Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.

TRIO is seeking a Clinical Research Associate (CRA) to join our Monitoring Resource team. This is a remote, part-time freelance opportunity on a 6-month contract, open to candidates based in Canada.

Responsibilities:

+ Performing data verification of source documents;

+ Conducting site visits, including pre-study, initiation, monitoring, and termination;

+ Confirming adherence to all FDA, ICH-GCP, and local regulations;

+ Ensuring implementation and compliance with FDA, and ICH-GCP guidelines

+ Participating in budget negotiation and follow-up where applicable

+ Assisting with data validation and query resolution

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