IQVIA LLC is seeking a site-based Clinical Research Associate to manage monitoring activities and ensure regulatory compliance across trials in Leeds. You will track submissions, site recruitment, data queries and documentation, while maintaining TMF/ISF and liaising with the study team.
The role requires at least 2 years of on-site monitoring experience, solid knowledge of GCP/ICH, and excellent English communication.
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Senior Clinical Research Associate: Site Management Lead 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.
