Associate Medical Director

Role Associate Medical Director, Clinical Development, supporting medical oversight of clinical trials for metabolic and endocrine disorder therapeutics. Responsibilities assist in protocol development contribute to clinical development plans review safety data and regulatory documents (INDs, CSRs) monitor ongoing studies serve as a medical contact for trial-related inquiries Provide medical input to cross-functional teams and CRO oversight support regulatory submissions assist with data presentation for scientific and regulatory meetings Qualifications MD, DO, PharmD, or equivalent 2-4 years of clinical or research experience, with late-phase (Phase 2/3) trial exposure preferred familiarity with GCP, regulatory reporting, and clinical data analysis High-Value expertise in metabolic/endocrine disorders, late-stage clinical development, regulatory documentation, and global safety standards. WorkSetup unspecified, with an emphasis on collaboration with internal teams and external partners. #J-18808-Ljbffr