Senior CRA: On-Site Monitoring & Study Leadership

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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