Clinical Research Coordinator (Research Institute)

McGill University Health Centre; Montreal; On-site; CAD 50,000 - 90,000; Full time

Job summary

An established industry player in biomedical research is seeking a dedicated full-time clinical research coordinator to join their dynamic team. This role involves collaborating on groundbreaking clinical studies focused on Tuberculosis treatment. You will play a vital role in participant recruitment, data management, and ensuring adherence to study protocols. Working closely with a passionate project team at prestigious institutions, you will contribute to impactful research that aims to improve patient outcomes. If you are organized, detail-oriented, and eager to make a difference in the field of clinical research, this opportunity is perfect for you.

Qualifications

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

Responsibilities

• Coordinate recruitment and follow-up for clinical research studies.
• Collaborate with project teams and TB clinic personnel.
• Complete case report forms and ensure protocol adherence.

Skills

Participant recruitment

Clinical research coordination

Data management

Protocol adherence

Education

Bachelor's degree in a relevant field

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

We are looking for a full-time clinical research coordinator who can help with recruitment and follow-up of participants for 2-3 clinical research studies. These projects are randomized trials of Tuberculosis treatment.

The incumbent, under the supervision of the site investigator and study manager, will assist in the execution of clinical studies at the Montreal Chest Institute and the Montreal Children’s Hospital (GLEN).

General Duties

1. Work in close collaboration with the project team.
2. Screen, recruit, and randomize participants in Montreal (at GLEN site).
3. Complete case report forms.
4. Collaborate with the personnel of the TB clinic for the follow-up of participants.
5. Follow all aspects of the study protocol.
6. Perform other related duties as required.