Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference!

RESEARCH INSTITUTE OF THE MUHC

The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal, Quebec, the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).

Position Summary

Department / Research Program: Department of Obstetrics and Gynecology The Endometriosis Research Program at the Research Institute of the McGill University Health Centre conducts patient-oriented clinical and epidemiological research aimed at improving the diagnosis, treatment and lived experience of people with endometriosis. Reporting to Drs. Andrew Zakhari, Dong Bach Nguyen and Basile Tessier-Cloutier, the clinician-scientists who lead the program, the incumbent is responsible for the scientific and operational management of the program’s portfolio of studies, from ethics submission and study registration through recruitment, data collection and analysis support, to publication and knowledge translation.



The incumbent is expected to work with a high degree of autonomy: setting priorities, anticipating deadlines and advancing projects independently rather than waiting for direction. The role combines regulatory and operational coordination with academic support (grant and manuscript preparation, communications, promotion dossiers) and genuine scientific participation in the design and interpretation of studies. This is a central position on a small, team-oriented team, and the incumbent will contribute to program planning and scientific discussion, not solely to execution.

General Duties

Regulatory affairs and research quality

- Prepare, submit and maintain research ethics board (REB) applications, including initial submissions, amendments, annual renewals and study closures, for all projects in the program,
- Ensure that all studies are conducted in accordance with ICH-GCP, TCPS 2, applicable Québec privacy legislation and RI-MUHC standard operating procedures,
- Register studies on public registries (ClinicalTrials.gov, PROSPERO, OSF) and keep registration records current,
- Maintain investigator study files, delegation logs and training records, prepare the team for audits, monitoring visits and inspections,
- Draft and maintain study protocols, standard operating procedures, consent forms, case report forms and data management plans.

Study conduct and participant management

- Identify, screen and recruit eligible participants, obtain and document informed consent,
- Schedule and coordinate study visits and serve as the primary point

📌 Clinical Research Coordinator – Endometriosis Research Program (Montreal)
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📍 Montreal