Compensation: CAD 28.18 - CAD 42.27 - hourlyCompany 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.Union: Non-UnionNumber of Vacancies: 3New or Replacement Position: NewSite: Princess Margaret Cancer CentreDepartment: Cancer Genomics ProgramReports to: Senior Program ManagerSalary Range: $28.18 - $42.27 per hourHours: 37.5 hours per weekShifts: Monday - FridayStatus: Temporary Full-time (1 year)Closing Date: November 9, 2026Position Summary: The Cancer Genomics Program (CGP) is a research program at the Princess Margaret Cancer Centre dedicated to advancing personalized cancer medicine through the identification of genetic mutations and molecular mechanisms that drive cancer. The program is supporting a large-scale, high-profile Molecular Residual Disease (MRD) study designed to inform treatment decisions and generate high-quality clinical and genomic data across a broad patient population. The CGP team is seeking Clinical Study and Regulatory Assistants whose primary responsibility will be the accurate, timely, and comprehensive curation of clinical data for this growing study. The role will also support study documentation, regulatory submissions, and related coordination activities.Duties:Curate clinical data as the primary responsibility, extracting and validating information from medical records and other source documents for a large-scale Molecular Residual Disease (MRD) studyEnter and maintain accurate, complete,



and timely study data in electronic case report forms (eCRFs) and other study databasesPerform ongoing data quality review, identify discrepancies and missing information, and resolve data queries in collaboration with study and clinical teamsMaintain study trackers; undertake longitudinal follow-up data entry to support complete and consistent participant recordsAssist in the preparation of Research Ethics Board (REB) submissions, amendments, and reportable eventsLiaise with interdisciplinary teams, including patient-facing clinical teams and biospecimen management teams, to coordinate data collection, clarify source information, and support study workflowsApply study protocols, privacy requirements, applicable regulations, hospital and departmental guidelines, and qualified standards to ensure compliant research conduct and data handlingAttend and contribute to program and study meetingsUndertake study-related administrative tasks such as organizing meetings, taking minutes, scanning documents, and obtaining signaturesQualificationsAt minimum, completion of Community college diploma in a health-related discipline, or equivalent requiredBachelor's degree in a health/science discipline, or equivalent, preferredClinical Research Graduate Certificate, preferredAt least 3 to 6 months related experience requiredClinical research experience preferredBachelor's degree in a health/science discipline, or equivalent (preferred)Clinical Research Graduate Certificate (preferred)Demonstrated relevant clinical research knowledgeHigh proficiency in Microsoft ExcelExperience in some or all of oncology, clinical trials, medical terminology, and regulatory issues involving human subjectsExcellent written and verbal communication skills, excellent organization, prioritization skills, computer skills,



ability to learn quickly and work independentlyExcellent interpersonal skillAbility to work under pressure and attend to detailsAbility to perform duties in a professional and courteous manner and produce high quality work while meeting deadlines in accordance with UHN standardsAbility to perform multiple concurrent tasksKnowledge of applicable legislative, UHN and/or departmental policiesSatisfactory attendanceCertification as a Clinical Research Professional an assetAdditional InformationIn 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.All applications must be submitted before the posting close date.UHN uses email to communicate with selected candidates. Please ensure you check your email regularly.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. 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.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.We thank all applicants for their interest, however, only those selected for further consideration will be contacted.

📌 Clinical Study And Regulatory Assistant (Toronto)
🏢 University Health Network
📍 Toronto