Job Description

About the Role

We are looking for a Freelance Site Activation Specialist based in Norway, Sweden or Denmark to support country-level clinical trial start-up and site management activities.

This role focuses on feasibility, site identification, regulatory submissions, and activation, with some involvement in maintenance activities. Candidates with experience in all three countries or exposure to the Nordics region are highly preferred.

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
  • Support contract and budget processes in collaboration with internal stakeholders
  • Maintain and update tracking tools...

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