Job Description
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.
Qualifications
College / University degree or an equivalent combination of education, training & experienceMinimum of 12 months experience in the clinical research industryKnowledge and experience with legal documents related to clinical trial sites.PC skills to be able to work with MS Word, Excel and PowerPointAbility to plan, multitask and work in a dynamic team environmentCommunication and collaboration skillsAdditional Information
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.