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.CaUnion: Non-UnionNumber of vacancies: 1New or Replacement Position: ReplacementSite: Princess Margaret Cancer CentreDepartment: Supportive CareReport to: Principal InvestigatorHours: 37.5 hours per weekSalary: $37.47 - $50.43 per hourStatus: Temporary full-time (1 year contract)Closing Date: October 7, 2026Position SummaryThe Department of Supportive Care at Princess Margaret Cancer Centre requires a Clinical Research Coordinator to lead one main study while also working across various research projects and initiatives. Working under the guidance of the Principal Investigator, the Clinical Research Coordinator collaborates with the Investigator to jointly assume responsibility for the overall management and coordination of supportive care clinical research studies and academic activities.This role requires previous experience in the coordination and administration of clinical studies (patient contact and informed consent; implements and coordinates all aspects of data collection and source documentation, as per UHN policy and ICH/GCP guidelines; identification of problems using assessment skills; and of execution study-related administrative tasks, such as collection of regulatory documents, research ethics board submissions, assessment of study-related literature). The role also requires experience in basic data analysis,



including descriptive analyses and T-tests, ANOVA, and chi-square tests.DutiesRecruitment of study participants (e.G. identify and screen potential subjects, obtain informed consent)Coordination of visits and data collection as per study protocolOther responsibilities may include planning, implementing, and coordinating aspects of data entry (e.G. in databases or Case Report Forms) and study-related administrative tasks, such as creation and maintenance of investigator study files, ethics submissions, meeting facilitation, etc.In addition to clinical research project activities, responsibilities include but are not limited to protocol development, manuscript and abstract preparation, conference preparation, basic statistical analyses, data collection and cleaning, and assistance with grant funding submission & managementThe Clinical Research Coordinator will also work with research students to provide guidance and supervision throughout various research projects and initiativesMinimum Bachelors degree, or recognized equivalent, in a health or science-related discipline, requiredAt least three (3) to five (5) years of clinical and/or qualified experience, requiredMinimum of one (1) to three (3) years clinical research experience, requiredExperience with patient contact including informed consent and questionnaire administration, requiredExperience with protocol and study document development, requiredDemonstrated ability to train other team members, requiredExcellent organizational and time management skills, requiredExperience with research ethics submissions and maintenance, requiredPrevious research in oncology, strongly preferredProficiency in basic medical terminology, preferredBackground or understanding of human anatomy, preferredExperience with grant management, and reporting, preferredKnowledge of ICH/GCP guidelines, preferred Certification as a Clinical Research Professional (e.G. SOCRA, ACRP),



assetExperienced with statistical software and ability to conduct statistical analysis independently, assetExperience using and managing research data collection platforms (e.G. REDCap), asset Demonstrate relevant clinical research funding/budgeting knowledge, assetExperience with manuscript preparation and scientific writing, assetExcellent interpersonal, verbal and written communication skills, requiredAbility to set priorities and work independently with accuracy in a multitasking environment Strong Proficiency with MS Office software, including Word, Excel, Outlook Authorized to work in Canada, requiredWhy join UHN?In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of benefits, programs and perks. It is the comprehensiveness of these offerings that makes it a differentiating factor, allowing you to find value where it matters most to you, now and throughout your career at UHN.Competitive offer packagesGovernment organization and a member of the Healthcare of Ontario Pension Plan (HOOPP https://hoopp.Com/)Close access to Transit and UHN shuttle serviceA flexible work environmentOpportunities for development and promotions within a large organizationAdditional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on-site gyms, etc.)Current UHN employees must have successfully completed their probationary period, have a good employee record along with satisfactory attendance in accordance with UHN's attendance management program, to be eligible for consideration.UHN is an equal opportunity employer committed to an inclusive recruitment process and workplace. Requests for accommodation can be made at any stage of the recruitment process. Applicants need to make their requirements known.Please be advised that a Criminal Record Check may be required of the successful candidate. Should it be determined that any information provided by a candidate be misleading, inaccurate or incorrect, UHN reserves the right to discontinue with the consideration of their application.We thank all applicants for their interest, however, only those selected for further consideration will be contacted.

📌 Clinical Research Coordinator I / Ii (Toronto)
🏢 University Health Network
📍 Toronto