University Health Network

Clinical Research Coordinator I


PayCompetitive
LocationToronto/Ontario
Employment typePart-Time

This job is now closed

  • Job Description

      Req#: 927456

      JOB TITLE: Clinical Research Coordinator I

      Job Posting #: 927456

      Site: Toronto Western Hospital

      Union: Non-Union

      Department: Al and Malka Green Artists' Health Centre

      Reports to: Program Development Lead

      Hours: 15 hours per week

      Salary: $35.33 - $44.16or hourly: To commensurate with experience and consistent with UHN compensation policy

      Status: Temporary Part-Time (1 year)

      Posted Date: January 10, 2024

      Closing Date: Until Filled

      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 Al & Malka Green Artists’ Health Centre is hiring a part-time Clinical Research Coordinator I (CRC I) to work with various research and quality improvement projects working under the direction of the Program Development Lead. As a pivotal member of our research team, you'll be at the forefront of the Centre’s initiatives aimed at enhancing the well-being of artists and contributing to the broader understanding of artists' health. The CRC I role will include study administration, preparing consent forms and paperwork required by the Research Ethics Board, facilitating community partnerships, coordinating patient engagement including training and survey development, and facilitating qualitative and quantitative data analysis. The CRPC will also assist in the preparation of study results, including presentations, progress reports, and manuscripts.

      DUTIES

      Responsibilities include but are not limited to:

      • Recruit study participants (e.g. identify and screen potential subjects, obtain informed consent)
      • Coordinate REB submission and revisions process.
      • Prepare REB protocols and associated materials.
      • Keep abreast of regulations and policies governing clinical research.
      • Encourage and foster collaborative relationships with community and patient partners.
      • Conduct literature reviews and keep current with study literature.
      • Attend and document outcomes of study team meetings.
      • Assist with design/development of promotional materials/newsletters.
      • Develop and monitor timelines for study.
      • Coordinate patient visit schedules as per study protocol
      • Conduct individual interviews and focus groups
      • Analyze quantitiatve and qualitative data and summarizing results
      • Participate in drafting of manuscripts, poster presentations, and oral presentations
      • Execution of various aspects of study visit. The CRC I performs source documentation in UHN’S EMR (Epic), PSS, OCEAN, and data collection according to UHNpolicy, ICH-GCP guidelines, and study protocol.
      • Other responsibilities may include planning, implementing, and coordinating aspects of data entry (e.g. in databases or Case Report Forms) and data management, supervision of students and volunteers, and study-related administrative tasks, such as creation and maintenance of investigator study files, ethics submissions, meeting facilitation, etc.

        QUALIFICATINS: