Key skills
Leadership
About this role
Role Overview
- serve as Medical Lead for clinical trials
- responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies
- collaborate with cross-functional stakeholders
- guide the Global Clinical Study Team to deliver high-quality trials on time
- oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance
- lead clinical study and protocol development and present to internal and external stakeholders
- provide clinical and scientific leadership for data review, study reports, and publications
- work closely with cross-functional partners to advance program goals and key deliverables
- collaborate with discovery teams to help shape future targets and development opportunities
Requirements
- An 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
Benefits
- annual bonuses or other incentive plans
- equity awards
- pension or retirement benefits
- 401(k) company match
- health and wellness programs
- fitness centers
- insurance benefits (e.g. medical, dental, vision, life and disability)
- paid time off
- family support benefits