Coordinate endometriosis research in Montreal using clinical research expertise, scientific writing, and patient-focused study management. This temporary full-time position is based at the Glen Site. The Clinical Research Coordinator supports the Endometriosis Research Program within the RI-MUHC Department of Obstetrics and Gynecology. You will manage studies from ethics submissions through recruitment, data collection, analysis support, publication, and knowledge translation. The work combines regulatory coordination, participant management, biobank operations, and academic support.

Key Responsibilities:

Prepare ethics submissions, amendments, renewals, and study closures

Recruit participants, obtain consent, and coordinate study visits

Manage EXCELLENT Biobank samples, inventories, and access requests





Build databases and prepare analysis-ready datasets

Prepare grants, manuscripts, abstracts, and progress reports

Requirements:

Bachelor's degree in health sciences or related discipline

Minimum one year of clinical or academic research coordination experience

Advanced written and oral French and English

Knowledge of ICH-GCP, TCPS 2, and ethics processes

Proficiency with LabKey, REDCap, Excel, and Office 365

Apply clinical research coordination, scientific communication, and autonomous project management skills to endometriosis studies at the RI-MUHC.

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📌 Clinical Research Coordinator - Full Time (Montreal)
🏢 RI-MUHC | Research Institute of the MUHC | #rimuhc
📍 Montreal