R|

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

Clinical Research Coordinator - Regulatory

On-site · Montréal

Conduct clinic interventions in accordance with study protocols, procedures, and internal standard operating procedures, and manage regulatory requirements for multiple studies. Obtain and maintain ethics approvals, maintain Investigator Study Files, coordinate site initiation and monitoring visits, follow up on identified issues, and liaise with sponsor representatives.

Research Assistant - Public Engagement

Hybrid · Montréal

Build relationships with community organizations, patients, public representatives, and healthcare professionals, and support CADeN’s public advisory committee. Develop, implement, and evaluate a nationwide medication-safety awareness campaign, and help plan events that include the perspectives of public partners and people with diverse lived experiences.

Clinical Research Coordinator

On-site · Montréal

Coordinate oncology clinical trial activities, including patient visits, protocol schedules, sample collection and shipment, and accurate, timely data entry. Maintain study records and laboratory kits, address sponsor queries, and communicate with investigators, physicians, and research staff to support protocol compliance.

Clinical Research Coordinator - Nurse (CIM)

On-site · Montréal

Coordinate multiple clinical research studies and support overall patient management in collaboration with investigators and healthcare personnel. Obtain consent, assess eligibility, monitor safety and medication compliance, maintain study documentation, coordinate data collection, and manage ethics submissions and study-related requests.

Clinical Trial Financial Control Analyst, Oncology Portfolio

Hybrid · Montréal

Reconcile Oncology clinical trial budgets with study activities, billing, sponsor payments, and cash collections, identifying and quantifying financial variances and risks. Prepare periodic and close-out reconciliation packages, maintain audit-ready records, and escalate material issues while supporting consistent financial controls.

Postdoctoral Fellow - Surgical and Interventional Sciences

On-site · Montréal

Lead independent research on fibrosis, tissue repair, or oral squamous cell carcinoma, investigating disease mechanisms and identifying and validating potential therapeutic targets. Design and analyze experiments, mentor trainees, maintain compliant laboratory records, and contribute to publications, presentations, and grant applications.

Clinical Research Coordinator

On-site · Montréal

Coordinate clinical interventions and study activities in accordance with protocols, procedures, and internal SOPs. Manage data collection and source documentation, coordinate protocol-related tests with research nurses, process and ship samples, maintain study kit inventory, and liaise with sponsor representatives.

Licensed Practical Nurse (LPN) or Research Nurse

On-site · Montréal

Recruit and enroll research participants, obtain informed consent, prepare study documents, and process blood samples, including performing blood draws and ECGs. Handle administrative duties and supply orders, provide vacation coverage for administrative tasks, and assist with other tasks as directed by the manager.

Animal Care Worker - Part-time occasional

On-site · Montréal

Provide husbandry and general care for laboratory animals, including cleaning and disinfecting cages and operating and monitoring relevant equipment. Record and report animal-care data, manage supplies and inventory, distribute linen and uniforms, and interact with researchers.

Clinical Research Coordinator – Nurse - CIM - Phase 1 Oncology

On-site · Montréal

Coordinate oncology clinical research studies and support overall patient management, including obtaining informed consent, assessing eligibility, monitoring safety and medication compliance, and coordinating protocol-related procedures. Maintain study documentation and data, respond to research queries, deliver protocol-specific training, and prepare Research Ethics Board submissions.

Clinical Research Coordinator - Regulatory Affairs (CIM)

On-site · Montréal

Review and revise sponsor informed consent forms, gather required study documents, and submit clinical research studies through Nagano for ethics and site-specific review. Coordinate communications among ethics committees, contracts, investigators, and sponsors throughout submission and renewal timelines, while helping optimize review times and serving as the primary stakeholder contact.

Clinical Research Nurse - Occasional Pool

On-site · Montréal

Conduct clinical evaluations, plan and prioritize patient care, provide treatments, and assess patient outcomes. Communicate with patients, families, and care teams while supporting clinical trial activities, including observations outside regular working hours.

Clinical Research Coordinator

Hybrid · Montréal

Coordinate a five-year study to improve access to hepatitis C treatment for people in three Montreal provincial prisons, serving as a link between the principal investigator, research team, recruitment sites, and community partners. Support study document development, ethics submissions, recruitment, data collection, records management, partner communications, and preparation of abstracts and manuscripts.

Receiving, Distribution and Package Delivery Clerk

On-site · Montréal

Receive, verify, sort, log, temporarily store, and deliver packages to laboratories and designated locations, prioritizing temperature-sensitive, regulated, and mission-critical items while maintaining cold-chain and custody records. Safely handle compressed gas cylinders and dry ice, communicate with research staff, support inventory tracking, and maintain clean, safe work areas.

Accounts Receivable Analyst

Hybrid · Montréal

Apply and code incoming payments, maintain accurate accounts receivable records, investigate payment discrepancies, and prepare correcting journal entries as needed. Monitor overdue balances, coordinate collections and reconciliations, prepare reports, support audits, and work with internal teams and external payers to resolve receivable issues.

Respiratory Therapist

On-site · Montréal

The posting does not specify the Respiratory Therapist's responsibilities. It describes the Research Institute of the McGill University Health Centre as focused on scientific discovery, innovation, and patient-centered medicine.

Research Associate

On-site · Montréal

Maintain and differentiate iPSCs, generate CRISPR-edited iPSC lines, and help oversee the iPSC platform and related research activities. Coordinate multidisciplinary projects, support planning and strategic initiatives, train and supervise student researchers, and contribute to grant writing.

Animal Health Technician - Part-time Occasional

On-site · Montréal

Provide health assessments, care, treatments, diagnostic tests, and routine or specialized procedures for laboratory animals, including surgical preparation and postoperative care. Support researchers through training and guidance, maintain animal-care supplies and equipment, and complete related administrative tasks.

Clinical Research Coordinator – Physiotherapist

On-site · Montréal

Assess and support the treatment of patients with endometriosis and other gynecologic conditions, including conducting protocol-specific assessments and interventions requiring physiotherapy expertise. Coordinate clinical research activities by screening and recruiting participants, obtaining informed consent, maintaining study documentation, and performing protocol-related tests.

Clinical Research Coordinator - Nurse

On-site · Montréal

Coordinate clinical research projects in inflammatory bowel disease, including ulcerative colitis and Crohn’s disease, and support patient screening, consent, follow-up, and care coordination. Administer investigational products, manage study documentation and data, process biological samples, coordinate imaging, and assist with ethics and regulatory requirements while following Good Clinical Practice.