Clinical Research Coordinator Trauma Department (Research Institute)
Clinical Research Coordinator Trauma Department (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 Québec - Santé (FRQS).
Position summary
Under the general supervision of Dr. Kosar Khwaja at the McGill University Health Centre the incumbent is responsible for the general coordination of clinical research projects in the Trauma Department at the Montreal General Hospital.
General Duties
Coordinate local and multi-centered research studies
Assist in the submission of documents to Ethics Boards Pharmacy Contract office and other relevant offices
Maintenance of all documentation of future ongoing and closed projects
Screening consenting and enrolling of patients into clinical studies
Data collection and entering data
Assist in the preparation of manuscripts presentations letters and other scientific reports
Prepare progress reports and statements for granting agencies
Organize investigators meetings and conference calls
Organize regular critical care clinical research meetings for the critical care group at the MUHC
Perform general clerical duties to include but not limited to: photocopying faxing mailing and filing.
Website of the organization
Required Skills
GCP certification and experience with clinical research an asset
Have good skills in written and spoken English and French
Have general knowledge of how hospitals function particularly intensive care units an asset
Knowledge of the Nagano platform for the submission of studies to the RI-MUHC ethics board an asset
Knowledge of the MSSS province-wide multi-centered study submission process an asset
Be capable of working independently with particular attention to detail
Good communication and organizational and interpersonal skills
Able to work with Microsoft Office suite (ACCESS WORD EXCEL and POWERPOINT)
Autonomous flexible sense of ethics and good judgment
Ability to work under minimal supervision
Clinical research experience is an asset.
Required Experience:
IC
Employment Type
Unclear
