Apply oncology monitoring expertise as a Clinical Research Associate with TRIO, working remotely across Western Canada on a one-year contract.

TRIO seeks a CRA for its Monitoring Resource team within a global academic clinical research organization. The position supports translational cancer research through site monitoring, regulatory compliance, data verification, and query resolution. Candidates need oncology experience and early-phase monitoring experience.

Key Responsibilities:

- Verify data against source documents
- Conduct pre-study, initiation, monitoring, and termination site visits
- Confirm FDA, ICH-GCP, and local regulatory adherence
- Assist with data validation and query resolution
- Mentor junior team members as required

Requirements:

- At least three years of oncology experience in clinical research
- At least one year monitoring early-phase clinical trials
- Science-related Bachelor's degree completion
- Solid ICH-GCP and clinical monitoring knowledge
- Ability to travel up to 60% on average

Bring oncology monitoring, regulatory, and data skills to TRIO's remote Clinical Research Associate team across Western Canada.

📌 Oncology Clinical Research Associate (Edmonton)
🏢 Freelance
📍 Edmonton