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Clinical Research Coordinator (Research Institute)

McGill University Health Centre

Montreal

On-site

CAD 45,000 - 60,000

Full time

29 days ago

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Job summary

The Research Institute of the McGill University Health Centre is seeking a clinical research coordinator to assist in various studies within the Allergy and Immunology department. This entry-level role involves patient enrollment, data collection, and ensuring follow-up visits, making it ideal for those looking to establish a career in clinical research.

Qualifications

  • Entry-level position suitable for individuals interested in clinical research.
  • Not for students; ideal for those pursuing a long-term career in clinical research.

Responsibilities

  • Enrolls patients and collects data for ongoing studies.
  • Ensures patient follow-up visits and organizes study documentation.
  • Assists in the organization of research projects.

Skills

Patient enrollment
Data entry
Patient follow-up
Medical chart reviews

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 incumbent will work in the department of Allergy and Immunology (IDIGH) for the principal investigator Dr. Moshe Ben-Shoshan. The incumbent will be responsible for enrolling patients, collecting patient data, data entry, ensuring patient follow up visits, as well as other various clinical related tasks for the department’s various ongoing studies. This is an entry level clinical research coordinator role and suitable for individuals who would like to learn and grow in the field of clinical research. This position is not for students, but for individuals who are interested in pursuing a longer-term career clinical research goal.

General Duties
• Assists in the organization of research projects,
• Obtains informed consent from patients for participation in research studies,
• Interviews patients to complete study questionnaires,
• Trains patients to complete electronic study surveys,
• Performs medical chart reviews,
• Performs data entry,
• Ensures patient follow-up visits are completed,
• Organizes and maintains study documentation at various study sites,
• Accomplishes any other related tasks as required by the immediate supervisor.
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