Senior Manager, Clinical Trial Supply Chain Management
vor 3 Wochen
Job Summary:
We are seeking a highly skilled Senior Manager, Clinical Trial Supply Chain Management to join our team at CSL Behring. This is an exciting opportunity to lead the clinical supply chain for assigned studies, ensuring compliant, on-time supply of study medication and ancillary materials for our patients.
Key Responsibilities:
Gives input to and oversees the implementation and execution of multi-year clinical supply strategies and plans for assigned simple to complex clinical studies.
Presents IMP related CTS topics in Study Execution Teams, Clinical Development Teams and Product Development Expert Team/Chemistry, Manufacturing, & Controls Team.
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 (e.g. Investigational Medicinal Product (IMP) Manuals, product preparation and administration videos).
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 for assigned clinical 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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