IC

Clinical Trial Manager

Montréal, Québec
On-site
Full-time
No salary posted3 days ago
Employment type
Full-time · On-site
Posted
November 10, 2026
Province
Quebec (QC)

Hiring confidence: Sparse posting · 22/100

This posting is missing most of the signals we look for, or shows patterns common to listings that are not actively being filled. Check with the employer before applying. How this is scored

Job Overview

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Clinical Operations Manager - Regulatory - Montreal At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. What You Will Be Doing This role is accountable for performance and compliance for assigned pro…

This role is based in Quebec. ICON Strategic Solutions 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 Trial Manager in Quebec

We do not have a salary benchmark for this title in Quebec yet. The posting does not state a salary either.

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

  • Clinical trial management experience
  • Knowledge of regulatory requirements and compliance
  • Understanding of GCP and ICH guidelines
  • Project management capabilities
  • Strong organizational skills

Fit check

Is this role right for you?

Top skills this posting asks for:

  • Clinical trial management
  • Regulatory compliance
  • Project management

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What you'll do

  • Manage performance and compliance for assigned protocols
  • Oversee clinical operations activities
  • Ensure regulatory compliance across trials
  • Coordinate with sponsor and internal teams
  • Monitor and report on trial progress
  • Maintain documentation and audit trails
  • Support patient treatment development initiatives

What you'll need

  • Clinical trial management experience
  • Knowledge of regulatory requirements and compliance
  • Understanding of GCP and ICH guidelines
  • Project management capabilities
  • Strong organizational skills
  • Ability to work in sponsor-dedicated model
  • Communication and coordination abilities

About the Company

IC

ICON Strategic Solutions