Clinical Research Clerk (Research Institute)

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

Job summary

Join a prestigious research institute in Montreal, dedicated to advancing healthcare through innovative research. This role focuses on supporting clinical research in gastroenterology, particularly in inflammatory bowel disease (IBD). You'll collaborate with a dynamic team, assisting with document management, ethics submissions, and the organization of clinical trials. This position offers a unique opportunity to contribute to impactful research while developing your skills in a supportive environment. If you're passionate about healthcare and research, this is the perfect opportunity to make a difference in patients' lives.

Qualifications

• Experience in clinical research and document management is essential.
• Strong communication skills are necessary for effective collaboration.

Responsibilities

• Maintain and organize filing for research projects.
• Assist with ethics submissions and research protocols.

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.