and support future launches while collaborating with sales teams 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><p><strong>Associate Product Manager, Oncology Marketing, France - Paris (H/F)</strong></p><p><strong>When & where:</strong></p><ul><li>France (Office-based - hybrid)</li><li>12-month fixed-term contract -CDD</li></ul><p><strong>Discover your role:</strong></p><ul><li>Support brand strategy through market analysis and customer insights</li><li>Drive execution of local brand plans and marketing initiatives</li><li>Develop promotional materials for sales force and digital channels</li><li>Collaborate with sales teams to optimize campaign execution</li><li>Partner with Sales Managers on field plans and communications</li><li>Prepare presentations for internal meetings and sales events</li><li>Ensure compliance with ethical and regulatory standards</li><li>You work collaboratively across teams to align and deliver outcomes</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree, preferably in a science-related field</li><li>2–4 years’ biotech or pharmaceutical marketing experience</li><li>Experience working within a France affiliate environment</li><li>Strong project management and multi-tasking capabilities</li><li>Knowledge of healthcare compliance codes and regulations</li><li>Excellent written and spoken French and English</li><li>Willingness to travel 20%</li><li>Experience in Oncology marketing (preferred)</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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 10:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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/ja/%E4%BB%95%E4%BA%8B/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[Sr Financial Analyst]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47488]]></requisitionid>
    <referencenumber><![CDATA[R47488]]></referencenumber>
    <apijobid><![CDATA[r47488]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47488/sr-financial-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>The Senior Financial Analyst 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[コーポレートファンクション]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Product Biochemistry]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48518]]></requisitionid>
    <referencenumber><![CDATA[R48518]]></referencenumber>
    <apijobid><![CDATA[r48518]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48518/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>Regeneron is seeking a highly motivated and passionate Associate Scientist to join our Product Biochemistry team. In this exciting role, you will play a critical part in implementing innovative biophysical assessment strategies to support a wide range of drug candidate modalities.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li>With supervisory direction and support, conducts biochemical and biophysical characterization experiments on therapeutic protein for late-stage development and regulatory submissions. </li><li>Provide input on experimental design and suggest modifications in protocols or methods to meet the needs of a particular program or molecule. </li><li>Will take on additional responsibilities in advanced method development to support efforts to enrich and characterize size/charge variants, protein-ligand complexes, and high concentration protein solutions of therapeutic protein drug candidates. </li><li>Documents experiments, results and findings in electronic laboratory notebook in a timely manner; 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>Maintain instruments, troubleshoot instrumental/experimental problems, and order/maintain supplies. Keen to follow procedures, guidance, and best practices for lab safety.</li></ul><p><strong>This Role Might Be For You If:</strong></p><ul><li>You have initiative and drive to complete meaningful tasks and learn new technologies.</li><li>You can work both independently and within a team environment on projects simultaneously</li><li>You contribute to lab equipment maintenance and safety to help create a safe, effective and efficient working environment.</li><li>You possess strong organizational, communication, analytical, computer, and technical writing skills.</li></ul><p>This role requires a BS/MS in Biochemistry/Biophysics, or related field plus 0-3 yrs+ experience. 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, protein-protein interaction and general biochemistry 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.</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.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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 15:56:07 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Regional Tumor Lead Marketing Oncology Lung]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48211]]></requisitionid>
    <referencenumber><![CDATA[R48211]]></referencenumber>
    <apijobid><![CDATA[r48211]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48211/regional-tumor-lead-marketing-oncology-lung/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Lung to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><p><br><strong>A Typical Day:</strong><br> </p><p>Leading country insight collection and prioritization to inform global brand strategy<br><br>Ensuring alignment of local priorities with global strategic direction<br><br>Developing the regional tactical plan, including budget alignment<br><br>Facilitating regional tumor marketing meetings to drive execution against plan<br><br>Reviewing country brand plans and sharing insights to improve execution quality<br><br>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes<br><br>Driving regional launch planning and optimization, supporting excellence in country</p><p><br><strong>This Role May Be For You, if you are:</strong></p><p><br>Energized by working with, leveraging and developing talents in countries<br><br>Enjoy connecting global strategy with local market realities<br><br>Comfortable prioritizing across countries and balancing trade-offs<br><br>Energized by guiding brand planning and execution at regional level<br><br>Enjoys shaping content strategies across multiple markets<br><br>Confident leading discussions and aligning diverse stakeholders<br><br>Motivated by improving execution through insights and performance data<br><br>Open to regular travel and engaging with teams across geographies<br><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>95,250 € - 186,125 €</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 05:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Hematology]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48212]]></requisitionid>
    <referencenumber><![CDATA[R48212]]></referencenumber>
    <apijobid><![CDATA[r48212]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48212/regional-tumor-lead-marketing-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Hematology to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br>A Typical Day:</p><ul><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><br><br>This Role May Be For You, if you are:</p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in hematology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</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[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Review Committee Senior Coordinator]]></title>
    <date><![CDATA[Tue, 16 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/ja/%E4%BB%95%E4%BA%8B/r48298/medical-review-committee-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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Associate Scientist, R&D Chemistry, Peptidomimetic Purification]]></title>
    <date><![CDATA[Tue, 16 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/ja/%E4%BB%95%E4%BA%8B/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>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[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 15:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Software Engineer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43915]]></requisitionid>
    <referencenumber><![CDATA[R43915]]></referencenumber>
    <apijobid><![CDATA[r43915]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r43915/principal-software-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 is one of the largest human genetics sequencing programs in the world. We study human DNA at massive scale to understand why diseases happen and how we can stop them. Using genetics to improve human health, our research has contributed directly to medicines helping patients today.</p><p>The RGC IT team builds and maintains shared services, platform tooling, and APIs that our research teams depend on. We approach development with an AI-first mindset, utilizing LLM-powered tooling to move faster, explore more ideas and quickly turn complex problems into working solutions for our scientists.</p><p><strong>A Typical Day As a Principal Software Engineer, you’ll contribute to:</strong></p><ul><li><p>API and service development across a shared platform that research teams use to access and work with large-scale genetic data.</p></li><li><p>Cloud-based data pipeline work on AWS, keeping high-volume genomic data moving reliably and performantly.</p></li><li><p>Integrating and applying AI tooling across development workflows — from LLM-assisted coding and review to building AI-powered capabilities into the platform itself.</p></li><li><p>Working directly with scientists and engineers to understand requirements and deliver meaningful solutions to improve our scientific discovery process.</p></li></ul><p><strong>This Role Might Be for You If You Have:</strong></p><ul><li><p>Strong fundamentals at the API and data layer. You’ve built production APIs, integration services, and pipelines in the cloud as microservices.</p></li><li><p>Comfortable with AI-first development. You use tools like Claude Code as a core part of how you work — not occasionally, but throughout planning, implementation, and review.</p></li><li><p>Technical depth across the stack. API design patterns, distributed systems, cloud-native development on AWS — you can contribute without needing everything handed to you.</p></li><li><p>Works well as part of a team. Decisions here are collaborative. You do good work in that kind of environment.</p></li><li><p>Takes quality seriously. You write things that can be tested and maintained, and you know why that matters at scale.</p></li></ul><p><strong>To be considered for this opportunity,</strong> you must have a Bachelor’s Degree or higher with at least 6 years of relevant IT experience building cloud-native applications. Candidates must have hands-on experience with:</p><ul><li><p>Languages & Runtimes: Python, TypeScript</p></li><li><p>API & Integration: REST API design and development, service integration patterns</p></li><li><p>AI Tooling: LLM-assisted development tools (e.g. Claude Code, GitHub Copilot), AI/ML service integration</p></li><li><p>Data & Databases: PostgreSQL or MySQL, Redshift or Snowflake, ETL orchestration</p></li><li><p>Infrastructure: Docker, AWS cloud services</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[研究と前臨床開発]]></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, Patent Attorney]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44376]]></requisitionid>
    <referencenumber><![CDATA[R44376]]></referencenumber>
    <apijobid><![CDATA[r44376]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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>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.<br><br><strong>As a Director Patent Attorney, a typical day may include:</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>Assisting in litigation activities as needed</p></li><li><p>Supporting due diligence projects, agreements and other transactional work, administrative initiatives, and policy questions.</p></li></ul><p><strong>This role might be for you if you have experience:</strong></p><ul><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>To be considered for this position, you must possess</strong> a 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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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, Epidemiology-Health Economics & Outcomes Research]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44671]]></requisitionid>
    <referencenumber><![CDATA[R44671]]></referencenumber>
    <apijobid><![CDATA[r44671]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r44671/director-epidemiology-health-economics-outcomes-research/]]></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 Director, Epidemiology (HEOR) you will develop and drive real world evidence (RWE) that influences the development and commercialization of our innovative therapies. You will lead high impact epidemiologic research, apply innovative methods, and work with rich real world data sources answering complex questions for patients, clinicians, regulators, and payers.</p><p>This position is located at our Sleepy Hollow, NY offices and will require you to be on-site 4 days week. If eligible, we can offer relocation benefits. We cannot offer a fully remote option. </p><p><strong>A typical day may include the following: </strong><br>• Generate high quality observational research using RWD to support development and commercial strategies.<br>• Apply epidemiologic expertise to clinical development and trial design discussions, including opportunities for external control arms or hybrid evidence approaches.<br>• Support global HTA, payer, and regulatory submissions by generating epidemiology and RWE inputs for reimbursement packages and regulatory and value dossiers.<br>• Synthesize and critically evaluate scientific evidence to generate epidemiologic evidence for regulatory and payer submissions, press releases, and internal needs.<br>• Evaluate and implement emerging design and analytic methods enhancing our RWE capabilities.<br>• Stay current with evolving regulatory and payer expectations for RWE, guiding internal teams on implications for evidence strategy and generation.<br>• Represent the organization in external scientific, industry, and other forums, including peer reviewed publications and conference presentations to strengthen external visibility.</p><p><strong>This may be for you if you:</strong> <br>• You thrive in a team first environment and want to see your work inform decision making at scale.<br>• Have an innovation approach and enjoy developing solutions to complex problems<br>• Are at ease with an abundance of detail and complexity, yet mindful of the big picture.<br>• Can operate successfully in a ‘rapid response” environment<br>• Exceptional communication abilities that allow you to translate complex designs and findings into clear, actionable insights for a wide range of audiences.</p><p>To be considered it is required to have a PhD in Epidemiology or a related subject area supported by 7+ years of experience across academia, pharma/biotech, or consulting. Hands on leadership in developing study protocols and statistical analysis plans using real world data sources with a record of peer-reviewed publications is required. Expertise in advanced analytical methods for large healthcare datasets to apply or expand skills in machine learning. Familiarity with global HTA and payer evidence is advantageous.<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[グローバル展開]]></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, Customer Insights & Analytics - Neurology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45023]]></requisitionid>
    <referencenumber><![CDATA[R45023]]></referencenumber>
    <apijobid><![CDATA[r45023]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45023/director-customer-insights-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 is seeking a Director, Insights & Analytics (I&A) to join our team! As part of an exciting upcoming launch in generalized myasthenia gravis (gMG), this role will play a critical role in shaping analytics, insights, and decision-making during a pivotal moment for the organization</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, I&A will report into an Executive Director, I&A within the Commercial Strategy and Insights and Analytics (CSI&A) department. This role will oversee a high-performing team (internal and external) responsible for generating actionable insights from a broad set of I&A sources, to inform business decisions. The role will partner with and serve as a strategic advisor to the Neurology Commercial Business Unit (CBU) and will partner with other leaders to grow and develop talent within the CSI&A team.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Lead</em></p><p>1) Lead the I&A Neurology team in providing business analytics, customer insights and competitive intelligence to address all commercialization needs</p><p>2) Collaborate with the ED, I&A to set the strategic I&A direction that aligns with overarching priorities and helps drive launch excellence</p><p><em>Develop</em></p><p>3) Foster innovative solutions and a design-thinking approach aligned with strategies for the Neurology business.</p><p>4) Develop people from both a functional skills and leadership perspective, with the goal of growing internal talent</p><p>5) Assess and implement novel methodologies and frameworks to <strong>a)</strong> garner meaningful insights to inform business decisions a rapidly developing Neurology CBU; and <strong>b)</strong> enhance brand differentiation and impact</p><p><em>Partnership and collaboration</em></p><p>6) Lead efforts to identify and crystalize insights that inform strategic plans</p><p>7) Collaborate with the Neurology CBU and other members of leadership to identify, predict and inform business decisions relating to the competitive outlook for gMG</p><p>8) 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>9) Coordinate alignment with stakeholders on all insights and analytics agendas</p><p>10) Work with other CSI&A leaders to develop standardized adoption of capabilities such as marketing mix, promotional optimization, data science, market structure analysis, patient/treatment flow modeling, analog modeling and ML/AI methodologies across I&A</p><p><em>Execute</em></p><p>11) Proactively communicate with the Neurology CBU and provide strategic recommendations and insights as well as anticipated future needs</p><p>12) Construct and deliver integrated business reviews, I&A summary overviews with leadership from Neurology and CSI&A</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum BS with 12+ (or MS with 10+) years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with market-leading brands required and neurology or rare disease experience is desired</p></li><li><p>Functional expertise in business analytics, HCP consumer/patient insights, primary research methods, analog forecast development and competitive intelligence</p></li><li><p>Prior experience managing I&A groups with responsibility for analytics, HCP consumer/patient 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></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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[IT Lead, Manufacturing GxP]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46064]]></requisitionid>
    <referencenumber><![CDATA[R46064]]></referencenumber>
    <apijobid><![CDATA[r46064]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46064/it-lead-manufacturing-gxp/]]></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 skilled IT professional to serve as the IT Lead for Regeneron's Cell Medicines (RCM) Manufacturing operation to support and maintain all Clinical Manufacturing Equipment and data acquisition/monitoring systems. This role will require strong management skills to effectively manage the support needed from multiple Regeneron Corporate IT services groups and external support vendors as needed, in addition to strong technical skills as the primary On-Site IT SME for the Clinical Manufacturing area.</p><p>This individual will ensure seamless communication, service delivery, and networking of points of contact across multiple IT groups and the business. The ideal candidate will have leadership and communication skills, experience in a GMP (Good Manufacturing Practices) environment, and the ability to troubleshoot on-site IT issues related to all Manufacturing and QC equipment and facilities IT systems.</p><p><strong>As an IT GxP Manufacturing Lead, a typical day may include: </strong></p><ul><li><p>Serve as the primary point of contact between RCM and Corporate IT, coordinating support across internal groups and external vendors.</p></li><li><p>Align IT services with RCM’s needs by facilitating clear stakeholder communication on requirements, timelines, and deliverables.</p></li><li><p>Lead planning and execution of IT projects and initiatives within a GMP environment, ensuring effective cross-team coordination.</p></li><li><p>Provide regular operational and project status updates, metrics, and risk/issue reports to leadership.</p></li><li><p>Manage and direct contracted IT personnel and oversee vendor performance for service delivery.</p></li><li><p>Troubleshoot and resolve on-site IT issues for manufacturing, QC equipment, and facilities systems (hardware/software), ensuring rapid restoration.</p></li><li><p>Ensure high availability and resilience of critical systems through monitoring, preventive maintenance, backups/archiving, and recovery readiness.</p></li><li><p>Develop and maintain GxP documentation, including specifications, test protocols, validation/CSV records, and system administration SOPs.</p></li><li><p>Support integration of equipment and systems with LIMS and other enterprise platforms in coordination with Corporate IT; supervise EMS for compliance and reliability.</p></li><li><p>Ensure GMP/regulatory compliance by partnering with QA, managing IT tasks in CMMS, maintaining audit readiness, and driving continuous improvement of workflows and support processes.</p></li></ul><p><strong>This role could be for you if you: </strong></p><ul><li><p>Strong management and leadership abilities.</p></li><li><p>Excellent written and verbal communication skills.</p></li><li><p>Ability to collaborate effectively with cross-functional teams.</p></li><li><p>Proven track record of collaborating with corporate IT teams.</p></li><li><p>Ability to adapt to a fast-paced, multifaceted work environment.</p></li></ul><p><strong>To be considered for this role, you must meet the following:</strong></p><ul><li><p>Bachelor’s degree in information technology, Computer Science, or a related field.</p></li><li><p>5 – 10 years' demonstrated ability in an IT role, preferably within a GMP-regulated environment.</p></li><li><p>Proficiency in troubleshooting all IT aspects of manufacturing/QC equipment and other data collection/monitoring systems (e.g. EMS)</p></li><li><p>Familiarity with GMP requirements and IT compliance standards.</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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Precision Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47135]]></requisitionid>
    <referencenumber><![CDATA[R47135]]></referencenumber>
    <apijobid><![CDATA[r47135]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47135/manager-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 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 Non-Immuno-Oncology (non-IO). 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><h3><strong>As a CLSM Manager, a typical day may include the following:</strong></h3><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><li><p>Provides guidance to clinical teams and clinical sites regarding collection and storage of samples acquired during clinical trials or other human sample acquisition projects</p></li><li><p>Works with scientists and clinical team to ensure sample collection and usage is in compliance with study protocol and applicable ICF</p></li></ul><br><h3><strong>This role may be for you if:</strong></h3><ul><li><p>You possess strong leadership tendencies, ability to proactively identify problems, determine resolutions, set priorities, and direct projects and work cross-functionally to manage expectations with excellent communication and collaborative skills and work well in a team-based environment. The CLSM Manager will be responsible for day-to-day oversight of multiple CLSMs, including responsibility for coaching, mentoring and performance management ensuring applicable key trial level milestones are achieved on schedule.</p></li><li><p>You demonstrate strong leadership skills and possess high level of emotional intelligence and effectively work collaboratively with colleagues, vendors and internally at Regeneron to ensure program success.</p></li></ul><p><strong>To be considered for this role,</strong> you must have a Bachelors, Minimum of 8 years pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams. Minimum of 5 years’ experience with Clinical Trials, focus on clinical sample collection. Extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested. We need a strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required. We are seeking clinical study knowledge, demonstrated by knowledge in science and technology.</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[研究と前臨床開発]]></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, GMP Counsel Regulatory]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46969]]></requisitionid>
    <referencenumber><![CDATA[R46969]]></referencenumber>
    <apijobid><![CDATA[r46969]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46969/senior-director-gmp-counsel-regulatory/]]></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 Senior Director, GMP Counsel Regulatory provides legal advice and counsel to global manufacturing operations (including Quality Assurance, Quality Control and other IOPS leadership) regarding GMP-related matters in Regeneron’s manufacturing, quality, and supply chain operations that constitute Regeneron’s Industrial Operations and Product Supply (“IOPS”) organization.</p><p>This role serves as a subject matter expert and key advisor on U.S. and global GMP legal and regulatory requirements, supporting GMP compliance across manufacturing, development, clinical, and commercial programs. The Senior Director partners closely with Quality (including Data Integrity), Manufacturing, Technical Operations (including Automation), IT (including AI), Supply Chain, Regulatory and other Law Department colleagues to support inspections, filings, and ongoing inspection readiness.</p><br><p><strong>A typical day may include:</strong></p><ul><li><p>Interpret and advise on GMP regulations to inform strategy and execution for manufacturing and quality-related regulatory activities throughout IOPS.</p></li><li><p>Counsel and apply U.S. and global GMP law regulations to business operations.</p></li><li><p>Serve as primary legal counsel on GMP compliance matters impacting development, clinical and commercial manufacturing across all operations - - bulk/API, fill-finish/packaging, etc.</p></li><li><p>Advise and support preparation, management, and response activities for regulatory GMP inspections and partner/collaborator audits.</p></li><li><p>Provide legal guidance on regulatory GMP inspection findings, CAPAs, remediation strategies, and enforcement risk mitigation.</p></li><li><p>Partner with IOPS key functions (e.g., QA, Manufacturing and Automation, IT) to ensure continuous inspection readiness.</p></li><li><p>Collaborate with QA, Manufacturing and Automation, IT, Supply Chain, Technical Operations, Regulatory and Law teams.</p></li><li><p>Advise internal stakeholders on legal regulatory risk, strategy, and compliance considerations related to GMP manufacturing operations and, as applicable, remediation and recall activity.</p></li></ul><br><p><strong>This role may be for you if you have:</strong></p><ul><li><p>Excellent oral and written communication skills with proven ability to present complex information accurately and concisely</p></li><li><p>Strong interpersonal communication skills and an ability to build trust and influence at all levels</p></li></ul><ul><li><p>Ability to handle multiple priorities in a dynamic and evolving environment</p></li><li><p>Strategic thinker with excellent analytical and problem-solving skills, focusing on practical solutions</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>JD required with significant experience in pharmaceutical, biotechnology, or highly regulated environment.</p></li><li><p>15+ years of progressive regulatory affairs legal counsel or related government (or industry) experience with significant GMP exposure.</p></li><li><p>5+ years of demonstrated experience supporting FDA and/or global regulatory inspections, 483 response and corrective actions/remediation, recall and other regulatory significant activity.</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>$203,000.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 Statistical Programming - Pharmacometrics]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47328]]></requisitionid>
