Site Activation Specialist / Contract Specialist
On-site · Paris, Île-de-France, France
Job Summary
Lead end-to-end contract and budget processes for site activation in clinical trials, including feasibility support, start-up planning, and site activation deliverables. Serve as primary contact for investigative sites, SAMs, project management teams, and relevant departments to ensure compliance with SOPs, regulatory requirements, and timelines. Perform quality control on site-submitted documents and engage sponsors for complex negotiations or contract strategy discussions. Develop and monitor project-specific contract and budget timelines, provide guidance on contracting processes, and coordinate cross-functional activities with regulatory, clinical operations, and project management teams. Requires a Bachelor’s degree in Life Sciences, Law, or a related field and at least 1 year of clinical research experience with direct site contract and budget negotiation exposure.
Required Qualifications
- Bachelor’s degree in Life Sciences, Law, or a related field (required)
- Minimum 1 years of experience in clinical research, with at least 6 months of direct experience in site contract and budget negotiations; or an equivalent combination of education, training, and relevant work experience
- Demonstrated experience in managing contract/budget negotiations and timelines within global or local clinical trial settings
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