Clinical Research Clerk (Research Institute)

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

Job summary

An established industry player in biomedical research seeks a dedicated individual to join their gastroenterology research team. This role focuses on clinical research related to inflammatory bowel disease (IBD), where you'll manage documents and data, assist in preparing ethics submissions, and support the coordination of clinical trials. Collaborating closely with physicians and research staff, you will play a vital role in ensuring the smooth operation of research projects. If you are organized, detail-oriented, and passionate about contributing to innovative research, this opportunity is perfect for you.

Qualifications

• Experience in clinical research, especially in gastroenterology.
• Strong organizational skills and attention to detail.

Responsibilities

• Maintain and organize filing for research projects.
• Assist with ethics submissions and research protocols.
• Coordinate industry-sponsored clinical trials.

Skills

Document management

Data management

Communication skills

Translation skills

Education

Bachelor's degree in a relevant 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.