Clinical Research Associate — Flexible Site Monitoring (UK)

IQVIA UK is seeking an experienced Clinical Research Associate for the South West England region. The role involves on-site monitoring visits, protocol training, and collaboration with study teams to ensure regulatory compliance and data integrity.

The candidate should have at least 2 years of independent on-site monitoring experience in interventional studies, with familiarity in start-up, enrolment, maintenance and close-out processes. UK right to work is required.

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