Clinical Research Analyst

*REPOST*

Union: Non-Union
New or Replacement: New
Number of Vacancies: 1
Site: Toronto General Hospital, University Health Network
Department: Living Donor Liver Transplant Program
Reports to: Directors of Living Donor Program & Clinical Research Manager
Department: HPB Oncology Research  
Hours: 37.5 hours per week
Salary Range: $33.80 - $42.25 per hour
Status: Temporary Full-Time (one year contract with possibility of extension)
Shifts: Days
Closing Date: May 31, 2026

Position Summary
This clinical research position is within the Living Donor Liver Transplant Research Program at the Ajmera Transplant Center, Toronto General Hospital, UHN.

Our portfolio includes epidemiological, translational and clinical research led by a multidisciplinary group of clinician investigators. Our high volume and world renowned program on living donor liver transplantation (largest program in the Western Countries) make this an exciting position for research personnel with translational and clinical knowledge/interests and opportunity to develop additional research skills as well as academic publications. This position offers an exciting research opportunity for an extremely organized, highly motivated, detail-oriented and hard-working individual, who possesses strong communication and interpersonal skills, and will enjoy the challenge of learning from and working with an interdisciplinary research team. 

Duties

• Recruitment of study participants (e.g., identifying and screening potential subjects and obtaining informed consent)
• Coordinating patient visit schedules as per study protocol
• Execution of various aspects of the study visit (e.g., recording adverse events and concomitant medications, monitoring patient safety, administering questionnaires/ePROs, and performing vital signs assessments)
• Supporting research projects being carried out by medical trainees, Fellows, and PIs
• Preparing CTA submissions for Investigator-initiated trials
• Preparing submissions for CAPCR
• Corresponding with study stakeholders
• Performing source documentation in UHN’s electronic medical record (Epic) and data collection according to UHN policy, ICH-GCP guidelines, and study protocol
• Other responsibilities include planning, implementing, and coordinating data entry (e.g., in databases or case report forms) and study-related administrative tasks, such as creating and maintaining investigator study files, meeting facilitation, etc.