IQVIA cFSP (sponsor-dedicated) seeks experienced Clinical Research Associates in the UK. The role involves on-site monitoring and site management to ensure protocol adherence, data quality and regulatory compliance across multiple UK sites.
Responsibilities include initiating and monitoring visits, training site staff, tracking recruitment, and managing trial documentation in TMF/ISF. 1+ year on-site experience preferred; English communication essential.
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Sponsor-Dedicated CRA 2 (UK) – On-Site Monitoring 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.
