Associate Director, Clinical Scientist, Ophthalmology
Regeneron
August 21, 2026
On-site
Tarrytown, NY
Clinical Research and Development
Discover Your Role
- May function as Clinical Scientist for program and/or delegate of Therapeutic area Clinical Scientist.
- Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings; represent function in cross-department activities.
- Maintain understanding of therapeutic disease biology, clinical manifestations, standard practice, and drug candidate/landscape (mechanism of action).
- Propose, design, and execute early and/or late-stage clinical research and development studies; communicate evidence-based strategy proposals.
- Develop Expanded Synopsis; author/review protocol and amendment scientific content; author/review medical monitoring plans, SAPs, informed consents, and Clinical Study Report clinical components; support regulatory documents; perform quality review/approval and resolve cross-functional comments.
- Plan and prepare materials for stakeholder meetings; present data to external investigators (SIV) and internal collaborators.
- Use analytical skills to understand how objectives/design impact data analysis; identify risks and mitigation strategies.
- Promote consistent first-line medical/clinical data review practices; review clinical data review plan and medical monitoring plan.
This Role Requires
- Advanced degree or equivalent in life science/healthcare preferred (PhD/PharmD/MSc).
- ≥10 years pharmaceutical clinical drug development experience, including basic Ophthalmology knowledge.
- Proficient in drug development process, Good Clinical Practice, study design, clinical research methodology; solid medical writing skills.
- Experience conducting global clinical trials and executing clinical programs.
- Strong team-player; confidence and diplomacy; ability to influence within and across functions.
Application Instructions
- Apply now.
- May function as Clinical Scientist for program and/or delegate of Therapeutic area Clinical Scientist.
- Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings; represent function in cross-department activities.
- Maintain understanding of therapeutic disease biology, clinical manifestations, standard practice, and drug candidate/landscape (mechanism of action).
- Propose, design, and execute early and/or late-stage clinical research and development studies; communicate evidence-based strategy proposals.
- Develop Expanded Synopsis; author/review protocol and amendment scientific content; author/review medical monitoring plans, SAPs, informed consents, and Clinical Study Report clinical components; support regulatory documents; perform quality review/approval and resolve cross-functional comments.
- Plan and prepare materials for stakeholder meetings; present data to external investigators (SIV) and internal collaborators.
- Use analytical skills to understand how objectives/design impact data analysis; identify risks and mitigation strategies.
- Promote consistent first-line medical/clinical data review practices; review clinical data review plan and medical monitoring plan.
This Role Requires
- Advanced degree or equivalent in life science/healthcare preferred (PhD/PharmD/MSc).
- ≥10 years pharmaceutical clinical drug development experience, including basic Ophthalmology knowledge.
- Proficient in drug development process, Good Clinical Practice, study design, clinical research methodology; solid medical writing skills.
- Experience conducting global clinical trials and executing clinical programs.
- Strong team-player; confidence and diplomacy; ability to influence within and across functions.
Application Instructions
- Apply now.