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Clinical Research Coordinator

Remote / Online - Candidates ideally in
Toronto, Ontario, C6A, Canada
Listing for: University Health Network
Full Time, Seasonal/Temporary, Remote/Work from Home position
Listed on 2026-09-16
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 37.47 - 46.84 CAD Hourly CAD 37.47 46.84 HOUR
Job Description & How to Apply Below
Position: Clinical Research Coordinator I

Company DescriptionUHN is Canada’s #1 hospital and the world’s #1 publicly funded hospital. With 10 sites and more than 44,000 TeamUHN members, UHN consists of Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute, The Michener Institute of Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care.

UHN has the largest hospital-based research program in Canada, with major research in neurosciences, cardiology, transplantation, oncology, surgical innovation, infectious diseases, genomic medicine and rehabilitation medicine. UHN is a research hospital affiliated with the University of Toronto.

Company DescriptionUHN is Canada’s #1 hospital and the world’s #1 publicly funded hospital. With 10 sites and more than 44,000 TeamUHN members, UHN consists of Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute, The Michener Institute of Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care.

UHN has the largest hospital-based research program in Canada, with major research in neurosciences, cardiology, transplantation, oncology, surgical innovation, infectious diseases, genomic medicine and rehabilitation medicine. UHN is a research hospital affiliated with the University of Toronto. UHN’s vision is to build A Healthier World and it’s only because of the talented and dedicated people who work here that we are continually bringing that vision closer to reality.

www.uhn.caJob Description

Union
:
Non-Union

Number of vacancies
: 1

New or Replacement Position
:
New

Site
:
Princess Margaret Cancer Centre (Research)

Department
:
Cancer Clinical Research Unit

Reports to
:
Clinical Research Manager

Salary
: $37.47 - $46.84 per hour

Hours
: 37.5 hours per week

Shifts
:
Day

Status
:
Temporary Full-Time (14 months)

Closing Date
:
September 20, 2026

Position Summary
:
The Cancer Clinical Research Unit requires a Clinical Research Coordinator I (CRC I) to work with various research projects within its oncology & hematology research portfolio. Working under the direction of the Clinical Research Manager, the CRC I collaborates and works very closely with the Principal Investigator, Clinical Research Nurses, and health care team to jointly assume responsibility for the frontline administrative management and coordination of clinical trials and research studies (interventional trials and non-therapeutic studies).

It is essential for the Clinical Research Coordinator I to be team oriented and contribute to the overall goals and tasks of the team, particularly with the Clinical Research Nurses. The CRC I will work collaboratively with data and regulatory teams to ensure the collection of high quality data and regulatory compliance through the trials. The CRC I will be a part of a larger CRC I team and may have the opportunity to participate in other team and CCRU initiatives.

The CRC I role is a primarily on-site position, with some flexibility for work from home as disease site clinical schedule and tasks allow, following UHN policies, and as approved by the Clinical Research Manager.

Duties
:

  • Administrative duties related to the frontline coordination of patient care on clinical trials
  • Recruitment of study participants (e.g. identify and screen potential subjects, obtain informed consent)
  • Coordination and execution of various aspects of patient visits schedules as…
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