Clinical Research Coordinator â Nurse (Pediatric and Adult Research) (Research Institute)
Clinical Research Coordinator â Nurse (Pediatric and Adult Research) (Research Institute)
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Job Description
Job Description
RESEARCH INSTITUTE OF THE MUHC
The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal Quebec the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Qubec - Sant (FRQS).
Position summary
Under the supervision of the Manager Pediatric and Adult Research Centre for Innovative Medicine (CIM) the Clinical Research Coordinator - Nurse is responsible for supporting the successful conduct of clinical research studies. The incumbent will collaborate with Investigators and health care personnel to assume responsibility for the overall patient management and the coordination of several clinical studies for the Pediatric and Adult Department of the RI-MUHC.
The Centre for Innovative Medicine is located in the Glen site hospital which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research.
More information on the CIM:
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 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
Responsible for the Research Ethics Board submissions
Conduct other related tasks as assigned by the supervisor.
Website of the organization
Required Skills
Bilingual: French and English spoken and written
Solid written and verbal communication skills
Able to work under minimal supervision
Self-directed flexible organized and sense of ethics
Clinical research experience is an asset
Knowledge of international federal and provincial laws and regulations governing clinical research (ICH-GCP) is an asset.
Required Experience:
IC
Employment Type
Unclear
