IQVIA is seeking a Senior Clinical Research Associate (CRA) to conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, GCP, ICH guidelines, and regulatory requirements. You will ensure patient safety, data integrity, protocol compliance, and study quality across sites in the UK.
You will build strong relationships with investigators, provide ongoing guidance and training, monitor progress, support recruitment strategies, and maintain
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Senior Clinical Research Associate - Onsite Monitoring Lead 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.
