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Top Benefits

Paid Sick Leave
Government Pension Plan
Vacation

About the role

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

https://rimuhc.ca/en

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.

Additional information

Status : Temporary Part-Time: 14 hours

Pay Scale: Commensurate with education and work experience.

Work Shift: Other or part-time

Other: Tuesday and Wednesday from 08:30am to 4:30 pm

Work Site: Glen Site, 1001 Decarie Blvd.

***If you wish to include a cover letter, please attach it with your resume in one document. ***

Why work with us?

3 days of paid sick leave per year, which includes a maximum of 1 personal day, RREGOP government pension plan (defined benefit plan), Vacation calculated on a pro-rata basis based on a percentage of your salary, 5.3% of your gross earnings will be added to your paycheque in lieu of statutory holidays.

https://rimuhc.ca/careers

To learn more about our benefits, please visit http://rimuhc.ca/en/compensation-and-benefits

THIS IS NOT A HOSPITAL POSITION.

Equal Opportunity Employment Program

The Research Institute of the McGill University Health Centre hires on the basis of merit and is strongly committed to equity, diversity and inclusion within its community. We welcome applications from all qualified candidates who self-identify as members of racialized groups/visible minorities, women, Indigenous persons, persons with disabilities, ethnic minorities, and 2SLGBTQIA+ persons. We also welcome candidates with the skills and knowledge to productively engage with diverse communities. Persons with disabilities who anticipate needing accommodations for any part of the application process may confidentially contact, research.talent@muhc.mcgill.ca

About RI-MUHC | Research Institute of the MUHC | #rimuhc

Research Services

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