IQVIA
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
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