IQVIA UK cFSP team is growing and seeking experienced Clinical Research Associates in South West England. The role involves on-site monitoring across the lifecycle of interventional studies, ensuring GCP/ICH compliance, trainee protocol delivery, and strong site collaboration.
Required are at least 2 years of independent on-site monitoring, a degree in a scientific field, and confidence with AI tools. UK right to work is required; visa sponsorship is not available.
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Clinical Research Associate - Site Monitoring & Compliance 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.
