About the Role
We are looking for a Freelance Site Activation Specialist based in Germany 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 Switzerland or exposure to the DACH region are highly preferred.
Key Responsibilities
Act as the primary point of contact for assigned investigative sitesExecute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelinesPrepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracySupport contract and budget processes in collaboration with internal stakeholdersMaintain and update tracking tools, timelines, and internal sys...