Clinical Study and Regulatory Assistant
University Health Network View all jobs
- Toronto, ON
- $53,747-80,621 per year
- Temporary
- Full-time
Number of Vacancies: 1
New or Replacement Position: New
Site: Princess Margaret Cancer Centre
Department: Radiation Medicine Program - Clinical Research Program (CRP)
Reports to: Clinical Research Manager
Salary Range: $53,747 - $80,621 Annually
Hours: 37.5 hours per week
Shifts: Monday - Friday
Status: Temporary Full-time (1-Year Contract)
Closing Date: April 24, 2026Position Summary:
We are seeking a highly motivated individual to work in the Radiation Medicine Program (RMP), joining our team of clinicians, scientists, and support personnel as a clinical research Regulatory Assistant. The ideal candidate is well organized and able to prioritize and multitask between multiple competing duties while contributing as an effective team player.Our portfolio of studies includes investigator-initiated studies and industry-sponsored trials, which provide the opportunity to apply a wide breadth of skills and knowledge in regulatory start-up activities and maintenance. Our team acts as the sponsor in several multi-site trials requiring strong project management skills.Duties:
- Organizes and conducts SIV and protocol reviews
- Participates in the planning and implementation of clinical research protocols
- Prepares submissions (amendments, reportable events, annual renewals, study closures) to REB
- Executes study-related administrative tasks, such as the collection and maintenance of regulatory documents, ethics submissions, protocols, staff training, and delegation logs in paper and electronic formats. Maintenance & modification of study-specific trackers and study tools
- Scheduling on-site/virtual monitoring visits and collecting necessary source documentation
- Liaises between the site and the sponsor to ensure that documentation and information are distributed to relevant staff
- Ensures and maintains regulatory compliance
- Coordinates the close-out phase of clinical study protocols as well as the archival of study documents
- Maintains annual renewal of REB's for the program portfolio
- Submission of retrospective studies into CAPCR
- Supports the trial activation process - following up with task assignments per the target timeframe and collation of documents
- Drafting Informed Consent Forms
- Set-up and maintenance of regulatory and study documentation
- Community college diploma in a health-related discipline, or equivalent (required)
- Completion of a Bachelor's degree program, or recognized equivalent in Health or Science-Related discipline, is preferred
- Clinical Research Graduate Certificate, preferred
- 6 months related experience in some or all of Oncology, Clinical trials, regulatory issues involving human subjects is required
- Demonstrated relevant clinical research knowledge
- Excellent written and verbal communication skills, excellent organization, prioritization skills, good computer skills, ability to learn quickly and work independently
- Excellent interpersonal skills
- Ability to work under pressure and attention to detail
- Ability to perform duties in a professional and courteous manner and produce high-quality work while meeting deadlines in accordance to UHN standards
- Ability to perform multiple concurrent tasks
- Knowledge of applicable legislative, UHN and/or departmental policies
- 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
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
- 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.)