Clinical Research Coordinator (Research Institute)

McGill University Health Centre; Montreal; On-site; CAD 55,000 - 75,000; Full time

Job summary

A world-renowned research institute is hiring a Clinical Research Coordinator in the Division of Neurology. The role focuses on managing clinical trials in pediatric neurosciences, ensuring patient safety, compliance, and effective data collection. Ideal candidates will have experience in clinical research and a strong understanding of pediatric care.

Qualifications

• Experience in clinical trials management.
• Strong understanding of pediatric neurosciences.
• Ability to conduct patient interviews and assess eligibility.

Responsibilities

• Manage the day-to-day operations of clinical trials in pediatric neurosciences.
• Obtain informed consent and assess patient eligibility.
• Monitor patient safety and medication compliance.

Skills

Patient Safety

Data Collection

Regulatory Compliance

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: Pediatrics, Division of Neurology

The incumbent will work under the supervision of the project manager and the Principal Investigator. The successful candidate will be responsible for the day-to-day management of clinical trials in pediatric neurosciences.

General Duties
• Obtains informed consent, assesses patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings,
• Maintains and completes concomitant medication, adverse events and questionnaires logs, forms and protocol specific source documentation,
• Monitors patient safety and medication compliance,
• Prepares orders for protocol-related requests and procedures, consults, requests for lab requisitions as needed,
• Coordinates all aspects of data collection and source documentation,
• Completes all research-related documents and responds to queries and requests for information,
• Participate on protocol specific and scientific trainings,
• Support the Research Ethics Board submissions,
• Conduct other related tasks as assigned by the project manager.