IQVIA is seeking a Clinical Monitoring Associate in the UK to perform site monitoring visits, ensure GCP/ICH compliance, and support trial deliverables. You will collaborate with cross-functional teams and manage site communications, with travel to sites as required.
The role requires at least 18 months of independent on-site monitoring, a life science degree or equivalent experience, and willingness to travel.
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Clinical Monitoring Associate — Site Monitoring & Trials in Wokingham 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.
