IQVIA cFSP (sponsor-dedicated) seeks experienced Clinical Research Associates in the UK to monitor sites, manage trials, and ensure regulatory compliance. You will collaborate with sites, coordinate training, and support recruitment plans to meet project needs.
The role requires working knowledge of GCP/ICH guidelines, a life science degree or equivalent experience, and willingness to travel to sites across the UK.
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Senior CRA – Sponsor-Dedicated, UK Travel 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.
