Site Activation Specialist (US Experience)
syneoshealth · ARG-Remote
Job description
About the role
Syneos Health is seeking a Site Activation Specialist with US experience to support clinical trial start‑up activities. The role ensures timely site activation, compliance with regulatory requirements, and accurate tracking of project milestones.
Key responsibilities
- Monitor forecasted submission and approval timelines, track milestone progress in real time, and provide rationale for any delays.
- Review and comply with SOPs and work instructions, maintain training records, and ensure timesheet compliance.
- Submit required documents to the Trial Master File according to company and sponsor SOPs.
- Prepare and submit Central and Local EC applications, regulatory authority submissions, and ongoing amendments.
- Act as liaison between investigational sites and functional leads, overseeing end‑to‑end site activation at the country level.
- Support site selection and feasibility activities with the lead and project manager.
- Assist with local investigator contract and budget negotiations, ensuring quality control and proper archival of contracts.
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syneoshealth
ARG-Remote