Clinical Research Supervisor, CIM (Adults & Pediatrics) (Research Institute)
Clinical Research Supervisor, CIM (Adults & Pediatrics) (Research Institute)
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Job Description
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 Qubec - Sant (FRQS).
Position summary
Under the supervision of the Manager of the Centre for Innovative Medicine (CIM) as well as following established governmental guidelines and regulations the incumbent is responsible for the supervision of the clinical research staff.
General Duties
Supervises clinical research staff
Assist the manager in overseeing study operations
Ensures study start up activities are in place (from the Confidential Disclosure agreement until the conduct of the initiation visit)
Assigns staff to studies and maintains a balanced staff/study ratio
Ensures that the research team meets the study recruitment objectives and implements solutions to meet the required objectives
Holds regular meetings with the staff to ensure that they meet quality standards and regulations
Provides the manager with bi-weekly reports on the status of the studies
Works closely with investigators including regular communications and troubleshoot when needed
Responsible for the onboarding and the training of new staff and ensuring that all internal and external training are up-to-date GCP SOP Health Canada Div 5 IATA Code Blue/Crash cart CPR etc
Responsible to put in place a back-up plan for all research projects to ensure studies are not interrupted
Responsible for staffs performance and conduct annual performance reviews
Participates in the interviews of new staff
Meets employees weekly or biweekly
Meets with his/her manager biweekly
Any other tasks requested by the Manager/Director of Operations.
Required Skills
Clinical research accreditation (SoCRA or ACRP)
Bilingual (French and English spoken and written)
Ability to work under pressure
Excellent organizational skills ability to multi-task and prioritizing time-sensitive issues
Experience working with electronic data management systems tools and technologies (EDC)
Experience working with Clinical Trial Management System (CTMS)
Excellent knowledge of international federal and provincial laws and regulations governing clinical research (ICH-GCP)
Self-directed and organized
Able to work as part of a team
Excellent interpersonal skills.
Required Experience:
Manager
Employment Type
Unclear
