Clinical Supply Chain Specialist

Role: Clinical Supply Chain Specialist managing drug supply activities for clinical trials, including planning, label development, packaging, and distribution. Responsibilities: develop and oversee supply plans, coordinate with internal teams and external vendors, optimize supply strategies, monitor production schedules, ensure label compliance, support IRT system activities, and manage shipments and import licenses. Requirements: Bachelor's degree in science, medicine, supply chain, or related field; 2+ years of supply chain experience within biotech, pharma, or CRO industries; proficiency in Microsoft Office; strong analytical, organizational, and communication skills. HighValue: focus on clinical trial supply management, collaboration with cross-functional teams (Clinical Operations, Regulatory, CMC), support for IRT systems, experience in biotech/pharma supply chain logistics. WorkSetup: not specified; likely hybrid or onsite based on typical industry practices.