Join our international team and be the key support to clinical research projects part of the startup team working in a dynamic multifunctional environment gaining unique skills from various disciplines relevant to clinical research.
This is an officebased position based in Toronto ON Canada. This position follows a hybrid schedule with officebased and homebased days.
The official job title for this role is Site Contract Specialist II.
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 sitespecific 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 & 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
Remote Work :
No
Employment Type :
Fulltime