    <referencenumber><![CDATA[R47328]]></referencenumber>
    <apijobid><![CDATA[r47328]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[MR（医薬情報担当者）- 皮膚領域　※千葉エリア]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48105]]></requisitionid>
    <referencenumber><![CDATA[R48105]]></referencenumber>
    <apijobid><![CDATA[r48105]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48105/medical-representative-mr-dermatology-starchiba-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>勤務地：</strong><br>千葉エリアを担当いただきます。<br>居住地は千葉または東京を想定しております。</p><p><br>Regeneronでは患者さまを第一に考え、情熱を持った医薬情報担当者を日本のDupixentコマーシャルチームに迎え入れたいと考えています。この役割では、皮膚科領域の販売目標を達成し、革新と卓越性に専念するチームと共に働くチャンスがあります。医療従事者や患者に価値を提供することに焦点を当てながら、このポジションはキャリアを成長させると同時に、人々の生活に変化をもたらす機会を提供します。</p><p><strong>1日の業務内容：</strong></p><ul><li><p>担当地域の予算とリソースを効果的に管理し、販売目標を達成する。</p></li><li><p>市場の洞察を取り入れ、マーケティング戦略と整合する年間の地域ビジネスプランを作成・実行する。</p></li><li><p>市場の変化に対応するため、ビジネスプランを定期的に更新する。</p></li><li><p>主要なデータソースを活用し、地域の戦略的アクションプランを作成する。</p></li><li><p>医療従事者と関わり、病気やコンセプトの販売を行い、個別のソリューションを提供する。</p></li><li><p>経費報告、マーケティングフィードバック、訪問記録作成などの管理業務を遂行する。</p></li><li><p>アライアンスパートナーと協力し、全体的な目標を達成し、規制ガイドラインを遵守する。</p></li><li><p>必要に応じて地域、国内、全国会議に出席し、Regeneronが提供するすべてのトレーニングプログラムを完了する。</p></li><li><p>会社の備品を適切に管理し、安全運転の実践を遵守する。</p></li></ul><p><strong>この役割に向いている方：</strong></p><ul><li><p>顧客との強固な関係を構築し、価値に基づいたソリューションを提供する能力がある。</p></li><li><p>戦略的思考に長け、目標を達成するために時間を効果的に管理できる。</p></li><li><p>独立した作業環境での業務を得意とし、タイトなスケジュールの中で計画を実行できる。</p></li><li><p>組織的で細部に注意を払い、管理業務に慣れている。</p></li><li><p>他者と協力して共有目標を達成することを楽しめる。</p></li><li><p>柔軟性があり、必要に応じて出張や夜間・週末勤務が可能である。</p></li></ul><p><strong>応募資格：</strong><br>応募者は、学士号（または同等の資格）を有し、製薬業界での営業経験が少なくとも5年以上必要です。有効な運転免許証とMR認定が必須です。英語の流暢さは歓迎されますが、この役割では必須ではありません。望ましい資格としては、皮膚科における治療分野の知識、生物学的製剤の販売経験、皮膚科の主要なリーダーとの確立された関係が含まれます。</p><p>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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 Data Reporting]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47785]]></requisitionid>
    <referencenumber><![CDATA[R47785]]></referencenumber>
    <apijobid><![CDATA[r47785]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Associate Director, Global Patient Safety Business Office]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47619]]></requisitionid>
    <referencenumber><![CDATA[R47619]]></referencenumber>
    <apijobid><![CDATA[r47619]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47619/associate-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 an Associate Director, Global Patient Safety Business Office to join our team!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Associate Director, GPS Business Office will help drive 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></p><ul><li><p>Partner directly with GPS LT to enable execution of GPS vision and strategic priorities </p></li><li><p>Facilitate 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>Maintain 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>Develop 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>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>Develop 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 10+ 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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[Sr. Associate Scientist, Drug Product Delivery Technologies (2 of 3)]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48242]]></requisitionid>
    <referencenumber><![CDATA[R48242]]></referencenumber>
    <apijobid><![CDATA[r48242]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48242/sr-associate-scientist-drug-product-delivery-technologies-2-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><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><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><strong>This Role Might Be For You if You:</strong></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>Possess strong ability to prioritize and manage multiple tasks effectively.</p></li><li><p>Are highly organized, detail-oriented, self-motivated, effective team player.</p></li><li><p>Have 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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 08:56:07 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Oncology Skin]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48192]]></requisitionid>
    <referencenumber><![CDATA[R48192]]></referencenumber>
    <apijobid><![CDATA[r48192]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48192/regional-tumor-lead-marketing-oncology-skin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Skin to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br><strong>A Typical Day:</strong><br><br><br>Leading country insight collection and prioritization to inform global brand strategy<br><br>Ensuring alignment of local priorities with global strategic direction<br><br>Developing the regional tactical plan, including budget alignment<br><br>Facilitating regional tumor marketing meetings to drive execution against plan<br><br>Reviewing country brand plans and sharing insights to improve execution quality<br><br>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes<br><br>Driving regional launch planning and optimization, supporting excellence in country</p><p><br><strong>This Role May Be For You, if you are:</strong></p><p><br>Energized by working with, leveraging and developing talents in countries<br><br>Enjoy connecting global strategy with local market realities<br><br>Comfortable prioritizing across countries and balancing trade-offs<br><br>Energized by guiding brand planning and execution at regional level<br><br>Enjoys shaping content strategies across multiple markets<br><br>Confident leading discussions and aligning diverse stakeholders<br><br>Motivated by improving execution through insights and performance data<br><br>Open to regular travel and engaging with teams across geographies<br><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>81,300 € - 160,000 €</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 04:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 12:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Director, Market Access Strategy (Ophthalmology)]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48344]]></requisitionid>
    <referencenumber><![CDATA[R48344]]></referencenumber>
    <apijobid><![CDATA[r48344]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48344/director-market-access-strategy-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[<h3>Build our future together:</h3><p>The Director of Market Access Strategy is a critical role on a fast-paced, energetic Market Access team. This team member will be responsible for leading and assisting in development/implementation of market access strategies across key segments of our business including: the Ophthalmology Account Director (OAD) team, Rebate Program Specialists (RPS), field reimbursement managers and sales. Primary responsibilities consist of leading and/or assisting in development, implementation and execution of market access initiatives and tactics. Additionally, this individual must maintain a high-level of collaboration and integration with Brand Marketing, I&A, Contract Strategy Operations and Pricing, Training, Trade and all field teams (OAD, Reimbursement, Sales and Payer).</p><h3>When & where:</h3><p>Sleepy Hollow, NY for 4 days a week</p><h3>Discover your role:</h3><ul><li>Leads the development of Market Access strategies and manages the execution of tactical plans aligned with EYLEA Market Access strategies for HCPs</li><li>Leads the GPO core team: facilitates the meetings including agenda and content development, meeting follow up and general correspondence, tracking and accountability</li><li>undefined</li><li>Leads the strategic and tactical development of various field-based resources to support field facing teams including Ophthalmology Account Directors (OAD), Rebate Program Specialists (RPS), Field Reimbursement Managers (FRM), and Sales teams</li><li>Continuously evaluates data and insights, changing market and competitive dynamics to inform short and long-term strategies including but not limited to GPO performance, contracting and pricing, competitive dynamics</li><li>Leads the management of key strategic partner relationships to ensure execution of the strategic vision and tactical goals as well as the timely completion of projects within budget</li><li>Collaborates with cross-functional internal teams (Customer Engagement, Trade, Contract Strategy and Pricing, Marketing, Patient Support Services, Insights and Analytics, Public Policy & Government Affairs, Trade, Medical Affairs and Training) to help inform comprehensive market access strategies and tactical plans</li><li>Ensures the development, production management and implementation of tactical components of the Market Access Strategy to support HCP GPO activities including but not limited to:</li><li>OAD and RPS account resources, initiatives, and partnership opportunities</li><li>Digital tools including websites</li><li>Print and digital market access promotional materials</li><li>Non-personal initiatives, media campaigns</li><li>Field team workshops / training</li><li>Meeting planning support and development of resources for conventions, speaker events, ad boards, POA meetings, etc.</li><li>POA meeting strategies, materials and workshops for the OAD and RPS teams</li><li>Manages OAD and RPS materials inventory, re-approvals, production grids, ISI updates</li></ul><h3>This role requires:</h3><ul><li>8-10+ years of “progressive” industry/relevant professional experienceundefined3-5+ years’ experience within the pharmaceutical/biopharmaceutical market including payer marketing, brand marketing, GPO analytics, contracting, account management, customer facing role, and/or health economics</li><li>Demonstrated background of strong planning and tactical development skills</li><li>Excellent project management skills, proven abilities to manage multiple partners, meet tight timelines and produce consistent, outstanding work products</li><li>Ability to manage multiple projects and tasks ensuring timing delivery while maintaining a high level of quality and on budget</li><li>Strong Teamwork, cross-functional collaboration, and leadership skills, including the ability to build collaborator trust, gain alignment and navigate ambiguity</li><li>Excellent understanding of the US market access landscape and the legal/regulatory environment for pharmaceuticals/biopharmaceuticals</li><li>Experience in the buy and bill space</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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 11:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Temp QC Analyst (HPLC)]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45672]]></requisitionid>
    <referencenumber><![CDATA[R45672]]></referencenumber>
    <apijobid><![CDATA[r45672]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45672/temp-qc-analyst-hplc/]]></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 perform a variety of chemical or biological analyses on raw materials, products, in-process materials, or stability samples in support of the company’s quality program.</p><p>This is a 12 month contract position.</p><p><br><strong>A typical day might include, but is not limited to, the following:</strong> </p><ul><li>Gathering data and documenting test results</li><li>Reviewing test results to ensure compliance with standards and reporting any quality anomalies</li><li>Complying with all pertinent regulatory agency requirements</li><li>Participating in required training activities</li><li>Maintaining laboratory supplies</li><li>Conducting testing on raw materials, in-process samples, product, stability samples, and/or research samples</li><li>Writing and revising control test procedures and SOPs</li><li>Completing test records and reviewing data</li><li>Calibrating or verifying the calibration of instruments/devices prior to use</li><li>Interacting with outside customers or functional peer groups</li><li>Maintaining responsibility for specific projects, where applicable</li><li>Devising or developing new analytical methods and techniques</li><li>Assisting in the validation of methods</li><li>Supporting the transfer of methodology from R&D</li></ul><p>To be considered for this opportunity, you should have a Bachelor’s degree in Life Sciences or a related field, or an equivalent combination of education and 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[産業オペレーションと製品供給]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Review Committee Senior Coordinator]]></title>
    <date><![CDATA[Tue, 16 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/ja/%E4%BB%95%E4%BA%8B/r48578/medical-review-committee-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, 17 Jun 2026 07:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Supervisor Process Maintenance, Wednesday-Saturday 2nd shift]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44046]]></requisitionid>
    <referencenumber><![CDATA[R44046]]></referencenumber>
    <apijobid><![CDATA[r44046]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r44046/supervisor-process-maintenance-wednesday-saturday-2nd-shift/]]></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 to add a Supervisor Process Maintenance to our growing team working a Wednesday-Saturday 2:00pm-12:30am schedule. This role primarily oversees the operations of the Large Scale 10k process area maintenance functions.</p><p>As a Supervisor Process Maintenance, a typical day might include the following:</p><ul><li>Planning and scheduling maintenance repairs/modifications of facility and process equipment.</li><li>Troubleshooting process equipment problems and making required changes.</li><li>Advising supervision of Regeneron Process Maintenance Technicians and Process Maintenance Leads to high performance goals in a cGMP - FDA regulated environment.</li><li>Leading team in continuous improvement, 5S, and Lean initiatives.</li><li>Coaching, counseling and managing performance of a team.</li><li>Reviewing departmental operations and recommending changes to management.</li><li>Forecasting resource requirements and submitting budget recommendations to management.</li><li>Supervising, coordinating and assuring compliance with contractors and Regeneron employees on all applicable codes and standards.</li><li>Supporting Deviation Management process including NOE, EOE and DNF investigations and reviews.</li></ul><p>This position might be for you if you:</p><ul><li>Have at least 3 years of leadership experience.</li><li>Consistently demonstrate adept interpersonal and communication abilities as a leader and provide thoughtful and decisive decision making.</li><li>Have a strong attention to detail including experience with budgeting management.</li><li>Are able to see the “Big Picture” and demonstrate the ability to respond accordingly.</li><li>Ensure the highest level of customer service for both internal and external customers.</li><li>Are skilled in the use of Microsoft office applications (Word, Excel, PowerPoint, Visio and Project) and other related software.</li></ul><p>To be considered for the Supervisor Production Maintenance position, you should have an AS in engineering, science or related field and 5+ years’ experience in pharmaceutical production operations for aseptic formulations, filling and lyophilization. Equivalent combination of education and experience may 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>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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 Scientist, Product Biochemistry (NMR)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46495]]></requisitionid>
    <referencenumber><![CDATA[R46495]]></referencenumber>
    <apijobid><![CDATA[r46495]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46495/associate-scientist-product-biochemistry-nmr/]]></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 Associate to join our dynamic and collaborative group. In this role, you will be responsible for implementing biophysical assessment strategies on different drug modalities such as oligonucleotides, peptides, and small molecule payloads, including collecting and analyzing NMR data, to support research and development efforts. You will play an integral part in technology innovation efforts aimed at enhancing our understanding of therapeutic agents through advanced NMR methodologies.</p><h3>A Typical Day as an Associate Scientist Looks Like:</h3><ul><li>Conduct NMR experiments and analyze data to elucidate the structural and chemical properties of oligonucleotide, peptide, and small molecule candidates.</li><li>Develop and optimize NMR protocols and methods to support both upstream and downstream research initiatives.</li><li>Document all analytical work in electronic laboratory notebooks according to defined protocols with accuracy and attention to detail.</li><li>Communicate experimental findings and data interpretation to supervisors and project teams.</li><li>Summarize results in a concise format for presentations and regulatory documents.</li><li>Present findings at group, departmental, and cross-functional meetings.</li><li>Maintain and troubleshoot instruments and other essential laboratory equipment.</li><li>Utilize additional analytical methods characterize therapeutic candidates alongside NMR studies, and participate in protein purification/enrichment activities.</li></ul><h3>This Role May Be for You If You Have:</h3><ul><li>Experience in the general operations of a laboratory and the ability to manage and organize scientific data under managerial supervision.</li><li>Technical competencies in NMR spectroscopy, with hands-on experience in collecting and interpreting NMR data on oligonucleotides, peptides, and small molecules.</li><li>Experience operating a range of NMR instruments and troubleshooting instrumentation issues.</li><li>Strong organizational skills and the ability to prioritize multiple tasks in a fast-paced environment.</li><li>Ability to contribute to lab equipment maintenance and safety to help create a safe, effective and efficient working environment.</li><li>Familiarity with related analytical techniques such as chromatography or mass spectrometry is a plus.</li></ul><p>This role requires a Bachelor’s or Master’s degree in Chemistry, Biochemistry, Biophysics, or a related field plus 0-3 yrs+ experience with an emphasis on NMR data collection and analysis of oligonucleotides, peptides, or small molecules. 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. Experience with SEC-MALS, iCE, CE-SDS, DSC, or general protein purification and chromatography techniques is highly desirable and considered a plus for this role.</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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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 (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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Scientist, Analytical Drug Product Development and Technology (DPDT)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46918]]></requisitionid>
    <referencenumber><![CDATA[R46918]]></referencenumber>
    <apijobid><![CDATA[r46918]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46918/scientist-analytical-drug-product-development-and-technology-dpdt/]]></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 Scientist to support the laboratory based analytical method development and qualification within the Drug Product Development and Technology (DPDT) group. The DPDT team supports all stages R&D work through commercial. You will be responsible for developing and qualifying analytical methods that will be assessing drug product stability of various drug products from pre-clinical to commercialization development.</p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li>Support analytical strategy development for drug products, with primary focus on peptides, and supporting focus on antibody–drug conjugates, siRNA, monoclonal antibodies, and bispecific antibodies</li><li>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.</li><li>Prepare, author, and review critical analytical technical documents, including analytical method procedures (SOPs), method performance reports, method transfer documents and chip into pharmaceutical development reports for completeness and correctness.</li><li>Guide and work with team members in conducting research and developmental activities. Investigates and solves problems related to the methods used to assess product quality and stability. Sets goals, assigns tasks, and provides performance management and development as needed.</li><li>Maintain full working knowledge of analytical techniques and instruments and applies appropriately to projects and identify and assess novel analytical methods and technologies.</li><li>Evaluate, interpret and present data at team meetings.</li><li>Collaborate with other team members in DPDT and other functional groups at Regeneron in supporting the program development.</li><li>Maintain accurate and complete laboratory record, participate in general lab instrument maintenance, and perform trouble shooting independently.</li></ul><h3><strong>This Role Might Be For You If You Have:</strong></h3><ul><li>Enthusiasm in science with a motivation for making contributions in a team environment is necessary.</li><li>Demonstrated communication skills, collaborative attitude and strong multi-tasking capabilities to thrive in matrix teams.</li><li>Strong collaboration, teamwork, and communication skills.</li><li>Independent, motivated, and detail-oriented with excellent problem-solving abilities.</li></ul><p>This role requires a BS degree in Chemistry, Chemical Engineering, Biochemistry, or related field with ≥7 years of research experience, or MS degree in the above mentioned fields with ≥ 5-years of hands-on research experience. Familiarity with the quantitative and qualitative techniques used in peptide and/or biologic drug products, including capillary and microchip electrophoresis, HPLC/UPLC, mass spectrometry. Experience in biophysical characterization techniques such as DLS, HIAC, fluorescent labeling assays s is a plus. The ability to work independently to design experiments, as well as interpret, document and communicate results 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>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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-Denver]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47329]]></requisitionid>
    <referencenumber><![CDATA[R47329]]></referencenumber>
    <apijobid><![CDATA[r47329]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47329/medical-specialist-ii-ophthalmology-denver/]]></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>Territory: Denver Territory (Colorado/Nebraska)</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.</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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 Pathology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47855]]></requisitionid>
    <referencenumber><![CDATA[R47855]]></referencenumber>
    <apijobid><![CDATA[r47855]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47855/associate-director-pathology/]]></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><p>DVM (or equivalent) with ACVP certification in Clinical Pathology (strong preference for PhD) </p></li></ul></div><div><ul><li><p>Minimum 3 years of experience interpreting GLP and non GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/ biotech or CRO setting. </p></li><li><p>Preferred qualifications: PhD in a scientific field and/or Certification in Anatomic Pathology </p></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[研究と前臨床開発]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Manager, Global Procurement]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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><br><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><br><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><br><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><br><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>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コーポレートファンクション]]></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, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47957]]></requisitionid>
    <referencenumber><![CDATA[R47957]]></referencenumber>
    <apijobid><![CDATA[r47957]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Senior Manager - Full Stack Developer- Clinical Data Operation]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47963]]></requisitionid>
    <referencenumber><![CDATA[R47963]]></referencenumber>
    <apijobid><![CDATA[r47963]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 - ATLANTA North, GA]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48026]]></requisitionid>
    <referencenumber><![CDATA[R48026]]></referencenumber>
    <apijobid><![CDATA[r48026]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48026/medical-account-specialist-ii-neurology-atlanta-north-ga/]]></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[<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: Atlanta North (Metro), GA</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><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>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 13:26:07 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Corporate Compliance Coordinator]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47662]]></requisitionid>
    <referencenumber><![CDATA[R47662]]></referencenumber>
    <apijobid><![CDATA[r47662]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47662/corporate-compliance-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>As a Corporate Compliance Coordinator, you will provide day-to-day operational and administrative support to the Global Corporate Compliance team. You will help maintain documentation, analyze compliance data, handle training systems, and assist with department projects and events.</p><p>Working in a highly collaborative, office-based environment, you will employ your proficiency with Microsoft Office, data analysis, and emerging AI tools to simplify workflows and produce high-quality materials for internal stakeholders. This <strong>entry-level </strong>role is ideal for a motivated professional eager to launch a career in corporate compliance.</p><p><strong>In this role, a typical day might include the following: </strong><br>- Updating compliance documentation, records, and tracking systems to ensure accuracy and readiness for audits <br>- Creating visually engaging presentations in PowerPoint for leadership briefings, employee training, and department communications <br>- Analyzing data in Excel, generating metrics dashboards, and preparing trend reports for management review <br>- Managing the Learning Management System (LMS/TalentHub) by enrolling users, tracking completions, and troubleshooting access issues <br>- Researching new AI and automation tools to improve compliance efficiency and communicating findings to the team <br>- Coordinating logistics for Ethics Day, national meetings, and other compliance-related events </p><p><strong>This job might be for you if you: </strong><br>- Take pride in organizing information and maintaining meticulous records <br>- Enjoy taking complex data into clear, compelling visuals and reports <br>- Are curious about using AI and technology to improve business processes <br>- Communicate clearly and professionally with stakeholders at all levels <br>- Thrive in a collaborative environment and value ethical decision-making <br>- Adapt quickly to shifting priorities and approach challenges with a problem-solving attitude </p><p><strong>In order to be considered for this role, you must have: </strong><br>- Bachelor’s degree in Business, Law, Life Sciences, or Communications preferred <br>- Demonstrated proficiency in Microsoft Excel (formulas, pivot tables) and PowerPoint design <br>- Familiarity with AI productivity tools (e.g., Microsoft Copilot, ChatGPT) and a interest in applying them to compliance operations</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[コーポレートファンクション]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 10 Jun 2026 11:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Regional Tumor Lead Marketing Oncology Lung]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48193]]></requisitionid>
