IQVIA UK’s cFSP team is expanding and seeks experienced Clinical Research Associates in the South West England to perform site monitoring visits in line with GCP/ICH guidelines and sponsor requirements. You will coordinate with sites, manage expectations, and support regulatory submissions throughout trials.
Join IQVIA for a mission to accelerate innovation for healthier outcomes, with flexible working, mentorship, and clear career development opportunities offered.
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Onsite Clinical Monitoring Associate – Interventional Trials in Pill 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.
