Coordonnateur(trice) de la documentation TMF II/TMF Document Coordinator II
- Employment type
- Full-time · On-site
- Posted
- September 26, 2026
- NOC code
- 14100 — General office support workers
- Province
- Quebec (QC)
Hiring confidence: Sparse posting · 11/100
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
This role is based in Quebec. The Canadian NOC code for this position is 14100 — General office support workers. Indero 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 Coordonnateur(trice) de la documentation TMF II/TMF Document Coordinator II 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
14100 — General office support workers. The National Occupational Classification code is what Express Entry, provincial nominee programs and Job Bank use to identify this occupation.
Typical qualifications for Canadian employers
- Knowledge of TMF structure and requirements
- Understanding of ICH-GCP guidelines
- Familiarity with clinical trial regulations and compliance standards
- Experience with quality control workflows
- Knowledge of study-specific SOPs
Fit check
Is this role right for you?
Top skills this posting asks for:
- Trial Master File (TMF) management
- Quality control and assurance
- Regulatory compliance
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What you'll do
- Maintain Sponsor's Trial Master File throughout clinical trial duration
- Review and process TMF records through quality control workflows
- Ensure TMF records meet quality, compliance, and regulatory standards
- Approve records into the TMF following study guidelines
- Ensure adherence to ICH-GCP requirements
- Support core TMF coordination functions
- Document processing and filing
What you'll need
- Knowledge of TMF structure and requirements
- Understanding of ICH-GCP guidelines
- Familiarity with clinical trial regulations and compliance standards
- Experience with quality control workflows
- Knowledge of study-specific SOPs
- Ability to review and process regulatory documents
- Experience in clinical trial environment