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Biotech
Support the Global Clinical Study Manager in global study delivery: set up and maintain study systems (eTMF, CTMS, SharePoint), track deliverables, assist study document reviews, coordinate cross‑functional teams, support vendor selection and budget/PO/payment tracking, contribute to data cleaning and Clinical Study Report activities, and help maintain TMF quality and compliance with ICH‑GCP.
Biotech
The Regional Clinical Compliance Manager ensures compliance in clinical activities, guiding study teams, managing inspections, tracking non-compliance issues, and developing training materials.
