Advance your career with TRIO as a Remote Clinical Research Associate, joining the Monitoring Resources team in Western Canada. Engage in vital clinical trials and support transformative cancer treatments.
TRIO is actively seeking a Clinical Research Associate to be a part of its agile Monitoring Resources team. You will conduct site visits, ensure compliance with regulations, and validate critical data across clinical trials. This role calls for a minimum of two years of CRA experience, particularly in monitoring phase 1 trials, and offers the flexibility of work from home.
Key Responsibilities:
• Conduct site visits, including monitoring and termination
• Confirm adherence to FDA, ICH-GCP, and local regulations




• Collect and complete necessary regulatory documents
• Verify source documents and ensure data integrity
• Mentor junior team members and assist with budget negotiations
Requirements:
• Bachelor’s Degree in allied health fields required
• Minimum of 2 years CRA experience necessary
• Solid knowledge of clinical monitoring processes
• Ability to travel up to 60% for site visits
• Fluent in English; French preferred
Elevate your expertise in oncology research while making a significant impact at TRIO.
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📌 Remote Clinical Research Associate In Oncology Edmonton
🏢 Translational Research in Oncology
📍 Edmonton