Clinical Research Coordinator - Nephrology (Research Institute)

McGill University Health Centre; Montreal; On-site; CAD 50,000 - 70,000; Full time

Job summary

A leading biomedical research institute is seeking a Clinical Research Coordinator to manage clinical studies focusing on virtual reality for physical exercise in patients undergoing hemodialysis. This role involves collaborating with a medical team, data collection, and maintaining compliance with research protocols. The ideal candidate should have strong communication skills and experience in clinical research.

Qualifications

• Experience in clinical research is preferred.
• Strong communication skills.
• Ability to work collaboratively with a diverse team.

Responsibilities

• Participate in all aspects of the project and collaborate with the medical team.
• Participate in data collection and maintain regulatory documents.
• Screen, consent, and enroll patients into clinical studies.

Skills

Collaboration

Data Collection

Patient Screening

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
The clinical research coordinator must ensure the smooth running of the clinical study on utilization of virtual reality for physical exercise in hemodialysis population.
The incumbent must work in collaboration with the members of the team, investigators and health care group.

General Duties
Working under the supervision of the project director, the incumbent will:
• Participate in all aspects of the project and collaborate with the members of the medical team,
• Participate in data collection and source documentation,
• Carry out protocol required assessments of study participants,
• Screen, consent, and enroll patients into clinical study,
• Maintain and update questionnaires and source documents, according to the protocol,
• Coordinate the tests required under the protocol,
• Maintain site’s essential and regulatory documents for the conduct of a clinical trial,
• Submit study protocols and maintaining communication with Research ethics Board about the studies.