Advance oncology trials remotely with TRIO as a Clinical Research Associate using clinical monitoring and ICH-GCP expertise. This freelance contract covers Western Canada.

TRIO seeks a Clinical Research Associate for its Monitoring Resource team on a remote, full time, one-year contract. The work supports translational cancer research through source verification, site visits, regulatory compliance, and data validation. Candidates need oncology experience and early-phase monitoring experience.

Key Responsibilities:
Verify source documents and resolve clinical trial data queries
Conduct pre-study, initiation, monitoring, and termination site visits
Confirm FDA, ICH-GCP, and local regulatory adherence
Collect regulatory documents and support compliance implementation




Mentor junior team members and participate in budget follow-up

Requirements:
At least three years of oncology CRA, coordinator, or nursing experience
At least one year monitoring early-phase clinical trials
Science-related Bachelor's degree and medical terminology knowledge
Solid ICH-GCP knowledge and clinical monitoring process expertise
English fluency, travel availability, and legal work authorization

Apply oncology monitoring expertise, regulatory knowledge, and data verification skills to TRIO's translational clinical research.
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📌 Oncology Clinical Research Associate Toronto (Canada)
🏢 Translational Research in Oncology
📍 Canada