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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, timelines, and internal sys...
About the Role
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
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