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University Health Network

Clinical Research Assistant I

Toronto, Ontario, CA Posted 2 days ago

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Sponsorship verdict

Sponsorship possible

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  • Employer is on a government sponsor recordThis employer appears on Canada’s positive-LMIA employer list.
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  • No salary bar for this routeCanada has no single salary bar: the employer usually needs a positive LMIA.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Employer is on a government sponsor record
This employer appears on Canada’s positive-LMIA employer list. Source: Positive LMIA employer list (Employment and Social Development Canada).
No salary bar for this route
Canada has no single salary bar: the employer usually needs a positive LMIA. Pay at or above the provincial median wage + 20% (e.g. C$36.92/h in Ontario) puts it in the high-wage stream. Source: https://www.canada.ca/en/employment-social-development/services/foreign-workers/median-wage.html, rules effective 2026-07-17.

Canada: Express Entry no longer awards ranking points for job offers (since 25 Mar 2025); a job offer still counts toward Federal Skilled Worker eligibility.

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About the role

Union: Non-union Number of vacancies:  2 Replacement or New:  New Site:  Toronto General Hospital & Toronto Western Hospital Department:  Emergency Medicine  Reports to:  Dr. Jennifer Hulme  Wage Range:  $27.56–$34.45 per hour Hours:  37.5 hours per week Shifts: Daytime, evening and weekend shifts as required Status:  Temporary Full-Time Closing Date: October 29, 2026 Position Summary The UHN Emergency Medicine Research Program supports a diverse portfolio of innovative and collaborative research across multiple areas, including clinical emergency medicine, addiction medicine and health equity, education, global health, health services delivery, injury prevention, palliative care, and quality improvement. The Emergency Medicine Research Program and Research Committee provide support and oversight for research involving patients, staff, trainees, and resources within the UHN Emergency Departments. Our program is committed to fostering a collaborative research environment that supports and mentors clinicians, researchers, and trainees; promotes interdisciplinary and multi-site collaboration; and advances emergency medicine and public health at local, national, and international levels. The Department of Emergency Medicine is currently seeking a Clinical Research Study Assistant to support a portfolio of clinical and health services research studies. The Clinical Research Study Assistant will provide participant-facing, research, organizational, and administrative support for ongoing research projects. Working under the direction and close supervision of Principal Investigators and senior research staff, the Clinical Research Study Assistant will assist with participant screening and recruitment, informed consent processes, data collection and entry, participant follow-up, research interviews and surveys, research ethics documentation, and day-to-day study operations. Depending on the assigned study, responsibilities may also include assisting with the collection, processing, labelling, storage, and preparation of biological specimens according to established study procedures and applicable training requirements. This is a fully in-person position based in the Emergency Departments at Toronto General Hospital and/or Toronto Western Hospital. Please note: Emergency Department research activities occur seven days per week. Research Assistants are scheduled across daytime, evening, and weekend shifts. The successful candidate must be available to work scheduled shifts of approximately 8–10 hours between 08:00 and 00:00, any day of the week, according to study and operational requirements Duties Participant Recruitment and Research Activities  • Assists the interprofessional research and clinical teams with study-specific activities according to approved research protocols and established procedures.  • Assists with screening and identifying potential research participants according to study eligibility criteria.  • Supports participant recruitment and informed consent processes under the direction of the Principal Investigator or designated senior research staff.  • Assists with participant interactions, including scheduling interviews, study visits, appointments, and follow-up activities.  • Administers surveys, questionnaires, structured interviews, telephone interviews, and other standardized data collection tools according to approved study protocols.  • Supports participant engagement in research activities, including co-design workshops, where applicable.  • Assists with participant compensation according to established study and UHN procedures.  • Travels to study or participant sites as required.  Data Collection and Documentation  • Collects and records study data using predefined data collection tools, work

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