Lead the design and implementation of clinical trial supply chain strategies across multiple global trials., Manage relationships with external vendors, including packaging, labeling, storage, and distribution partners., Lead demand forecasting and inventory management to ensure uninterrupted supply of trial materials to clinical sites., Ensure that all supply activities are compliant with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and local/international regulatory requirements., Identify and proactively manage risks associated with clinical supply, including potential supply chain disruptions, regulatory hurdles, or quality issues., Manage clinical supply budgets, optimizing resources, controlling costs, and ensuring timely reporting on budget performance., Partner closely with clinical operations, quality assurance, regulatory affairs, and project management teams to ensure the clinical supply strategy continuously aligns with study requirements., Lead initiatives to streamline supply chain processes, enhance operational efficiencies, and implement best practices across the clinical supply chain., Provide regular updates to senior leadership on supply chain progress, risks, and opportunities.