    <referencenumber><![CDATA[R48193]]></referencenumber>
    <apijobid><![CDATA[r48193]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48193/regional-tumor-lead-marketing-oncology-lung/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Lung to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br><strong>A Typical Day:</strong></p><ul><li><p>​Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><br><strong>This Role May Be For You, if you are:</strong></p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</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[Mon, 15 Jun 2026 04:26:12 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Associate Scientist, Formulation Development (DPDT)]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46169]]></requisitionid>
    <referencenumber><![CDATA[R46169]]></referencenumber>
    <apijobid><![CDATA[r46169]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46169/associate-scientist-formulation-development-dpdt/]]></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 and Technology Group is seeking an <strong>Associate Scientist</strong> to support all stages of pre-clinical, clinical, commercial formulation, and drug product development for various drug product modalities. In this role, you may develop, qualify, and 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><strong>A Typical Day in the Role of Associate Scientist May Include the Following:</strong></p><ul><li><p>Design and execute phase-appropriate formulation development studies, such as formulation screening, stability, and compatibility studies, to support formulation and drug product development for early and late-stage development programs.</p></li><li><p>Conduct biochemical and biophysical assessments and pre-formulation studies to support evaluation of preclinical drug candidates.</p></li><li><p>Characterize drug product (lyophilized or liquid) formulation to support process development and manufacturing of clinical drug substances and drug products.</p></li><li><p>Provide technical support for development, technology transfer and manufacture of drug substance and drug products and collaborate with cross-functional teams.</p></li><li><p>Develop and qualify analytical methods for critical quality attributes to support formulation development, drug product process development, and stability testing for programs in all development stages. </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>Author protocols, technical documents for internal use and support regulatory filings.</p></li><li><p>Participate in meetings and present study results in department meetings or cross-functional team meetings.</p></li><li><p>Take part in the general laboratory and instrument maintenance.</p></li></ul><p><strong>This Role Might Be for You If:</strong></p><ul><li><p>You are highly organized, detail-oriented, self-motivated, and passionate about science and innovation.</p></li><li><p>You excel when working in a fast-paced environment and can manage multiple tasks effectively.</p></li><li><p>You are a strong team player.</p></li><li><p>You have excellent interpersonal, oral, and written communication skills.</p></li></ul><p>This role requires a B.S or MS degree in Pharmaceutical Sciences, Chemistry, Biochemistry, Biophysics, Biomedical Engineering, Analytical Chemistry, Chemical Engineering, or a related discipline with 0-3 years of hands-on laboratory experience. Relevant industry or intern experience is preferred. 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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 12:56:09 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/ja/%E4%BB%95%E4%BA%8B/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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers)]]></title>
    <date><![CDATA[Mon, 08 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/ja/%E4%BB%95%E4%BA%8B/r42074/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[<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[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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, Predictive Analytics]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45118]]></requisitionid>
    <referencenumber><![CDATA[R45118]]></referencenumber>
    <apijobid><![CDATA[r45118]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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, IT Product Management – Source to Pay]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45507]]></requisitionid>
    <referencenumber><![CDATA[R45507]]></referencenumber>
    <apijobid><![CDATA[r45507]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45507/associate-director-it-product-management-source-to-pay/]]></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, IT Product Management – Source to Pay, you will lead the IT execution, delivery, and operational ownership of Regeneron’s Source-to-Pay (S2P) capabilities within a modern, global ecosystem. This role is accountable for translating product strategy and roadmap direction into high-quality, scalable, and compliant solutions that support Global Procurement, Finance, and Supply Chain operations.</p><p>Success in this role requires not only deep Oracle EBS and Fusion S2P expertise, but also deep Procurement industry knowledge.</p><div></div><div></div><p>A typical day in this role might look like:</p><ul><li>Serve as IT Product Owner for Oracle EBS and Fusion Cloud Source-to-Pay and associated boundary systems, including but not limited to Procurement (Direct and Indirect), Purchasing, Sourcing/eRFx, Supplier Portal, Supplier Qualification Management, Third Party Risk Management initiatives and Accounts Payable.</li><li>Be a Strategic and trusted IT Partner to business to understand Global Procurement, AP, and Supplier (including ASL and Qualification Management) needs in support of the digital strategy, corporate objectives, and functional priorities.</li><li>Drive S2P end-to-end process, supplier master data and governance (along with Supply Chain) and technology deliverables supporting global growth including standardization.</li><li>Lead IT deliverables for multi-year Procurement Technology Transformation Roadmap and Strategy, deliver on Business outcomes</li><li>Partnering strategically with business for Vendor Selections, RFPs, Cost benefit analysis, application rationalization on an ongoing basis.</li><li>Prepare and maintain project and day-to-day business requirements, functional and system designs, solution documentation, and test plans.</li><li>Provide oversight of system integrators and vendors, ensuring delivery aligns with enterprise standards, Oracle best practices, and future‑state architecture.</li><li>Execute and enforce application, integration, and data architecture standards.</li><li>Partner with technical leads on integrations and extensions involving OIC, APIs, file-based integrations, and data exchanges with upstream and downstream systems.</li><li>Provide techno-functional ownership and oversight for procurement-related boundary systems including Icertis (contract management), ORO (procurement orchestration), Sievo (spend analytics), and Trustpair (supplier bank validations).</li><li>Lead participation in Integration Testing, SIT, UAT, regression testing, and quarterly Oracle patch impact assessments for all P2P-related functionality.</li><li>Maintain strong Identity and Access Management controls (RBAC / ABAC) across sensitive procurement and financial systems.</li><li>Partner with Infosec and other technology teams to ensure alignment with Regeneron security standards and ensure compliance on ERP platforms, SaaS, and third-party applications for patching, data security, privacy.</li></ul><p>This role might be for you if you have:</p><ul><li>Proven experience delivering global S2P implementations, ERP modernizations, or complex rollouts.</li><li>Experience across Oracle ERP Procurement, Finance, and Supply Chain applications.</li><li>Deep experience with Direct Procurement and Supplier Onboarding specifically related to complex ASL and Supplier Qualification process.</li><li>Oracle Fusion Cloud Procure-to-Pay process areas.</li></ul><p>In order to be considered for this position, you must hold a Bachelor’s degree in a related field (Business, Finance, Supply Chain, Information Systems) and 10+ years of experience across Oracle ERP Procurement, Finance, and Supply Chain applications with deep experience with Direct Procurement and Supplier Onboarding specifically related to complex ASL and Supplier Qualification process plus 4+ years of hands-on experience with Oracle Fusion Cloud Procure-to-Pay process areas.</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[コーポレートファンクション]]></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-Pulmonology-Dayton, OH/Northern Cincinnati]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45789]]></requisitionid>
    <referencenumber><![CDATA[R45789]]></referencenumber>
    <apijobid><![CDATA[r45789]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45789/medical-specialist-i-pulmonology-dayton-ohnorthern-cincinnati/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dayton]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Dayton, OH/Northern Cincinnati -representative must reside within or close to the territory.</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>As a Medical Specialist, a typical day might include the following:</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 may be for you if you:</strong></p><ul><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></ul><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. Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches. 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. 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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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 GMP Compliance and Inspections]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46546]]></requisitionid>
    <referencenumber><![CDATA[R46546]]></referencenumber>
    <apijobid><![CDATA[r46546]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46546/manager-gmp-compliance-and-inspections/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>We are seeking a Manager for GMP Compliance & Inspections who will work with cross-functional teams to drive activities that will ensure a state of continuous GMP compliance in Regeneron. This individual will play a leading role in the preparation and execution of regulatory inspections, partner audits and internal audits, as well as follow up post audit/inspection on any items requiring response and action. This role will also promote and drive compliance by building inspection readiness processes across the organization. </p></div><div></div><div><p><strong>As the Manager GMP Compliance & Inspections a typical day might include the following: </strong></p></div><div><ul><li><p>Ensuring readiness for regulatory inspections and partner/other audits in the creation, maintenance and management of inspection content, ensuring it is organized, current and readily accessible at all times</p></li></ul></div><div><ul><li><p>Planning all inspection and audit logistics and scenarios: communication plan, room allocations, backroom/frontroom configuration, technology checks & personnel assignments</p></li></ul></div><div><ul><li><p>Performing a lead role in the audit/inspection Backroom and responding to incoming requests during inspections and audits and ensuring timely and accurate responses</p></li></ul></div><div><ul><li><p>Evaluating outcomes of regulatory authority inspections/partner and other audits to identify near misses, lessons learned and other best practices and working cross-functionally to ensure identified process or system improvement opportunities are sustainably implemented</p></li></ul></div><div><ul><li><p>Coordinating inspection/audit responses and actively managing commitments to regulatory authorities/audit bodies in response to inspection/audit findings</p></li></ul></div><div><ul><li><p>Working collaboratively with commitment owners to ensure that all commitment timelines are met via proactive CAPA tracking, and confirming their timely closure and ensuring suitable effectiveness checks are in place</p></li></ul></div><div><ul><li><p>Maintaining and enhancing communication processes to site management on the status of regulatory inspection readiness and CAPA commitments, including development of appropriate KPIs</p></li></ul></div><div><ul><li><p>Generating, developing and reporting metrics / trends for program adherence to requirements and effectiveness </p></li></ul></div></div><div><div><ul><li><p>Participating in proactive evaluation and education of site GMP compliance against current and emerging regulatory trends</p></li></ul></div><div><ul><li><p>Utilising strong critical thinking skills to serve as a thought partner to the GMP Compliance and Inspections leadership with regard to complex problems</p></li></ul></div><div><ul><li><p>Supporting and leading teams implementing practices and improvements to make IOPS inspection-ready at all times</p></li></ul></div><div><ul><li><p>Building and implementing tools to improve IOPS inspection readiness; determining system improvements through effective project management</p></li></ul></div><div><ul><li><p>Developing and delivering training on inspection conduct, backroom/frontroom protocols, and regulatory expectations</p></li></ul></div><div><ul><li><p>Working with department leaders and cross functional teams to educate, building and maintaining an inspection readiness structure across the organization</p></li></ul></div><div><ul><li><p>Liaising with partners on audit/inspection and quality related matters to provide guidance and advice</p></li></ul></div><div><ul><li><p>Participating on internal committees/teams, as required</p></li></ul></div><div><ul><li><p>Cross-site support of inspection readiness and inspection activities</p></li></ul></div><div><ul><li><p>Coordinating Regeneron information to support regulatory requests for paper inspections and/or observation responses</p></li></ul></div><div><ul><li><p>Additional duties may be assigned as required. </p></li></ul></div><div><p><strong>This role might be for you if:</strong></p><ul><li>You have strong project management, interpersonal, cross- cultural, communication, negotiation, and problem-solving skills</li><li>You understand and listen to team members and stakeholders while fostering a productive team environment to one common objective</li><li>You are driven for proactive resolution of issues with tact, diplomacy and composure</li><li>You show resiliency and flexibility in the face of challenges and adversarial situations</li><li>You are able to provide clear direction to others in ambiguous situations and environments</li><li>You possess knowledge of industry practices and regulations</li></ul></div><div><p>To be considered for this role you should have a BA/BS degree in Life Sciences and the following minimum years of relevant experience for each level: </p></div><div><ul><li><p>Assoc Manager: 6+ years of relevant experience, preferably in the pharmaceutical or biotech industries or related field or equivalent combination of education and experience. </p></li></ul></div><div><ul><li><p>Manager: 7+ years of relevant experience, preferably in the pharmaceutical or biotech industries or related field or equivalent combination of education and experience. </p></li></ul><p>Level will be determined based on qualifications and experience relevant to the role.</p><p>#IRELIM #JOBSIEST #LI-Onsite</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>€74,000.00 - €120,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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, Global Commercial Strategy & Operations - Immunology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47419]]></requisitionid>
    <referencenumber><![CDATA[R47419]]></referencenumber>
    <apijobid><![CDATA[r47419]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47419/associate-director-global-commercial-strategy-operations-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><em>This position is required on-site at Sleepy Hollow, currently 4 days per week with 1 day work from home. A fully remote role is not possible. This role cannot be based in Tarrytown NY nor Basking Ridge NJ.</em></p><p>The Associate Director, Global Commercial Strategy & Operations Immunology will work closely with Global Senior Brand Leadership including SVP, CBU VPs and cross-functional teams to support strategic planning and execution. This role will support the integration and coordination of franchise business planning and analytics, develop global and market brand strategies and lead strategic projects. This role will be based in Sleepy Hollow NY and will report to the Senior Director, Global Commercial Strategy.</p><h3><strong>A Typical Day May Look Like:</strong></h3><ul><li>Support Global, Cross-Functional and Cross-Regional Immunology Commercial integration efforts. Responsible for maintaining cross brand alignment of indications in the U.S., key international markets and HQ teams.</li><li>Evaluate and provide brand leadership with key trends, industry/category/ performance data to support delivery of brand performance against forecasts and assumptions. Helps guide adaptation as necessary to deliver on key brand objectives.</li><li>Support efforts to expand the global impact and reach of product by providing analytic support, investment, strategy, and planning.</li><li>Synthesize data available and build data driven models where needed to analyze and gather insights to help senior leaders better understand business potential for new indications in a given market.</li><li>Lead analysis to measure global business performance by providing valuable insights and recommendations backed by data/</li><li>Collaborate with global leadership on establishing and tracking global performance incentives (including consolidation / calculation).</li><li>Support Immunology Global and U.S. strategic projects in support of overall Immunology brand goals and objectives.</li><li>Participate and where needed lead key partnering meetings, activities and actions.</li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li>You have familiarization with commercial strategy, deep understanding in analytics and proven track record in operations with new product indications and/or launch experience preferred.</li><li>You bring strong analytic skills, learning agility, excellent verbal and written communication skills. Data driven with the ability to visualize, articulate and derive insights by making decisions that are sensible given available information.</li><li>You are able to build positive, productive and sustainable work relationships with internal partners and working with cross functional matrix team across various organizational functions; alliance experience preferred.</li><li>You can operate and define priorities based on business with a result focused approach.</li></ul><p>To be considered, we expect you to have Bachelor’s degree ideally in a scientific field with 10+ years of progressive consulting and/or industry/relevant professional experience including pharmaceutical/biotech. MBA strongly preferred. We also expect you to have the ability to travel 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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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-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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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-New York]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47625]]></requisitionid>
    <referencenumber><![CDATA[R47625]]></referencenumber>
    <apijobid><![CDATA[r47625]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47625/medical-account-specialists-hematology-new-york/]]></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>Geography: New York, 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 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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Scientist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47982]]></requisitionid>
    <referencenumber><![CDATA[R47982]]></referencenumber>
    <apijobid><![CDATA[r47982]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47982/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>Join our fast-paced Regeneron Genetic Medicines team as an <strong>Associate Scientist</strong> supporting pre-clinical gene therapy programs. In this hands-on role, you’ll be involved in the characterization of genetic cargos, complete in vivo studies, and generate high-quality data that informs discovery through early clinical development.</p><p><strong>As an Associate Scientist, a typical day might include:</strong></p><ul><li><p>Characterize and validate genetic cargos both in-vitro and in-vivo</p></li><li><p>Support mice in vivo studies, including blood collection, dosing of viral vectors, antibody oligonucleotide conjugates, and other compounds</p></li><li><p>Participate in necropsies and process various tissues samples for downstream analysis</p></li><li><p>Assess biodistribution through molecular and immunohistochemistry readouts</p></li><li><p>Evaluate efficacy through in-life functional measurements</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You enjoy working with animals and are enthusiastic about translational research —studies that move discoveries from the lab bench to the clinic to benefit patients</p></li><li><p>You are meticulous, take excellent notes, and communicate professionally with both junior and senior colleagues.</p></li><li><p>You are comfortable with quickly shifting priorities and thrive in a collaborative, fast-paced, team driven environment</p></li><li><p>You are curious, proactive, and are looking for an opportunity to grow your skills across multiple gene therapy technologies.</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 a related field.</p></li><li><p>1+ year of proven experience. Must-have experience should include mouse handling, familiarity with various rodent injection and blood collection techniques, and experience with collection and preparation of multiple rodent tissue types for histological analysis.</p></li><li><p>Comfortable asking questions, taking notes, and summarizing high-level takeaways</p></li><li><p>Able to work on multiple projects at once.</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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Reimbursement Business Manager-(Gastro-Pulm)-Tallahassee, FL, Montgomery, AL & Mobile, AL]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47237]]></requisitionid>
    <referencenumber><![CDATA[R47237]]></referencenumber>
    <apijobid><![CDATA[r47237]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47237/reimbursement-business-manager-gastro-pulm-tallahassee-fl-montgomery-al-mobile-al/]]></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><strong>Field Reimbursement Manager, Immunology – Pulmonology and Gastroenterology (Tallahassee, FL - Montgomery, AL - Mobile, AL) </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>A typical day may include the following:</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 may be for you if:</strong> </p><ul><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><li><p>Maintain knowledge base necessary to ensure support of all access and patient/payer support programs and resources offered for all products.</p></li><li><p>Assist in providing appropriate field insights throughout the development of Market Access marketing support materials as needed</p></li><li><p>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</p></li><li><p>Ensure training is completed and kept up to date with appropriate clinical knowledge of the respective products</p></li><li><p>Develop and execute annual budget, with allocation within respective territory</p></li></ul><p>To be considered for this opportunity, you will possess the following:</p><p>A Minimal educational requirement: 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. Experience working with products delivered through a Specialty Pharmacy network is critical. Knowledge of CMS policies and processes with expertise in Part D (Pharmacy Benefit design and coverage policy).This is a field-based position. Candidates must live within the geographical territory that includes Tallahassee, FL, Montgomery, AL, and Mobile, AL. </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>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 18 May 2026 09:56:07 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Field Reimbursement Manager  - Neurology (NY, NY)]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48126]]></requisitionid>
    <referencenumber><![CDATA[R48126]]></referencenumber>
    <apijobid><![CDATA[r48126]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48126/field-reimbursement-manager-neurology-ny-ny/]]></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[コマーシャル]]></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[MR（医薬情報担当者）- 皮膚領域　※岡山西/広島東エリア]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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>勤務地：</strong><br>岡山西部および広島東部エリアを担当いただきます。<br>居住地は岡山（倉敷）または広島（福山）を想定しております。</p><p><br>Regeneronでは患者さまを第一に考え、情熱を持った医薬情報担当者を日本のDupixentコマーシャルチームに迎え入れたいと考えています。この役割では、皮膚科領域の販売目標を達成し、革新と卓越性に専念するチームと共に働くチャンスがあります。医療従事者や患者に価値を提供することに焦点を当てながら、このポジションはキャリアを成長させると同時に、人々の生活に変化をもたらす機会を提供します。</p><p><strong>1日の業務内容：</strong></p><ul><li><p>担当地域の予算とリソースを効果的に管理し、販売目標を達成する。</p></li><li><p>市場の洞察を取り入れ、マーケティング戦略と整合する年間の地域ビジネスプランを作成・実行する。</p></li><li><p>市場の変化に対応するため、ビジネスプランを定期的に更新する。</p></li><li><p>主要なデータソースを活用し、地域の戦略的アクションプランを作成する。</p></li><li><p>医療従事者と関わり、病気やコンセプトの販売を行い、個別のソリューションを提供する。</p></li><li><p>経費報告、マーケティングフィードバック、訪問記録作成などの管理業務を遂行する。</p></li><li><p>アライアンスパートナーと協力し、全体的な目標を達成し、規制ガイドラインを遵守する。</p></li><li><p>必要に応じて地域、国内、全国会議に出席し、Regeneronが提供するすべてのトレーニングプログラムを完了する。</p></li><li><p>会社の備品を適切に管理し、安全運転の実践を遵守する。</p></li></ul><p><strong>この役割に向いている方：</strong></p><ul><li><p>顧客との強固な関係を構築し、価値に基づいたソリューションを提供する能力がある。</p></li><li><p>戦略的思考に長け、目標を達成するために時間を効果的に管理できる。</p></li><li><p>独立した作業環境での業務を得意とし、タイトなスケジュールの中で計画を実行できる。</p></li><li><p>組織的で細部に注意を払い、管理業務に慣れている。</p></li><li><p>他者と協力して共有目標を達成することを楽しめる。</p></li><li><p>柔軟性があり、必要に応じて出張や夜間・週末勤務が可能である。</p></li></ul><p><strong>応募資格：</strong><br>応募者は、学士号（または同等の資格）を有し、製薬業界での営業経験が少なくとも5年以上必要です。有効な運転免許証とMR認定が必須です。英語の流暢さは歓迎されますが、この役割では必須ではありません。望ましい資格としては、皮膚科における治療分野の知識、生物学的製剤の販売経験、皮膚科の主要なリーダーとの確立された関係が含まれます。</p><p>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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[Senior Manager EDC Development]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47771]]></requisitionid>
    <referencenumber><![CDATA[R47771]]></referencenumber>
    <apijobid><![CDATA[r47771]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Los Angeles, CA)]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48128]]></requisitionid>
    <referencenumber><![CDATA[R48128]]></referencenumber>
    <apijobid><![CDATA[r48128]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48128/field-reimbursement-manager-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[<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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 14:56:09 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/ja/%E4%BB%95%E4%BA%8B/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[Field Reimbursement Manager  - Neurology (Austin, TX)]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48132]]></requisitionid>
    <referencenumber><![CDATA[R48132]]></referencenumber>
