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RI-MUHC | Research Institute of the MUHC | #rimuhc

Verified Job Source

Biomedical research to improve human health.

Montreal, Quebec

Research Services
1,001–5,000 people

About

The Research Institute of the McGill University Health Centre (The Institute) brings together pediatric and adult research programs, accelerating the translation of biomedical research to improve human health.

Open positions

Animal Care Worker - Part-time occasional

On-site · Montréal

The candidate performs animal husbandry, technical procedures, and administrative duties for laboratory animals across RI-MUHC sites. Responsibilities include cleaning cages, managing inventory, and interacting with researchers.

Clinical Research Nurse - Occasional Pool (Research Institute)

On-site · Montréal

Perform clinical evaluations and provide care planning and treatments for patients within clinical trials. Support the Centre for Innovative Medicine by assisting with trial-related activities, particularly outside of regular working hours.

Clinical Research Coordinator – Nurse - CIM - Phase 1 Oncology

On-site · Montréal

The coordinator is responsible for the overall patient management and coordination of clinical research studies in oncology. Key duties include obtaining informed consent, monitoring patient safety, and managing Research Ethics Board submissions.

Clinical Research Coordinator - Nurse

On-site · Montréal

The coordinator is responsible for participant recruitment, vaccine administration, and the collection of clinical data and biospecimens. They ensure strict compliance with study protocols, regulatory guidelines, and institutional policies to maintain data integrity and participant safety.

Clinical Research Coordinator - CIM

On-site · Montréal

The incumbent supports the submission of clinical research studies to the Centre of Applied Ethics and other site-specific assessments. Key duties include revising informed consent forms, coordinating with sponsors and investigators, and managing submissions through the Nagano system.

Animal Resources Division Manager – Montreal General Hospital Site

On-site · Montréal

The manager is responsible for overseeing research animal facilities at the Montreal General Hospital, including staff management, budgeting, and operational support for investigators. Key duties include implementing policies, managing capital resources, and formulating strategic business plans.

Budget Specialist - CIM

On-site · Montréal

The incumbent is responsible for reviewing, analyzing, and negotiating research study budgets with industry partners. This includes developing detailed budgets from protocols and collaborating with internal departments to finalize contract agreements.

Infusion Nurse - Research

On-site · Montréal

The infusion nurse administers and adjusts chemotherapy and immunotherapy treatments for cancer patients within a research setting. They are responsible for evaluating patient health status and ensuring proper documentation for clinical research studies.

Medical Writer, Scientific Projects – Pre-Awards Office

Hybrid · Montréal

The role involves drafting, editing, and managing scientific grant proposals to help researchers secure funding from various agencies. Additionally, the incumbent identifies funding opportunities and coordinates institutional events and meetings to enhance research visibility.

Research Assistant

On-site · Montréal

The candidate will maintain iPSC cultures, generate CRISPR edited lines, and differentiate cells into various CNS types including oligodendrocytes and neurons. Additionally, they will supervise student researchers and contribute to the writing of research grants.

Research Assistant

Hybrid · Montréal

The role involves supporting studies on genetic services for hereditary kidney disease, including developing protocols and managing ethics submissions. Key duties include participant recruitment, data collection, and assisting in the preparation of research manuscripts and abstracts.

Supervisor, Finance – Clinical Research Portfolio

Hybrid · Montréal

The role involves monitoring and analyzing the financial performance of a clinical research portfolio and maintaining financial dashboards. It also includes supervising the Billing and Financial Control team to ensure quality and timeliness of outputs.

Clinical Research Manager

On-site · Montréal

Lead and manage clinical research activities and staff within the McGill Division of Thoracic Surgery, focusing on surgical oncology. Oversee site operations, regulatory submissions, and the design of clinical databases and biobanks.

Science Lead, Knowledge Mobilization

Hybrid · Montréal

The role involves designing and implementing knowledge mobilization strategies and funding opportunities aligned with the ICRH mandate. The incumbent will lead scientific projects, identify research gaps, and foster partnerships with national stakeholders to translate research into impact.

Research Assistant

Hybrid · Montréal

The incumbent will coordinate a 5-year CIHR-funded study on HIV prevention and treatment access for migrants in Montreal. Responsibilities include managing study protocols, participant recruitment, data collection, and acting as a liaison between investigators and community partners.

Clinical Research Coordinator – Nurse - CIM - Oncology

On-site · Montréal

The role involves coordinating clinical research studies in oncology, including patient recruitment, obtaining informed consent, and managing data collection. The coordinator is also responsible for monitoring patient safety and handling Research Ethics Board submissions.

Clinical Research Coordinator

On-site · Montréal

The coordinator will screen, recruit, and randomize participants for tuberculosis treatment clinical trials. They are responsible for completing case report forms and collaborating with clinic personnel for participant follow-up.

Clinical Research Coordinator

On-site · Montréal

The coordinator manages complex cellular therapy clinical trials, specifically CAR-T studies, ensuring compliance with federal regulations and GCP guidelines. They serve as the primary liaison between investigators, sponsors, and clinical teams to coordinate patient procedures and regulatory documentation.