IQVIA UK's RWE team is seeking a Clinical Research Associate II to support Phase 3b and 4 studies across therapeutic areas. The CRA will cover sites in the UK & Ireland, with 6-7 site visits per month, requiring on-site monitoring and strong regulatory knowledge.
The candidate should have 1–2 years of on-site monitoring experience, a degree in a scientific discipline or healthcare, and a solid grasp of GCP/ICH guidelines to maintain trial quality and site compliance.
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CRA II: UK & Ireland Site Monitoring & Study Execution in Taunton 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.
