Medical Director, Clinical Development, Endocrinology
When & Where
4 days a week on-site in Tarrytown, NY, Washington, D.C., or Cambridge, Massachusetts
Role Summary
You guide the Global Clinical Study Team to deliver high-quality trials on time. You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance. You lead clinical study and protocol development and present to internal and external stakeholders. You provide clinical and scientific leadership for data review, study reports, and publications. You work closely with cross-functional partners to advance program goals and key deliverables. You collaborate with discovery teams to help shape future targets and development opportunities in the field.
Requirements
- M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable.
- At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered).
- Experience in rare disease drug development strongly preferred.
- Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage.
Qualifications
- Highly performing and highly passionate physician scientist.
- Clinical role model for the team.
- Outstanding clinical scientific knowledge applicable to clinical research.
Skills
- Strong communication and collaboration skills.
- Ability to work independently and as part of a team.
- Expertise in clinical study design and execution.
- Knowledge of regulatory guidelines and processes.
Pay
$284,900.00 - $385,700.00 annually
Schedule
4 days a week on-site in Tarrytown, NY, Washington, D.C., or Cambridge, Massachusetts