The role oversees global clinical bioanalytical lab operations for Phase I-III trials, focusing on biospecimen management, vendor oversight, and operational efficiency while ensuring compliance with regulatory standards.

Lead clinical data management strategy and execution across global clinical programs. Oversee DM processes (database development, review, cleaning, lock), vendor/CRO oversight, regulatory compliance, inspection readiness, resource and budget planning, and cross-functional collaboration. Implement data visualization and reporting, ensure DM plans and metrics, and represent the function in industry groups to drive best practices.