Medical Director, Clinical Development, Endocrinology
Regeneron
June 27, 2026
On-site
Tarrytown, NY
Clinical Research and Development
Role: Medical Director (Endocrinology) — Clinical Development Unit
Responsibilities
- Guide the Global Clinical Study Team to deliver high-quality trials on time.
- Oversee medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance.
- Lead clinical study and protocol development; present to internal and external stakeholders.
- Provide clinical and scientific leadership for data review, study reports, and publications.
- Work closely with cross-functional partners to advance program goals and key deliverables.
- Collaborate with discovery teams to shape future targets and development opportunities.
Qualifications / Requirements
- M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred (relevant experience acceptable).
- At least 2 years pharmaceutical industry experience (equivalent academic research considered).
- Experience in rare disease drug development strongly preferred.
- Previous interactions with regulatory agencies or prior CTD (“dossier”) submission in an ICH region is an advantage.
Benefits (if included)
- Comprehensive total rewards package may include annual bonuses/incentives, equity awards, pension/retirement benefits, 401(k) match, health and wellness programs, insurance (medical/dental/vision/life/disability), paid time off, and family support benefits.
Application
- Apply now to take your first step toward living the company’s way.
Location
- 4 days per week on-site in Tarrytown, NY, Washington, D.C., or Cambridge, MA.
Responsibilities
- Guide the Global Clinical Study Team to deliver high-quality trials on time.
- Oversee medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance.
- Lead clinical study and protocol development; present to internal and external stakeholders.
- Provide clinical and scientific leadership for data review, study reports, and publications.
- Work closely with cross-functional partners to advance program goals and key deliverables.
- Collaborate with discovery teams to shape future targets and development opportunities.
Qualifications / Requirements
- M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred (relevant experience acceptable).
- At least 2 years pharmaceutical industry experience (equivalent academic research considered).
- Experience in rare disease drug development strongly preferred.
- Previous interactions with regulatory agencies or prior CTD (“dossier”) submission in an ICH region is an advantage.
Benefits (if included)
- Comprehensive total rewards package may include annual bonuses/incentives, equity awards, pension/retirement benefits, 401(k) match, health and wellness programs, insurance (medical/dental/vision/life/disability), paid time off, and family support benefits.
Application
- Apply now to take your first step toward living the company’s way.
Location
- 4 days per week on-site in Tarrytown, NY, Washington, D.C., or Cambridge, MA.