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Translational Research in Oncology·Montreal, Quebec
Clinical Research Associate · CA$105,000 - CA$140,000/yr
Computed from live listings
Shaded band: the middle 50% of posted healthcare roles in Montreal, Quebec salarys. This role sits in the 88th percentile.
Pay for this role is about 54% above the Montreal, Quebec median for similar positions.
The Clinical Research Associate is responsible for conducting site visits, including pre-study, initiation, monitoring, and termination. They must ensure compliance with FDA and ICH-GCP regulations while managing regulatory documentation and data verification.
If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!
Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting.
Our passionate team is committed to providing cancer treatments of the future to the world of today.
TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team.
Reporting to a CRA Line Manager, this position will be home-based in Canada.
Conducting site visits, including pre-study, initiation, monitoring and termination; Confirming adherence to all FDA, ICH-GCP and local regulations; Ensuring the completion and collection of regulatory documents; Performing data verification of source documents; Ensuring implementation and compliance with FDA, ICH-GCP guidelines; Participating in budget negotiation and follow-up where applicable; Assisting with data validation and query resolution; Mentoring junior team members as required.
A minimum of 2 years of monitoring experience in oncology trials Fluent in English and French Experience monitoring phase 1 trials An advanced level of oncology knowledge Completion of a science-related Bachelor’s degree Excellent knowledge of medical terminology and clinical monitoring process Strong ICH-GCPs knowledge Experience with clinical trial information systems Ability to travel up to 60% on average Fluent in both English and French What TRIO Can Offer You: Competitive salary 3 weeks of vacation plus paid Christmas Closure 2 weeks paid personal/sick time Health, Dental, Vision & Life Insurance premiums paid by TRIO Flexible working hours Monthly internet allowance Up to 5% RRSP Matching Program Pay Range $105,000.00 to $140,000.00 annually - Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.
Prior to applying please review TRIO's Applicant Information Notice To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.
To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience. Teamwork · Passion · Integrity · Innovation
Candidates must have a minimum of 2 years of monitoring experience in oncology trials and a science-related Bachelor’s degree. Proficiency in both English and French is required, along with the ability to travel up to 60% of the time.
Market context
Clinical Research Associate roles in Quebec are typically driven by ongoing clinical trial activity, especially in oncology, where sponsors look for candidates who can monitor sites and keep studies compliant. Competition is often strongest for applicants with direct oncology monitoring experience, strong ICH-GCP knowledge, and flexibility to travel frequently. Review the AI-summarized requirements and benefits here to quickly compare fit before applying, then confirm your travel availability and relevant study-monitoring background.
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