Clinical Research Coordinator (Research Institute)
Clinical Research Coordinator (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
Cardiac Electrophysiology. Cardiovascular Health Across the Lifespan Program.
Under the supervision of the manager of the Clinical Research Unit in cardiac electrophysiology and the Principle Investigator
Investigator the incumbent will be responsible for supporting the successful conduct of clinical research studies.
General Duties
Assists in the planning/organization of research projects
Recruitment of study participants (e.g. Identify and screen potential subjects obtain informed consent.) coordination of study visits as per study protocol
Execution of all aspects of study visit(e.g. adverse events safety questionnaires sample collection including processing and shipment of samples according to clinical protocol)
Clinical evaluation of subjects according to protocol requirements
Provide coordination and timely completion of all aspects of data collection and sources documentation
Timely completion of electronic CRFs as for clinical trial requirements
Respond promptly to queries and requests for information
Conduct other related tasks as assigned by supervisor.
Website of the organization
Required Skills
Bilingual (excellent French and English spoken and written)
Autonomous flexible sense of ethics and good judgment
Excellent organizational time management skills ability to multi-task and prioritizing time sensitive issues
Excellent interpersonal skills
Ability to work under minimal supervision
Ability to generate and maintain accurate records
Strong analytical and problem solving skills
Decision making:
- Planning implementing and evaluating patient care.
- While the investigator is the main responsible for his/her study the incumbent must ensure protocol compliance including participant eligibility.
Clinical research experience is an asset.
Required Experience:
IC
Employment Type
Unclear
