Coordinate clinical research submissions in Montreal using Nagano, informed consent review, and bilingual communication at the RI-MUHC Glen site.
Reporting to the Manager, Clinical Research Administration Centre for Innovative Medicine, this temporary full-time position supports studies submitted to ethics and site-specific reviewing committees. You will coordinate sponsors, investigators, contracts, and ethics contacts while maintaining submission and renewal timelines. The work supports patient-centered biomedical research at the Research Institute of the McGill University Health Centre.
Key Responsibilities: Review and revise sponsor informed consent forms
Obtain required documents from sponsors and study teams
Submit studies through Nagano to reviewing committees




Communicate with ethics, contracts, investigators, and sponsors
Optimize study review time and support assigned tasks
Requirements: Diploma of College Studies in Science
Minimum one year in ethics or regulatory submissions is an asset
Knowledge of clinical research
Advanced oral and written French and English
Solid organization, communication, computer, Word, Excel, and PowerPoint skills
Apply clinical research knowledge, submission coordination, and bilingual communication to support studies at the RI-MUHC.

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📌 Clinical Research Submissions Coordinator (Quebec City)
🏢 RI-MUHC | Research Institute of the MUHC | #rimuhc
📍 Quebec City