Senior Manager, Clinical Scientist, Hematology Full-time

Senior Manager, Hematology Clinical Sciences

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Hematology Clinical Sciences to join our Clinical Sciences team, supporting our hematology clinical programs in a matrixed, cross-functional environment. In this role, you will contribute to the planning, execution, and data interpretation of clinical studies across early and late phase development, helping ensure the integrity of study data and the safety of patients. You will collaborate closely with Medical Directors and cross-functional partners as a member of the Clinical Study Team and Global Clinical SubTeam. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

• Location: Tarrytown, NY, Warren, NJ, or Cambridge, MA
• Work model: Primarily on-site with hybrid flexibility

Discover your role:

• Partner with Medical Directors to provide the scientific expertise needed to design and deliver clinical studies and programs
• Contribute to program team meetings, advisory boards, steering committees, and data/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, 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 with clear, concise communication and creative problem-solving

This role requires:

• Advanced degree in life science or healthcare (PhD, MD, PharmD, or MSc) and 8+ years of pharmaceutical clinical drug development experience (other levels 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 experience working cross-functionally, with strong organizational awareness
• Preferred: Proven track record of clinical trial process improvements