Associate Director, Clinical Scientist, Hematology

Regeneron Pharmaceuticals • Warren, MI

1d • 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. 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.
• 10 or more years of pharmaceutical clinical drug development experience; other levels may be considered depending on experience.
• Basic knowledge of oncology or hematology.
• Proven leadership and accomplishment 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 informed by disease biology, the drug landscape, and current literature.
• Develop Expanded Synopses 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 develop 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

• Annual bonuses or other incentive plans, depending on country and role.
• Equity awards, depending on country and role.
• Pension or retirement benefits, depending on country and role.
• 401(k) company match.
• Health and wellness programs.
• Fitness centers.
• Insurance benefits, including medical, dental, vision, life, and disability insurance.
• Paid time off.
• Family support benefits.

What This Job Offers

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