Senior Manager, Clinical Scientist, Hematology
About The Position
Regeneron is seeking a Senior Manager, Clinical Scientist to join its Hematology Clinical Sciences team. The role supports hematology clinical programs in a matrixed, cross-functional environment and contributes to planning, execution, and interpretation of clinical studies across early- and late-phase development. The position helps ensure study data integrity and patient safety, collaborating closely with Medical Directors and cross-functional partners as part of the Clinical Study Team and Global Clinical SubTeam. The role 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.
- At least 8 years of pharmaceutical clinical drug development experience; other levels may be considered depending on experience.
- 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 the design and delivery of clinical studies and programs.
- Contribute to program team meetings, advisory boards, steering committees, and data and safety monitoring meetings.
- Build and maintain understanding 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
- 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.
- Medical, dental, vision, life, and disability insurance benefits.
- Paid time off.
- Family support benefits.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Senior
