About the Role
We are looking for a Freelance Site Activation Specialist based in France to support country-level clinical trial start-up and site management activities.
This role focuses on EU CTR package preparations, site outreach, document collection and review, ICF adaptations.
Key Responsibilities
Act as the primary point of contact for assigned investigative sitesExecute 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 with Site Activation Managers, Project Manageme...