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Senior Medical Director, Clinical Development, Genetics Medicines (Neurology)

Regeneron
United Statesfull_timeVerifiedPosted 18 Mar 2026
💰 CA$450,900/yr(CA$333,300/yrCA$450,900/yr)

About the role

The Senior Medical Director, Regeneron Genetic Medicines Clinical Development Unit (RGM CDU) is a qualified physician scientist with significant pharmaceutical/biotechnology sector and exceptional clinical trials experience. With oversight from Vice President manager, the Senior Medical Director works with other members of the cross-functional team to deliver translational and clinical programs from target nomination to registration.  

A typical day in the life may include the following responsibilities: 

  • Serves as the clinical champion for research programs from target nomination to clinical candidate selection and contributes to the evaluation of novel targets and modalities 

  • Leads the Global Clinical Sub-Team to deliver clinical programs from development candidate selection to registration 

  • Designs human studies, including first-in-human, proof-of-concept, and registrational studies 

  • Leads Cross-Functional Study Teams to deliver human studies 

  • Maintains a high-trust, collaborative environment with team members at partner biotech companies across co-development programs 

  • Mentors and develops team members 

  • Contributes to RGM activities by interacting with scientists across the RGM Clinical Development Unit, Regeneron Genetics Center, and RGM Therapeutic Functional Area, presenting project work, fostering cross-project learning, best-practice adoption, and a culture of scientific excellence 

This job may be for you if you have the following: 

  • M.D. degree. (MD/Ph.D. preferred) Board Certification/Eligibility in a relevant therapeutic area (Neurology, NeuroPsychiatry, Pediatric Neurology) preferred 

  • At least 4 – 8 years of clinical development pharmaceutical industry experience 

  • Has authored and published in medical/scientific peer-reviewed journals. Interactions with Regulatory agencies or Common Technical Document (CTD or “dossier”) submission in any ICH region are an advantage 

  •  Effective communications (verbal & written) and presentation skills are essential 

  •  Must be able to work productively in a fast-paced collaborative environment 

  • Demonstrated critical thinking skills and sound decision-making 

  • Prior experience with mentoring and leading cross functional teams 

This role is based on-site in Tarrytown 4 days/week. 

#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location.  In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.  For other countries’ specific benefits, please speak to your recruiter.
Please be advised that at Regeneron, we believe we are most successful and work best when we are together.  For that reason, many of Regeneron’s roles are required to be performed on-site.  Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.
 

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, nationality, national or ethnic origin, civil status, age, citizenship status, memb

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Company

Regeneron

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