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...