IQVIA is seeking experienced Clinical Research Associates in the UK to perform on-site monitoring, ensure GCP/ICH compliance, and drive site recruitment plans. The role involves regular site visits, training, and close collaboration with the study team across diverse sites.
Candidates should have independent monitoring experience, strong GCP/ICH knowledge, and flexibility to travel. This is a sponsor-dedicated CRA position based in the UK.
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UK CRA – Sponsor-Dedicated, On-Site Monitoring in Reading employer: IQVIA, Inc.
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous learning opportunities and the chance to work with cutting-edge technology in the heart of the healthcare industry. Join us in a role that not only challenges you but also allows you to make a meaningful impact on global health outcomes.
