Clinical Research Coordinator , CIM PediatricsAdults (Research Institute)
Clinical Research Coordinator , CIM PediatricsAdults (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 Québec - Santé (FRQS).
Position summary
Under the supervision of the Supervisor/Manager Pediatrics/Adult Clinical Research at the Centre for Innovative Medicine (CIM) the Clinical Research Coordinator is responsible for supporting the successful conduct of CIM Pediatrics/Adults clinical research studies. The person will collaborate with Investigators and health care personnel to assume responsibility for the overall patient management and coordination of several clinical studies for 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.
General Duties
Recruits research participants prescreens patients and obtains informed consent assesses patients for protocol eligibility through personalized interviews and/or medical record review in in-patient and out-patient settings
Maintains and completes (either in paper or electronic formats) medication adverse events and questionnaires logs forms and protocol specific source documentation ensures ethical approvals are continued throughout the study
Monitors patient safety and medication compliance
Completes all follow-ups as per special protocol requirements: patient visits/status disease site active trial lists and completes clinical notes
Coordinates orders for protocol related requests and procedures: consultations requests for pathology diagnostic and analytical laboratories etc
Coordinates all aspects of data collection and source documentation
Completes all research related documents and responds to queries and requests for information
Collaborates with the Monitor the Quality Assurance and any resource assigned to the Pediatrics/Adult team
Supports the team with the Research Ethics Board submissions
Conduct other related tasks as assigned by the Supervisor/manager of phase I to IV.
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 and compliance
Knowledge of regulations governing clinical research (ICH-GCP) H-C FDA is an asset.
Required Experience:
IC
Employment Type
Unclear
