Clinical monitoring expertise takes center stage at TRIO, with work from home based in Western Canada and travel across clinical trial sites. Support oncology research through site visits, regulatory compliance, and source data verification.

TRIO seeks a Clinical Research Associate for its Monitoring Resources team, reporting to the CRA Line Manager. The position requires at least two years of CRA experience, phase 1 trial monitoring, ICH-GCP knowledge, and clinical trial information systems experience. A bachelor’s degree in an allied health field is required.

Key Responsibilities:

- Conduct pre-study, initiation, monitoring, and termination site visits
- Confirm adherence to FDA, ICH-GCP, and local regulations
- Complete and collect required regulatory documents




- Verify source documents and assist with query resolution
- Mentor junior team members and support budget follow-up

Requirements:

- At least two years of previous CRA experience
- Experience monitoring phase 1 clinical trials
- Bachelor’s degree in medical, nursing, pharmacy, or health science
- Excellent medical terminology and clinical monitoring knowledge
- Ability to travel up to 60% and communicate fluently in English

Apply clinical monitoring, regulatory, and data verification expertise to advance translational cancer research with TRIO across Western Canada.

📌 Clinical Research Associate Western Canada (Montreal)
🏢 S.i. Systems
📍 Montreal