Research Assistant
On-site · Montréal
Perform advanced genetic manipulations and molecular biology techniques to investigate rare neurogenetic disorders. Manage day-to-day laboratory operations, including reagent ordering and student supervision.
R|
RI-MUHC | Research Institute of the MUHC | #rimuhc
Verified Job SourceBiomedical 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
Research Assistant
On-site · Montréal
The Research Assistant will coordinate study visits, recruit participants, and manage the collection of clinical and biospecimen data. They are also responsible for REB submissions, data entry in REDCap, and assisting in the preparation of manuscripts and grant applications.
Research Data Manager
Hybrid · Montréal
The role involves managing technical data harmonization and integration for multidisciplinary epidemiological research projects. Key duties include validating external data, maintaining R packages, and ensuring project deliverables and budgets are met.
Program Manager, Metabolic Disorders and Complications Program (MeDiC)
On-site · Montréal
The Program Manager facilitates scientific and administrative activities for the Metabolic Disorders and Complications Program, acting as a liaison between leadership and research teams. Key duties include leading major funding requests, managing budgets, and implementing strategic goals through internal committees and seminars.
Research Data Manager
Hybrid · Montréal
The role involves managing technical data harmonization and integration for multidisciplinary epidemiological projects. Responsibilities include validating external data, developing methodological tools, and contributing to scientific publications and grant applications.
Programmer
On-site · Montréal
Establish and maintain MLOps and CI/CD pipelines for conversational AI and digital health projects. Manage cloud-based containerized environments and ensure the reliability and performance of AI/ML systems.
Clinical Research Coordinator
On-site · Montréal
The coordinator will manage participant recruitment, obtain research consent, and handle the collection and management of clinical and molecular data. They will also coordinate research visits and maintain the study's REDCap database.
Multicenter Research Assistant – BRIGHT Coaching Study
Hybrid · Montréal
Coordinate the implementation and sustainability of the BRIGHT Coaching Study across multiple Canadian provinces. Manage daily operations, regulatory compliance, stakeholder engagement, and financial tracking for the research project.
Receiving, Distribution and Package Delivery Clerk
On-site · Montréal
Responsible for receiving, verifying, and distributing temperature-sensitive and mission-critical packages to laboratories. The role also involves handling compressed gas cylinders, dry ice, and contributing to inventory tracking.
Ophthalmic Research Specialist
On-site · Montréal
Perform a wide range of visual and retinal testing for blindness treatments in children and adults. Coordinate patient recruitment, obtain informed consent, and manage study documentation and multicenter collaborations.
MRI Technologist
On-site · Montréal
Operate MRI scanners for human imaging following research protocols and perform equipment quality control. Provide technical support for cardiovascular research, including participant preparation and contrast media injection.
Postdoctoral Fellow
On-site · Montréal
Lead multi-omic analyses and integrate molecular findings with clinical and vascular phenotyping data to investigate cardiovascular disease. Prepare manuscripts for peer-reviewed journals and mentor graduate and undergraduate students.
Clinical Research Coordinator
Hybrid · Montréal
The coordinator will support a research study on early psychological intervention for young adults in the Psychiatric Emergency Department. Key duties include recruiting participants, collecting and organizing research data, and ensuring protocol compliance.
Administrative Assistant
Hybrid · Montréal
Provides comprehensive administrative support to the CHILD-BRIGHT Network, including meeting coordination, documentation management, and operational follow-up. Additionally, supports implementation science-related research projects through logistical coordination and record maintenance.
Community Research Liaison- Nunavik TB Declaration
Remote · Montreal, Quebec, Canada
Facilitate public consultation sessions and community discussions to inform the Nunavik TB Declaration. Document participant feedback, coordinate logistics for meetings, and collaborate with the research team to summarize findings.
Clinical Research Coordinator
On-site · Montréal
The coordinator is responsible for conducting clinic interventions according to protocols and internal SOPs. They also manage the integration of clinical data into database platforms and coordinate participant tests and sample shipments.
MRI Technologist
On-site · Montréal
Operate MRI scanners for human imaging following research protocols and perform equipment quality control. Provide technical support for cardiovascular research, including participant preparation and contrast media injection.
Research Associate
On-site · Montréal
The Research Associate will execute activities involving iPSC maintenance, differentiation into CNS cell types, and the creation of 3D organoids. They will also oversee multidisciplinary research projects, supervise students, and contribute to grant writing.
Laboratory Manager
Hybrid · Montréal
The Lab Manager will oversee day-to-day operations and coordinate research projects focused on equity in dementia care. Key duties include designing study protocols, managing research teams, and collaborating with community partners and stakeholders.
Clinical Research Coordinator - Regulatory
On-site · Montréal
The coordinator is responsible for conducting clinic interventions according to protocols and managing the regulatory aspects of multiple studies. Key duties include obtaining ethics committee approvals and maintaining the Investigator Study File.