IQVIA cFSP is seeking experienced Clinical Research Associates in the UK to perform on-site monitoring visits and support trial management. The role requires independent monitoring experience, site training, and strong GCP/ICH knowledge.
Travel to diverse investigative sites is expected as part of the role, with access to IQVIA’s training and development resources to advance your clinical research career.
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On-Site Clinical Monitoring Specialist | 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.
