Clinical Research Coordinator - Baccalaureate Nurse

Description du poste

Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference!

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.

Website of the organization

Education / Experience

Education: Bachelor's Degree
Field of Study: Nursing

Work Experience: Minimum of 15 years, experience in clinical trials an asset

Professional Membership: ☒ Yes: Member of the Ordre des infirmières et infirmiers du Québec

Required Skills

• This position requires an advanced knowledge of oral and written French.
• An advanced knowledge of oral and written English is required, as the position requires regular and complex contact with patients, researchers or international students who are exclusively proficient in English. The position also requires complex writing or in-depth analysis of documents in English related to a research project.
• Excellent communication and interpersonnel skills,
• Analytical skills and attention to details,
• Demonstrates adaptability skills,
• Capacity to work autonomously or with teams with minimum supervision,
• Proficiency in Microsoft Office (Word, Excel, Teams, Outlook) and Adobe.