    <apijobid><![CDATA[r48132]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48132/field-reimbursement-manager-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[<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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 12:56:11 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Manager, Market Access (Temp)]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48312]]></requisitionid>
    <referencenumber><![CDATA[R48312]]></referencenumber>
    <apijobid><![CDATA[r48312]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48312/manager-market-access-temp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Belgium]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a dynamic professional to join our team as a Market Access Manager, overseeing end-to-end management of HTA submissions, price negotiations, and tender strategies in Belgium. This pivotal role ensures strategic alignment with both affiliate and global teams to optimise market access for our innovative products.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Collaborate with HEOR and Global Market Access to prepare and submit robust dossiers to HTA bodies.</p></li><li><p>Develop and align market access and pricing strategies with affiliate commercial teams.</p></li><li><p>Communicate payer needs to global/local teams to inform evidence generation and value dossier development.</p></li><li><p>Support strategies to secure optimal pricing and access, and operationalise these strategies through final negotiations.</p></li><li><p>Contribute to global price-setting and support local price negotiations with innovative solutions.</p></li><li><p>Develop tender strategies and manage submissions in the Belgian market.</p></li><li><p>Track and report performance against market access plans using KPIs and dashboards.</p></li></ul><p><strong>This Role May Be For You If you:</strong></p><ul><li><p>Have extensive experience in a Market Access role within the Pharma sector.</p></li><li><p>Are familiar with the Belgian markets and have a strong track record in HTA submissions.</p></li><li><p>Excel in devising market access strategies and delivering compelling value propositions.</p></li><li><p>Have a proven ability to drive price execution for optimal commercial returns.</p></li><li><p>Are skilled in developing KPIs and dashboards to support growth and performance.</p></li></ul><p><strong>To Be Considered:</strong></p><p>Applicants must have experience in a multidisciplinary, matrix, and global context within the Pharma sector, particularly in the Belgian market. A post-graduate qualification such as an MBA or MSc is highly desirable. Experience in Oncology/Haematology and a good scientific awareness of drug development are preferred.</p><p>Join us in making a meaningful impact on healthcare in Belgium. We look forward to your application!</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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 - 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 -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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 - 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Reimbursement Business Manager - New Jersey]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48456]]></requisitionid>
    <referencenumber><![CDATA[R48456]]></referencenumber>
    <apijobid><![CDATA[r48456]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48456/reimbursement-business-manager-new-jersey/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New Jersey]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><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 customers, sales teams, Payer teams, Alliance partners, HUBs, etc. The Field Reimbursement Management reports to the District Manager of Field Market Access.</p><h3>When & where:</h3><p>Location, Work Model & Travel %, contract duration (for temporary positions only) + flexibility</p><h3>Discover your role:</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. Complete 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>Complete established performance parameters and monitor personal performance against these agreed parameters: Work closely with partners as assigned; District Sales Managers, Medical Specialists, other FRM, Reimbursement, Marketing and Access team members in assigned geographical areas to insure efficient coverage and customer knowledge of this process and all REGN patient services within defined accounts</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, in efforts to streamline the coverage and specialty pharmacy processes to acquire alliance products</li><li>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</li></ul><h3>This role requires:</h3><ul><li>You have a bachelor's degree at a minimum and 5 years of Pharmaceutical Sales or Reimbursement experience</li><li>You have biologic expertise (Specialty Pharmacy/Buy & Bill)</li><li>You are a standout colleague and able to collaborate</li><li>You can optimally communicate across multiple regions via different mediums</li><li>You can get results with your activity</li><li>You are capable with meeting the expectations of internal and external customers</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[コマーシャル]]></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 Director, Clinical Scientist, Ophthalmology]]></title>
    <date><![CDATA[Tue, 16 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/ja/%E4%BB%95%E4%BA%8B/r48582/associate-director-clinical-scientist-ophthalmology/]]></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>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>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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 17 Jun 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Control Analyst]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48421]]></requisitionid>
    <referencenumber><![CDATA[R48421]]></referencenumber>
    <apijobid><![CDATA[r48421]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48421/quality-control-analyst/]]></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 to for a Quality Control (QC) Analyst with a 1st shift, Sunday-Thursday, 8am-4:30pm schedule to join our Gels Team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. The QC Analyst will be part of the lot release for market use of our products. They will perform a variety of biochemical analyses on products, in-process materials or stability samples in support of the company’s quality programs. </p><p>As a QC Analyst, a typical day might include the following: </p><ul><li>Develops and maintains efficient processes to support commercial testing in laboratory functions. Examples include management of materials, reagents, equipment, electronic systems, documents, laboratory safety and inspection readiness. </li></ul><ul><li>Conduct testing on in-process, product, stability and/or research samples. </li></ul><ul><li>Executes and/or coordinates the completion of lab operations activities. </li></ul><ul><li>Ensures timely completion of activities impacting the QC commercial operations. </li></ul><ul><li>Review test results to ensure compliance with standards; report any quality anomalies. </li></ul><ul><li>Perform laboratory OOT, atypical and OOS investigations. </li></ul><ul><li>Writes and revises control test procedures and SOPs. </li></ul><ul><li>Conduct efforts to continuously improve processes while maintaining GxP compliance and keeping tasks on track. </li></ul><ul><li>May be responsible for maintain a specific project. </li></ul><ul><li>May devise and develop new analytical methods and techniques. </li></ul><ul><li>May assist in validation of methods. </li></ul><ul><li>May be involved in establishing the transfer of methodology from R&D. </li></ul><p>This role might be for you if you: </p><ul><li>Are able to maintain integrity and honesty at all time. </li></ul><ul><li>Enjoy working independently or as part of a team. </li></ul><ul><li>Thrive in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients. </li></ul><ul><li>Have effective time management skills to work on multiple projects. </li></ul><ul><li>Have strong interpersonal skills. </li></ul><ul><li>Have excellent written and verbal communication skills </li></ul><p>To be considered for the QC Analyst position you must be willing and able to work 1st shift, Sunday-Thursday, 8am-4:30pm. You must have a BS/BA in Biochemistry, Biology, Chemistry or related field. Or AS/AAS Degree/Certificate in Biotechnology/Biological Science, or an equivalent combination of education and experience. Level is 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 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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 IT Applications Analyst - Labware]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45599]]></requisitionid>
    <referencenumber><![CDATA[R45599]]></referencenumber>
    <apijobid><![CDATA[r45599]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45599/senior-it-applications-analyst-labware/]]></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 Senior IT Applications Analyst is responsible for the configuration, implementation, maintenance, and ongoing support of various IT applications and systems. This role will be primarily focused on performing System Administration, Application troubleshooting, solution design and implementation, and ensuring adherence to compliant processes with some software development opportunities as projects arise.</p><p>As a Senior IT Applications Analyst, a typical day might include the following:</p><ul><li>Develop software and enterprise system solutions by studying information needs, analyzing user requirements, assessing impact and integration with existing information flow between Systems, following the Regeneron software development lifecycle (SDLC).</li><li>Coordinates across business departments and stakeholders, gathering, and implementing requirements and enhancement requests for various applications.</li><li>Responsible for IT Applications documentation, including, converting User Requirement Specifications to a Detail Design Specification, Configuration Test Plans, and Summary Reports.</li><li>Perform design, code, and architecture reviews, processes IT Applications change control requests.</li><li>Providing end-user support for IT Applications including troubleshooting problems at the application, server, and infrastructure level.</li><li>Coordinates with other IT Application team members to administer and support production systems in an efficient and compliant manner.</li><li>Participates or may lead IT Applications systems security access and periodic audit trail reviews.</li><li>Performs recurring system administrative tasks and assists with the maintenance of existing AWS infrastructure.</li><li>Monitoring of development and production service issues to assist support teams.</li><li>Writes and executes queries against large-scale enterprise-level databases.</li><li>Configures reports (tabular, trend, and labels).</li></ul><p>This role may be for you if you have:</p><ul><li>Enjoy both collaborating with a team as well as working independently to develop solutions to complex problems.</li><li>Enjoy driving a creative mindset and collaborating to design, implement, and modify code or configuration, or discover ways to simplify business processes.</li><li>Exhibit a degree of ingenuity, creativity, and resourcefulness in an evolving and sometimes ambiguous environment.</li><li>Have strong analytical and organizational skills, as well as excellent written and verbal communication skills.</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 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><li>Certificates in LabWare Configuration Using LIMS Basic and/or LabWare ELN V4: Experiments, Templates and Configuration 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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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,  Scientific Communications ( Oncology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46060]]></requisitionid>
    <referencenumber><![CDATA[R46060]]></referencenumber>
    <apijobid><![CDATA[r46060]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46060/associate-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>We are seeking an Associate Director, Scientific Communications, to join our dynamic Global Medical Affairs team supporting out Oncology portfolio. In this pivotal role, you will shape and implement comprehensive scientific communication strategies for oncology, ensuring alignment with therapeutic goals and delivering impactful educational materials. This position offers the opportunity to collaborate within a matrix organization, influence medical communications globally, and contribute meaningfully to advancing patient care. </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><strong>A typical day may include the following: </strong><br>• Developing and maintaining scientific communication platforms, lexicons, and disease-state education materials.<br>• Collaborating with Medical Affairs Franchise Directors aligning on congress deliverables and educational content.<br>• Driving quality control and endorsement of scientific assets like program slides and publication updates.<br>• Leading projects through medical review committees to ensure compliance and scientific accuracy.<br>• Managing vendor interactions to ensure timely delivery of high-quality materials.<br>• Creating innovative digital scientific assets for diverse medical channels, including portals and social media.<br>• Assessing internal and external medical education needs to develop impactful educational activities.<br>• Supervising budget allocations and ensuring systematic tracking of expenditures.<br>• Maintaining centralized, searchable resource repositories to support internal teams.</p><p><strong>This may be for you if you:</strong> <br>• Are highly self-motivated with a hands-on execution mentality and a “can-do” spirit. <br>• Excel in a fast-paced, constantly evolving organization and value adaptability. <br>• Are passionate about ensuring scientific integrity and accuracy in all medical and scientific assets. <br>• Enjoy collaborating across multifunctional teams and driving innovative approaches to medical education. <br>• Are committed to ethical standards and prioritize patient-first values in your work. <br>• Are adept at using digital channels to enhance the reach and impact of scientific communications. </p><p>To qualify for this position, you must hold a PhD, MD, or PharmD and have a minimum of 6 years of experience in the pharmaceutical industry, including at least 4 years in Scientific Communications or Medical Affairs. A strong background in oncology and general medicines is essential. Preferred qualifications include proficiency in managing vendor relationships, developing innovative digital assets, and navigating medical review processes. <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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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, Biostatistics - Genetic Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46282]]></requisitionid>
    <referencenumber><![CDATA[R46282]]></referencenumber>
    <apijobid><![CDATA[r46282]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Sourcing Specialist Global Procurement]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46412]]></requisitionid>
    <referencenumber><![CDATA[R46412]]></referencenumber>
    <apijobid><![CDATA[r46412]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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-Allergy/ENT-Las Vegas]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47199]]></requisitionid>
    <referencenumber><![CDATA[R47199]]></referencenumber>
    <apijobid><![CDATA[r47199]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47199/medical-specialist-i-allergyent-las-vegas/]]></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[<p><strong>Geography: Las Vegas (Allergy/ENT)</strong></p><p>Key Markets include Las Vegas, Henderson, Reno, Sparks, Carson City</p><p>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists, and ENTs 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 act. 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> As an Allergy/ENT Medical Specialist, a typical day might include the following:</p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology/ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/ENT 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>This role may be for you if:</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 states, treatment options and healthcare trends</p></li><li><p>You can 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’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology/ENT experience preferred. We need someone with demonstrated 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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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, Clinical Scientist, Genetics Medicine]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47576]]></requisitionid>
    <referencenumber><![CDATA[R47576]]></referencenumber>
    <apijobid><![CDATA[r47576]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47576/senior-manager-clinical-scientist-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>We are seeking a Senior Manager to join our Clinical Sciences team within Regeneron Genetics Medicine. Qualified scientist with training in the pharmaceutical/biotechnology sector, or academic or clinical setting. You will work closely with supervisor and other members of the cross-functional team, contributes to early development and clinical experimentation for projects for discovery phase through Proof of Concept (POC). </p><p>As a Senior Manager, a typical day may include the following:</p><p><br>- Supports the cross-functional study team on the following activities, including but not limited to: </p><p>- Contributes to the writing of sections of Clinical Study Concepts (CSCs) and Clinical Study Protocols (CSPs) and amendments.</p><p>- Assists with identifying key internal and external collaborators/advisors, organizes consultations with global subject matter experts</p><p>- Represents the clinical genetics medicine function on clinical study teams, contributing medical/scientific knowledge to timely and compliant clinical trial execution and quality of deliverables</p><p>- Works alongside Clinical Trial Manager to provide day-to-day clinical input to the study team</p><p>- Drafts portions of the clinical sections in regulatory and clinical documents such as: regulatory agency briefing books, IND/IMPD submissions, investigator’s brochure, informed consent forms, IRB/IEC submissions, clinical study reports, abstracts/manuscripts for publication, etc.</p><p>- Reviews study related documents such as: medical monitoring plans, statistical analysis plans, data management plan, eCRF completion guidelines, data validation manuals, database UAT, etc</p><p>- Trains and support study team and CRO personnel regarding clinical aspects of trial</p><p>- Assist with medical monitoring, raising and responding to investigator queries, writing safety narratives, analysis of trends of safety and efficacy, etc.</p><p>- Organizes steering committees, advisory boards, and data safety monitoring boards as required</p><p>- Identifies program, trial or data risks, creates and implements mitigation strategies</p><p>- Ensures Clinical Team compliance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety.</p><p>- Provides background literature searches in support of:</p><p>- Early clinical strategy in terms of indication selection, study rationale, scientific/clinical endpoints</p><p>- POC-enabling human studies, First-In-Human (FIH) studies, clinical experimental studies as per clinical strategy</p><p>This role may be for you if:</p><p><br>- Effective communications (verbal & written) and presentation skills are essential</p><p>- Must be able to work productively in a fast-paced collaborative environment</p><p>- Demonstrated/potential for critical thinking skills and sound decision-making</p><p>To be considered for this role, you must have a Bachelor’s degree. Ph.D., PharmD. or Master’s degree in biomedical subject. Additionally, we are seeking 8 years of clinical research/development 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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[Sales Manager（営業所長）- 呼吸器領域　※中国・四国エリア]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45705]]></requisitionid>
    <referencenumber><![CDATA[R45705]]></referencenumber>
    <apijobid><![CDATA[r45705]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45705/sales-manager-respiratory-chugoku-and-shikoku-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>勤務地:</strong><br>中国地方および四国地方をご担当いただきます。<br>居住地は広島または岡山が望ましいですが、兵庫または大阪についても相談可能です。</p><p>ダイナミックなイミュノロジーチームで、リードし、インスパイアし、成果を生み出す準備はできていますか？<br>Regeneronでは、私たちのビジョン、価値観、戦略的方向性に沿った高パフォーマンスチーム文化を共に創造し、それを浸透させる営業マネージャーを募集しています。チームの重要な一員として、指定された地域内で営業スペシャリストのグループを管理し、目標達成のための指導とパフォーマンス管理を行います。この役割は、製薬業界で成長と革新を促進しながら、意味のある影響を与える絶好の機会を提供します。</p><p><strong>1日の業務内容:</strong><br>営業マネージャーとして、日々の業務は挑戦に満ち、意義のある貢献が求められます。以下のような業務を担当します：</p><ul><li><p>営業スペシャリストチームをリードし、商業的目標達成を指導する。</p></li><li><p>明確な戦術的戦略を持つ地域およびローカルアカウント計画を策定・実行する。</p></li><li><p>主要業績指標（KPI）を監視し、必要に応じて戦略を調整する。</p></li><li><p>地域全体で投資利益率（ROI）を示すために予算を効果的に管理する。</p></li><li><p>共同商業化パートナーや主要な医療専門家（HCP）との生産的な関係を構築する。</p></li><li><p>業界規範および会社の手続きに完全に準拠することを保証する。</p></li><li><p>関連するビジネス機能にパフォーマンス概要を提供し、組織の成功を支援する。</p></li><li><p>チームのパフォーマンスと協力を向上させるためのベストプラクティスを特定し、共有する。</p></li></ul><p><strong>この役割があなたに向いている理由:</strong><br>リーダーシップの役割で活躍し、このポジションで成功するための資質をお持ちの方。以下に該当する場合、この役割はあなたにぴったりです：</p><ul><li><p>製薬業界での1stラインマネジメントの経験をお持ちの方（優遇）。</p></li><li><p>チームを指導し、最善を尽くすように育成することに情熱を持っている方。</p></li><li><p>強い商業的洞察力とアカウント管理の専門知識を持っている方。</p></li><li><p>戦略的計画、優先順位付け、目標達成の実行に優れている方。</p></li><li><p>ネットワーキングや影響力を発揮し、高い信頼性のある関係を築く能力を持っている方。</p></li><li><p>ビジネスチャンスを見つけ、それを解決策に変える能力を持っている方。</p></li><li><p>協力を重視し、クロスファンクショナルチームでの経験をお持ちの方。</p></li><li><p>頻繁な出張や多様な環境への適応に自信のある方。</p></li></ul><p><strong>応募資格:</strong><br>応募資格を満たす方は、ライフサイエンス、薬学、化学、生物学の学士号をお持ちで、少なくとも7年以上の業界経験を積んでいる必要があります。MR認定資格と有効な運転免許証が必要です。データ、CRMシステム、ExcelやPowerPointなどのツールを使用する能力が必須です。<br>望ましい資格には、呼吸器および耳鼻咽喉科の治療分野の知識、生物学的製剤の販売経験、これらの分野の重要な意見リーダーとの確立された関係が含まれます。英語の流暢さは有利ですが、必須ではありません。</p><div></div><p>免疫学の未来を形作る旅に参加し、あなたのリーダーシップで革新と成功を促進してください。今すぐ応募して、Regeneronの変革の旅の一員になりましょう！</p><p>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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>Identify and maintain relationships with medical and therapeutic area experts, investigators, and other stakeholders.</li><li>Respond to scientific and clinical inquiries in compliance with industry regulations.</li><li>Perform disease management and therapeutic area education for practitioners, payers, and researchers.</li><li>Attend medical conferences to gather and report scientific, clinical, and competitive intelligence.</li><li>Collaborate with investigators and internal medical affairs teams to support investigator-initiated studies (IIS).</li><li>Assist in the development and communication of clinical data through abstracts, posters, presentations, and manuscripts.</li><li>Support site initiation and enrollment activities for clinical trials.</li><li>Ensure adherence to company policies, procedures, and compliance standards.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You are passionate about oncology and have deep knowledge in lung cancer, solid tumors, or hematology oncology.</li><li>You thrive in a collaborative, matrix organization and enjoy building relationships in academic and clinical practice settings.</li><li>You have excellent communication skills and are fluent in both Japanese and English.</li><li>You are experienced in immuno-oncology and clinical trials, and possess a strong commitment to compliance.</li><li>You are comfortable traveling 30–50% of the time to engage with stakeholders and attend conferences.</li></ul><p><strong>To Be Considered:</strong><br>We’re looking for healthcare or scientific professionals with:</p><ul><li>A PhD, PharmD, or MD preferred, though a Master’s Degree with extensive oncology experience may be considered.</li><li>At least 6 years of relevant experience in pharmaceutical industry or clinical settings, such as drug information or disease management programs.</li><li>Proven expertise in oncology, particularly lung cancer, solid tumors, or hematology oncology.</li><li>Immuno-oncology experience is preferred.</li></ul><p>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Front Office Administrator]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47563]]></requisitionid>
    <referencenumber><![CDATA[R47563]]></referencenumber>
    <apijobid><![CDATA[r47563]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47563/front-office-administrator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Bengaluru]]></city>
    <state><![CDATA[Karnātaka]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<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 Admin Coordinator, you will play a key role in ensuring smooth day-to-day office operations. You will be responsible for managing administrative processes, supporting employee experience, and maintaining an organized, efficient, and welcoming workplace environment.</p><h3><strong>A typical day may include the following:</strong></h3><ul><li><p>Managing office attendance records and ensuring adherence to working schedules</p></li><li><p>Welcoming and assisting visitors, ensuring a professional and organized reception experience</p></li><li><p>Monitoring and maintaining office supplies, inventory, and essential resources</p></li><li><p>Coordinating with housekeeping teams to maintain a clean and well-organized office environment</p></li><li><p>Managing inventory records in Excel for stationery, food supplies, and office materials</p></li><li><p>Placing orders for office essentials such as food, water, and other supplies as needed</p></li><li><p>Maintaining invoice records and supporting bill processing activities</p></li><li><p>Supporting employee onboarding activities including preparation of welcome kits and ID cards</p></li><li><p>Maintaining employee databases with accurate and updated information</p></li><li><p>Coordinating cab bookings and supporting transport-related activities</p></li><li><p>Managing courier services for documents, laptops, and related materials</p></li><li><p>Supporting employee engagement activities in coordination with HR and operations teams</p></li><li><p>Handling reception calls and directing them to the appropriate stakeholders</p></li><li><p>Assisting with documentation, printing, and filing activities in an organized manner</p></li><li><p>Coordinating with building management for facility-related issues and follow-ups</p></li></ul><h3><strong>This job may be for you if you have:</strong></h3><ul><li><p>Strong organizational and multitasking skills</p></li><li><p>Good understanding of office administration and operations processes</p></li><li><p>Proficiency in Microsoft Excel and basic office tools</p></li><li><p>Strong attention to detail and record-keeping skills</p></li><li><p>Effective communication and interpersonal skills</p></li><li><p>Ability to coordinate with multiple teams and stakeholders</p></li><li><p>A proactive and problem-solving mindset</p></li></ul><h3><strong>To be considered for this role, you must have:</strong></h3><ul><li><p>3+ years of experience into front office Administration</p></li><li><p>Bachelor’s degree in any discipline</p></li><li><p>Prior experience in administrative, office coordination, or operations support roles preferred</p></li><li><p>Ability to handle multiple responsibilities in a fast-paced environment</p></li><li><p>Strong coordination and execution skills</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[コーポレートファンクション]]></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[Senior Clinical Data Reporting Specialist]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48291]]></requisitionid>
    <referencenumber><![CDATA[R48291]]></referencenumber>
    <apijobid><![CDATA[r48291]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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  - Neurology (Chicago, IL)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48127]]></requisitionid>
    <referencenumber><![CDATA[R48127]]></referencenumber>
