Clinical Research Coordinator

4 weeks ago

Toronto, Ontario, Canada PSI CRO Full time
Key Responsibilities

As a Clinical Research Coordinator at PSI CRO, you will play a crucial role in supporting clinical research projects. Your key responsibilities will include:

  • Reviewing and negotiating site budgets to ensure compliance with company policies and industry standards.
  • Facilitating the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site.
  • Customizing and preparing contractually binding site-specific documents in cooperation with PSI Legal.
  • Tracking CTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS).
  • Preparing the executable version of the contract, including grants, and coordinating the signature process.
  • Filing executed contracts in the Trial Master File and maintaining local documentation.
  • Liaising with the project team, translation, and legal departments on site contracting and grant negotiation matters.
Qualifications

To be successful in this role, you will need:

  • A college or university degree or an equivalent combination of education, training, and experience.
  • A minimum of 12 months of experience in the clinical research industry.
  • Knowledge and experience with legal documents related to clinical trial sites.
  • Proficiency in MS Word, Excel, and PowerPoint.
  • Excellent communication and collaboration skills.
About the Role

This is an exciting opportunity to advance your career in clinical research and work in a dynamic team environment. As a Clinical Research Coordinator, you will have the opportunity to learn new skills and grow with the company.

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