IQVIA is seeking a Clinical Monitoring Associate in the United Kingdom to perform on-site monitoring visits, ensure adherence to GCP and ICH guidelines, and support project management across multiple sites.
You will collaborate with investigative sites, administer protocol training, track recruitment, and maintain essential trial documentation. Flexibility to travel is required as projects span diverse sites with regulatory expectations.
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Clinical Monitoring Associate - On-Site, UK Travel in Reading 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.
