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
