Medical Director, Clinical Development, Obesity
Regeneron
June 25, 2026
Remote friendly (Tarrytown, NY)
United States
Clinical Research and Development
Medical Director, Clinical Development, Obesity
Role Summary
- Serve as Medical Lead for clinical trials in the Clinical Development Program (CDP) and responsible for designing clinical study concepts leading to clinical trial protocols. Act as a clinical role model and demonstrate outstanding clinical scientific knowledge applicable to clinical research.
Responsibilities
- Act as medical expert and lead interactions with external stakeholders.
- Define clinical trial-related CDP goals and objectives.
- Collaborate with discovery teams to provide input on next-generation targets.
- Ensure relevance and accuracy of medical science underpinning clinical study concepts via scientific review and consultation.
- Review and finalize clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance.
- Lead the Global Clinical Study Team to deliver high-quality program outputs on schedule.
- Own medical content of clinical study reports, clinical data analysis, safety monitoring, and activities/procedures ensuring patient safety.
Qualifications
- M.D. (or equivalent) with board eligibility/certification in Pediatric Endocrinology preferred (relevant experience acceptable).
- At least 2 years pharmaceutical industry experience (academic equivalent research considered).
- Experience in metabolic disorders drug development strongly preferred.
- Prior regulatory agency interactions or CTD/dossier submission in an ICH region advantageous.
Role Summary
- Serve as Medical Lead for clinical trials in the Clinical Development Program (CDP) and responsible for designing clinical study concepts leading to clinical trial protocols. Act as a clinical role model and demonstrate outstanding clinical scientific knowledge applicable to clinical research.
Responsibilities
- Act as medical expert and lead interactions with external stakeholders.
- Define clinical trial-related CDP goals and objectives.
- Collaborate with discovery teams to provide input on next-generation targets.
- Ensure relevance and accuracy of medical science underpinning clinical study concepts via scientific review and consultation.
- Review and finalize clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance.
- Lead the Global Clinical Study Team to deliver high-quality program outputs on schedule.
- Own medical content of clinical study reports, clinical data analysis, safety monitoring, and activities/procedures ensuring patient safety.
Qualifications
- M.D. (or equivalent) with board eligibility/certification in Pediatric Endocrinology preferred (relevant experience acceptable).
- At least 2 years pharmaceutical industry experience (academic equivalent research considered).
- Experience in metabolic disorders drug development strongly preferred.
- Prior regulatory agency interactions or CTD/dossier submission in an ICH region advantageous.