    <apijobid><![CDATA[r48127]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48127/field-reimbursement-manager-neurology-chicago-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[<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[コマーシャル]]></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[Drug Production, Associate Manufacturing Specialist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46370]]></requisitionid>
    <referencenumber><![CDATA[R46370]]></referencenumber>
    <apijobid><![CDATA[r46370]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46370/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 Drug Production, Associate Manufacturing Specialist in the Global Manufacturing department. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment. Please continue to review the job duties if you are interested in working 3rd shift (10pm-8:30am) with the potential for weekends.</p><p>A typical day for a Drug Production, Associate Manufacturing Specialist might include:</p><ul><li><p>Performing all aspects 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></ul><p>This role might be for you if you:</p><ul><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>Value trust and transparency in everyday work</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><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>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>Shift & Physical Requirements</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>To enable a healthy work life balance we offer multiple shifts that are 4 working days (10 hours) to support 24/7 production.</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>To be considered for this role you must meet the below minimum education and experience requirements:</p><p>Drug Production, Associate Manufacturing Specialist:</p><ul><li><p>HS diploma + 4 years of relevant work experience <strong>or</strong></p></li><li><p>AS, BS or BA in Life Sciences or related field</p></li><li><p>Able to work 3rd shift (10pm-8:30am) with the potential for weekends</p></li></ul><p>Regeneron offers an exciting and competitive benefits package! For details check out: <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</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[産業オペレーションと製品供給]]></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[Executive Assistant]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48249]]></requisitionid>
    <referencenumber><![CDATA[R48249]]></referencenumber>
    <apijobid><![CDATA[r48249]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48249/executive-assistant/]]></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 R&D, Regulatory and Commercial — 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.</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>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><li><p>Proactively identify opportunities for continuous improvement to current processes.</p></li><li><p>Communicate exceptionally well, whether orally or in writing.</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>Eight or more years of administrative experience required, with at least four 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[コーポレートファンクション]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 20:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Pharmaceutical Sales Specialist Immunology - Alsace]]></title>
    <date><![CDATA[Mon, 08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 08 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Hematology]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48194]]></requisitionid>
    <referencenumber><![CDATA[R48194]]></referencenumber>
    <apijobid><![CDATA[r48194]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48194/regional-tumor-lead-marketing-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Hematology to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br>A Typical Day:</p><ul><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><br><br>This Role May Be For You, if you are:</p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in hematology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</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 02:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 02:56:07 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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 Principal Disaster Recovery Architecture & Engineering]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47450]]></requisitionid>
    <referencenumber><![CDATA[R47450]]></referencenumber>
    <apijobid><![CDATA[r47450]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47450/senior-principal-disaster-recovery-architecture-engineering/]]></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 IT Disaster Recovery (DR) Architecture & Engineering Lead to mature and scale our global DR and resilience capabilities. With a decade of infrastructure-operations experience—including at least five years defining DR architectures and engineering standards—you will develop technical strategy, champion Tier 0 (core-infrastructure) recoverability, and deliver innovative solutions across on-prem, cloud, and hybrid environments. Your leadership will ensure that Regeneron’s critical systems remain available, secure, and compliant as the organization continues to grow.</p><p>Success in this role hinges on deep technical expertise, strategic vision, and the ability to collaborate across engineering, application, and business teams in a highly regulated life-sciences' setting.</p><p><strong>In this role, a typical day might include the following: </strong></p><p>- Driving Tier 0 resiliency roadmaps — compute, storage, network, cloud, security, and automation frameworks </p><p>- Representing DR at Solution Design Engineering Reviews to embed recovery standards into every new or changed system </p><p>- Authoring recovery architectures for cyber-resilience, including offline/ransomware-protection strategies </p><p>- Leading enterprise-wide tabletop and hands-on recovery tests; analyzing results and closing gaps </p><p>- Developing RFPs and evaluating innovative technologies to improve recovery speed, scale, and automation </p><p><strong>This job might be for you if you: </strong></p><p>- Thrive on translating sophisticated technical challenges into practical, scalable recovery solutions </p><p>- Enjoy partnering with diverse teams in a matrix environment to influence architecture decisions </p><p>- Communicate crisply with engineers, executives, and vendors—tailoring your message to each audience </p><p>- Stay calm and decisive while directing high-pressure recovery events or cyber-incident responses </p><p>- Relish process improvement and leverage infrastructure-as-code, automation, and multi-cloud design </p><p>- Value compliance and quality in a pharmaceutical manufacturing context </p><p><strong>In order to be considered for this role, you must have:</strong> </p><p>- 10+ years of IT infrastructure operations experience, and 5+ years leading enterprise DR architecture/engineering initiatives </p><p>- Expert knowledge of DR tools, VMware HA/SRM, multi-cloud (AWS, Azure, GCP) design, cloud recovery architectures, and infrastructure-as-code (Terraform, CloudFormation).</p><p>- Working familiarity with zero-trust concepts.</p><p>- Proven ability to lead recovery testing, influence stakeholders across levels, and perform command-and-control leadership during planned and unplanned events.</p><p>- A Bachelor’s degree in Computer Science, or related field 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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コーポレートファンクション]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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 System Administrator]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43991]]></requisitionid>
    <referencenumber><![CDATA[R43991]]></referencenumber>
    <apijobid><![CDATA[r43991]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r43991/principal-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 a Senior 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 the following minimum relevant experience for each level:</p><ul><li>Senior Automation System Administrator: 5+ years</li><li>Principal Automation System Administrator: 8+ years</li><li>Equivalent combination of education and experience may be considered. Level will be 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[産業オペレーションと製品供給]]></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 Operations Specialist (IT Business Process Automation)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44091]]></requisitionid>
    <referencenumber><![CDATA[R44091]]></referencenumber>
    <apijobid><![CDATA[r44091]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r44091/principal-operations-specialist-it-business-process-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Principal Operations Specialist (IT Business Process Automation) to lead workflow automation across ServiceNow and ProcessX, partnering with IAM and QAR stakeholders to streamline processes, strengthen compliance, and improve reliability. You’ll own the end-to-end lifecycle—from design and integration to operations, incident response, and audit readiness—so teams can move faster with confidence.</p><p>As a Principal Operations Specialist, a typical day might include the following:</p><ul><li>Design, build, and maintain automated workflows in ServiceNow and ProcessX to improve operational efficiency and service delivery.</li><li>Identify, scope, and prioritize automation opportunities across IAM and QAR aligned to business goals and regulatory standards.</li><li>Optimize platform configurations and integrations for performance, scalability, and compliance, following ITIL and GxP best practices.</li><li>Monitor and continuously improve service availability, reliability, and throughput against defined SLAs/OLAs; publish clear metrics and dashboards.</li><li>Define and enforce operational guardrails, SOPs, CSV/validation artifacts, and documentation to ensure GxP, security, and audit readiness.</li><li>Lead major incident response for automation services; coordinate triage, stakeholder communications, root cause analysis, and post-incident reviews.</li><li>Create and execute Service Improvement Plans; use data and analytics to measure impact and recommend enhancements.</li><li>Act as a trusted advisor—translate requirements into practical roadmaps and automation solutions; align platform capabilities with stakeholder needs.</li><li>Partner with Security, QA, and Compliance to meet requirements such as data integrity, access controls, and change governance.</li><li>Own the automation platform roadmap; evaluate new features, apps, and integrations that extend value across the enterprise.</li></ul><p>This role may be for you if you have:</p><ul><li>Deep hands-on experience with ServiceNow workflow configuration, Flow Designer, IntegrationHub, CMDB, and custom development/integrations.</li><li>Proven success implementing automation that improves efficiency and compliance in GxP contexts; familiarity with 21 CFR Part 11 and Annex 11.</li><li>Strong familiarity with IAM and QAR processes in regulated environments and experience operating validated systems using GAMP 5 concepts.</li><li>Expertise with core ITIL disciplines: Incident, Problem, Change, Request, Monitoring/Reporting; strong operational rigor.</li><li>Experience creating validation packages and audit-ready documentation; understanding of data integrity controls and operational guardrails.</li><li>Service management operations at scale, including escalation procedures and on-call/major incident leadership.</li><li>Technical breadth across operating systems (Windows, Linux), virtualization (VMware), and monitoring/security tools (e.g., Splunk, Claroty, next-gen OT tools).</li><li>ServiceNow certifications (e.g., CSA, CAD, CIS in relevant modules) or equivalent demonstrable expertise.</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: 5 years of experience delivering IT/OT services to business or consumers.</li><li>Principal: 8 years of experience delivering IT/OT services to business or consumers.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Strong GxP experience and proven experience in highly regulated environments required.</li><li>Service Management or support in a large-scale and diverse environment of incident management, escalation procedures and related disciplines.</li><li>Experience with delivering projects and initiatives in the IT or OT space.</li><li>Deep experience with ITIL disciplines.</li><li>Experience with operating systems (Microsoft Windows & Linux), VMware.</li><li>Experience with monitoring and security tools such as Splunk, Claroty and next Gen OT 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>€54,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></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 Statistical Programmer]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44611]]></requisitionid>
    <referencenumber><![CDATA[R44611]]></referencenumber>
    <apijobid><![CDATA[r44611]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Délégué(e) Hospitalier(e) Oncologie - Bourgogne Franche-Comté]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45656]]></requisitionid>
    <referencenumber><![CDATA[R45656]]></referencenumber>
    <apijobid><![CDATA[r45656]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45656/delegue-e-hospitalier-e-oncologie-bourgogne-franche-comte/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></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>As an Oncology Pharmaceutical Sales Representative, you will play a pivotal role in driving our commercial goals and encouraging a high-performance culture, while covering <strong>Bourgogne Franche-Comté</strong>. You will be responsible for running your territory, ensuring professional account planning and management of all key accounts and implementing a professional targeting & segmentation approach.</p><p><strong>Oncology Pharmaceutical Representative - Bourgogne Franche-Comté</strong></p><p><strong>As an Oncology Pharmaceutical Representative, a typical day might include the following:</strong></p><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><li><p>Consistently deliver on the value proposition for the brand through key message communication to HCPs.</p></li><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><li><p>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs.</p></li><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><li><p>Report results and developments proactively and clearly to the Immunology leadership team</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You are passionate about ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</p></li><li><p>You are committed to work in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</p></li><li><p>You are thrilled about handling multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</p></li><li><p>You can operate effectively in a “start-up” model as this is a completely new team.</p></li></ul><p>To be considered for this opportunity you must hold a Carte Professionnelle with minimum <strong>5+ years of pharmaceutical sales experience in Oncology</strong>. You are happy with regular travel and have a valid driver's license. Conversational English would be desirable, but not required.</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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Global Finance Operations & Technology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46449]]></requisitionid>
    <referencenumber><![CDATA[R46449]]></referencenumber>
    <apijobid><![CDATA[r46449]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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>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><em><strong>This role will require 4 days per week onsite at our Campus in Sleep Hollow, NY. This is not available as a fully remote / hybrid work.</strong></em></p><p><strong>A typical day may include:</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>Mentor and develop managers and senior individual contributors, building digital fluency and operational excellence across the organization.</p></li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li><p><strong>Finance Technology & Transformation Leadership:</strong> Ability to bridge strategy and execution across finance systems and operations.</p></li><li><p><strong>Global Systems Expertise:</strong> Experience supporting multi‑country finance platforms and operating models.</p></li><li><p><strong>ERP & Cloud Platforms:</strong> Hands‑on experience with modern ERP solutions (e.g., Oracle Fusion, Workday) and cloud‑native technologies.</p></li><li><p><strong>Data & Analytics Enablement:</strong> Experience building dashboards, operational metrics, and insight‑driven reporting capabilities.</p></li><li><p><strong>Architecture & Integration:</strong> Working knowledge of finance system architecture, integrations, and data flows.</p></li><li><p><strong>Change & Talent Development:</strong> Passion for building high‑performing teams and fostering a culture of innovation and continuous improvement.</p></li></ul><p><strong>To be considered for this role you must possess:</strong></p><ul><li><p>Bachelor’s degree in Finance, Accounting, Information Systems, or related field; MBA preferred</p></li><li><p><strong>10+ years</strong> 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[コーポレートファンクション]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Mgr. Accounting Operations]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47280]]></requisitionid>
    <referencenumber><![CDATA[R47280]]></referencenumber>
    <apijobid><![CDATA[r47280]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47280/mgr-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[コーポレートファンクション]]></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, Biostatistics - Medical Affairs]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47321]]></requisitionid>
    <referencenumber><![CDATA[R47321]]></referencenumber>
    <apijobid><![CDATA[r47321]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Field Reimbursement Manager-Oncology-Atlanta, GA/Jacksonville, FL]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48113]]></requisitionid>
    <referencenumber><![CDATA[R48113]]></referencenumber>
    <apijobid><![CDATA[r48113]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48113/field-reimbursement-manager-oncology-atlanta-gajacksonville-fl/]]></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>This position is a critical front-line member of the Regeneron Field Access & Reimbursement team. The primary purpose of this role is to support Physician offices in obtaining appropriate reimbursement and to support the company and divisional reimbursement strategy for Regeneron products within various payer segments.</p><p><strong>When & where: </strong></p><ul><li><p>Hybrid role</p></li><li><p>Location: Atlanta, GA/Jacksonville, FL</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Work cross-functionally and collaboratively with multiple field teams (Regional Directors, Oncology Medical Specialists from multiple teams, Key Account & Payer teams) to act as Reimbursement/Payer Subject Matter Expert, in efforts to support the healthcare provider segment.</p></li><li><p>Provide reimbursement support services/activities in concert with multiple field teams, to educate physician offices on payer policies, billing &coding and Regeneron Patient & Practice services, in efforts to streamline the acquisition and reimbursement processes for Regeneron products. </p></li><li><p>Establish a working relationship within targeted healthcare provider offices to assist healthcare professionals in resolving prior authorization and reimbursement issues that may be barriers to product access in a manner that complies with Regeneron policies, processes, and standard operating procedures.</p></li><li><p>Assist healthcare providers in identifying claims, coding issues and process changes to provide guidance on claims appeal processes within provider offices.</p></li><li><p>Individual must be acutely aware of reimbursement requirements and environmental changes to coverage policies set forth by federal and state governments and managed care organizations.</p></li><li><p>Individual must be flexible to anticipate and adapt to customer reimbursement and support needs, as well as market changes and challenges.</p></li><li><p>Ability to build foundational relationships within payer segments to ensure appropriate product education and overall product support.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor’s degree. At least five years of field reimbursement experience. Buy and Bill market experience. Oncology experience is preferred.</p></li><li><p>Responsible for submitting individual development goals, territory business plan, monthly activity reports, expense reports and other reports as requested by the Regional Director</p></li><li><p>Complete assignments projects as directed and in a timely manner.</p></li><li><p>Demonstrate appropriate territory planning and time management skills by effectively covering the specific geographical area of responsibility.</p></li><li><p>Meet or exceed the standard level of performance in target account activity.</p></li><li><p>Provide sales support via distribution of reimbursement materials and assistance to physician offices and Medical Specialists. Work with Director of Reimbursement Services to track and report on trends within territory assist hotline staff in addressing coding, coverage, or reimbursement resolutions, appeals for authorization and payment as directed. Constantly evaluate levels of customer support delivered and work with department personnel toward improving customer support.</p></li><li><p>Work collaboratively within the various Regeneron departments to facilitate, implement, and execute the overall divisional and corporate goals and 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>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Associate Scientist - Sample Management]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47259]]></requisitionid>
    <referencenumber><![CDATA[R47259]]></referencenumber>
    <apijobid><![CDATA[r47259]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47259/associate-scientist-sample-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>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 Sample Management Group, supporting biobanking operations efficiently and effectively while beginning to independently manage sample data processes. Possesses a thorough knowledge and understanding of clinical/non-clinical study protocols and associated documentation. Is fully capable of multi-tasking across assignments. Works with clients directly in a team environment. The incumbent may help in assessing and investigating new opportunities that will lead to increased efficiencies and improved productivity with regards to biobanking operations.</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>Trains on clinical/non-clinical study protocols and associated study documentation to build knowledge of study conduct as it pertains to biospecimen management. Executes study reference file creation by interpreting protocols and other applicable data inputs with guidance.</li><li>Performs the accessioning and receipt of non-clinical/clinical samples by assessing and verifying data, both manually and with automated platforms such as Microsoft VBA and Streamlit. May identify and communicate issues with automated platforms to drive resolution.</li><li>Executes necessary operations in applicable software systems (e.g., LIMS, ELN, etc.) to perform specimen and data management. Has the ability to identify and troubleshoot routine challenges.</li><li>Fulfills clinical/non-clinical sample requests to support bioanalysis deliverables as well as company-wide research initiatives.</li><li>Facilitates the completion and review sample transfer documentation, as applicable.</li><li>Responsible for assigning and coordinating sample management activities for assigned programs under limited guidance.</li><li>Under supervision, executes the reconciliation and data cleaning of biospecimens to drive deliverables forward.</li><li>May be responsible for the review of study documents to support study start up and protocol amendments.</li><li>Provides cross-functional support to other sample management teams, as needed.</li><li>May assist with the training of other laboratory staff.</li><li>Participates in sub-group meetings and may shares results or progress of work with others.</li><li>Ensures compliance and proper documentation in accordance with SOPs, and applicable regulations.</li><li>Communicates effectively with his/her manager and actively seeks out feedback to deepen self-development.</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>This Role May Be for You If You Have Experience:</strong></p><ul><li>Collaborates and maintains effective verbal and written communication with internal and/or external stakeholders to facilitate data discrepancy resolution. Communicates with CRO’s and third-party vendors to support biospecimen operations.</li><li>Is capable of identifying and troubleshooting problems pertaining to clinical/non-clinical protocols and associated documents as well as routine sample management processes and/or procedures.</li><li>Ensures a state of audit readiness. Assists in the preparation of supporting documents for Quality Audits, as applicable. May participate in study audit activities.</li><li>Handles high priority and high volume tasks within the appropriate timeframe while maintaining accuracy. Adapts to changing priorities. Is capable of multi-tasking across assignments.</li><li>Has an in-depth knowledge of Microsoft Excel and can analyze discrepancies in sample metadata using complex formulas with limited guidance.</li></ul><p><strong>The role requires: </strong></p><ul><li>Bachelor’s degree</li><li>0-4 years of relevant post-degree laboratory experience for Bachelor’s degree</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>$66,300.00 - $98,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Dallas/Houston, TX)]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48129]]></requisitionid>
    <referencenumber><![CDATA[R48129]]></referencenumber>
    <apijobid><![CDATA[r48129]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48129/field-reimbursement-manager-neurology-dallashouston-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[<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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (San Francisco, CA)]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48130]]></requisitionid>
    <referencenumber><![CDATA[R48130]]></referencenumber>
    <apijobid><![CDATA[r48130]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48130/field-reimbursement-manager-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 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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Animal Research Associate]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47955]]></requisitionid>
    <referencenumber><![CDATA[R47955]]></referencenumber>
    <apijobid><![CDATA[r47955]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47955/animal-research-associate/]]></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 Animal Research Associate to join the VelociGene team. This person would manipulate, observe and care for genetically altered rodents to prepare them for study. <br> <br><strong>In this role, a typical day may include: </strong> <br>• Performs certain basic tasks vital for the processing of genetically altered rodents such as animal identification by marking, breeding, weaning, and collection of tissue samples for DNA or RNA analysis. <br>• Performs a natural history analysis when requested. <br>• Records crucial data in the Velocigene Data Management System. <br>• Handles other responsibilities including, but not limited to, the breeding of rodents serving as embryo donors and recipients. <br>• Performs husbandry (cage changing) duties. <br>• Performs additional responsibilities related to the packing and shipping of rodents as well as some basic vivarium tasks such as ordering supplies, and general maintenance when needed. <br> <br><strong>This role may be for you if you: </strong> <br>• Are looking to further their skills and knowledge in lab animal medicine. <br>• Have strong oral and written communication skills. <br> <br>To be considered for this role, you must have a minimum of an A.A. degree with some biology course work or a minimum of 2 years experience working with laboratory animals preferred. Previous work with the handling of laboratory rodents is preferred. The execution of above tasks will be guided by the Velocigene Data Management System and by instruction from the Vivarium manager.</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>$26.35 - $41.15]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47182]]></requisitionid>
