Clinical Research Coordinator (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 is seeking a dedicated clinical research coordinator. This full-time role involves collaborating with a dynamic project team to recruit and follow up with participants in clinical studies focused on Tuberculosis treatment. You will play a crucial role in ensuring the smooth execution of randomized trials at renowned institutions, contributing to impactful research that aims to improve patient outcomes. If you are passionate about clinical research and eager to make a difference, this opportunity is perfect for you.

Qualifications

• Experience in clinical research coordination and participant recruitment.
• Strong organizational and data management skills.

Responsibilities

• Collaborate with the project team for clinical studies.
• Screen and recruit participants for randomized trials.

Skills

Clinical Research Coordination

Participant Recruitment

Data Management

Education

Bachelor's Degree in Health Sciences or related 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 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.