The Clinical Supply Manager will be responsible for ensuring the clinical supplies needed for all clinical studies managed by Rho are provided on time, within budget, and in accordance with protocol and applicable regulatory requirements. This includes management and oversight of the planning, forecasting, sourcing, packaging, labeling, distribution and return of clinical supplies for commercial and government sponsored Phase 1 - 4 clinical trials. The successful applicant will collaborate closely as a member of cross-functional study teams which include Project Management, Clinical Operations, Client Support Services, and IRT Software Development.
Clinical Trial Supply Management (General):
Packaging and Labeling
IRT (Interactive Response Systems)