Clinical Research Coordinator

2 days ago


Toronto, Ontario, Canada PSI CRO Full time

Clinical Research Opportunities

**About the Role**

We are seeking a skilled Clinical Research Coordinator to join our team at PSI CRO. As a key member of our start-up team, you will play a vital role in supporting clinical research projects. This is an office-based position based in Toronto, ON, Canada, with a hybrid schedule that includes both office-based and home-based days.

**Key Responsibilities**

* Review and negotiate site budgets to ensure seamless project execution
* 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 coordinate the signature process
* File executed contracts in the Trial Master File and maintain local documentation
* Liaise with the project team, translation, and legal departments on site contracting and grant negotiation matters

**Requirements**

* 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

**Career Advancement**

At PSI CRO, we offer opportunities for career growth and development in clinical research. As a Clinical Research Coordinator, you will have the chance to coordinate a variety of tasks, learn new skills, and advance your career in a dynamic and supportive environment.



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