Associate Director, Clinical Scientist, Hematology

Regeneron Pharmaceuticals

3d • $176,100 - $287,300 • Hybrid

About The Position

Regeneron is seeking an Associate Director, Clinical Sciences to join its Hematology/Oncology Clinical Sciences team. The role supports clinical programs in a matrixed, cross-functional environment and leads the design, execution, and scientific interpretation of hematology/oncology clinical studies across early- and late-phase development, while ensuring study data integrity. The position collaborates closely with Medical Directors and cross-functional partners and may manage one or more clinical scientists. The role is based in Tarrytown, NY; Warren, NJ; or Cambridge, MA, with a primarily on-site work model and hybrid flexibility.

Requirements

• Advanced degree in life science or healthcare: PhD, MD, PharmD, or MSc; other levels may be considered depending on experience.
• 10 or more years of pharmaceutical clinical drug development experience.
• Basic knowledge of oncology or hematology.
• Proven leadership and accomplishment in conducting global clinical trials and executing clinical programs.
• Proficient knowledge of the drug development process, Good Clinical Practice, study design, and clinical research methodology.
• Solid medical writing skills.
• Strong direct-line and cross-functional management, interpersonal, and problem-solving skills.

Responsibilities

• Lead or support clinical science strategy for a program, serving as Lead Clinical Scientist or delegate to the Therapeutic Area Lead.
• Partner with Medical Directors to design and deliver clinical studies grounded in disease biology, the drug landscape, 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.
• Lead planning for and present at program team meetings, advisory boards, steering committees, Data Monitoring Committees (DMCs), regulatory authority meetings, and investigator meetings.
• Promote consistent clinical data review practices across studies, identify risks, and design mitigation strategies.
• Manage and mentor clinical scientists and junior colleagues, serving as a peer coach.
• Influence across functions with confidence, creativity, and professional diplomacy while driving process improvements.

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.

What This Job Offers

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