Join our international team and be the key support to clinical research projects, part of the start-up team, working in a dynamic multi-functional environment, gaining unique skills from various disciplines relevant to clinical research.
This is an office-based position based in Toronto, ON, Canada. This position follows a hybrid schedule with office-based and home-based days.
The official job title for this role is Site Contract Coordinator.
You will:
- 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
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.
