Senior Director, Clinical Supply Chain

Role: Senior Director, Clinical Supply Chain, responsible for developing and executing strategies for clinical supply management supporting small molecule and biologics projects from development through commercial launch. Responsibilities include overseeing supply forecasting, inventory management, labeling, packaging, distribution, procurement of comparator and placebo products, and ensuring GMP compliance. The role requires collaboration with CMC, Clinical, and non-clinical teams to support global Phase I-III trials and investigator-sponsored studies. The position involves leading supply chain infrastructure, vendor sourcing, and managing a team, with a focus on uninterrupted supply continuity and regulatory compliance. Requirements: Bachelor's degree with 15+ years (or advanced degree with 12+ years) in drug manufacturing, analytical testing, or related fields; extensive experience in clinical supply chain for multiple trial phases; strong knowledge of GMP/GCP/GLP/GDP regulations; strategic decision-making skills; ability to lead cross-functional teams; proficiency in supply chain planning tools and MS Office. HighValue: Expertise in biologics and small molecules, global clinical trial supply management, GMP compliance, and vendor oversight. WorkSetup: On-site with 20% travel to vendor sites and team meetings.