Senior Medical Director, Clinical Development, Ophthalmology
Regeneron
August 06, 2026
On-site
Tarrytown, NY
Clinical Research and Development
Discover Your Role
- Act as medical expert and leader in interactions with external stakeholders, internal stakeholders, and decision boards
- Develop innovative clinical strategies to shorten development cycles amid an evolving regulatory landscape
- Design efficient, robust Phase 1, 2, and 3 programs
- Partner with research and discovery teams to inform the next generation of targets in the field
- Safeguard patient safety in clinical studies and support signal detection from post-marketing surveillance
- Ensure the quality of clinical documents (investigator brochures, protocols, study reports, and regulatory submission materials)
- Draft responses to regulatory agency questions and prepare regulatory submission documents
- Build consensus and drive sound decision-making across dynamic, matrixed clinical teams
This Role Requires
- MD (or equivalent medical degree), with board certification or eligibility in Ophthalmology
- Minimum 4 years of industry experience in early or late clinical development (strong academic backgrounds with less experience may be considered)
- Experience leading proof-of-concept and/or registrational clinical trials, including protocol design and study execution
- Solid knowledge of global regulatory requirements (ICH) for pharmaceutical development
Application Instructions
- Apply now.
- Act as medical expert and leader in interactions with external stakeholders, internal stakeholders, and decision boards
- Develop innovative clinical strategies to shorten development cycles amid an evolving regulatory landscape
- Design efficient, robust Phase 1, 2, and 3 programs
- Partner with research and discovery teams to inform the next generation of targets in the field
- Safeguard patient safety in clinical studies and support signal detection from post-marketing surveillance
- Ensure the quality of clinical documents (investigator brochures, protocols, study reports, and regulatory submission materials)
- Draft responses to regulatory agency questions and prepare regulatory submission documents
- Build consensus and drive sound decision-making across dynamic, matrixed clinical teams
This Role Requires
- MD (or equivalent medical degree), with board certification or eligibility in Ophthalmology
- Minimum 4 years of industry experience in early or late clinical development (strong academic backgrounds with less experience may be considered)
- Experience leading proof-of-concept and/or registrational clinical trials, including protocol design and study execution
- Solid knowledge of global regulatory requirements (ICH) for pharmaceutical development
Application Instructions
- Apply now.