Freelance Site Activation Specialist – France (Home-Based)
About this role
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, and ICF adaptations. What You'll Do
- Act as the primary point of contact for assigned investigative sites
- Execute 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
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