Advance cancer research with TRIO as a remote Clinical Research Associate in Western Canada. This role focuses on site visits, regulatory compliance, and supporting clinical trials.
TRIO is seeking a dedicated Clinical Research Associate to enhance its Monitoring Resources team. Ideal candidates will have a Bachelor’s Degree in allied health and at least two years of CRA experience, particularly with phase 1 trials. This position involves ensuring adherence to FDA and ICH-GCP guidelines while mentoring junior staff and facilitating data verification.
Key Responsibilities:
• Conduct site visits for pre-study and monitoring phases
• Confirm adherence to regulations and guidelines
• Verify source documents and manage data validation
• Mentor junior team members for qualified growth
• Participate in budget negotiations and follow-ups
Requirements:
• Bachelor's Degree in Health Sciences or equivalent
• Minimum 2 years CRA experience
• Strong knowledge of ICH-GCP standards
• Experience in clinical trial information systems
• Fluency in English; French preferred
Leverage your CRA expertise to empower transformative cancer treatments at TRIO in a remote setting.
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