    <referencenumber><![CDATA[R47182]]></referencenumber>
    <apijobid><![CDATA[r47182]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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, Uxbridge, UK</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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 07:56:09 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 07:56:09 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Senior Manager, Clinical Study Lead, Internal Medicine]]></title>
    <date><![CDATA[Sun, 14 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/ja/%E4%BB%95%E4%BA%8B/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, Uxbridge, UK</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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 15 Jun 2026 09:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 - 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 Manager - Data Quality & Governance]]></title>
    <date><![CDATA[Fri, 12 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47659]]></requisitionid>
    <referencenumber><![CDATA[R47659]]></referencenumber>
    <apijobid><![CDATA[r47659]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47659/senior-manager-data-quality-governance/]]></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 – Data Quality & Governance, you will play a critical leadership role in shaping and executing the organization’s data governance and data quality strategy. You will serve as a key liaison across global teams, ensuring the implementation of robust, scalable, and compliant data practices. This role is responsible for driving enterprise-wide data quality frameworks, governance policies, metadata management, and data access controls, with a strong focus on enabling analytics, regulatory compliance, and AI readiness across the organization.</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 strategic point of contact for data governance and quality initiatives across regional and global collaborators.</p></li><li><p>Define and implement enterprise data quality frameworks, including rules, standards, monitoring, and remediation processes.</p></li><li><p>Lead the design and deployment of data quality capabilities within platforms such as Snowflake, ensuring alignment with regulatory and governance standards.</p></li><li><p>Establish and maintain data governance artefacts including data quality rule registers, metadata standards, and audit-ready documentation.</p></li><li><p>Oversee data cataloguing and lineage initiatives, ensuring transparency, traceability, and usability of data assets across platforms.</p></li><li><p>Partner with business, technology, and analytics teams to ensure data is governed, trusted, and accessible for decision-making.</p></li><li><p>Define and govern access control models (RBAC/ABAC), ensuring compliance with internal policies and regulatory requirements.</p></li><li><p>Monitor data quality metrics and develop dashboards and scorecards to provide insights to senior leadership.</p></li><li><p>Serve as a blocking issue point for data quality and governance-related issues, ensuring timely resolution and risk mitigation.</p></li><li><p>Drive continuous improvement initiatives to enhance governance maturity, operational efficiency, and data product adoption.</p></li></ul><p><strong>This Role May Be for You If You Have:</strong></p><ul><li><p>Strong experience in data governance, data quality management, or metadata management within global or regulated environments.</p></li><li><p>Deep understanding of data quality dimensions, governance frameworks, data lineage, and access control principles.</p></li><li><p>Proven ability to work in a matrix organization and collaborate with cross-functional and global collaborators.</p></li><li><p>Excellent collaborator management, communication, and influencing skills at senior leadership levels.</p></li><li><p>A structured, detail-oriented approach with strong problem-solving and analytical capabilities.</p></li><li><p>Experience leading teams or mentoring junior members while driving strategic initiatives.</p></li></ul><p><strong>To Be Considered for This Role:</strong></p><ul><li><p>8–10+ years of relevant experience in data governance, data quality, or related domains, preferably within a multinational or GCC environment.</p></li><li><p>Bachelor’s degree required; advanced degree (master’s or equivalent) preferred.</p></li><li><p>Strong experience working with modern data platforms such as Snowflake and tools supporting data governance and lineage.</p></li><li><p>Proficiency in SQL and familiarity with automation tools (e.g., Python, dbt) for data quality processes.</p></li><li><p>Experience in pharmaceutical, biotech, or other highly regulated industries (GxP environment) is preferred.</p></li><li><p>Proven experience supporting audit readiness and regulatory compliance (e.g., FDA, 21 CFR Part 11) is highly desirable.</p></li><li><p>Ability to work effectively in a global environment with strong communication and collaboration 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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Oncology Skin]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48204]]></requisitionid>
    <referencenumber><![CDATA[R48204]]></referencenumber>
    <apijobid><![CDATA[r48204]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48204/regional-tumor-lead-marketing-oncology-skin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Skin to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br><strong>A Typical Day:</strong><br><br><br>Leading country insight collection and prioritization to inform global brand strategy<br><br>Ensuring alignment of local priorities with global strategic direction<br><br>Developing the regional tactical plan, including budget alignment<br><br>Facilitating regional tumor marketing meetings to drive execution against plan<br><br>Reviewing country brand plans and sharing insights to improve execution quality<br><br>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes<br><br>Driving regional launch planning and optimization, supporting excellence in country</p><p><br><strong>This Role May Be For You, if you are:</strong></p><p><br>Energized by working with, leveraging and developing talents in countries<br><br>Enjoy connecting global strategy with local market realities<br><br>Comfortable prioritizing across countries and balancing trade-offs<br><br>Energized by guiding brand planning and execution at regional level<br><br>Enjoys shaping content strategies across multiple markets<br><br>Confident leading discussions and aligning diverse stakeholders<br><br>Motivated by improving execution through insights and performance data<br><br>Open to regular travel and engaging with teams across geographies<br><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>95,250 € - 186,125 €</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[Mon, 15 Jun 2026 04:26:12 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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, Statistical Programming]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43877]]></requisitionid>
    <referencenumber><![CDATA[R43877]]></referencenumber>
    <apijobid><![CDATA[r43877]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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, Clinical Data Management]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44832]]></requisitionid>
    <referencenumber><![CDATA[R44832]]></referencenumber>
    <apijobid><![CDATA[r44832]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Preclinical Operations Associate II]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47267]]></requisitionid>
    <referencenumber><![CDATA[R47267]]></referencenumber>
    <apijobid><![CDATA[r47267]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47267/preclinical-operations-associate-ii/]]></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 Preclinical Operations Associate II provides cross-functional program management support across <strong>Preclinical Operations (PCO)</strong>, <strong>Bioanalytical Sciences (BAS)</strong>, <strong>Scientific Writing (SW)</strong>, and <strong>Drug Safety and Pharmacometrics (DSP)</strong>. This role enables effective planning, alignment, execution, and communication of PCO, BAS, SW and DSP activities in support of development programs.</p><p><strong>Responsibilities during a typical day might include the following:</strong></p><ul><li>Independently deliver comprehensive program management support to PCO, BAS, SW, and DSP functions.</li><li>Facilitate the development, alignment, and execution of nonclinical cross-functional plans, timelines, and deliverables for assigned program(s).</li><li>Integrate nonclinical activities into the broader project plan to ensure alignment with overall development objectives.</li><li>Proactively monitor progress against approved plans, identifying and communicating risks, issues, dependencies, and variances.</li><li>Lead and coordinate appropriate Sub-Team(s) for assigned program(s), ensuring clear objectives, accountability, and effective decision-making.</li><li>Build and maintain strong working relationships with functional and cross-functional stakeholders to influence outcomes and gain alignment.</li><li>Maintain accurate, current nonclinical program information in corporate planning and collaboration tools (e.g., Planisware, SharePoint, Teams, MS Project).</li><li>Contribute to process improvement initiatives by identifying opportunities, proposing solutions, and supporting implementation.</li><li>Provide limited operational or systems support, as needed, to enhance communication, collaboration and efficiency across supported functions.</li><li>Offer constructive feedback and collaborate with team members and functional colleagues to address project and team challenges.</li></ul><p><strong>This role may be for you, if you: </strong></p><ul><li>Bachelor’s or Master’s degree in a relevant scientific or technical field.</li><li>Minimum of 2 years of project or program management experience.</li><li>Strong communication, collaboration, and stakeholder engagement skills.</li><li>Demonstrated ability to learn quickly and adapt to new processes, tools, and systems.</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>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 Process Maintenance]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47325]]></requisitionid>
    <referencenumber><![CDATA[R47325]]></referencenumber>
    <apijobid><![CDATA[r47325]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47325/manager-process-maintenance/]]></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 Manager Process Maintenance to join our growing team. This person will provide leadership, management, and technical consultation to our facilities employees across a team of skilled technicians for day-to-day operations of the Process Maintenance Group. You will oversee contracts for process maintenance projects and coordinate work with appropriate internal departments, contractors, and external agencies, while maintaining department compliance to all regulatory requirements</p><p>As Manager Process Maintenance, a typical day might include the following:</p><ul><li>Managing and leading a Process Maintenance Group and outside contractors/vendors to maintain assets in a state of compliance and control to support the production schedule</li><li>Developing and implementing changes to the Preventive Maintenance (PM) and Predictive Maintenance (PdM) Programs to ensure full compliance to company guidelines</li><li>Collaborating with other department managers in order to maintain Process Equipment, while promoting and ensuring a safe working environment</li><li>Participating in and providing leadership for the development of people, policies and procedures for department, division and organization</li><li>Supervising and maintaining all corrective and preventative maintenance programs for process areas and equipment, while overseeing resolution of Process Maintenance issues</li><li>Managing investigations, coordinating study teams and completing investigation documentation</li></ul><p>This role might be for you if you:</p><ul><li><p>Have demonstrated leadership experience and enjoy mentoring and developing a team in a dynamic, fast paced environment supporting a 24/7 operation</p></li><li>Are capable of interacting with and presenting to senior leadership and confidently communicating with business partners and/or auditors/inspectors</li><li>Build and maintain strong working relationships across the business and with external partners, while providing exceptional customer service</li><li>Can demonstrate excellent analytical, negotiation, and influencing skills</li><li>Have a continuous improvement mentality to identify and implement improvement opportunities</li><li>Have strong time management and organizational skills to balance multiple activities and priorities</li></ul><p>To be considered for this position, you should ideally have an Associate’s degree in engineering or other technical field and the following experience for each level:</p><ul><li>Associate Manager: 8+ years as a maintenance professional, 4+ years in a pharmaceutical or other cGMP environment, 4+ years in a leadership role</li><li>Manager: 9+ years as a maintenance professional, 5+ years in a pharmaceutical or other cGMP environment, 5+ years in a leadership role</li><li>Senior Manager: 10+ years as a maintenance professional, 6+ years in a pharmaceutical or other cGMP environment, 6+ years in a leadership role</li></ul><p>Equivalent combination of education and industry experience may be considered. 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>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 Pharmacology (Oncology)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47422]]></requisitionid>
    <referencenumber><![CDATA[R47422]]></referencenumber>
    <apijobid><![CDATA[r47422]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47422/associate-director-clinical-pharmacology-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 looking for an Associate Director for our Clinical Pharmacology group. The incumbent will provide strategic and scientific expertise, as well as represent Clinical Pharmacology at relevant meetings. This position will provide Clinical Pharmacology subject matter support to new and on-going clinical programs primarily in the Oncology area.</p><p><strong>This role is onsite 4-days per week at either our Tarrytown, NY, Warren, NJ or Cambridge, MA location. </strong></p><p><strong>A day in the life of an Associate Director may look like:</strong></p><ul><li><p>Proactively-identify and provide significant PMx contributes potentially of a complex nature for research and development programs that address strategically important program needs, and that represent scientific advancements of one or more programs and/or aptly address significant regulatory hurdles.</p></li><li><p>Is regarded as an expert in the field; as such is able to contribute to the overall strategic program development and is able to communicate complex PMx strategies and results in an influential manner to the development team.</p></li><li><p>Independently designs and conducts or otherwise oversees the development of PMx analysis plans and applies standardized or advanced scientific techniques to conduct PK, PD, and/or other types of quantitative analyses. Informs PMx management of results and issues in a timely manner.</p></li><li><p>Advanced knowable of the field and know willingness to provide mentorship, is regarded as a scientific leader in PMx.</p></li><li><p>Responsible for the preparation and timely delivery of accurate and well-articulated nonclinical or clinical study reports and regulatory submission documents as appropriate.</p></li></ul><p><strong>This may be the right role for you if you:</strong></p><ul><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>Want to work in cross-functional teams with forward-thinking, passionate, and driven teammates</p></li></ul><p><strong>In Order to be considered qualified for this role you must have:</strong></p><p>A PhD in Biology, Pharmacology, Engineering, Pharmacy (Pharm.D.) or Medicine (MD) with at least 6+ years of relevant Clinical Pharmacology experience. Oncology experience is strongly 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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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 Quantitative Pharmacologist (Pharmacometrician)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47819]]></requisitionid>
    <referencenumber><![CDATA[R47819]]></referencenumber>
    <apijobid><![CDATA[r47819]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47819/principal-quantitative-pharmacologist-pharmacometrician/]]></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 Principal Quantitative Pharmacologist in Pharmacometrics (PMx), this individual is encouraged to provide contributions to PMx results in support of programs. Is further able to prospectively provide PMx contributions in support of longer-term development strategies implemented over the course of multiple experiments, studies, and/or clinical trials.</p><p><strong>In this role, a typical day might include the following: </strong> </p><ul><li><p>Prospectively designs and conducts quantitative or other PMx analyses of a sophisticated nature or otherwise appropriate that is consistent with and encouraging of the program development strategy for one or more program.</p></li><li><p>Keeps PMx management advised of significant PMx results.</p></li><li><p>As a PMx Program Representative on program teams, efficiently communicate sophisticated PMx results in colloquial terms that are understandable across the development teams.</p></li><li><p>Implements PMx management strategic or otherwise impactful changes to the program strategy, direction, and/or regulatory interactions.</p></li><li><p>As a PMx Program Representative, with limited mentorship from PMx management is responsible for, authoring PMx contributions to regulatory documentation, such as IB’s, as well as briefing document for; pre-IND, EOP2, and other global Health Authority (HA) meetings.</p></li><li><p>Is responsible for the preparation and timely delivery of accurate and well-articulated study reports was well as regulatory submission documents as appropriate.</p></li><li><p>Contributes accurate tables and figures for inclusion in slides for senior management presentations.</p></li><li><p>Is able to independently draft and review documentation for accuracy, clarity and messaging to ensure documents are appropriate for further PMx management review.</p></li><li><p>Performs additional analyses as required to support regulatory interactions.</p></li><li><p>Share scientific ideas and contribute to the mentoring of PMx staff.</p></li><li><p>With some supervision is able to competently represents PMx at pre-IND, Type C, pre- BLA, and other HA meetings.</p></li></ul><p><strong>This role may be for you if you have</strong> :</p><ul><li><p>Understanding of PMx concepts and techniques, compartmental modeling, translational modelling/pharmacology, Exposure-Responses analysis methods, Nonlinear Mixed Effects modeling (population PK/PD), logistic regression, survival analysis, Bayesian approaches, disease modelling/QSP*.</p></li><li><p>Knowledge of advanced PMx methodologies applicable to clinical trials, such as survival analysis, stratified or covariate analyses, and strategies for handling missing data.</p></li><li><p>Has regulatory experience through authoring of regulatory briefing books, CTD summaries, contribution at HA meetings, HA negotiations through regulatory review and approval of BLA or equivalent.</p></li><li><p>Proficient in use of analysis tools such as: MS-Excel, R, R-Studio, Phoenix WinNonlin, NLME, NonMem, STAN.</p></li></ul><p><strong>To be considered for this opportunity you will need:</strong> </p><ul><li><p>PhD with 4+ years or an MS degree with relevant industry experience. We expect this experience to include advanced pharmacokinetics, advanced pharmacological principles, non-compartmental analysis methods. Familiarity with other methodologies such as exposure-Response analysis methods, translational modelling/pharmacology, nonlinear Mixed Effects modeling, logistic regression, survival analysis, Bayesian approaches, disease modelling/QSP is also 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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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 Staff Engineer, Data Management (DEA)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47989]]></requisitionid>
    <referencenumber><![CDATA[R47989]]></referencenumber>
    <apijobid><![CDATA[r47989]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47989/sr-staff-engineer-data-management-dea/]]></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, is a multi-functional team that drives PAPD’s digitalization efforts by making data usable and useful!</p><p>The Data Management Architect defines and governs the end-to-end architecture of data systems that power preclinical science and operations. You will architect domain-driven data models, curated datasets, and integration patterns across data lakes, lab systems and analytical tools, while enabling self-service visualizations. You will drive data quality, lineage, metadata and data catalog standards, and platform patterns. To accomplish this, you will partner with numerous teams and departments and deliver value through Agile approaches.</p><p><strong>A Typical Day in the Role Might Involve:</strong></p><ul><li><strong>Enterprise Data Architecture (Preclinical):</strong><br>Define data models for preclinical entities (samples, assays, lots, batches, instruments, methods), harmonized across the data ecosystem; establish golden‑record, lineage, and System or record.</li><li><strong>Data Platform Design:</strong><br>Partner with IT teams to continue our journey to a central data platform like the Research data lake or connected data marts. Partner with data engineering teams to design streaming and batch data flow (ETL vs ELT) patterns and deliver such solutions.</li><li><strong>Visualization & Semantics:</strong><br>Publish governed, analysis‑ready semantic layers and reusable data marts; define KPI/metric definitions; enable self‑service in <strong>Spotfire</strong>/<strong>Tableau</strong> with certified data sources and good performance.</li><li><strong>Data Management & Governance:</strong><br>Stand up data catalog/metadata standards, reference/master data strategies, quality controls, and lifecycle policies; partner with business data stewards in PAPD.</li><li><strong>LIMS/ELN Architecture and Solution Delivery:</strong><br>Partner with platform owners and lab teams to model experiment workflows, capture structured context at source, and ensure compliant, scalable Lab platforms like <strong>Benchling or LabWare LIMS.</strong></li><li><strong>SAFe Ways of Working:</strong><br>Act as the overall product manager and program Lead – define our roadmap and continuous delivery mechanism using Scaled Agile Frameworks.</li><li><strong>Collaboration & Change Enablement:</strong><br>Co‑create roadmaps with PAPD functional leads and department data experts; conduct design reviews; mentor engineers and citizen developers.</li></ul><p><strong>Minimum Qualifications</strong></p><ul><li><strong>Education:</strong> Ph.D. with 6+ years OR Master’s with 12+ years in Computer Science, Data Science, Data Engineering, Applied Mathematics, Bioinformatics, or related discipline.</li><li>Strong understanding of <strong>LIMS/ELN</strong> systems like <strong>Benchling</strong>, <strong>LabWare</strong> or similar <strong>is mandatory.</strong></li><li><strong>Experience:</strong> 8+ years in data architecture/engineering in a scientific or manufacturing context; proven delivery in hybrid cloud/on‑prem data lakes/warehouses.</li><li><strong>Cloud data platforms: </strong>Expertise in AWS, Snowflake, Databricks or comparable cloud data platforms and ecosystems.</li><li><strong>Database Platforms:</strong> Expertise in NoSQL, in-memory, Graph and relational databases, which form the backbone of our operations.</li><li><strong>Tooling & Platforms:</strong> Expert in <strong>data lake</strong> architectures (curation/serving layers), metadata/catalog tools, ELT/ETL data transformation frameworks;</li><li><strong>Analytics Enablement:</strong> Delivered governed, reusable datasets powering visualization tools like <strong>Spotfire</strong>, <strong>Tableau or Power BI</strong>;</li><li><strong>Ways of Working:</strong> Working knowledge of <strong>Scaled Agile (SAFe)</strong> - backlog refinement, PI planning and release management.</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>Experience in <strong>preclinical/bioprocess</strong> domains (samples, assays, batches, equipment, methods).</li><li>Experience with Lab Systems for bioprocessing. </li><li>Prior work aligning data standards across R&D, QA, and Manufacturing (data integrity, traceability).</li></ul><p><strong>Core Competencies</strong></p><ul><li>Build<strong> Data Architectures</strong> that span lab, data, and analytics ecosystems.</li><li>Strong<strong> Communications</strong></li><li>Ability to <strong>Influence</strong>:</li><li>Build <strong>Roadmaps</strong>.</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[研究と前臨床開発]]></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 Group, Quantitative Pharmacology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47970]]></requisitionid>
    <referencenumber><![CDATA[R47970]]></referencenumber>
    <apijobid><![CDATA[r47970]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47970/senior-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>We are looking for a<strong> Senior Group Director</strong> in Quantitative Pharmacology. This individual will be responsible for managing a team functioning in one or more therapeutic focus area. In this capacity the SGD is accountable for the successful and timely completion of QP 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>A day in the life of a Senior Group Director may look like:</strong></p><ul><li><p>Managing and mentoring a broad spectrum of individual contributing scientists.</p></li><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></ul><p><strong>This may be the right role for you, if you:</strong></p><ul><li><p>Can inspire and lead colleagues to deliver PMx and company goals.</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>In order to be considered qualified for this role, you must have:</strong></p><ul><li><p>10+ years of industry experience (with a Ph.D.) or 12+ years (with an M.S.), 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[研究と前臨床開発]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Senior Director Clinical Data Management]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45840]]></requisitionid>
    <referencenumber><![CDATA[R45840]]></referencenumber>
    <apijobid><![CDATA[r45840]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Senior Specialist, EDC Administration]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47959]]></requisitionid>
    <referencenumber><![CDATA[R47959]]></referencenumber>
    <apijobid><![CDATA[r47959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Neurology Account Director - West]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48153]]></requisitionid>
    <referencenumber><![CDATA[R48153]]></referencenumber>
    <apijobid><![CDATA[r48153]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48153/neurology-account-director-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 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: West (California, Oregon, Washington)</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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 15:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Boston, MA)]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48125]]></requisitionid>
