JOB POSTING #909537
Position: Clinical Research Coordinator I
Site: Princess Margaret Cancer Centre
Department: Gynecologic Oncology
Reports to: Clinical Research Manager
Salary Range: $65,910 - $82,388 per annum (Commensurate with experience and consistent with UHN Compensation Policy)
Hours: 37.5 hours per week
Status: Permanent Full-time
University Health Network (UHN) is looking for an experienced professional to fill the key role of Clinical Research Coordinator I.
Transforming lives and communities through excellence in care, discovery and learning.
The University Health Network, where "above all else the needs of patients come first", encompasses Toronto Rehabilitation Institute, Toronto General Hospital,Toronto Western Hospital, Princess Margaret Cancer Centre and the Michener Institute of Education at UHN. 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.
University Health Network (UHN) is a research hospital affiliated with the University of Toronto and a member of the Toronto Academic Health Science Network. The scope of research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care. Research across UHN's five research institutes spans the full spectrum of diseases and disciplines, including cancer, cardiovascular sciences, transplantation, neural and sensory sciences, musculoskeletal health, rehabilitation sciences, and community and population health.
The Clinical Research Coordinator I will support various clinical research studies within the Division of Gynecologic Oncology at Princess Margaret Cancer Centre. Responsibilities include, but are not limited to: recruitment of study participants (e.g. identifying, screening potential participants & obtaining informed consent); data collection; coordination of participant visit schedules, as per study protocol; biospecimen coordination; liaising with sponsors and stakeholders; management of study databases; execution of study-related administrative tasks (e.g., completion of relevant study logs, trackers, etc.; maintenance of regulatory files; preparation of ethics submissions). Other research related tasks may be asked of the CRCI, as applicable.
Qualifications:
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