University Health Network

Clinical Research Coordinator II


PayCompetitive
LocationToronto/Ontario
Employment typeFull-Time

This job is now closed

  • Job Description

      Req#: 928143

      JOB TITLE: Clinical Research Coordinator II

      Job Posting #: 928143

      Site: Toronto General Hospital

      Department: Medicine/Lung Transplant Program

      Reports to: Principal Investigator

      Hours: 35 Hrs. per week

      Salary: $69,204 - 86,505 annually: To commensurate with experience and consistent with UHN compensation policy

      Status: Permanent Full-Time

      Posted Date: January 25, 2024

      Closing Date: February 24, 2024

      The University Health Network, where “above all else the needs of patients come first”, encompasses Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute and the Michener Institute of Education. The breadth of research, the complexity of the cases treated, and the magnitude of its educational enterprise has made UHN a national and international resource for patient care, research and education. With a long tradition of ground breaking firsts and a purpose of “Transforming lives and communities through excellence in care, discovery and learning”, the University Health Network (UHN), Canada’s largest research teaching hospital, brings together over 16,000 employees, more than 1,200 physicians, 8,000+ students, and many volunteers. UHN is a caring, creative place where amazing people are amazing the world.

      Position Summary

      The Toronto Lung Transplant program is one of the world’s foremost programs, renowned for cutting edge research and clinical practice. Working under the direction of the Principal Investigator, the Clinical Research Coordinator II collaborates with MDs and the multidisciplinary health care team in the recruitment of study participants.

      Duties

      • Identifies and screens potential subjects, obtains informed consent, conducts pre-testing and administers questionnaires or other data collection tools;
      • Plans, implements, and coordinates all aspects of data collection and source documentation, as per UHN policy and ICH/GCP guidelines;
      • Identifies problems using assessment skills and reports any abnormalities to MD or health care team member;
      • Executes study-related administrative tasks, such as collection of regulatory documents, ethics submissions, etc.;
      • Conducts telephone and/or clinical recruitment interviews to collect data using established criteria;
      • Coordinates patient visit schedule as per study protocol;
      • Executes all aspects of study visit (e.g., assessment, adverse events, monitoring safety, medication, questionnaires, sample collection, processing and transportation/shipment of samples according to clinical protocol);
      • Assesses study-related literature; and liaises with sponsor for monitoring/audits.

        Qualifications