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Science
Clinical Research
Job Description & How to Apply Below
Coordinate clinical research submissions in Montreal using French, English, and detailed regulatory communication at the RI-MUHC Glen site. This is a temporary full-time assignment.
Under the Manager, Clinical Research Administration Centre for Innovative Medicine, you will support studies submitted to the Centre of Applied Ethics and site-specific reviewing committees. The work includes informed consent review, sponsor coordination, Nagano submissions, and renewal communication. Knowledge of clinical research supports this position.
Key Responsibilities:- Review and revise sponsor informed consent forms
- Obtain required documents from sponsors and study teams
- Submit studies through Nagano to reviewing committees
- Coordinate communication with Ethics, Contracts, Investigators, and Sponsors
- Serve as the primary stakeholder contact
- Diploma of College Studies in Science
- Minimum one year of ethics or regulatory submissions experience
- Advanced oral and written French and English
- Strong organization, communication, and prioritization skills
- Computer skills including Word, Excel, and Power Point
Support ethical clinical research submissions with bilingual communication, organization, and Nagano knowledge at the RI-MUHC.
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