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
Recruit participants for cardiology research studies, obtain informed consent, prepare study documents, process blood samples, and perform 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.
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.
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.
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 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
Coordinate oncology clinical research studies, including patient screening, informed consent, safety monitoring, and protocol-related care. Maintain study documentation and data, prepare protocol-related requests, provide study training, and manage Research Ethics Board submissions.
On-site · Montréal
Coordinate and oversee clinical research projects in inflammatory bowel disease, including screening and consenting participants, coordinating follow-up and care, administering investigational drugs, and monitoring safety. Maintain study documentation and data, process biological samples, coordinate imaging, support ethics and regulatory tasks, and collaborate with research teams, physicians, sponsors, and patients.
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 coverage for teammates, and assist with other tasks as directed by the manager.
On-site · Montréal
Operate MRI scanners for human research imaging according to study protocols, including participant preparation, safety screening, and contrast administration when applicable. Perform equipment warm-up and quality-control procedures, report incidents, maintain familiarity with relevant procedures and standards, and coordinate with supervisors, investigators, and research teams.
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, coordinate data collection, respond to study queries, and prepare Research Ethics Board submissions.
On-site · Montréal
Assess and support the treatment of patients with endometriosis and related gynecologic conditions, including conducting protocol-specific assessments and interventions requiring physiotherapy expertise. Support clinical research by screening and recruiting participants, obtaining informed consent, coordinating study procedures, and maintaining accurate patient and study documentation.
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, manage samples and imaging processes, monitor safety, and support regulatory and ethics activities in compliance with Good Clinical Practice.
On-site · Montréal
Operate MRI scanners for human research imaging according to study protocols, perform equipment warm-up and quality control, prepare and screen participants, and administer contrast media when required. Follow safety and procedural requirements, report incidents, maintain availability, and work with the CMR supervisor, project manager, investigators, and study teams.
On-site · Montréal
Assess and treat patients with endometriosis and other gynecologic conditions, including conducting protocol-specific assessments and interventions requiring physiotherapy expertise. Support clinical research by screening and recruiting participants, obtaining informed consent, maintaining study documentation, and coordinating protocol-related tests.
On-site · Montréal
Coordinate oncology clinical research studies and manage patient-related study activities, including informed consent, eligibility assessment, safety monitoring, and protocol compliance. Maintain study documentation and data, prepare protocol-related requests, conduct training, and manage Research Ethics Board submissions.
On-site · Montréal
Recruit and enroll participants in clinical research studies, obtain informed consent, prepare study documents, and process blood samples. Handle administrative tasks and supply orders, provide vacation coverage for administrative duties, and assist with other tasks as directed by the manager.
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 and data, respond to research queries, provide protocol training, and prepare Research Ethics Board submissions.
On-site · Montréal
Assess and treat patients with endometriosis and related gynecologic conditions, including conducting protocol-specific assessments and interventions requiring physiotherapy expertise. Support clinical research by screening and recruiting participants, obtaining informed consent, maintaining study documentation, and coordinating protocol-related tests.
On-site · Montréal
Recruit and support research participants, obtain informed consent, prepare study documents, and process blood samples, including performing blood draws and electrocardiograms. Handle administrative duties and supply orders, provide vacation coverage for administrative tasks, and assist with other team needs as directed by the manager.