Associate Director, Clinical Scientist, Genetics Medicine

Regeneron Pharmaceuticals

8d • $176,100 - $287,300 • Hybrid

About The Position

Regeneron is seeking an Associate Director, Clinical Sciences to join its Clinical Development Unit and support clinical programs in a matrixed, cross-functional environment. The role leads the design, execution, and scientific interpretation of clinical studies across early- and late-phase development while ensuring study-data integrity and patient safety. The Associate Director collaborates with Medical Directors, regulatory teams, and other partners to advance clinical candidates. The position is based in Tarrytown, NY; Warren, NJ; or Cambridge, MA, with primarily on-site work and hybrid flexibility.

Requirements

• Bachelor’s degree.
• 10 or more years of pharmaceutical clinical drug development experience; other levels may be considered depending on experience.
• Proficient knowledge of the drug development process, ICH/GCP guidelines, study design, and clinical research methodology.
• Demonstrated leadership in conducting global clinical trials and executing clinical programs.
• Strong cross-functional leadership, interpersonal, and problem-solving skills in a matrix environment.
• Solid medical writing skills.

Nice To Haves

• Advanced degree in life science or healthcare, such as a PhD, MD, PharmD, or MSc.
• Proven track record of clinical trial process improvements.
• Experience across early- and late-phase development.

Responsibilities

• Lead or support clinical science strategy for a program, serving as lead Clinical Scientist or as a delegate to the Therapeutic Area Lead.
• Partner with Medical Directors to design and deliver clinical studies informed by disease biology and current literature.
• Develop the Expanded Synopsis and author or review clinical sections of protocols, amendments, and study reports.
• Prepare medical monitoring plans, statistical analysis plans (SAPs), and informed consents, and resolve cross-functional comments with minimal guidance.
• Review clinical data and monitor safety to protect patients and ensure data integrity.
• Present at program team meetings, advisory boards, steering committees, data monitoring committees (DMCs), and investigator meetings.
• Identify risks, develop mitigation strategies, and drive process improvements across studies.
• Influence across functions and mentor junior colleagues with confidence, creativity, and professional diplomacy.

Benefits

• Competitive and comprehensive total rewards package, which may include annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, medical, dental, vision, life and disability insurance, paid time off, and family support benefits, depending on country and role.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior