Location: United Kingdom (Home-Based)Contract Type: FreelanceFTE: 1.0Start: ImmediateDuration: Approximately 3–6 monthsAbout the RoleWe are seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial start-up and site activation activities.The primary focus of this role will be UK submission document collection and preparation, site document review, Informed Consent Form (ICF) adaptations, and regulatory submission support. The successful candidate will work closely with investigative sites and internal study teams to ensure submission packages are complete, compliant, and delivered according to project timelines.Key ResponsibilitiesCollect, review, and prepare site and regulatory documentation required for UK clinical trial submissionsSupport the preparation and submission of regulatory packages in accordance with study requirements and local regulationsPerform and coordinate Informed Consent Form (ICF) adaptations and associated document updatesReview essential site documentation to support Regulatory Green Light readinessLiaise directly with investigative sites to obtain, track, and resolve outstanding documentationEnsure the completeness, accuracy, and quality of submission packagesMaintain study tracking systems, timelines, and submission recordsSupport site activation activities and monitor progress against project milestonesCollaborate closely with Site Activation Managers, Regulatory Affairs, Project Management, and other cross-functional teamsEnsure compliance with ICH-GCP, local UK regulations, and study-specific requirementsRequirementsBased in the United KingdomMinimum 2–3 years of experience in Site Activation, Study Start-Up, Regulatory Affairs, or Clinical ResearchStrong experience with site document collection, review, and submission preparationExperience supporting clinical trial regulatory submissions in the UKExperience performing ICF adaptationsSolid understanding of site activation and study start-up processesStrong attention to detail and ability to manage multiple priorities and timelinesBachelor's degree in Life Sciences or a related fieldFluent English communication skills, both written and verbalIf this role sounds of interest, please apply today!#LI-DNP#LI-CES#LI-HCPN#LI-XSIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.