Associate Director, Clinical Scientist, Genetics Medicine

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About the role

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 Clinical Development Unit, supporting our clinical programs in a matrixed, cross-functional environment. In this role, you will lead the design, execution, and scientific interpretation of clinical studies across early and late phase development, ensuring the integrity of study data and the safety of patients. You will collaborate closely with Medical Directors, regulatory, and other cross-functional partners to move promising candidates forward. 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, 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 and current literature • Develop the Expanded Synopsis and author or review the clinical sections of protocols, amendments, and study reports • Prepare medical monitoring plans, SAPs, and informed consents, and resolve cross-functional comments with minimal guidance • Perform clinical data review and safety monitoring to protect patient safety and data integrity • Present at program team meetings, advisory boards, steering committees, DMCs, and investigator meetings • Identify risks, design mitigation strategies, and drive process improvements across studies • Influence across functions and mentor junior colleagues with confidence, creativity, and professional diplomacy This role requires: • Bachelor’s degree and 10+ years of pharmaceutical clinical drug development experience (other levels considered depending on experience) • Proficient knowledge of the drug development process, ICH/GCP guidelines, study design, and clinical research methodology • Demonstrated leadership in conducting global clinical trials and executing clinical programs • Strong cross-functional leadership, interpersonal, and problem-solving skills in a matrix environment • Solid medical writing skills • Preferred: Advanced degree in life science or healthcare (PhD, MD, PharmD, or MSc) • Preferred: Proven track record of clinical trial process improvements and experience across early and late phase development Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.   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 skil

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