The Clinical Research Director (CRD) is the Clinical Operations lead in a country or cluster and is responsible for the execution of all clinical trials in scope for GCTO country operations. Adherence to GCP, local and global policies and procedures to conduct high‑quality, inspection‑ready studies is essential. The position is accountable for trial quality, audit responses and completion of CAPAs. The incumbent ensures a single point of contact for managing clinical trial execution in all its aspects across phases within the GCTO cluster.
Division/Area: Clinical Operations
Reports to: GCTO Regional Research Director (RRD) or Cluster Clinical Research Director
Extent of Travel: up to 30%
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