Compensation: CAD 37.47 - CAD 50.43 - hourly 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.

New or Replacement Position: Replacement Site: Princess Margaret Cancer Centre Supportive Care Salary: $37.47 - $50.43 per hour Temporary full-time (1 year contract) The 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; 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. Coordination of visits and data collection as per study protocol Other 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 & management The Clinical Research Coordinator will also work with research students to provide guidance and supervision throughout various research projects and initiatives Minimum Bachelors degree, or recognized equivalent, in a health or science-related discipline, required Minimum of one (1) to three (3) years clinical research experience,



required Experience with research ethics submissions and maintenance, required Previous research in oncology, strongly preferred Proficiency in basic medical terminology, preferred Knowledge of ICH/GCP guidelines, preferred Certification as a Clinical Research Professional (e.g.

SOCRA, ACRP), asset Experienced with statistical software and ability to conduct statistical analysis independently, asset Experience using and managing research data collection platforms (e.g. REDCap), asset Demonstrate relevant clinical research funding/budgeting knowledge, asset Experience with manuscript preparation and scientific writing, asset Ability 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, required In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of perks, programs and perks. Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP ) A flexible work environment Additional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on-site gyms, etc.) At University Health Network (UHN), artificial intelligence technologies may be used to assist in the screening, assessment, and selection of candidates for this position.

Please be advised that a Criminal Record Check may be required of the successful candidate. Requests for accommodation can be made at any stage of the recruitment process.

📌 Clinical Research Coordinator - Full Time (Toronto)
🏢 University Health Network
📍 Toronto