University Health Network
Healthcare
ClinicalResearchStudyAssistant
Neural analysis suggests this role is
optimal for not-applicable candidates.
“Clinical Research Study Assistant at University Health Network. Skills: Clinical research, Data collection, Study coordination. Support clinical trials. Recruit study participants”
Industry & Context.
Problem-solving skills
Criminal Record Check
What They're Looking For.
Must Have
1-2 years relevant experience, Bachelor's degree in life sciences, Bachelor's degree in oncology, Bachelor's degree in health-related disciplines, Bachelor's degree in science-related disciplines, Interpret applicable regulations, Ensure compliance during study conduct, Work within tight deadlines, Manage competing demands, Independently coordinate tasks, Independently prioritize tasks, Excellent computer skills, Microsoft Office Suite proficiency, Problem-solving skills, Ability to learn new concepts, Ability to learn new techniques, Critical mindset, Attention to detail, Work in fast-paced team environment, Work independently
Nice to Have
Master's degree in similar fields
What You'll Do.
Support clinical trials
Recruit study participants
Identify potential participants
Screen potential participants
Obtain informed consent
Coordinate patient visit schedules
Document adverse events
Administer questionnaires
Assess study-related information
Liaise with stakeholders
Liaise with clinical care
Implement data collection
Coordinate data collection
Execute study-related administrative tasks
Complete study trackers
Complete study databases
Maintain regulatory files
Coordinate operations of virtual cancer
Manage financial budgets
Manage communications with patients
Manage communications with clinical care
Produce scientifically accurate documents
Conduct literature reviews
Prepare comprehensive reports
Assist with data collection
Assist with data analysis
Support manuscript preparation
Perform transcriptions
Perform thematic analysis
Collaborate with providers
Collaborate with experts
Collaborate with educators
Understand programmatic needs
Execute strategic initiatives
Perform cross-functional duties
How You'll Work.
Team & Collaboration
Clinical care providers; Subject matter experts; Researchers; Educators; Clinical care team
Communication Scope
Written communication; Verbal communication; Communicate effectively; Translate scientific information; Adapt writing style
Full Job Description
UHN 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.ca](https://www.uhn.ca/) Union: Non-Union Number of Vacancies: 1 New or Replacement Position: Replacement Site: Princess Margaret Cancer Centre Department: Surgical Oncology Reports to: Principal Investigator Salary Range: $53,747 - $67,184 Per Year Hours: 37.5 Hours Per Week Shifts: Monday - Friday Status: Temporary, Full-Time (1 year contract) Closing Date: June 9, 2026 Position Summary: The Clinical Research Study Assistant's primary role is supporting clinical trials pertaining to virtual cancer care, biomarker analysis, surgical techniques and more. Primary responsibilities will include, but are not limited to, recruitment of study participants (e.g. identifying, screening potential participants & obtaining informed consent); coordinating patient visit schedules as per study protocol; executing/coordinating all aspects of study visits (e.g. and as applicable, documentation of adverse events & medications, administration of questionnaires, reviewing & assessing study-related
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