IQVIA UK is seeking experienced Clinical Research Associates to join the cFSP team in the South West England. The role focuses on on-site monitoring, recruitment planning, regulatory compliance, and site training to ensure trial integrity and patient safety.
Candidates should have at least 2 years of independent monitoring experience in interventional studies, with knowledge of GCP/ICH and UK regulatory requirements.
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Clinical Research Associate - On-site Monitor in Bath 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.
