Senior Medical Director, Clinical Development, MASH

Start free →

Or apply yourself on the official page →

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 a Senior Medical Director, Clinical Sciences, MASH to join our Genetic Medicines clinical development team. In this role, you will lead one or more MASH clinical programs from first-in-human through registration-enabling studies while collaborating with research, the Regeneron Genetics Center, regulatory affairs, clinical operations, and other partners. Evolving Genetic Medicines modalities include RNA interference (RNAi), gene editing, viral vector gene delivery, and others. 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 Discover your role: • Lead one or more MASH clinical programs and serve as the clinical expert with regulators, key opinion leaders, and advisory boards • Design and execute innovative Phase 1, 2, and 3 studies, from first-in-human through registration-enabling • Develop clinical strategies that shorten development timelines in an evolving regulatory landscape • Partner with discovery scientists and translational geneticists to evaluate emerging genetic medicines targets and shape clinical experiments • Provide input to research teams on the next generation of targets in metabolic diseases • Safeguard patient safety in clinical studies and review post-marketing signals alongside Global Patient Safety • Ensure the quality of clinical documents and prepare responses to regulatory agency questions and submissions • Build consensus across matrixed, multi-disciplinary teams and serve as a clinical role model This role requires: • M.D., D.O., or equivalent medical degree and relevant specialized fellowship/residency training (MD/PhD preferred) • Minimum of 3-4 years of industry clinical development experience with a track record of conducting clinical trials and/or leading clinical programs • Solid knowledge of compliance and global regulatory requirements (ICH) for pharmaceutical development • Strong understanding of operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out) • Experience leading cross-functional or similarly diverse teams • Excellent interpersonal and stakeholder management skills • Preferred: Clinical development experience in MASH • Preferred: Research experience in an academic setting #MDJOBSCD, #MDJOBS 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 skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influenc

View the official posting →