Clinical Supply Chain Director

Role: Clinical Supplies Director responsible for developing and executing clinical supply chain strategies and infrastructure supporting small molecule and biologics projects across development and commercialization phases. Responsibilities: lead procurement, labeling, packaging, distribution, and inventory management for clinical trials; oversee vendor capabilities and ensure GMP compliance; forecast supply needs; and maintain regulatory records. Collaborates with cross-functional teams and manages CMO vendors, providing mentorship within a matrix environment. Requirements: BS/BA with 13+ years, MS/MA with 11+ years, or PhD with 8+ years in related fields; extensive experience in drug manufacturing, analytical testing, and GMP/GCP/GLP regulations; proven track record in clinical supply management for Phases I-III. HighValue: focus on biologics and small molecules, clinical development stages (Phases I-III), regulatory compliance, CMO oversight, supply chain infrastructure, and team leadership. WorkSetup: 20% travel; office environment.