UK Site Activation Specialist - Remote Freelance

IQVIA

Greater London

Remote

GBP 76,000 - 90,000

Full time

8 hours ago

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Job summary

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, working with sites and internal study teams to ensure timely, compliant submissions.

The candidate will manage documentation, timelines, and cross-functional collaboration to ensure Green Light readiness and

Qualifications

Minimum 2–3 years of experience in Site Activation, Study Start-Up, Regulatory Affairs, or Clinical Research.
Strong experience with site document collection, review, and submission preparation.
Fluent English communication, both written and verbal.

Responsibilities

Collect, review, and prepare site and regulatory documentation required for UK clinical trial submissions.
Support the preparation and submission of regulatory packages in line with local regulations.
Perform and coordinate Informed Consent Form (ICF) adaptations and updates.
Review essential site documentation to support Regulatory Green Light readiness.
Liaise with investigative sites to obtain, track, and resolve outstanding documentation.
Ensure completeness, accuracy, and quality of submission packages.