Associate Medical Director/Medical Director, Endocrinology and Metabolism

Associate Medical Director/Medical Director — key participant in the medical and scientific oversight of clinical studies in endocrinology and metabolism.

Responsibilities:
- Participate in the design, development, and execution of clinical studies across the development life cycle (Phase 1–3)
- Write and review clinical protocols, investigator brochures, clinical study reports, and other documents
- Provide medical oversight and safety monitoring for clinical trials (review AEs/SAEs) and participate in the safety committee
- Analyze, interpret, and present clinical data
- Collaborate with development functions (clinical operations, safety, biometrics, regulatory, medical writing) to achieve project objectives
- Establish relationships with external scientific experts (principal investigators and opinion leaders) to facilitate excellence in clinical trials
- Serve as liaison to the commercial team on medical and scientific issues
- Participate in regulatory discussion and activities, including filing INDs, CTXs, and NDA/MAAs
- Provide ongoing disease area and scientific training to clinical team members
- Other duties as assigned

Preferred Skills, Qualifications, and Technical Proficiencies:
- Strong clinical and scientific knowledge
- Excellent communicator with proven leadership skills; able to interact in a cross-functional environment
- Agility to adjust workload based on changing priorities
- Ability to drive timelines while maintaining quality and GCP compliance

Preferred Education and Experience:
- MD or equivalent; board eligible or certified in internal medicine or internal medicine subspecialty preferred
- 2+ years clinical development experience in biotech/pharma or an academic clinical trial unit
- Publications in peer-reviewed journals preferred

Application instructions:
- Applicants must be currently authorized to work in the United States on a full-time basis.