Medical Director, Clinical Development, Genetics Medicine, MASH
$284,900–$385,700 year
On-siteTarrytown, New York, United States
Job Summary
Lead cross-functional study teams to craft novel clinical development strategy for genetic medicines from First in Human through Phase 3. Author and finalize protocols, amendments, monitoring plans, SAPs, and regulatory submissions while evaluating therapeutic candidates to inform program decisions. Oversee trial execution, including adverse event review and ongoing monitoring of patient health and data quality, ensuring full compliance with FDA, EMA, ICH, and GCP guidelines. Conduct literature reviews to identify development opportunities and represent clinical science in communications with regulatory agencies. Collaborate closely with discovery scientists, translational researchers, and regulatory colleagues to support MASH and metabolism programs.
Required Qualifications
- M.D. degree
- Board Certification/Eligibility in a relevant therapeutic area (Hepatology, Gastroenterology, Endocrinology, or Nephrology)
- 2-3+ years of clinical practice or industry experience
- Track record of success in clinical or scientific research settings
- On-site four days per week
- 10% to relevant conferences/congresses
Desired Qualifications
- M.D./Ph.D. or prior research experience preferred
- Hepatology, Gastroenterology, Endocrinology, or Nephrology preferred
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