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.

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