University Health Network

Clinical Research Coordinator I


PayCompetitive
LocationToronto/Ontario
Employment typeFull-Time

This job is now closed

  • Job Description

      Req#: 929362

      JOB TITLE: Clinical Research Coordinator I

      Job Posting #:929362

      Union: Non-Union

      Site: Princess Margaret Cancer Centre

      Department: Department of Medical Oncology & Hematology

      Reports to: Principal Investigator

      Hours: 35 hours per week

      Salary range: $68,890 - $86,112 per annum: To commensurate with experience and consistent with UHN compensation policy

      Status: Temporary Full Time (1 year)

      Posted Date: March 4, 2024

      Closing Date: March 18, 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.

      Job Summary:

      A Clinical Research Coordinator I position is available at the Princess Margaret Cancer Centre / University Health Network in Toronto, Canada. This role will encompass a variety of cancer genetics and genomics research studies in hereditary cancer early detection. Reporting to Dr. Raymond Kim, Medical Geneticist and Medical Director – Cancer Early Detection, the Clinical Research Coordinator I collaborates with the Manager, Principal Investigator and research health care team to assume responsibility for the overall coordination and management of a variety of hereditary cancer syndrome projects.

      Duties

      • Identification of patients fulfilling hereditary genetic testing criteria and assist in organizing clinical genetic testing for their patients
      • Enrollment of patients into tumour profiling studies
      • Coordinating liquid biopsy studies for patients with hereditary cancer syndromes
      • Recruitment of study participants (e.g. identify and screen potential subjects, coordinate for blood tests and tissue bank, coordinate patient visits, obtain informed consent, execution of study visit) for multiple studies
      • Planning, implementing and coordinating all aspects of data collection, source documentation and data entry per UHN policy and ICH/GCP guidelines
      • Assisting with implementation of universal germline genetic testing for the breast site
      • Collaborating with team members on tasks related to participant recruitment, data generation and updating
      • Coordinating with the Project Manager to execute administrative tasks, such as collection of regulatory documents, ethics submissions and general paperwork

        Qualifications:

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