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

Department / Research Program: IDIGH / CVIS

The Chronic Viral Illness Service Research team has an active research program, conducting numerous clinical trials each year to provide innovative research to their patients. Under the immediate supervision of the CVIS Research Director and the CVIS Project Manager, the incumbent will be directly involved in several PI-Initiated and industry clinical trials and research studies, related to chronic viral illnesses such as HIV, HBV, HCV, STIs, and liver diseases. The Clinical Research Coordinator-Nurse (DEC) will complete the below listed tasks at the Chronic Viral Illness Service of the McGill University Health Center.

General Duties

• Recruits research participants,

• Coordinate and perform study visits and protocol procedures as per study protocol, coordinating with clinic staff to ensure proper documentation and timing of research-related procedures,

• Maintains, completes and updates concomitant medication log, adverse event log, questionnaires and protocol specific source documentation,

• Timely completion of all study documentation forms, including case report forms (CRFs), adverse events reports, queries and other study specific documents,

• Review subject’s information, medical charts and laboratory reports in preparation for the investigator’s review,

• Administer investigational products,

• Monitors patient safety and medication compliance, completes patient charting accordingly,

• Coordinates protocol related tests according to clinical protocol and manuals,

• Verifies medication compliance and patient diaries,

• Creates study specific source documentation,

• Provides coordination of all aspects of data collection and source documentation,

• Participate to monitoring visits and comply with monitoring reports,

• Planning, implementation, and maintaining of data collection and analysis systems in support of research protocol,

• Sample collection and clinical follow-up of research participants according the study protocol,

• Participating in research team meetings, trials related meetings including but not limited to Investigator meeting,

• Performing miscellaneous job-related duties as assigned by supervisor, including support to other coordinator and research nurses.