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
- Robust organization, communication, computer, Word, Excel, and PowerPoint skills

Apply clinical research knowledge, submission coordination, and bilingual communication to support studies at the RI-MUHC.

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