Director, Clinical Supplies

Role: Director of Clinical Supplies overseeing the labeling, packaging, and distribution of clinical trial materials through third-party CSPs for global trials. Main objectives include ensuring uninterrupted supply, managing CSP relationships, and controlling budgets in compliance with GMP and clinical standards. Responsibilities: direct forecasting, quoting, and monitoring of supply chain activities; manage inventory via IRT systems; support deviations and investigations; oversee budgets, expenditures, and performance; collaborate with Clinical Operations to align supplies with trial protocols; provide forecasts for current and future studies. Qualifications: Bachelor's or Master's in Engineering, Biological Sciences, or Business; 10+ years in clinical study product supply management; 3-5 years managing third-party providers; Project Management Certification preferred; proficiency in IRT systems, MS Office, and project tools. High-Value: experience with global clinical trial supply, GMP/GDP compliance, supply chain logistics, and budget management; familiarity with clinical development processes. Work setup and travel details are not specified.