Clinical Development Senior Medical Director- gMG

Role: Senior Medical Director responsible for defining and leading clinical development strategy for a biopharma asset, including study design, protocol development, and regulatory documentation. Responsibilities: oversee clinical trial execution, medical monitoring, and regulatory interactions; serve as Medical Lead for trials; collaborate with cross-functional teams on project and strategic planning; contribute to IND/CTA submissions and safety reports; participate in business development activities; act as liaison with external medical professionals. Requirements: MD, DO, or equivalent; approximately 12 years' experience in pharmaceutical/biotech clinical development, including trial management and regulatory interactions; board certification/eligibility in a specialty preferred. HighValue: global clinical research experience; interaction with regulatory authorities; leading development programs possibly in innovative modalities; emphasis on cross-functional leadership and strategic planning. WorkSetup: hybrid or on-site, with flexibility.