Clinical Research Associate (Canada)
- Employment type
- Full-time · On-site
- Posted
- November 11, 2026
- Salary range
- $74,700–$136,700 CAD per year
- Province
- Quebec (QC)
Hiring confidence: Some gaps · 51/100
Some signals are missing from this posting. It may well be genuine, but it is worth confirming the role is still open before you invest time in applying. How this is scored
Job Overview
This role is based in Quebec. IQVIA is hiring for this full-time position through Jobily, where you can check how well your resume matches the posting before you apply.
Market context
About this role in Quebec
Average salary for Clinical Research Associate (Canada) in Quebec
We do not have a salary benchmark for this title in Quebec yet. The posting advertises $74,700–$136,700.
NOC code
This posting has not been matched to a NOC 2021 unit group yet. Use the NOC finder to identify the code from the duties listed above.
Typical qualifications for Canadian employers
- Knowledge of Good Clinical Practice (GCP) guidelines
- Understanding of International Conference on Harmonization (ICH) regulations
- Familiarity with study protocols and regulatory requirements
- Ability to conduct site monitoring visits
- Knowledge of applicable regulations and sponsor requirements
Fit check
Is this role right for you?
Top skills this posting asks for:
- Clinical research monitoring
- Site management
- Good Clinical Practice (GCP)
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What you'll do
- Perform site monitoring visits including selection, initiation, monitoring, and close-out visits
- Ensure sites are conducting studies according to study protocol
- Verify that study data is reported as required
- Monitor compliance with applicable regulations and guidelines
- Ensure adherence to sponsor requirements
- Perform site management work
- Execute work within contracted scope and regulatory requirements
What you'll need
- Knowledge of Good Clinical Practice (GCP) guidelines
- Understanding of International Conference on Harmonization (ICH) regulations
- Familiarity with study protocols and regulatory requirements
- Ability to conduct site monitoring visits
- Knowledge of applicable regulations and sponsor requirements
- Based in or able to work in Canada