Job Description

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...
            

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Senior Site Activation Specialist - Belgium

Job Description

Apply for This Position