Remote UK Site Activation Specialist

IQVIA is seeking an experienced Freelance Site Activation Specialist in the United Kingdom to support clinical trial start-up and site activation. Focus on UK document collection, site review and regulatory submissions, with ICF adaptations and regulatory support across project timelines.

The role requires home-based UK work, immediate start, approximately 3–6 months, and collaboration with cross-functional teams to ensure compliant submission packages and Green Light readiness.

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