Fortrea Development India Private Limited in London is seeking a Study Start‑Up PM to lead country‑level submissions, approvals and site readiness for a global, client‑dedicated program. You will oversee regulatory submissions, IRB/IEC interactions, and local documentation while coordinating with cross‑functional teams.
The role requires 5+ years in clinical research with regulatory exposure, strong knowledge of UK regulations, and the ability to manage multiple protocols in a hybrid
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Contact Details:
Fortrea Development India Private Limited Recruitment Team
