RESEARCH INSTITUTE OF THE MUHC
Position summary
Under the supervision of the Manager of Oncology Research, Centre for Innovative Medicine (CIM), the Clinical Research Coordinator -- Nurse is responsible for supporting the successful conduct of clinical research studies in oncology. The incumbent will collaborate with Investigators and health care personnel to assume responsibility for overall patient management and the coordination of several clinical studies for the CIM-Oncology Department of the RI-MUHC.
The Centre for Innovative Medicine is located in the new Glen site hospital which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research.
More information on the CIM:
http://rimuhc.ca/web/research-institute-muhc/centre-for-innovative-medicine
General Duties
• Obtains informed consent, assesses patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings,
• Maintains and completes concomitant medication, adverse events and questionnaires logs, forms and protocol specific source documentation,
• Monitors patient safety and medication compliance,
• Prepares orders for protocol related requests and procedures, consults, prescriptions, requests for pathology slides and blocks as needed,
• Coordinates all aspects of data collection and source documentation,
• Completes all research related documents and responds to queries and requests for information,
• Conducts protocol specific and scientific trainings,
• Creates protocol specific nursing alerts/feasibilities for the oncology day center
• Responsible for assisting with the submission of serious adverse events to the Research Ethics Board,
• Conduct other related tasks as assigned by supervisor. #J-18808-Ljbffr
