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!
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 is responsible for supporting the successful conduct of clinical research
studies. The person will have to collaborates with investigators and health care teams to assume responsibility for the overall patient
management and coordination of several clinical studies at the RI-MUHC.
General Duties
Under the direction of Dr Amine Benmassaoud, the incumbent :
- Executes all aspects of study visits and collaborate with the entire medical care team.
- Performs clinical evaluation of the participants according to the protocol requirements,
- Recruits research participants :
- Maintains, completes and updates : adverse event log, questionnaires and protocol specific source documentation,
- Coordinates protocol related tests and processes and ships samples according to clinical protocol and manuals,
- Creates study specific source documentation,
- Provides coordination of all aspects of data collection and source documentation,
- Performs any other duties as assigned by the immediate supervisor.
Website of the organization
Education / Experience
Education : Diploma of College Studies (DEC)
Work Experience : Two (2) years of related experience
Professional Membership : Yes No
Other Requirements :
- Clinical research experience is an asset,
- Experience working with electronic data management systems, tools and technologies (EDC) is an asset,
- Experience working with Clinical Trial Management System (CTMS) is an asset,
- Knowledge of international, federal and provincial laws and regulations governing clinical research (ICHGCP) is an asset,
- Bilingual (French and English, spoken and written),
- Autonomous, flexible, sense of ethics and good judgment,
- Good organizational, time management skills, and ability to multi-task and prioritizing time-sensitive issues,
- Interpersonal skills.
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