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
Manage the operational lifecycle of multicentre clinical research studies, including site start-up, monitoring, recruitment, regulatory and safety oversight, data systems, budgets, and close-out. Coordinate investigators, sponsors, sites, vendors, laboratories, and study teams while tracking risks, timelines, documentation, and study deliverables.
On-site · Montréal
Coordinate and oversee clinical research projects in inflammatory bowel disease, including patient screening, consent, trial follow-up, care coordination, investigational drug administration, and safety monitoring. Maintain study documentation and data, coordinate imaging and biological sample shipments, and support research staff with ethics, regulatory, and sponsor-related tasks.
On-site · Montréal
Assess patients for study eligibility and provide physiotherapy-related assessments and interventions for endometriosis and other gynecologic conditions. Coordinate research procedures, recruit and consent participants, and maintain study documentation, patient charts, and safety logs.
On-site · Montréal
Conduct clinic interventions in accordance with study protocols, procedures, and internal SOPs, 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.
On-site · Montréal
Triage and recruit participants for a study evaluating virtual reality exposure therapy for anxiety and related disorders, and manage study data through entry and database maintenance. Prepare and submit Research Ethics Board applications and renewals, and assist with other research tasks while ensuring timely data collection and professional interactions.
On-site · Montréal
Coordinate oncology clinical research studies and support patient management, including obtaining informed consent, assessing protocol eligibility, and monitoring patient safety and medication compliance. Maintain study documentation and data, prepare protocol-related requests, conduct training, and manage Research Ethics Board submissions.
Hybrid · Montréal
Reconcile Oncology clinical trial budgets with study activities, billing, and sponsor payments, identifying and quantifying financial variances and risks. Prepare periodic and close-out reconciliations, maintain audit-ready records, and escalate material issues while supporting consistent financial controls.
On-site · Montréal
Coordinate ethics submissions and approvals, including initial applications, amendments, renewals, safety reports, and study close-outs, while supporting clinical trial start-up and site initiation. Maintain regulatory files and training records, advise research teams on compliance, coordinate monitoring and audits, and liaise with internal and external stakeholders.
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 laboratory kit inventory, and liaise with sponsor representatives.
On-site · Montréal
Coordinate multiple clinical research studies and support overall patient management in collaboration with investigators and healthcare personnel. Obtain informed consent, assess eligibility, monitor safety and medication compliance, maintain study documentation, coordinate data collection, and manage research ethics submissions.
On-site · Montréal
Coordinate the Endometriosis Research Program’s clinical and epidemiological studies, including ethics submissions, participant recruitment and follow-up, biobank operations, data management, and research quality. Support grants, publications, communications, and team planning while contributing to study design, interpretation, and project advancement.
Hybrid · Montréal
Support the coordination and successful conduct of a five-year study to improve access to hepatitis C treatment in three Montreal provincial prisons, serving as a link between the principal investigator, research team, study sites, and community partners. Assist with study documents and ethics submissions, recruitment, data collection, research records, partner communications, and preparation of abstracts and manuscripts.
Remote · Montreal, Quebec, Canada
Coordinate multiple clinical research studies in collaboration with investigators and healthcare teams, including planning projects, recruiting and consenting patients, managing data, and ensuring follow-up. The role also supports team administration through student onboarding and supervision, team activity coordination, website content and communications, and staff education about ongoing studies.
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, sponsor communications, and related assigned tasks.
On-site · Montréal
Coordinate multiple clinical research studies and support overall patient management in inpatient and outpatient settings. Obtain consent, assess eligibility, monitor safety and medication compliance, maintain study documentation and data, respond to research queries, conduct protocol training, and prepare Research Ethics Board submissions.
On-site · Montréal
Coordinate clinical interventions and research activities in accordance with study protocols, procedures, and internal standard operating procedures. Manage data collection and source documentation, coordinate protocol-related tests with research nurses, process and ship samples, maintain laboratory kit inventory, and liaise with sponsor representatives.
Hybrid · Montréal
Reconcile Oncology clinical trial budgets, performed activities, billing, and sponsor payments, identifying and quantifying discrepancies and financial risks. Prepare periodic and close-out reconciliation reports, maintain audit-ready records, and escalate material issues while supporting consistent financial controls.
On-site · Montréal
Coordinate ethics and regulatory activities for clinical trials and research studies, including submissions, approvals, amendments, renewals, regulatory documentation, and investigator site files. Support study start-up and training, liaise with internal and external stakeholders, assist with monitoring visits, and prepare for institutional, sponsor, and health agency audits.
On-site · Montréal
Manage the operational lifecycle of multicentre clinical research studies, including start-up, site oversight, monitoring, recruitment, regulatory and safety activities, data systems, budgets, and close-out. Coordinate investigators, sponsors, sites, vendors, laboratories, and cross-functional teams while tracking study risks, timelines, documentation, and deliverables.
On-site · Montréal
Triage and recruit participants for a study evaluating virtual reality exposure therapy for anxiety and related disorders, and manage study data through entry and database maintenance. Prepare and submit Research Ethics Board applications and renewals, and assist with other research tasks while maintaining timely data collection and professional interactions.