IQVIA LLC is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across the UK & Ireland. The CRA will perform 6–7 site visits per month, ensure GCP/ICH compliance, and collaborate with study teams for successful trial execution.
The role requires 1–2 years of on-site monitoring experience, a degree in a scientific discipline or healthcare, and the ability to manage site communications and regulatory activities. Visa sponsorship is not offered.
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CRA II: On-Site Monitoring & Study Oversight (UK & Ireland) 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.
