Senior Manager, Clinical Scientist, Genetics Medicine

Regeneron Pharmaceuticals • Warren, MI

6d • Hybrid

About The Position

Regeneron is seeking a Senior Manager to join the Clinical Sciences team within Regeneron Genetics Medicine, supporting early clinical development in a fast-paced, collaborative environment. The role contributes to clinical strategy and study execution from discovery through Proof of Concept, helping translate genetic insights into potential treatments. The position collaborates closely with a supervisor, Clinical Trial Managers, and cross-functional study teams. It is based in Tarrytown, NY; Warren, NJ; or Cambridge, MA, and is primarily on-site with hybrid flexibility.

Requirements

• Bachelor’s degree.
• 8+ years of clinical research/development experience.
• Training as a scientist in the pharmaceutical or biotechnology sector, or in an academic or clinical setting.
• Effective verbal and written communication and presentation skills.
• Ability to work productively in a fast-paced, collaborative environment.
• Demonstrated or potential critical thinking skills and sound decision-making.

Nice To Haves

• PhD, PharmD, or Master’s degree in a biomedical subject.
• Experience in early-phase development, including First-In-Human and Proof of Concept studies.

Responsibilities

• Represent the clinical genetics medicine function on study teams, contributing medical and scientific expertise to compliant, high-quality trial execution.
• Contribute to Clinical Study Concepts, protocols, and amendments, supported by literature research on indication selection, rationale, and endpoints.
• Draft clinical sections of regulatory and clinical documents, including briefing books, IND/IMPD submissions, investigator’s brochures, consent forms, and study reports.
• Review key study documents such as medical monitoring plans, statistical analysis plans, and data management materials.
• Partner with Clinical Trial Managers to provide day-to-day clinical input and train study team and CRO personnel on clinical aspects of the trial.
• Support medical monitoring, investigator queries, safety narratives, and trend analysis of safety and efficacy data.
• Organize steering committees, advisory boards, data safety monitoring boards, and consultations with global subject matter experts.
• Identify program, trial, and data risks and implement mitigation strategies while ensuring compliance with FDA, EMEA, ICH, and GCP guidelines.

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, insurance benefits (medical, dental, vision, life, and disability), paid time off, and family support benefits.

What This Job Offers

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