SeniorSiteActivationSpecialist

## **Freelance Senior Site Activation Specialist – Belgium (Home-Based)** Location: Belgium (home-based) Contract type: Freelance FTE: 1.0 - full time Start: immediately Duration: around 6 month **About the Role** We are looking for a Freelance Senior Site Activation Specialist based in Belgium to support country-level clinical trial start-up and site management activities. This role focuses on **EU-CTR compilation, submission documents, regulatory submissions, ICF adaptions, packages and activation.** ### **Key Responsibilities** * Act as the primary point of contact for assigned investigative sites * Execute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelines * Prepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracy * Maintain and update tracking tools, timelines, and internal systems with accurate project data * Monitor and report on site activation progress and performance metrics * Ensure compliance with ICH-GCP, local regulations and study requirements * Collaborate closely with Site Activation Managers, Project Management, and cross-functional teams ### **Requirements** * **Based in Belgium** with strong understanding of the local regulatory environment * **2–3 + years of experience** in site activation, study start-up, or clinical research * Bachelor’s degree in Life Sciences or related field * Solid knowledge of clinical trial start-up processes and regulatory requirements * Experience managing site documentation and submission processes * Strong attention to detail and ability to manage multiple sites and timelines * **Fluent in Dutch or French and English (written and spoken)** If this role sounds of interest, please apply today! #LI-DNP #LI-CES #LI-HCPN #LI-NS1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent