Clinical Research Coordinator - CIM (Phase 1)

Description du poste

Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference!

Recherche Institut de la 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).

Résumé du poste

Under the general supervision of the Manager Phase 1, for the Centre for Innovative Medicine (CIM), the incumbent is responsible to conduct clinic interventions following protocols, procedures and internal SOPs.

The Centre for Innovative Medicine is located at the McGill University Health Centre (Glen Site), which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research.

Responsabilités générales

• Obtains ethics committee approval of Phase 1 protocols and ensures ethical approvals throughout the study,
• Maintenance of the Investigator Study File (ISF),
• Recruits participants for studies, obtains informed consent, assesses subjects for protocol eligibility, and obtains medical history of the subject with consent,
• Updates and completes forms for any adverse events or side effects, questionnaires and protocol-specific source documentation, Completes all follow-ups as per protocol requirements: visits and patient status,
• Coordinates requisitions for requests and procedures related to protocols: consultation, pathology, diagnostic and analytical laboratories, etc.,
• Coordinates all aspects of data collection and source documentation,
• Completes all documents related to the study and respond to all queries,
• Collaborates with the Study Monitor, Quality Assurance and Phase 1 Team,
• Performs any other tasks identified by the Phase 1 Manager.

Site web de l’organisation

CIM video

Éducation / Expérience

Education: Diploma of College Studies (DEC)

Work Experience: Minimum of two (2) years of clinical research experience

Compétences requises

• Advanced knowledge of oral and written French is required,
• An advanced knowledge of oral and written English is required, as the position requires regular and complex contact with researchers or international students who are exclusively proficient in English,
• Strong written and verbal communication skills,
• Ability to work with minimum supervision,
• Independent, flexible, organized and ethical and compliant,
• Knowledge of regulations, Health Canada, FDA, related to clinical research (ICH-GCP).