Clinical Research Coordinator

4 weeks ago


Toronto, Ontario, Canada PSI CRO Full time

Job Title: Clinical Research Coordinator

Job Summary: We are seeking a highly skilled Clinical Research Coordinator to join our team at PSI CRO. As a key member of our start-up team, you will play a crucial role in supporting clinical research projects.

Key Responsibilities:

  • Review and negotiate site budgets to ensure compliance with regulatory requirements.
  • 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.
  • Liaise 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.

About PSI CRO: PSI CRO is a dynamic and growing company that offers a unique opportunity to advance your career in clinical research. As a Clinical Research Coordinator, you will have the chance to work on a variety of tasks, learn new things, and grow with the company.



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