Job opportunity
Clinical Research Coordinator Oncology
RI-MUHC | Research Institute of the MUHC | #rimuhc
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.
#J-18808-Ljbffr
Apply on source site 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.
#J-18808-Ljbffr