Medical Director, Clinical Development, Genetic Medicines, Neurology
About The Position
Regeneron is seeking a Medical Director, Clinical Development to join its Genetic Medicines Clinical Development Unit (RGM CDU). The role serves as a clinical champion for genetic medicine programs from target nomination through human studies, helping shape how novel targets and modalities move into clinical development. The Medical Director collaborates with Research, the Regeneron Genetics Center, cross-functional study teams, external institutions, investigators, experts, and biotech partners. The position is based in Tarrytown, New York, with a four-days-per-week work model and approximately 10% travel to relevant conferences. It offers the opportunity to contribute to a growing, science-driven organization focused on developing medicines for serious diseases. Regeneron describes its total rewards package as potentially including annual bonuses or other incentive plans, equity awards, pension or retirement benefits, a 401(k) company match, health and wellness programs, fitness centers, insurance benefits, paid time off, and family support benefits. The package may vary by country and role.
Requirements
- M.D. or M.D./Ph.D. with Board Certification or Eligibility in neurology or psychiatry.
- 1–3 years of clinical research experience in the pharmaceutical industry, or significant academic clinical trials/research experience.
- Authorship of peer-reviewed medical or scientific publications.
- Strong written and verbal communication and presentation skills.
- Sound critical thinking and decision-making in a fast-paced, collaborative environment.
Responsibilities
- Serve as the clinical champion for research programs from target nomination to clinical candidate selection.
- Provide clinical input on disease areas and indications, and evaluate novel targets and modalities.
- Partner with Research, the Regeneron Genetics Center, and external institutions on emerging targets and indications.
- Design first-in-human, proof-of-concept, and registrational studies with scientific rigor and medical relevance.
- Lead cross-functional study teams, providing medical leadership and driving timely, high-quality execution.
- Lead benefit-risk assessments and safety monitoring to protect patient safety.
- Identify trial, program, and data risks early and implement mitigation strategies.
- Build strong relationships with key investigators, external experts, and partner biotech teams.
Benefits
- Competitive and comprehensive total rewards package, which may include annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, medical, dental, vision, life and disability insurance, paid time off, and family support benefits.
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What This Job Offers
Job Type
Full-time
Career Level
Director
Education Level
Ph.D. or professional degree
