Senior Manager, Clinical Scientist, Hematology
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.
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
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$150,500.00 - $245,500.00
