Biomedical research to improve human health.
Montreal, Quebec
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.
On-site · Montréal
Operate MRI scanners for human research imaging according to study protocols, perform quality control and equipment warm-up procedures, prepare and screen participants, and administer contrast media when required. Work under the supervision of the CMR supervisor and project manager, report incidents, and maintain familiarity with relevant technical, safety, and procedural documents.
Hybrid · Montréal
Apply and reconcile incoming payments, maintain accurate accounts receivable records, investigate discrepancies, and prepare correcting entries as needed. Monitor overdue balances, coordinate follow-up with internal teams and external payers, prepare reports, and support audits and finance projects.
On-site · Montréal
The posting does not describe specific responsibilities. The role is with the Research Institute of the McGill University Health Centre, an organization focused on biomedical research and patient-centered medicine.
On-site · Montréal
Coordinate clinical interventions and study activities in accordance with protocols, procedures, and internal SOPs, including participant testing, data collection, and source documentation. Integrate clinical data into database platforms, process and ship samples, maintain laboratory kit inventories, and liaise with sponsor representatives.
On-site · Montréal
Maintain and differentiate iPSC cultures, generate CRISPR-edited iPSC lines, and oversee the iPSC platform and related research activities. Coordinate multidisciplinary projects, support planning and strategic initiatives, supervise and train student researchers, and contribute to grant writing.
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, respond to study queries, and prepare ethics submissions.
On-site · Montréal
Assess and treat patients with endometriosis and other gynecologic conditions, including conducting protocol-related assessments and interventions requiring physiotherapy expertise. Support clinical research by screening and recruiting participants, obtaining informed consent, maintaining study documentation and logs, and coordinating protocol-related tests.
On-site · Montréal
Coordinate oncology clinical research studies, including obtaining informed consent, assessing patient eligibility, and managing patient safety and protocol compliance. Maintain study documentation and data, prepare protocol-related requests, conduct training, and manage Research Ethics Board submissions.
Hybrid · Montréal
Support Principal Investigators with research data strategy, protocol and measurement-tool review, REDCap implementation, and data management throughout the study lifecycle. Develop platform policies and resources, provide training and technical support, and collaborate with research, biostatistics, IT, and other institutional teams.
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 inclusive network events.
On-site · Montréal
Coordinate the Endometriosis Research Program’s studies from ethics submissions and registration through participant recruitment, data and biobank management, analysis support, and publication. Contribute to scientific planning and interpretation while managing grants, communications, collaborators, and project timelines with a high degree of autonomy.
On-site · Montréal
Assist with preparing and setting up research materials and equipment, administrative tasks, and recording study results. Enter data and participate in lab meetings supporting clinical and basic research studies focused on vascular health and cardiovascular disease.
On-site · Montréal
Build and maintain MLOps and CI/CD pipelines, cloud environments, containerized services, and automated deployment, monitoring, and maintenance processes for digital health applications. Collaborate with researchers, clinicians, and engineers to deploy and manage AI/ML components, contribute to model development and evaluation as needed, and document technical processes.
On-site · Montréal
Process human, louse, and other research specimens; perform DNA extraction, PCR/qPCR, and immunofluorescence testing; and contribute to the development, validation, optimization, and quality control of diagnostic assays. Maintain laboratory records, research databases, specimen inventories, and equipment, while supporting a safe and organized laboratory and collaborating with research partners.
On-site · Montréal
Coordinate participant triage and recruitment for a study evaluating virtual reality exposure therapy for anxiety and related disorders in psychiatric outpatients. Enter and manage study data, prepare and submit Research Ethics Board applications and renewals, and assist with other research tasks.
On-site · Montréal
Coordinate clinical research studies in inflammatory bowel disease, including screening and consenting participants, patient follow-up, care coordination, and investigational drug administration. Maintain study documentation and data, coordinate imaging and biological sample processes, address safety issues, and support ethics, regulatory, and sponsor-related activities in accordance with Good Clinical Practice.
On-site · Montréal
Conduct clinic interventions in accordance with study protocols, procedures, and internal standard operating procedures. Manage regulatory requirements for multiple studies, including ethics approvals, investigator study files, site visits, follow-up on identified issues, and communication with sponsor representatives.
Hybrid · Montréal
Reconcile Oncology clinical trial budgets, study activities, billing, and sponsor payments; analyze variances and identify financial risks throughout the study lifecycle. Prepare periodic and close-out reconciliation packages, maintain audit-ready records, and escalate material issues while supporting consistent financial controls.
On-site · Montréal
Manage the Montreal General Hospital research animal facilities, including staff, budgets, operations, resources, infrastructure, and equipment, while ensuring effective support for investigators and research personnel. Develop and implement facility policies and strategic plans, oversee staffing and performance, manage budgets and procurement, coordinate renovations, and participate in committees and other assigned projects.
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 conduct experiments, analyze and communicate findings, mentor trainees, maintain compliant laboratory records, and contribute to publications and grant applications.
