Associate Director, Clinical Supply

Role: Associate Director of Clinical Supply Chain Management overseeing planning, execution, and compliance of clinical supply operations for biopharma programs. Responsibilities: lead demand forecasting, procurement, packaging, labeling, distribution, and vendor management; collaborate with Clinical Operations, CMC, QA, RA; ensure documentation, quality assurance, and regulatory compliance; drive process improvements and resource planning. Requirements: Bachelor's in a scientific or healthcare field; 10+ years in regulated pharma or biotech, including 8+ years in global clinical supply chain and 5+ years of managerial experience; thorough knowledge of FDA, cGMPs, GxP, and IRT systems; APICS certification advantageous. HighValue: extensive clinical supply chain experience in biotech, regulatory compliance expertise, vendor/vendor management skills, familiarity with clinical trial logistics, and cross-functional collaboration. WorkSetup: not specified; likely hybrid or on-site based on location.