Medical Director, Clinical Development, Obesity
Regeneron
August 08, 2026
On-site
Tarrytown, NY
Clinical Research and Development
Discover Your Role
- 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.
- Collaborate with cross-functional partners to advance program goals and key deliverables.
- Collaborate with discovery teams to help shape future targets and development opportunities in the field.
This Role Requires
- M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable.
- At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered).
- Previous interactions with regulatory agencies or common technical document (CTD/dossier) submission in an ICH region is an advantage.
When & Where
- Location: Tarrytown, NY or Warren, NJ.
- Travel: 10% to relevant conferences.
- 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.
- Collaborate with cross-functional partners to advance program goals and key deliverables.
- Collaborate with discovery teams to help shape future targets and development opportunities in the field.
This Role Requires
- M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable.
- At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered).
- Previous interactions with regulatory agencies or common technical document (CTD/dossier) submission in an ICH region is an advantage.
When & Where
- Location: Tarrytown, NY or Warren, NJ.
- Travel: 10% to relevant conferences.