Senior Manager, Clinical Supply

The Senior Manager, Clinical Supply is responsible for leading global clinical supply strategies and execution for clinical development programs across multiple phases of development. This role ensures uninterrupted supply of investigational medicinal products (IMPs), comparators, ancillary materials, and clinical trial supplies while maintaining compliance with regulatory requirements, GMP standards, and company policies. Responsibilities Clinical Supply Strategy & Planning Develop and execute end-to-end clinical supply strategies for Phase I–III clinical studies. Create demand forecasts and supply plans based on study protocols, enrollment assumptions, and country-specific requirements. Determine proper use of materials as required by the governing regulatory agencies. Perform risk assessments and mitigation planning. Optimize inventory and minimize waste. Supply Chain Management Manage packaging, labeling, distribution, returns, and destruction activities. Manage label text development. Coordinate global supply distribution. Monitor inventory levels. Ensure clinical trial materials have proper and complete documentation and correct and up-to-date information. Support vendor engagement activities, including contracts, meetings, invoices, and deliverables. Collaborate with Clinical Operations, Regulatory Affairs, Quality, and Pharmaceutical Development and Operations teams. Other duties as assigned. Qualifications Bachelor’s degree in natural sciences, or related field;