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Experienced CRA – On-site Monitoring & Study Leadership
Job Description & How to Apply Below
IQVIA is seeking experienced Clinical Research Associates in the United Kingdom to conduct on-site monitoring visits in line with GCP/ICH guidelines. The role involves overseeing site performance, coordinating with sites on recruitment plans, and ensuring proper documentation and regulatory compliance across multiple studies.
Travel to clinical sites is required, with flexibility to work across diverse sites.
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