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Sr Clinical Trial Manager
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- The position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out, including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources, budgets, contracts, and timelines.
- Manage and/or support global clinical trials (Phase 1-3) in oncology indications, ensuring that studies are carried out in accordance with the clinical development plan, ICH-GCP, and FDA/other regulatory agency requirements.
- Setup and manage study vendors (e.g., CRO, IRT, laboratories, central ECG/imaging).
- Assist in IRT design and development.
- Provide TMF oversight to ensure inspection readiness.
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