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Associate Medical Director, Clinical Sciences, Early Clinical Development

Job Description

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The Associate Medical Director is a qualified physician-scientist with experience in the pharmaceutical/biotechnology sector, or academic clinical setting. The Associate Medical Director works with supervisor and other members of the cross-functional study team to author/contribute to early clinical development protocols and facilitate execution of study activities and data summarization. Early Clinical Development and Experimental Sciences (ECDES) is uniquely poised to shepherd our internal discovery portfolio and external collaboration programs through clinical proof of concept (POC). In close partnership with Regeneron Labs, ECDES uses human clinical studies to inform upon biology and identify which candidates have the most promise as new medicines. ECDES has core functional capabilities to enable the sustainable delivery of the early development strategy including Clinical Science, Precision Medicine & Operations, and Clinical Imaging. Together with Regeneron’s technology platforms, ECDES effectively integrates genetic and molecular characterization of human disease biology to advance our clinical studies.

As an Associate Medical Director, a typical day may include the following:

  • Facilitates/leads the cross-functional study team on the following activities, including but not limited to:

  • Designs POC-enabling human studies, First-In-Human (FIH) studies, POC (clinical and/or pharmacologic) studies as per clinical strategy.

  • Responsible for the relevance and accuracy of medical science underpinning of clinical study based on thorough scientific review and consultation with internal and external experts

  • Reviews, edits and finalizes clinical trial plans

  • Organizes and conducts consultations with global opinion leaders

  • Reviews and finalizes the medical and scientific portions of clinical study concepts (CSCs) and clinical study protocols (CSPs) and amendments.

  • Reviews and edits documents related to trials, such as monitoring plans, SAPs, amendments, IRB/IEC submissions and regulatory submissions

  • Responsible for oversight of cross-functional study team and provides medical guidance to the clinical study teams

  • Accountable, with input from Clinical Trial Management and Biostatistics and Data Management for timely clinical trial execution and quality of deliverables

  • Leads and supervises the Clinical Team to produce high quality program deliverables on schedule

This role may be for you if:

  • Effective communications (verbal & written) and presentation skills are essential.

  • Must be able to work productively in a fast-paced collaborative environment.

  • Demonstrated critical thinking skills and sound decision-making

To be considered for this role, you must have an M.D. Degree (M.D./Ph.D. Degree preferred) Board Certification/Eligibility in a relevant therapeutic area preferred, along with relevant industry experience. A minium of 2-3yr (Associate Director), 4-8yr (Director) prior industry experience or practice experience, preferably in a research/academic setting. Experience in analysis of clinical and basic research information from a wide range of topics.


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 including health and wellness programs, fitness centers and equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an 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.
The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

Salary Range (annually)

$234,000.00 - $286,000.00