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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Senior Clinical Research Associate - Site Monitoring & QA employer: Parexel International
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative and inclusive work environment where your expertise is highly valued. As a Senior Statistical Programmer, you'll have the opportunity to work on groundbreaking projects while enjoying professional growth, flexible working hours, and a strong commitment to work-life balance. Join us in the UK, Poland, Serbia, or Hungary, and unlock your full potential with our dedication to employee development and quality management.
