Medical Director, Clinical Development, Obesity
Core
Medical Lead for clinical trials in the Clinical Development Program (CDP), responsible for designing clinical study concepts and protocols for metabolic disorders.
Role type
Senior IC physician scientist (Medical Director)
Builds
Clinical study concepts, protocols, and high-quality program deliverables for metabolic disorder drug development.
Domain
Pharmaceutical industry, metabolism, obesity, Type 2 diabetes
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial design, medical science review, safety monitoring, regulatory agency interaction, CTD/dossier submission, team leadership, stakeholder management
Preferred skills
Board certification in Pediatric Endocrinology, experience in metabolic disorders drug development, prior interactions with regulatory agencies
Technologies
Clinical Development Program (CDP), Common Technical Document (CTD)
Responsibilities
Define CDP goals and objectives, review and finalize clinical study concepts, lead the Global Clinical Study Team, ensure patient safety and data analysis accuracy, act as medical expert with external stakeholders
Seniority
Director level, hands-on IC
