CU

Clinical Research Coordinator – Nurse - CIM - Phase 1 Oncology

Montréal, Québec
On-site
Contract
$57K – $106K CAD
1 weeks ago
Employment type
Contract · On-site
Posted
September 26, 2026
Salary range
$57,093–$105,997 CAD per year
Province
Quebec (QC)

Hiring confidence: Some gaps · 40/100

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 is only part of this posting — the job board it came from publishes a short summary. Read the full posting.
Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference! Job Description RESEARCH INSTITUTE OF THE MUHC The Research Institute of the McGill University Health Centre (RI-MUHC) i…

This role is based in Quebec. CUSM is hiring for this contract 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 Coordinator – Nurse - CIM - Phase 1 Oncology in Quebec

We do not have a salary benchmark for this title in Quebec yet. The posting advertises $57,093–$105,997.

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

  • Nursing license or certification
  • Experience in clinical research
  • Knowledge of Phase 1 oncology trials
  • Understanding of regulatory requirements
  • Ability to work in a research environment

Fit check

Is this role right for you?

Top skills this posting asks for:

  • Clinical research coordination
  • Nursing
  • Patient care

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What you'll do

  • Coordinate Phase 1 oncology clinical trials
  • Manage patient recruitment and enrollment
  • Conduct patient assessments and monitoring
  • Collect and document clinical trial data
  • Ensure compliance with regulatory requirements
  • Communicate with research team and patients
  • Maintain electronic health records
  • Support scientific discovery initiatives

What you'll need

  • Nursing license or certification
  • Experience in clinical research
  • Knowledge of Phase 1 oncology trials
  • Understanding of regulatory requirements
  • Ability to work in a research environment
  • Strong organizational skills
  • Attention to detail

About the Company

CU

CUSM