The Cancer Clinical Research Unit requires a Clinical Research Coordinator I (CRC I) to work with various research projects within its oncology & hematology research portfolio. Working under the direction of the Clinical Research Manager, the CRC I collaborates and works very closely with the Principal Investigator, Clinical Research Nurses, and health care team to jointly assume responsibility for the frontline administrative management and coordination of clinical trials and research studies (interventional trials and non-therapeutic studies). It is essential for the Clinical Research Coordinator I to be team oriented and contribute to the overall goals and tasks of the team, particularly with the Clinical Research Nurses. The CRC I will work collaboratively with data and regulatory teams to ensure the collection of high quality data and regulatory compliance through the trials. The CRC I will be a part of a larger CRC I team and may have the opportunity to participate in other team and CCRU initiatives. The CRC I role is a primarily on-site position, with some flexibility for work from home as disease site clinical schedule and tasks allow, following UHN policies, and as approved by the Clinical Research Manager.
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Job Type
Full-time
Career Level
Entry Level