IQVIA UK’s Site Management team is expanding to include experienced Clinical Research Associates. The role focuses on on-site monitoring visits, site management, and collaboration with study teams to ensure protocol compliance and safe, efficient trial conduct.
Ideal candidates will have proven independent monitoring experience, familiarity with GCP/ICH, and a life science degree. Travel to sites will be required, and visa sponsorship is not available for this position.
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Senior CRA: On-Site Monitoring & Study Leadership in Manchester 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.
