IQVIA UK is seeking experienced Clinical Research Associates to perform site monitoring visits (selection, initiation, monitoring and close-out) in line with GCP/ICH requirements. You will drive subject recruitment plans, administer protocol training, and maintain open communication with sites to ensure project success.
Role requires at least 2 years of on-site monitoring experience in interventional studies and a strong knowledge of regulatory requirements. UK right to work is essential.
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Senior Clinical Research Associate: Site Monitoring & GCP/ICH 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.
