This position provides comprehensive information regarding clinical trial protocols to medical and nursing staff. Responsible for evaluating and assessing eligibility of potential candidates for clinical research studies, study compliance, assessing toxicities to treatments, collecting and submitting data, assisting other research staff and principal investigators in the coordination of treatments such as laboratory studies, radiological studies and other designated procedures for protocol compliance. Serves as a clinical liaison between the research department and other patient care departments within CHH, ECCC and externally with other health care providers. Responsible for maintaining high levels of accuracy in order to assure compliance with all parties involved in monitoring clinical research activities.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree