Senior Clinical Research Associate – Site Monitoring & QA

Parexel FSP is seeking an experienced Senior CRA to join a large Sponsor’s EU project. The role focuses on site management, monitoring and close-out of investigator sites to ensure patient safety and high-quality study execution.

Key responsibilities include site activation through database lock, adherence to monitoring plans, and collaboration with study teams, vendors and Drug Safety for SAE follow-up. Oncology experience is preferred.

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