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.
Are you ready to take on the Senior Clinical Research Associate
- Site Monitoring & QA role at Parexel International?
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Clinical Research Associate
- Site Monitoring & QA role in the description above.
We appreciate your interest in this position.
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