    <referencenumber><![CDATA[R48125]]></referencenumber>
    <apijobid><![CDATA[r48125]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48125/field-reimbursement-manager-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[<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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 05 Jun 2026 15:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II-Oncology-Las Vegas, NV]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46212]]></requisitionid>
    <referencenumber><![CDATA[R46212]]></referencenumber>
    <apijobid><![CDATA[r46212]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46212/medical-account-specialist-ii-oncology-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[<p><strong>Geography: Las Vegas, NV</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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 23 Apr 2026 16:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Neurology Account Director - Mid South]]></title>
    <date><![CDATA[Fri, 05 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48152]]></requisitionid>
    <referencenumber><![CDATA[R48152]]></referencenumber>
    <apijobid><![CDATA[r48152]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48152/neurology-account-director-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 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: Mid South (North Carolina, Virginia, South Carolina, Tennessee)</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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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 Specialist–Full Stack Developer- Clinical Data Operation]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48286]]></requisitionid>
    <referencenumber><![CDATA[R48286]]></referencenumber>
    <apijobid><![CDATA[r48286]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 09 Jun 2026 06:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Country Manager Immunology DACH (f/m/d)]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46508]]></requisitionid>
    <referencenumber><![CDATA[R46508]]></referencenumber>
    <apijobid><![CDATA[r46508]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46508/country-manager-immunology-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>At Regeneron, we’re driven by a passion for innovation and making a difference in patients’ lives. As our Country Manager Immunology (f/m/d) for the DACH region, you’ll play a pivotal role in shaping the success of our immunology portfolio. This role includes leading the commercial execution and co-promotion of immunology therapies across multiple indications, driving strategic initiatives, and leading a high-performing team in Germany, Switzerland, and Austria.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Leading and managing the commercial execution and co-promotion of the immunology portfolio for multiple indications</p></li><li><p>Developing and implementing strategic and annual business plans for the DACH region in collaboration with alliance partners</p></li><li><p>Overseeing operational responsibilities, including financial performance, budget and oversight of broad commercial functions including primarily sales force, commercial operations, training, sales force analytics, commercialization and in total a team of ~150 FTEs</p></li><li><p>Preparing for potential future launches of Regeneron’s immunology pipeline</p></li><li><p>Attracting, developing, and retaining a high-performing multidisciplinary team</p></li><li><p>Providing input into strategies for marketing, market access, pricing, and reimbursement led by alliance partners</p></li><li><p>Advocating Regeneron’s vision and mission to medical, patient, and business communities</p></li><li><p>Promoting the company’s profile and ensuring productive and legally compliant relations with business partners, customers, patients, and country authorities</p></li><li><p>Acting as a core member of Regeneron’s international leadership team, contributing to strategies across major markets outside the U.S.</p></li></ul><ul><li><p>Assuming full accountability for the DACH immunology commercial operations including:</p><ul><li><p>Ensuring that the operating objectives and standards of performance are understood and owned by the management team and employees</p></li><li><p>Ensuring consistency between local and global policies and SOPs including adherence to all relevant compliance principles</p></li></ul></li></ul><ul><li><p>Driving affiliate implementation and adherence to the Regeneron mission and values</p></li><li><p>Developing effective relationships with Regeneron’s collaboration partner</p></li></ul><p><strong>This Role May Be For You, If You:</strong></p><ul><li><p>Bring clear patient focus and passion to make a difference in patients’ lives</p></li><li><p>Have demonstrated strategic thinking</p></li><li><p>Champion fact-based, analytical decision making</p></li><li><p>Have the ability to establish goals to guide action and objectively measure performance</p></li><li><p>Have problem solving abilities and critical thinking</p></li><li><p>Demonstrate superior ability to communicate in a multicultural environment in proficient German and English</p></li><li><p>Are results and performance driven</p></li><li><p>Are an excellent team player and collaborator inter- and intra-organizationally</p></li><li><p>Have inspiring leadership presence and a positive mindset</p></li><li><p>Act with transparency and integrity</p></li><li><p>Are ready to travel ~20% of the time</p></li><li><p>Bring international cultural awareness and sensitivity</p></li></ul><p><strong>To Be Considered:</strong></p><p>You’ll need a minimum of 15 years of progressive management experience in the pharmaceutical or biotech sector, with significant experience in sales leadership. An advanced degree in science and/or business is required with an MBA preferred. Proven expertise in leading successful product launches, particularly in immunology or biologics, is highly valued. You bring demonstrated experience driving significant results in a high-performance, rapid-growth innovative enterprise. You have a proven track record of achieving short and long-term objectives and results through the implementation of highly-collaborative, cross-functional teams and infrastructure. Outstanding knowledge of the pharmaceutical specialty market in DACH and experience with co-promoted products with significant aptitude for managing intercompany relationships in alliance structures will set you apart.</p><p><strong>Salary Range (annually)</strong></p><p>157,500 € - 328,750 €</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[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 11 Jun 2026 12:26:08 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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[Regional Tumor Lead Marketing Oncology Skin]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47469]]></requisitionid>
    <referencenumber><![CDATA[R47469]]></referencenumber>
    <apijobid><![CDATA[r47469]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47469/regional-tumor-lead-marketing-oncology-skin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Skin to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><h3>A Typical Day:</h3><ul><li></li><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><h3>This Role May Be For You, if you are:</h3><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</p><div><p><strong>Salary Range (annually)</strong></p><p>101,500€ - 200,400€</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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 12 Jun 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Oncology Skin]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48207]]></requisitionid>
    <referencenumber><![CDATA[R48207]]></referencenumber>
    <apijobid><![CDATA[r48207]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48207/regional-tumor-lead-marketing-oncology-skin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Skin to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br><strong>A Typical Day:</strong><br><br><br>Leading country insight collection and prioritization to inform global brand strategy<br><br>Ensuring alignment of local priorities with global strategic direction<br><br>Developing the regional tactical plan, including budget alignment<br><br>Facilitating regional tumor marketing meetings to drive execution against plan<br><br>Reviewing country brand plans and sharing insights to improve execution quality<br><br>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes<br><br>Driving regional launch planning and optimization, supporting excellence in country</p><p><br><strong>This Role May Be For You, if you are:</strong></p><p><br>Energized by working with, leveraging and developing talents in countries<br><br>Enjoy connecting global strategy with local market realities<br><br>Comfortable prioritizing across countries and balancing trade-offs<br><br>Energized by guiding brand planning and execution at regional level<br><br>Enjoys shaping content strategies across multiple markets<br><br>Confident leading discussions and aligning diverse stakeholders<br><br>Motivated by improving execution through insights and performance data<br><br>Open to regular travel and engaging with teams across geographies<br><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>84,675 € - 167,125 €</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 04:56:08 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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[Regional Tumor Lead Marketing Hematology]]></title>
    <date><![CDATA[Sun, 14 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48214]]></requisitionid>
    <referencenumber><![CDATA[R48214]]></referencenumber>
    <apijobid><![CDATA[r48214]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48214/regional-tumor-lead-marketing-hematology/]]></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 Regional Tumor Lead Marketing Hematology to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br><strong>A Typical Day:</strong></p><ul><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><br><br><strong>This Role May Be For You, if you are:</strong></p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in hematology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</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[Mon, 15 Jun 2026 04:26:12 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/ja/%E4%BB%95%E4%BA%8B/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[Quality Control Scientist]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45797]]></requisitionid>
    <referencenumber><![CDATA[R45797]]></referencenumber>
    <apijobid><![CDATA[r45797]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45797/quality-control-scientist/]]></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 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 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 Quality Control Scientist (Chemistry) Technical Resources role you must have a BS in Chemistry, Biochemistry, Biology, or a related field, and 4+ 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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational 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[産業オペレーションと製品供給]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Assoc Scientist- Biomolecular Interactions/Kinetics]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41252]]></requisitionid>
    <referencenumber><![CDATA[R41252]]></referencenumber>
    <apijobid><![CDATA[r41252]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r41252/sr-assoc-scientist-biomolecular-interactionskinetics/]]></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>We are seeking a motivated Sr Assoc Scientist to join the High Throughput Antibody Screening and Biomolecular Interaction Group within the Therapeutic Proteins team.</strong> You will support Therapeutics Protein activities by implementing methods to characterize protein interaction kinetics and biochemical properties using SPR, BLI, ITC, and other analytical technologies in support of our VelocImmune fully-human antibody pipeline.</p><p><strong>As a Sr Assoc Scientist, a typical day might include:</strong></p><ul><li><p>Conducting experiments including antibody characterization, method development, and analytical support for biologics development using biochemical and biophysical methods</p></li><li><p>Troubleshooting established test methods used in development and release testing of screening reagents</p></li><li><p>Tabulating results and writing summary reports of assay development</p></li><li><p>Presenting findings at group and interdepartmental meetings</p></li><li><p>Maintaining lab supplies and equipment</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Can work independently, show initiative to design and carry out experiments based on protocols</p></li><li><p>Manage and organize data independently, as well as have decision-making capabilities but know when to reach out for support</p></li><li><p>Can troubleshoot methodological and technical issues</p></li><li><p>Enjoy working in a fast-paced and deadline driven team environment and are capable of multi-tasking across assignments</p></li><li><p>Have excellent communication skills</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS with 4+ years of relevant lab experience. We need someone with a foundational knowledge in structural biology, biophysics, or chemical biology. Must have experience in protein chemistry techniques (HPLC, FLPC, ion-exchange, affinity, size exclusion chromatography, and protein conjugation chemistry) and protein analysis (SDS-PAGE, Western-blot, ELISA). Knowledge and experience in using biophysical methodologies such as Biacore, Octet, or ITC to study protein/small molecule or protein/protein interactions and binding kinetics 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>$79,100.00 - $129,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></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 Automation System Specialist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43990]]></requisitionid>
    <referencenumber><![CDATA[R43990]]></referencenumber>
    <apijobid><![CDATA[r43990]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r43990/senior-automation-system-specialist/]]></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 a Senior Automation System Specialist (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><p>Administering system applications including user control access; adding, modifying, and removing users; defining user types, user groups and security settings.</p></li><li><p>Monitoring data backup or archival to ensure systems can meet defined RTO (Recovery Time Objective) and RPO (Recovery Point Objective).</p></li><li><p>Utilizing configuration management and recipe/method management.</p></li><li><p>Authoring documents such as impact statements, Configuration Specifications, risk assessments, Standard Operating Procedures, Work Instructions, Policies, and corrective/prevention action plans.</p></li><li><p>Supporting system SAT (Site Acceptance Testing) / FAT (Factory Acceptance Testing), validation and qualification efforts.</p></li><li><p>Conducting system integration with existing systems (e.g. LIMS, Historian).</p></li><li><p>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.</p></li><li><p>Providing end-user support including system functionality training, solving problems at the application level and hardware troubleshooting (includes working with vendors to resolve issues).</p></li><li><p>Participating in, leading, or authoring investigations and root cause analysis for issues of non-compliance.</p></li><li><p>Leading aspects of the work for contractors and providing guidance as applicable.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Have experience with a combination of the following: Ignition, MQTT brokers, HiveMQ, HighByte, or other similar platforms.</p></li><li><p>Have interest in manufacturing process within a regulated technical environment.</p></li><li><p>Have a solid understanding of System Design Lifecycle and Quality Risk Management.</p></li><li><p>Enjoy designing and implementing sustainable technical\procedural solutions in a complex environment.</p></li><li><p>Understand process control systems and product release testing systems.</p></li><li><p>Are familiar with regulatory and quality policies, procedures, documentation methods.</p></li><li><p>Enjoy working independently as part of a broader team with a proven focus on customer service and maintaining compliance.</p></li><li><p>Enjoy project management and have strong organizational skills.</p></li><li><p>Are motivated to participate in continuous process improvement.</p></li></ul><p>Applicants ideally should have a BS/BA in Science, Engineering or related field and the following minimum relevant experience for each level:</p><ul><li><p>Senior Automation System Specialist (Administrator): 5+ years</p></li><li><p>Principal Automation System Specialist (Administrator): 8+ years</p></li></ul><p>Equivalent combination of education and experience may be considered. 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>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[産業オペレーションと製品供給]]></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 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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, AI Engineering (Global Development)]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44760]]></requisitionid>
    <referencenumber><![CDATA[R44760]]></referencenumber>
    <apijobid><![CDATA[r44760]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Reimbursement Business Manager-Dermatology-Columbus, OH]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45962]]></requisitionid>
    <referencenumber><![CDATA[R45962]]></referencenumber>
    <apijobid><![CDATA[r45962]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r45962/reimbursement-business-manager-dermatology-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>Field Reimbursement Manager - Dermatology (Columbus, OH)</strong></p><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><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>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</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 (Dupixent).</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 aligns with Regeneron policies, processes, and standard operating procedures</p></li><li><p>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</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</p></li><li><p>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.</p></li><li><p>You possess excellent organizational, project management, and communication skills.</p></li><li><p>Experience working with products delivered through a Specialty Pharmacy network is essential.</p></li><li><p>Collaboration and proactive communication skills.</p></li><li><p>Background in leadership and effective cross functional partnership a plus.</p></li><li><p>Established ability to work within an Account Management based structure.</p></li></ul><p>To be considered for this opportunity, you will possess the following:</p><p>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. Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors. Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</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>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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 Clinical Data Management Study Lead]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46045]]></requisitionid>
    <referencenumber><![CDATA[R46045]]></referencenumber>
    <apijobid><![CDATA[r46045]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r46045/senior-manager-clinical-data-management-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></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[グローバル展開]]></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[Associate Director, Finance & Administration - Canada]]></title>
    <date><![CDATA[Mon, 08 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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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, Customer Master & CRM Data Management]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47203]]></requisitionid>
    <referencenumber><![CDATA[R47203]]></referencenumber>
    <apijobid><![CDATA[r47203]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47203/director-customer-master-crm-data-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>Regeneron is seeking a Director, Customer Master & CRM Data Management to join our Commercial Organization! <br> </p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, Customer Master & CRM Data Management will report into the Executive Director, Commercial Data Management within the Commercial Strategy, Insights & Analytics (CSI&A) organization at Regeneron Pharmaceuticals, Inc. This role serves as the Commercial Customer Data Owner accountable for the integrity, quality, governance, and strategic evolution of Regeneron’s commercial customer master data spanning HCP, HCO, address, affiliation, and hierarchy domains. The Director will also oversee overall commercial business needs related to a next-generation master data management (MDM) platform, as well as the insights and analytics (I&A) needs for Regeneron’s next-generation customer relationship management (CRM) platform, while also ensuring continuity and excellence of data quality on the current platforms. The ideal candidate brings deep expertise in pharmaceutical customer data management, MDM & CRM platforms, and cross-functional stakeholder engagement, with the leadership presence to chair the Customer Master Data Council and drive commercial-wide alignment.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Lead</em></p><p>1) Serve as the strategic Customer Data Owner for the commercial customer master, as well as the business owner of the MDM platform, setting the vision, standards, and roadmap for HCP, HCO, address, affiliation, and hierarchy data across all therapeutic areas and commercial systems (CRM, commercial data warehouse [CDW], and downstream platforms)</p><p>2) Chair the Customer Master Data Council; establish governance cadences, decision rights, and RACI frameworks across CSI&A, Commercial IT (CIT), and business stakeholders in alignment with the data governance operating model</p><p>3) As the business owner, in collaboration with CIT, define and drive the Commercial team’s MDM platform transition through requirements definition, phased implementation, UAT, and go-live; own the ongoing customer master capability roadmap from a Commercial business perspective, including near-real-time CM-CRM-CDW synchronization, canonical data feeds, and next-gen identity resolution frameworks</p><p><em>Develop</em></p><p>4) Build and formalize the Customer Master Data Governance program, including data dictionaries, Critical Data Element (CDE) catalogs, data quality (DQ) rule catalogs, and controlled field and intake channel standardization; establish and continuously improve data quality KPIs, SLA frameworks, and closed-loop remediation processes with dashboards providing transparent DQ and data change request (DCR) metrics to all stakeholders</p><p>5) Lead organizational change management associated with the MDM platform transition, including stakeholder communication, training, and adoption planning for internal teams and downstream system owners</p><p><em>Partnership and Collaboration</em></p><p>6) Partner closely with CIT & Commercial platform leads (e.g., CRM, CDW), CRM product owners, CDW owners, and 3rd-party data vendors (IQVIA, MedPro) to ensure customer data flows correctly and consistently across all commercial systems</p><p>7) Manage external data vendor relationships including contract oversight, SLA enforcement, data delivery quality reviews, and issue escalation for customer master data sources</p><p>8) Oversee and mentor a team of data stewards (Lead Business Data Steward and TA/Brand-level stewards); foster a culture of data ownership, accountability, and continuous improvement in data quality practices</p><p><em>Execute</em></p><p>9) Oversee day-to-day DCR governance, ensuring single intake, search-before-create enforcement, auto-approval thresholds, and timely SLA compliance</p><p>10) Perform and direct data analytics to troubleshoot customer master issues, quality-check system changes, validate affiliation and hierarchy integrity, and respond to ad hoc stakeholder questions</p><p>11) Document, maintain, and update all standard operating procedures (SOPs) and workflows related to customer master data management; ensure proper version control and cross-functional accessibility</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>BA/BS required; advanced degree (MBA, MS) preferred</p></li><li><p>12+ years of progressive experience in commercial data management within pharmaceutical or biotechnology (or 10+ years with MBA/MS); at least 3 years in a director-level or senior leadership role</p></li><li><p>Deep expertise in pharmaceutical customer master data including HCP/HCO identity, affiliation management, hierarchy maintenance, address validation, and DCR governance processes</p></li><li><p>Demonstrated experience leading or serving as business lead for an MDM platform implementation or major system transition (e.g., Reltio, Veeva Network, IQVIA OCE, Informatica MDM, or equivalent)</p></li><li><p>Strong working knowledge of commercial customer data vendors and sources including IQVIA OneKey and MedPro, and their integration into commercial customer master platforms</p></li><li><p>Experience establishing and operating data governance frameworks including data quality KPIs, SLA management, DQ rule catalogs, CDEs, and stewardship programs</p></li><li><p>Proficiency with data management and analytics tools (SQL, Snowflake, Databricks, or equivalent); ability to perform analytics to diagnose and resolve data quality issues</p></li><li><p>Proven ability to translate complex business requirements into technical specifications and manage cross-functional delivery with IT partners</p></li><li><p>Strong executive communication and presentation skills; demonstrated experience influencing senior stakeholders and chairing governance forums</p></li><li><p>Demonstrated ability to lead, develop, and mentor a team; experience building stewardship programs and driving adoption of data governance practices</p></li><li><p>Familiarity with privacy and compliance requirements applicable to commercial customer data (HIPAA, state-level HCP data regulations, aggregate spend reporting)</p></li></ul><p>Preferred Skills</p><ul><li><p>Experience with mainstream biotech commercial platforms (CRM, CDW) </p></li><li><p>Background in commercial operations roles (field force data, sales operations, analytics) providing appreciation for the downstream impact of customer master data quality</p></li><li><p>Familiarity with IQVIA LAAD/APLD or other secondary HCP-level datasets and their relationship to customer master identity resolution</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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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 Paralegal - R&D and Regulatory]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47214]]></requisitionid>
    <referencenumber><![CDATA[R47214]]></referencenumber>
