IQVIA UK Site Management team seeks junior and experienced Clinical Research professionals to perform on-site monitoring visits across multiple sponsors. You will drive subject recruitment plans, train site staff on the protocol, and ensure regulatory compliance throughout the study lifecycle.
The role requires independent monitoring experience, strong GCP/ICH knowledge, and willingness to travel between sites. UK visa sponsorship is not available for this position.
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Site Monitoring CRA II — GCP/ICH Expert in Leeds 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.
