Senior Manager, Clinical Scientist, Hematology

Regeneron Pharmaceuticals • Village of Tarrytown, NY

3d • $150,500 - $245,500 • Hybrid

About The Position

Regeneron is seeking a Senior Manager, Hematology Clinical Sciences to join its Clinical Sciences team and support hematology clinical programs in a matrixed, cross-functional environment. The role contributes to the planning, execution, and interpretation of clinical studies across early- and late-phase development, helping maintain study-data integrity and patient safety. The position collaborates closely with Medical Directors and cross-functional partners as part of the Clinical Study Team and Global Clinical SubTeam. It is based in Tarrytown, New York; Warren, New Jersey; or Cambridge, Massachusetts, and is primarily on-site with hybrid flexibility.

Requirements

• Advanced degree in life science or healthcare (PhD, MD, PharmD, or MSc).
• Eight or more years of pharmaceutical clinical drug development experience; other levels may be considered depending on experience.
• Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology, and medical writing.
• Strong analytical, presentation, interpersonal, and problem-solving skills.
• Significant cross-functional experience and strong organizational awareness.

Nice To Haves

• Proven track record of clinical trial process improvements.

Responsibilities

• Partner with Medical Directors to provide scientific expertise for designing and delivering clinical studies and programs.
• Contribute to program team meetings, advisory boards, steering committees, and data and safety monitoring meetings.
• Build and maintain knowledge of the disease area, drug candidate, mechanism of action, and drug landscape.
• Assist with developing the Expanded Synopsis and author or review clinical sections of protocols, amendments, and study reports.
• Author or review medical monitoring plans, statistical analysis plans (SAPs), and informed consents, and support regulatory document development.
• Perform clinical data review and safety monitoring, promoting consistent review practices across assigned studies.
• Identify critical risks and recommend mitigations while maintaining compliance with FDA, EMEA, ICH, and GCP guidelines.
• Influence within and across teams through clear, concise communication and creative problem-solving.

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