    <apijobid><![CDATA[r47214]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47214/senior-paralegal-rd-and-regulatory/]]></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 R&D Regulatory law group is seeking a <strong>Senior Paralegal </strong>to join our legal team. The Senior Paralegal will play an important role in various R&D and regulatory-related activities. The ideal candidate will possess excellent organizational skills and be motivated to learn about drug development regulations. </p><p>This role functions as a senior manager-level individual contributor, providing sustained ownership of complex R&D regulatory contract processes and exercising independent judgment in a high-risk, highly regulated environment, without people management responsibilities.</p><p><strong>In this role, a typical day might include the following:</strong> </p><ul><li><p>Support maintenance of contract playbooks, templates, and internal clinical research documents</p></li><li><p>Work with R&D attorneys to review contracts and other regulatory forms</p></li><li><p>Partner with R&D attorneys to formulate and communicate compliant and practical solutions that meet business objectives</p></li><li><p>Assist with fact-gathering to support legal advice</p></li></ul><p><strong> </strong></p><p><strong>This role might be for you if have experience with :</strong></p><ul><li><p>Strong organizational skills; able to effectively manage projects and responsibilities by applying prioritization skillset and sound judgment</p></li><li><p>Demonstrated ability to work accurately and effectively</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>BA/BS required</p></li><li><p>8 or more years of progressive paralegal work experience</p></li><li><p>Previous experience in a pharmaceutical company or biotech and knowledge of issues related to clinical research 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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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 Disaster Recovery Governance]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47449]]></requisitionid>
    <referencenumber><![CDATA[R47449]]></referencenumber>
    <apijobid><![CDATA[r47449]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47449/assoc-dir-disaster-recovery-governance/]]></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 IT Disaster Recovery (DR) Governance Lead to improve and run the company’s enterprise-wide DR and resilience program. Drawing on 10–15 years of IT infrastructure and business-operations expertise—including at least 5 years leading DR planning—you will design governance frameworks, drive continuous improvement, and ensure that recovery capabilities keep pace with evolving business, technology, and regulatory requirements.</p><p>Success in this role requires strategic leadership, hands-on proficiency in DR tools and cloud technologies, and the ability to influence cross-functional teams, vendors, and senior executives within a highly regulated environment.</p><p><strong>In this role, a typical day might include the following: </strong></p><p>- Representing DR during Solution Design Engineering Reviews to align new systems with recovery objectives </p><p>- Governing CMDB/DR metadata, application mapping, and interdependency documentation in ServiceNow </p><p>- Developing and enforcing DR policies, standards, and SOPs, while supervising compliance metrics and key performance indicators</p><p>- Coordinating quarterly and annual recovery tests, analyzing results, and driving corrective actions </p><p>- Partnering with engineering teams and SaaS vendors to close capability gaps, negotiate SLAs, and automate DR processes </p><p>- Acting as command-and-control lead during planned and unplanned recovery events </p><p><strong>This job might be for you if you: </strong></p><p>- Excel at translating sophisticated technical requirements into clear, actionable recovery strategies </p><p>- Enjoy collaborating with infrastructure, application, and business teams in a matrix environment </p><p>- Communicate confidently with everyone from hands-on engineers to C-suite executives </p><p>- Thrive on improving processes, measuring outcomes, and using data to drive decisions </p><p>- Remain calm and decisive during high-pressure incidents and recovery exercises </p><p>- Value regulatory rigor and have a passion for protecting critical operations in life-sciences manufacturing </p><p> - Excel at tracking indicators and reporting program health to senior leadership and governance boards </p><p><strong>In order to be considered for this role, you must have: </strong></p><p>- A Bachelors Degree in Computer Science, or related field.</p><p>- 5+ years leading enterprise DR governance, plus 10–15 years in IT infrastructure or related fields </p><p>- Validated expertise with DR planning tools and CMDB/BCM platforms (ServiceNow preferred) </p><p>- Strong organizational, analytical, and interpersonal skills with the ability to influence 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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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/ja/%E4%BB%95%E4%BA%8B/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[研究と前臨床開発]]></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[Temp Talent Acquisition Specialist]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47858]]></requisitionid>
    <referencenumber><![CDATA[R47858]]></referencenumber>
    <apijobid><![CDATA[r47858]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47858/temp-talent-acquisition-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p> Are you passionate about connecting top talent with impactful opportunities? Join our dynamic Global Recruiting Team and contribute to the growth and innovation of one of the most exciting organisations in the Biotech/Pharma industry. </p><p>In this role, you will play a key role in executing on our recruiting strategies and delivering outstanding candidate and hiring manager experiences. This position partners closely with various groups within our organisation, driving full-cycle recruitment processes and ensuring we attract and hire the best talent for our thriving organisation. </p><p><strong>As a Temp Talent Acquisition Specialist, a typical day might include the following:</strong> </p><ul><li><p>Source, screen, and lead candidates through the full recruitment lifecycle, providing outstanding candidate experience</p></li><li><p>Build and sustain proactive pipelines for various roles both temporary and full time through various search techniques, Talent Relationship Management tools (Beamery), and professional networks</p></li><li><p>Be responsible for candidate experience initiatives, ensuring consistent and high-quality touchpoints across the recruitment lifecycle</p></li><li><p>Collaborate with hiring managers to define roles, responsibilities, and draft compelling job postings that reflect organisational objectives and attract top talent</p></li><li><p>Partner with leaders across the various teams to implement recruiting strategies that meet each function’s talent needs</p></li><li><p>Outstanding stakeholder management with the ability to influence; you have a history of building trust and credibility with leaders</p></li><li><p>Stay current on industry trends, labor market conditions, and recruiting best practices to continuously improve strategies</p></li><li><p>Handle candidate activity within the applicant tracking system (ATS) and TRM system (Beamery)</p></li></ul><p><strong>This role might be for you if you:</strong> </p><ul><li><p>Are a self-motivated, and proactive professional who thrives in a fast-paced, collaborative environment</p></li><li><p>Excel at building rapport, balancing multiple priorities, and getting results</p></li><li><p>Display strong problem-solving skills and the ability to navigate ambiguity with confidence</p></li><li><p>Have excellent written and verbal communication skills, with a talent for providing clear and insightful updates to candidates, colleagues, and business partners</p></li><li><p>Demonstrate proficiency in Microsoft Word, Excel, and Outlook</p></li></ul><p>To be considered for this position you should have a Bachelor’s degree in Human Resources, Industrial-Organisational Psychology, or a related field and at least 2+ years of full-cycle recruiting experience</p><p>#IRELIM #JOBSIEST #LI-Onsite </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[コーポレートファンクション]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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 Medical Affairs Senior Manager, Haemato-Oncology]]></title>
    <date><![CDATA[Mon, 08 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48108]]></requisitionid>
    <referencenumber><![CDATA[R48108]]></referencenumber>
    <apijobid><![CDATA[r48108]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48108/field-medical-affairs-senior-manager-haemato-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></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. Join our <strong>UK Medical Affairs</strong> team as <strong>Senior Manager, Field Medical Affairs, Haemato-Oncology</strong>, supporting national field engagement across haematological malignancies. In this role, you will exchange scientific and medical information with key opinion leaders, healthcare professionals, researchers and population-based decision makers, while bringing field insights on research developments, the treatment landscape and opportunities that build medical strategy. This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide. </p></div><div><p><strong>When & where: </strong></p></div><div><ul><li><p><strong>Location:</strong> Field based, UK </p></li></ul></div><div><p><strong>Discover your role: </strong></p></div><div><ul><li><p>Build peer relationships with key opinion leaders in haematological malignancies. </p></li></ul></div><div><ul><li><p>Act as a clinical and scientific resource for healthcare professionals. </p></li></ul></div><div><ul><li><p>Support company-sponsored clinical trials, including investigator selection and enrolment activities. </p></li></ul></div><div><ul><li><p>Collaborate with Clinical Development and trial teams to execute medical plans. </p></li></ul></div><div><ul><li><p>Identify medical insights, research gaps and opportunities with investigators. </p></li></ul></div><div><ul><li><p>Present scientific and clinical data in response to appropriate information requests. </p></li></ul></div><div><ul><li><p>You communicate complex data clearly to varied scientific and clinical audiences. </p></li></ul></div><div><ul><li><p>You balance field work, projects and changing priorities with sound judgement. </p></li></ul></div><div><p><strong>This role requires: </strong></p></div><div><ul><li><p>Bachelor’s degree (preferably in a science-related field) and 4+ years of relevant experience, including 2+ years as a Medical Science Liaison in biotech or pharmaceutical oncology/haematology. </p></li></ul></div><div><ul><li><p>Knowledge or experience in the oncology/haematology therapeutic area. </p></li></ul></div><div><ul><li><p>Understanding of treatment guidelines, clinical research processes, European Union regulations and compliant pharmaceutical practices. </p></li></ul></div><div><ul><li><p>Experience in lymphoma and/or multiple myeloma preferred. </p></li></ul></div><div><ul><li><p>Established relationships with key opinion leaders in malignant haematology and knowledge of relevant institutions. </p></li></ul></div><div><ul><li><p>Drug launch experience 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[グローバル展開]]></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[Senior Manager, Global Patient Safety]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[グローバル展開]]></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[Associate Manager, Market Access]]></title>
    <date><![CDATA[Tue, 09 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/ja/%E4%BB%95%E4%BA%8B/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>私たちの企業理念であるRegeneron Way。私たちが目指す理想へと続くこの道を私たちと共に歩む、その第一歩を踏み出してみませんか？ご興味をお持ちいただけましたら、ぜひともご応募ください。私たちは、インクルーシブな文化を持つ職場づくりに取り組んでいます。Regeneronは、応募者、従業員の皆様に平等な機会を提供する企業 （いわゆる Equal Opportunity Employer ）であり、応募者の皆様は選考過程において、人種、肌の色、宗教または信条（またはその有無）、性別、性的指向、ジェンダー・アイデンティティまたはジェンダー表現、性別再割当、婚姻状況または法的に承認されたパートナーシップ関係 （いわゆるシビル・パートナーシップ）の有無、個人の法的な地位、妊娠または育児に関する状況、年齢、障がい、国籍、市民権の状態、出身民族または出身国、トラベラー・コミュニティへの所属、家族構成、遺伝情報、軍歴または退役軍人であること、および適用法令による保護の対象となるその他の特性に由来する差別を受けることはありません。なお、応募者の方で、障がいや慢性疾患をお持ちの皆様には、募集・選考過程において、社会通念上適切な合理的配慮を必要に応じて提供させていただきます。</p><p>当社は、事業を展開するすべての国において、必要に応じて各職種の給与レンジを開示しております。最終的なオファーは、勤務国、具体的な職位レベル、ならびにご経験・スキルに基づき、該当するレンジ内で決定させていただきます。一部の国では、団体交渉協約（CBA）が適用され、これにより報酬や福利厚生が何らかの影響をこうむる場合がございます。またRegeneronは、あらゆる側面から皆様をサポートすべく、魅力的な福利厚生、トータル・リワード・パッケージをご提供いたしております。年次ボーナス等のインセンティブ・プラン、株式報酬、年金または退職給付、401(k) への会社拠出、健康およびウェルネス・プログラム、フィットネス・センター、保険給付（医療、歯科、視力、生命保険、障がい保険など）、有給休暇、家族支援給付などをご用意させていただいております。（なお、提供される内容は国や職種等により異なりますのでご了承ください。）米国における Regeneron の福利厚生に関する詳細につきましては、<a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> をご参照ください。その他の地域に関する詳細情報につきましては、選考過程におきましてご提供させていただきます。ご不明点等ございましたら、担当のリクルーターまでお問い合わせください。</p><p>Regeneron では、従業員が同じ職場で一緒に働いてこそ最高の成果を出すことができると考えております。そのため、多くの職種ではオフィス等指定の職場にご出勤いただいたうえで職務に従事していただく、いわゆるオンサイトでの勤務が求められております。皆様ご自身の職種および勤務地に対応したオンサイト勤務に関する要件につきましては、担当のリクルーターおよび採用担当マネージャーまでお問い合わせください。</p><p>採用プロセスの一環といたしまして、バックグラウンド・チェックを実施する場合がございます。本チェックは雇用開始前に、本人確認、就労資格、学歴などの必要な情報を確認することを目的としており、該当する国の法令に従って実施されます。なにとぞご理解、ご協力のほどお願い申し上げます。</p><p>カナダでの募集職種について：本求人は既存のポジションに関するものです。</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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[Associate Director–Data Lake Operations]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47775]]></requisitionid>
    <referencenumber><![CDATA[R47775]]></referencenumber>
    <apijobid><![CDATA[r47775]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Senior Manager Clinical Data Management Tech Solutions]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47796]]></requisitionid>
    <referencenumber><![CDATA[R47796]]></referencenumber>
    <apijobid><![CDATA[r47796]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/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><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 Senior Manager, AI Agents and Workflow, you will lead the design and deployment of LLM-powered automation solutions that transform clinical data operations across the trial lifecycle. You will partner closely with cross-functional teams to deliver scalable, production-grade AI capabilities that reduce manual effort, accelerate data processes, and enhance data quality and reliability.</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 the strategy and execution of AI-driven automation initiatives across Clinical Data Management operations</p></li><li><p>Designing and implementing LLM-powered agents to automate workflows across data ingestion, quality management, reporting, and study operations</p></li><li><p>Driving automation of complex clinical data processes such as query generation, reconciliation, deviation detection, and reporting workflows</p></li><li><p>Embedding AI capabilities into regulatory and inspection readiness processes to ensure compliance and auditability</p></li><li><p>Building scalable data workflows to process and harmonize data from multiple sources including EDC systems and external vendors</p></li><li><p>Leading development of advanced analytics capabilities such as anomaly detection, predictive modeling, and data quality insights</p></li><li><p>Collaborating with IT and platform teams to integrate AI solutions into clinical systems and data platforms</p></li><li><p>Partnering with Data Management, Biostatistics, and Clinical teams to identify high-impact automation opportunities</p></li><li><p>Establishing governance frameworks for AI solutions, including validation, auditability, and compliance with regulatory requirements</p></li><li><p>Leading and mentoring a team of AI engineers and data scientists, ensuring high-quality delivery and alignment with business priorities</p></li></ul><h3><strong>This job may be for you if you have:</strong></h3><ul><li><p>Strong expertise in AI/ML, large language models (LLMs), and agent-based workflow automation</p></li><li><p>Experience working with LLM platforms and agent frameworks (e.g., OpenAI, Anthropic, LangChain, or similar)</p></li><li><p>Good understanding of clinical data management, EDC systems, and clinical trial workflows</p></li><li><p>Familiarity with CDISC standards and regulatory requirements in a GxP environment</p></li><li><p>Strong programming skills in Python and SQL, with experience in data engineering and AI pipelines</p></li><li><p>Proven ability to lead cross-functional initiatives and manage technical teams</p></li><li><p>Strong problem-solving, stakeholder management, and communication skills</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>8–10+ years of experience in AI/ML, data science, or related fields</p></li><li><p>At least 3+ years of people management experience</p></li><li><p>Experience building and deploying AI or LLM-based solutions, preferably in a regulated industry</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[グローバル展開]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[産業オペレーションと製品供給]]></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[Sales Specialist Immunology (f/m/d) - Parental leave cover until July 31, 2028]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48248]]></requisitionid>
    <referencenumber><![CDATA[R48248]]></referencenumber>
    <apijobid><![CDATA[r48248]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48248/sales-specialist-immunology-fmd-parental-leave-cover-until-july-31-2028/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>For a parental leave cover, we are looking for a Sales Specialist Immunology (f/m/d), fixed-term until July 31, 2028, covering the territory of Bielefeld, Gelsenkirchen, Gütersloh, Detmold, Paderborn, and Ahlen.</p><p><strong>Discover your role:</strong></p><ul><li><p>Provide advice and support to relevant specialist physicians, both in the hospital setting and in outpatient care</p></li><li><p>Build and maintain strong, long-term customer relationships – in person and through digital channels</p></li><li><p>Lead focused, content-driven discussions that emphasize customer value and patient benefit</p></li><li><p>Work closely with the Medical Affairs team to implement regional programs and key activities supporting HCP needs</p></li><li><p>Independently manage your territory, including account analysis, route planning, and documentation of activities in the CRM system</p></li><li><p>Participate in trade fairs and congresses, and independently plan, coordinate, and deliver training events and scientific presentations</p></li><li><p>Provide regular, proactive, and structured reporting to the local leadership team</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Completed medical, pharmaceutical, or scientific training (e.g., certified Pharmaceutical Sales Representative), or a relevant degree (scientific or health economics) in accordance with §75 of the German Medicines Act (AMG)</p></li><li><p>Experience in field sales of prescription (Rx) pharmaceuticals</p></li><li><p>Strong knowledge of immunology indications and / or an established network in this field</p></li><li><p>Good understanding of hospital sales processes and reimbursement mechanisms within the German healthcare system</p></li><li><p>Entrepreneurial mindset with the ability to identify win-win opportunities</p></li><li><p>Results-driven approach, with initiative, flexibility, and strong time management skills</p></li><li><p>Proficiency in Microsoft Office and common software tools</p></li><li><p>Engaging, personable demeanor and a strong passion for field sales</p></li><li><p>Valid Class B/3 driver’s license</p></li><li><p>Fluency in German with good command of English</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>64.125,00 € - 106.875,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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 - ATLANTA South, GA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48027]]></requisitionid>
    <referencenumber><![CDATA[R48027]]></referencenumber>
    <apijobid><![CDATA[r48027]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48027/medical-account-specialist-ii-neurology-atlanta-south-ga/]]></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[<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: Atlanta South (Metro), GA</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[コマーシャル]]></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 -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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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- TAMPA, FL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48033]]></requisitionid>
    <referencenumber><![CDATA[R48033]]></referencenumber>
    <apijobid><![CDATA[r48033]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48033/medical-account-specialist-ii-neurology-tampa-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>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: Tampa (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[コマーシャル]]></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[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/ja/%E4%BB%95%E4%BA%8B/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[コーポレートファンクション]]></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[Regional Tumor Lead Marketing Oncology Skin]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48205]]></requisitionid>
    <referencenumber><![CDATA[R48205]]></referencenumber>
    <apijobid><![CDATA[r48205]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48205/regional-tumor-lead-marketing-oncology-skin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Skin to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.<br><br><strong>A Typical Day:</strong><br><br><br>Leading country insight collection and prioritization to inform global brand strategy<br><br>Ensuring alignment of local priorities with global strategic direction<br><br>Developing the regional tactical plan, including budget alignment<br><br>Facilitating regional tumor marketing meetings to drive execution against plan<br><br>Reviewing country brand plans and sharing insights to improve execution quality<br><br>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes<br><br>Driving regional launch planning and optimization, supporting excellence in country</p><p><br><strong>This Role May Be For You, if you are:</strong></p><p><br>Energized by working with, leveraging and developing talents in countries<br><br>Enjoy connecting global strategy with local market realities<br><br>Comfortable prioritizing across countries and balancing trade-offs<br><br>Energized by guiding brand planning and execution at regional level<br><br>Enjoys shaping content strategies across multiple markets<br><br>Confident leading discussions and aligning diverse stakeholders<br><br>Motivated by improving execution through insights and performance data<br><br>Open to regular travel and engaging with teams across geographies<br><br><br>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p><strong>Salary Range (annually)</strong></p><p>79,800 € - 156,375 €</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 05:26:09 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/ja/%E4%BB%95%E4%BA%8B/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[コマーシャル]]></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, 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/ja/%E4%BB%95%E4%BA%8B/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[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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></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[Associate Scientist - Bioanalytical Science]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47951]]></requisitionid>
    <referencenumber><![CDATA[R47951]]></referencenumber>
    <apijobid><![CDATA[r47951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r47951/associate-scientist-bioanalytical-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 Associate Scientist to join our Clinical Bioanalysis department.</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>Train on bioanalytical methods (manual, hybrid, and automated) and completes methods to perform bioanalysis for clinical studies under supervision.</li><li>Analyze multiple plates within the same day and may perform multiple assays within the same day.</li><li>Interpret data to assess plate acceptance criteria and adjust sample dilutions accordingly.</li><li>Complete vital operations in LIMS (requesting samples, building analysis plates, tracking sample movement, tracking pending analysis and performing data entry). Uses the ELN for data documentation purposes.</li><li>Prepares and qualifies reagents, and re-orders laboratory supplies and reagents, as needed.</li><li>Ensures compliance, as appropriate, for all laboratory work and documentation in accordance with working practices, company SOPs, bioanalytical method procedures (BMPs), and regulations.</li></ul><p><strong>This Role May Be for You If You Have Experience:</strong></p><ul><li>Can manage, organize, and interpret data more independently.</li><li>Possess a knowledge of the basic principles of immunoassays</li></ul><p><strong>The role requires: </strong></p><ul><li>BS degree or MS degree in a scientific field</li><li>0–3 years of relevant experience (industry or academic)</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[研究と前臨床開発]]></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[Senior Principal Disaster Recovery Architecture & Engineering]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48539]]></requisitionid>
    <referencenumber><![CDATA[R48539]]></referencenumber>
    <apijobid><![CDATA[r48539]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/ja/%E4%BB%95%E4%BA%8B/r48539/senior-principal-disaster-recovery-architecture-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an IT Disaster Recovery (DR) Architecture & Engineering Lead to mature and scale our global DR and resilience capabilities. With a decade of infrastructure-operations experience—including at least five years defining DR architectures and engineering standards—you will develop technical strategy, champion Tier 0 (core-infrastructure) recoverability, and deliver innovative solutions across on-prem, cloud, and hybrid environments. Your leadership will ensure that Regeneron’s critical systems remain available, secure, and compliant as the organization continues to grow.</p><p>Success in this role hinges on deep technical expertise, strategic vision, and the ability to collaborate across engineering, application, and business teams in a highly regulated life-sciences' setting.</p><p><strong>In this role, a typical day might include the following: </strong></p><p>- Driving Tier 0 resiliency roadmaps — compute, storage, network, cloud, security, and automation frameworks </p><p>- Representing DR at Solution Design Engineering Reviews to embed recovery standards into every new or changed system </p><p>- Authoring recovery architectures for cyber-resilience, including offline/ransomware-protection strategies </p><p>- Leading enterprise-wide tabletop and hands-on recovery tests; analyzing results and closing gaps </p><p>- Developing RFPs and evaluating innovative technologies to improve recovery speed, scale, and automation </p><p><strong>This job might be for you if you: </strong></p><p>- Thrive on translating sophisticated technical challenges into practical, scalable recovery solutions </p><p>- Enjoy partnering with diverse teams in a matrix environment to influence architecture decisions </p><p>- Communicate crisply with engineers, executives, and vendors—tailoring your message to each audience </p><p>- Stay calm and decisive while directing high-pressure recovery events or cyber-incident responses </p><p>- Relish process improvement and leverage infrastructure-as-code, automation, and multi-cloud design </p><p>- Value compliance and quality in a pharmaceutical manufacturing context </p><p><strong>In order to be considered for this role, you must have:</strong> </p><p>- 10+ years of IT infrastructure operations experience, and 5+ years leading enterprise DR architecture/engineering initiatives </p><p>- Expert knowledge of DR tools, VMware HA/SRM, multi-cloud (AWS, Azure, GCP) design, cloud recovery architectures, and infrastructure-as-code (Terraform, CloudFormation).</p><p>- Working familiarity with zero-trust concepts.</p><p>- Proven ability to lead recovery testing, influence stakeholders across levels, and perform command-and-control leadership during planned and unplanned events.</p><p>- A Bachelor’s degree in Computer Science, or related field 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>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[研究と前臨床開発]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 12:56:09 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/ja/%E4%BB%95%E4%BA%8B/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[グローバル展開]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 16 Jun 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
</source>