- Review and negotiate site budgets
- Facilitate the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site.
- Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal.
- Track CTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS).
- Prepare the executable version of the contract, including grants, and coordinates the signature process.
- File executed contracts in the Trial Master File and maintains local documentation.
- Liase with the project team, translation, and legal departments on site contracting and grant negotiation matters.
- College/University degree or an equivalent combination of education, training & experience
- Minimum of 12 months experience in the clinical research industry
- Knowledge and experience with legal documents related to clinical trial sites.
- PC skills to be able to work with MS Word, Excel and PowerPoint
- Ability to plan, multitask and work in a dynamic team environment
- Communication and collaboration skills
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then this is the right choice for you.
