Clinical Research Coordinator (Research Institute)

McGill University Health Centre; Montreal; On-site; CAD 50,000 - 80,000; Full time

Job summary

Un institut de recherche de premier plan au Canada, affilié à l'Université McGill, recherche un candidat pour gérer des essais cliniques en neurologie pédiatrique. Ce rôle implique des responsabilités variées allant de l'obtention du consentement éclairé à la supervision de la sécurité des patients. Le candidat idéal doit posséder une formation pertinente et une expérience antérieure dans des essais cliniques.

Qualifications

• Expérience dans la gestion d'essais cliniques ou dans un environnement de recherche.
• Capacité à obtenir le consentement éclairé et évaluer l'éligibilité des patients.
• Compétences en documentation et collecte de données.

Responsibilities

• Gestión quotidienne des essais cliniques en neurosciences pédiatriques.
• Surveillance de la sécurité des patients et de la conformité aux médicaments.
• Coordination de toutes les facettes de la collecte de données et de la documentation.

Skills

Patient Safety

Clinical Trials Management

Data Collection

Documentation

Education

Bachelor's degree in a 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
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.