Senior Site Activation Specialist - Belgium

IQVIA • Charleroi, Région wallonne • Posted June 23, 2026

About the Role

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 wi...