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 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, quality, and required documentation.
On-site · Montréal
Coordinate investigator-initiated and industry research studies for the Orthopaedic Trauma team, including ethics submissions, sponsor communication, budgets, contracts, patient recruitment and follow-up, and study documentation. Maintain data quality and study records, provide status and account updates, support investigators with grants and publications, and help ensure research certifications and ethical standards are current.
On-site · Montréal
Coordinate clinical interventions in accordance with study protocols, procedures, and internal SOPs, and integrate clinical data into database platforms. Manage data collection and source documentation, coordinate participant testing with research nurses, process and ship samples, maintain study kit inventory, and liaise with sponsors.
On-site · Montréal
Coordinate the clinical component of the genCARE-QC study, including learning the protocol, screening and recruiting participants, obtaining informed consent, and scheduling and conducting study visits and assessments. Support participants, evaluate their health status, and ensure accurate, timely case report forms and complete research documentation.
On-site · Montréal
Coordinate oncology clinical research studies, including patient consent and eligibility assessment, patient management, safety monitoring, and protocol-related procedures. Maintain study records and data, complete research documentation, respond to information requests, provide protocol-specific training, and prepare Research Ethics Board submissions.
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 protocol and document development, ethics submissions, study logistics, participant recruitment, data collection, research records, and preparation of abstracts and manuscripts.
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 assessing eligibility, recruiting participants, obtaining informed consent, maintaining study documentation, and performing protocol-related tests.
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
Coordinate day-to-day patient activities and clinical trial visits, prepare study documents and kits, and collect, process, and ship pathology and blood samples. Maintain accurate study data and research records, manage laboratory kits, address sponsor queries, and support protocol compliance in collaboration with investigators and clinical teams.
On-site · Montréal
Coordinate the Endometriosis Research Program’s studies from ethics submissions and registration through participant recruitment, data collection, biobank operations, and analysis support. Contribute to grants, publications, communications, team planning, and scientific discussions while independently managing timelines and research quality.
On-site · Montréal
Coordinate clinical research studies and manage patient-related activities in collaboration with investigators and healthcare personnel. Obtain consent, assess eligibility, monitor safety and medication compliance, maintain study documentation, coordinate data collection, and handle ethics submissions and research queries.
Hybrid · Montréal
Reconcile Oncology clinical trial budgets, performed activities, billing, and sponsor payments, identifying and quantifying variances and financial risks. Prepare periodic and close-out reconciliations, maintain audit-ready records, and escalate material issues while supporting consistent financial controls.
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, process biological samples, coordinate imaging, and support ethics and regulatory activities in accordance with Good Clinical Practice.
Hybrid · Montréal
Reconcile Oncology clinical trial budgets, clinical activities, billing, and sponsor payments, identifying and quantifying discrepancies and financial risks. Prepare periodic and close-out reconciliations, maintain audit-ready records, and escalate material issues while supporting consistent financial controls.
On-site · Montréal
Assess and treat patients with endometriosis and other gynecologic conditions, including conducting protocol-specific assessments and interventions that require physiotherapy expertise. Support clinical research by screening and recruiting participants, obtaining informed consent, coordinating study procedures, and maintaining accurate clinical and research documentation.
On-site · Montréal
Coordinate the clinical component of the genCARE-QC study, including learning the protocol, screening and recruiting participants, obtaining informed consent, and scheduling and conducting protocol-based assessments. Support participants, evaluate their health status, and ensure accurate, timely case report forms and research documentation.
On-site · Montréal
Coordinate clinical research projects in inflammatory bowel disease, including ulcerative colitis and Crohn’s disease, and manage study documentation and data. Screen and follow up with participants, support consent and investigational drug administration, complete study records, coordinate samples and imaging, and assist with regulatory and ethics tasks.
On-site · Montréal
Coordinate oncology clinical research studies, including obtaining informed consent, assessing patient eligibility, and supporting patient management and safety. Maintain study documentation and data, prepare protocol-related requests, conduct training, and manage Research Ethics Board submissions.
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, logistics, recruitment, data collection, research records, and preparation of abstracts and manuscripts.
On-site · Montréal
Conduct clinical evaluations, plan and prioritize patient care, provide treatments, and evaluate patient outcomes. Communicate with patients, families, research and clinical teams, and support staff while assisting with clinical trial activities, including work outside regular hours.