We are looking for a proactive and organized professional to support our client with clinical projects and help manage documentation for clinical sites.

What you will do:

• Prepare and review regulatory documents for clinical sites
• Assist with site contract and budget negotiations
• Support the team in project planning and tracking progress
• Ensure document quality and compliance with GCP standards
• Provide feedback and support to the project team and management
• Participate in site selection and other project activities as needed

Start date: immediately

Contract for limited period with possibility of prolongation