Senior Manager - Clinical Supply Chain Operations

Senior Manager – global Clinical Supply Chain Operations – fully remote working £90 per hour (experience dependent) + min 12-month contract with excellent possibility of permanent opportunity thereafter + immediate start available + 100% remote working + collaborative global team environment Senior Manager – global Clinical Supply Chain Operations key responsibilities include: * Investigational material activities for global Trial Phases I-IV, including coordination of packaging, labeling, and distribution. * Collaborate with medical, regulatory, and clinical experts to ensure that quality Clinical Supplies are provided. * Interact with internal and external supply chain and logistics personnel in the procurement of clinical drug supplies. * Technical assessment and selection of contract packaging vendors; review and approve contracts for packaging and labeling activities and monitor budget. * Coordinate QP release of investigational materials to be used in the EU. * Review and approve IVRS specifications from investigational materials perspective. * Forecast and order bulk drugs from manufacturing vendors and other suppliers. * Responsible for development of clinical supply plan and packaging design. * Co-ordinate the design of clinical labels to meet protocol, FDA, EU and country specific requirements. * Write /review the Study Medication Sections of the protocol and IND as required. * Monitor Investigational Materials inventories and expiry/retest dates supplies. Senior Manager – global Clinical Supply Chain Operations profile: * BSc Degree or related scientific discipline. * Min 6+ years pharmaceutical industry experience in global clinical supplies. * Extensive experience in the management of multiple studies globally. * Comprehensive operational experience in R&D Clinical Supplies and related areas. * Highly experienced in investigational material activities for global trial phases I-IV, including coordination of packaging, labeling and distribution. * Excellent knowledge of GMP (current Good Manufacturing Practices for Finished Pharmaceuticals) and EU / country specific regulations regarding clinical studies. * Thorough understanding of the development and clinical supplies process. * Extensive Vendor management experience; excellent interpersonal & planning skills. The above contract role is an opportunity to join a forward thinking & fast-paced global pharmaceutical business, serving as a core member for clinical projects around the world. If you are available at relatively short notice, then please send your profile and one of our team will be in touch