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
- Strong 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.

📌 Oncology Clinical Research Associate (Vancouver)
🏢 Translational Research in Oncology
📍 Vancouver