Coordinate hepatitis C research in Montreal using participant recruitment and clinical study organization skills. This temporary full time role offers hybrid work.
At the Research Institute of the McGill University Health Centre, support a five-year study improving treatment access for people in three provincial prisons. Under the principal investigator, coordinate research activities across CVIS / IDIGH. Serve as the direct link among the research team, recruitment sites, and community partners. The work requires organized study coordination, participant-focused communication, and accurate documentation.
Key Responsibilities: Assist with protocols, consent forms, questionnaires, and study documents
Support ethics submissions and protocol amendments
Coordinate logistics and communication among study partners




Assist participant recruitment, data collection, and document storage
Prepare abstracts and manuscripts for submission
Requirements: Bachelor's degree in public health, epidemiology, or related field
Minimum two years of academic or clinical research experience
Advanced written and oral French and English
Excellent communication, organization, and interpersonal skills
Access to a vehicle for required travel
Apply clinical research coordination, bilingual communication, and careful documentation skills to this Montreal hepatitis C study.

#J-18808-Ljbffr

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