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 sitesExecute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelinesPrepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracyMaintain and update tracking tools, timelines, and internal systems with accurate project dataMonitor and report on site activation progress and performance metricsEnsure compliance with ICH-GCP, local regulations and study requirementsCollaborate closely wi...