Freelance UK Site Activation Specialist

IQVIA is seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial start-up and site activation activities. The role focuses on UK submission document collection, site document review, ICF adaptations, and regulatory submission support to ensure timely, compliant submissions.

You will collaborate with investigative sites and internal study teams to maintain quality submission packages, manage timelines, and ensure regulatory readiness