Manager, Clinical Supplies
Provides operational cross-functional support of clinical trial material supply planning and distribution. Actively manages the coordination, and implementation of clinical supplies for multiple projects involving global distribution. This position plans and coordinates the efficient movement of materials through the development and execution of operational strategies for the designated programs. Actual title may vary depending on experience. Reports to Associate Director, Clinical Supplies.
•Coordination and tracking of shipments to clinical sites
•Coordination and tracking of shipments to depots
•Coordination and tracking of temperature excursions
•Track inventories across sites and depots
•Document creation/collection for regulatory submissions and QP release
•Communicate with contract packager/labeler/depot
•Communicate with CRO/Depot regarding study drug needs
•Study drug label review and management
•Drug return, reconciliation, and destruction management
•Clinical Supplies functional representative on Study Team(s)
•Bachelor’s degree, preferably in a scientific discipline; a combination of relevant education and applicable job experience may be considered.
•4+ years clinical supplies experience
•GMP experience and training
•Global trial experience
•Experience on studies where drug is prepared in the pharmacy
The content of this position description provides a summary of the general nature of the job and may include other duties as assumed or assigned. The Company reserves the right to change this description at any time and require the employee to perform other tasks as required due to business needs.
Cidara Therapeutics is an E-Verify Company