University Health Network·Toronto, Ontario
The Clinical Research Analyst supports the conduct and management of clinical trials by preparing regulatory submissions and maintaining Research Ethics Board applications. They also assist in participant recruitment, data collection, and the execution of study-related administrative tasks.
Company 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
Job Description: Union: Non-Union
1 New or Replacement Position: Replacement Site: Toronto Western Hospital Department: The Rheumatology Clinical Trials Unit Reports to: Principal Investigator
$33.80 - $42.25 per hour Hours: 37.5 hours per week Shifts: Day Status: Temporary Full-time
Closing Date: September 9, 2026
The Rheumatology Clinical Trials Unit at the Toronto Western Hospital/Schroeder Arthritis Institute is seeking a highly motivated individual to join our team. We are a busy clinical trial unit with a focus on Systemic Lupus Erythematosus, Psoriatic Arthritis, Osteoarthritis, Rheumatoid Arthritis and Sjogren’s Syndrome trials. Working under supervision of multiple principal investigators, the Clinical Research Analyst will support the conduct and management of clinical trials, assist in facilitating and coordinating daily study activities, and play a critical role in the overall execution of the study.
Working under the directions of the Director and co-Director of the Rheumatology Clinical Trial Unit, Clinical Research Manager and other senior research staff members, the Clinical Research Analyst's responsibilities include but are not limited to: Prepare, submit, and maintain Research Ethics Board (REB) applications, track ethics approvals, and regulatory submissions during and post study conduct, including but not limited to, SAEs, End of Study Notifications, Amendments, Renewals, responses to other submissions queries/questions/observations, etc. Prepare regulatory documents for REB submission Prepare Investigator site file binders as per sponsor policies Assist in study participant recruitment by identifying and screening potential subjects, obtaining informed consent, conducting pre-testing, and administering questionnaires or other data collection tools Assist in data collection, source documentation and data entry following UHN policy and ICH/GCP guidelines Identify problems using assessment skills and report any abnormalities to the Clinical Research Manager Execute study-related administrative tasks, including the collection of regulatory documents and ethics submissions Conduct telephone and/or clinical recruitment interviews Perform various study-related tasks during study visits, such as basic administration, collecting, processing and shipping samples according to the trial protocol, archiving close-out studies, lab kit disposal and IP destruction
Bachelor’s degree, or recognized equivalent, in a health or science-related discipline At minimum, 1 to 2 years of related experience is required; clinical trial research experience is preferred Understanding of ICH-GCP guidelines, TCPS2 standards, and Health Canada regulations Experience with electronic data capture systems (Medidata Rave, Veeva Vault, RedCap) and skilled in query resolution and data quality assurance Understanding of study protocols, case report forms (CRFs), and source documentation Ability to coordinate with nurses, physicians, pharmacists, and study coordinators Experience with lab techniques, sample handling, and safety protocols Attention to detail and commitment to maintaining data integrity and confidentiality Ability to work independently and collaboratively in a fast-paced environment Ability to multi-task and perform in a fast-paced environment Excellent interpersonal, verbal and written communication skills, required Proficiency with MS Office software (Outlook, Word, Excel, PowerPoint) Excellent organizational and time management skills Well-developed critical reasoning skills Client service oriented, with the ability to effectively work with diversity and appreciate that people with different opinions, backgrounds and characteristics bring richness to the challenge or situation at hand
Why 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 packages Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP https://hoopp.com/) Close access to Transit and UHN shuttle service A flexible work environment Opportunities for development and promotions within a large organization Additional 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.
Candidates must hold a bachelor's degree in a health or science-related discipline with at least 1 to 2 years of related experience. Proficiency in ICH-GCP guidelines, electronic data capture systems, and strong organizational skills are required.
Market context
In Ontario, Clinical Research Analyst roles are often driven by ongoing activity in hospitals, academic centers, and life sciences organizations, where employers look for candidates who can support compliant study operations and accurate data handling. This role is competitive because employers typically want a health or science degree, 1 to 2 years of related experience, and working knowledge of ICH-GCP and electronic data capture systems. If you are applying, review the original posting carefully and tailor your resume to show research coordination, documentation, and data-quality experience; this platform’s job requirements and benefits are AI-summarized from the original description, which can save time when comparing roles.