Coordinate oncology clinical research at Montreal’s Glen Site, applying protocol compliance, participant recruitment, and informed consent procedures.

At the Research Institute of the McGill University Health Centre, this full time coordinator supports the Centre for Innovative Medicine under oncology management supervision. The work includes ethics approvals, Investigator Study File maintenance, protocol eligibility assessment, medical history collection, and follow-up coordination. You will also manage source documentation, study data, requisitions, and protocol queries while collaborating with monitors, Quality Assurance, and the Phase 1 Team.

Key Responsibilities:

- Obtain and maintain ethics approvals for oncology protocols
- Maintain Investigator Study Files throughout clinical studies




- Recruit participants and obtain informed consent
- Assess eligibility and collect authorized medical histories
- Coordinate protocol visits, procedures, documentation, and follow-ups

Requirements:

- Diploma of College Studies
- Minimum two years of clinical research experience
- Advanced oral and written French and English
- Strong written and verbal communication skills
- Knowledge of Health Canada, FDA, and ICH-GCP regulations

Support oncology studies through ethical coordination, accurate documentation, participant recruitment, and compliant clinical research practices.

📌 Clinical Research Coordinator Oncology (Montreal)
🏢 RI-MUHC | Research Institute of the MUHC | #rimuhc
📍 Montreal