IQVIA LLC in the United Kingdom is seeking a Clinical Research Associate to perform site monitoring visits in line with GCP/ICH and contracted scope. You will collaborate with sites to drive recruitment plans and ensure protocol training and regular communication.
The role focuses on evaluating site practices, managing regulatory submissions, and maintaining TMF/ISF documentation, with close collaboration across the study team to support project execution.
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Clinical Monitoring Associate – Site & Study Operations employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
