Clinical Research Clerk (Research Institute)

McGill University Health Centre; Montreal; On-site; CAD 60,000 - 80,000; Full time

Job summary

Join a prestigious biomedical research institute in Montreal, where you will play a vital role in clinical research focused on inflammatory bowel disease. This position offers the opportunity to work alongside leading physicians and research professionals, assisting with the organization and implementation of vital research projects. Your contributions will include managing documents and data, preparing ethics submissions, and supporting industry-sponsored clinical trials. This role is perfect for individuals passionate about advancing medical research and eager to make a meaningful impact in the healthcare field.

Qualifications

• Experience in clinical research and data management is essential.
• Strong organizational skills and attention to detail are required.

Responsibilities

• Maintain and organize filing for research projects.
• Assist with ethics submissions and research protocols.
• Communicate effectively with staff and assist with administrative tasks.

Skills

Document management

Data management

Communication skills

Translation skills

Education

Bachelor's degree in a related field

Tools

Excel

RedCap

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: Gastroenterology

The incumbent will be involved with clinical research in gastroenterology and more specifically inflammatory bowel disease (IBD). Document and data management is an essential part of this position. The incumbent will work closely with the project manager, IBD physicians as well as with gastroenterology research nurses and coordinators mainly on clinical study protocols.

The incumbent will also help to initiate industry sponsored clinical trials including assisting with REB documents, coordination, regulatory work, advertising, and accounting.

General Duties

1. Maintain and organize filing.
2. Assist with preparation of ethics submissions, updates, and renewals.
3. Assist with organization and implementation of research projects.
4. Maintain databases (Excel/RedCap/Other study-clinic related).
5. Assist with ethics submissions, research protocols and study-related documents.
6. Attend videos and teleconferences regarding projects.
7. Communicate rapidly and effectively with staff through email or other strategies.
8. Translate, edit, and format documents.
9. Assist with other administrative tasks as required.