Senior Manager, Clinical Trial Supply Chain
vor 2 Wochen
CSL Behring is seeking a highly skilled Senior Manager, Clinical Trial Supply Chain to lead the end-to-end supply chain for assigned clinical studies. The successful candidate will be responsible for managing the depot network, distribution to clinical sites, and ensuring final return and destruction of study medication and ancillary materials.
Key Responsibilities:
- Gathers and documents requirements for clinical supplies based on protocol attributes and clinical assumptions.
- Leads demand forecasting for study(ies) and adjusts plans monthly based on actual consumption and changes to clinical and/or supply assumptions.
- Establishes and monitors global network of regional and global depots to distribute drug supplies and ancillary supplies to countries and sites in assigned clinical studies.
- Develops clinical trial supply documents and training to support study execution for clinical sites and patients.
- Ensures compliance of all clinical study activities with SOPs and regulations for assigned studies.
- Creates and updates budgets for complex studies including product and packaging and labeling costs, storage and distribution costs, and comparator and ancillary material costs.
- Ensures study reconciliation, returns, destructions are complete and leads lessons learned sessions.
Requirements:
- University degree (BSc, MSc, PhD) in life sciences, engineering, logistics or equivalent experience.
- Minimum of 7 years' experience in biopharmaceutical R&D or supply chain including 4 years' experience in clinical trial supplies leading global studies.
About CSL Behring:
CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
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