Associate Director, Clinical Scientist, Hematology

Regeneron Pharmaceuticals, Inc; Cambourne; Hybrid; GBP 142,000 - 172,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking an Associate Director, Clinical Sciences to join the Hematology/Oncology Clinical Sciences team. You will lead design, execution, and interpretation of hematology/oncology studies across early and late phase development, ensuring data integrity.

You will collaborate with Medical Directors, mentor junior staff, and drive cross-functional program strategies in a fast-growing science-driven environment.

Qualifications

• Advanced degree in life science with 10+ years pharmaceutical clinical drug development experience.
• Proven leadership in conducting global clinical trials and executing clinical programs.
• Proficient knowledge of Good Clinical Practice, study design, and clinical research methodology.
• Solid medical writing 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 grounded in disease biology, the drug landscape, and current literature.
• Develop the Expanded Synopsis and author or review clinical sections of protocols, amendments, and study reports.
• Prepare medical monitoring 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, DMCs, regulatory authority meetings, and investigator meetings.
• Promote consistent clinical data review practices across studies, and identify risks and design 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.

Skills

Leadership

Clinical strategy

Mentoring

Education

PhD in life sciences

Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Clinical Sciences to join our Hematology/Oncology Clinical Sciences team, supporting our clinical programs in a matrixed, cross-functional environment. In this role, you will lead the design, execution, and scientific interpretation of hematology/oncology clinical studies across early and late phase development, while ensuring the integrity of study data. You will collaborate closely with Medical Directors and cross-functional partners, and may manage one or more clinical scientists. 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/flexibility: Primarily on-site with hybrid flexibility

Discover your role:

• 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 grounded in disease biology, the drug landscape, and current literature
• Develop the Expanded Synopsis and author or review clinical sections of protocols, amendments, and study reports
• Prepare medical monitoring 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, DMCs, regulatory authority meetings, and investigator meetings
• Promote consistent clinical data review practices across studies, and identify risks and design 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

This role requires:

• Advanced degree in life science or healthcare (PhD, MD, PharmD, or MSc) and 10+ years of pharmaceutical clinical drug development experience, including basic knowledge of oncology or hematology (other levels considered depending on experience)
• Proven leadership and accomplishment in 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