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| Job Location | Winnipeg, MB |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Full Time |
SummaryResponsible for the supervision of Clinical Staff for their assigned studies, organisation of study documentation and execution of study protocols in Clinical Research Environment under the direction of the Principal Investigator and or the Site Manager/ Site Director.The Study Supervisor will report directly to the Site Director & Site Manager giving weekly updates on their assigned studies, apprising them of any issues, seeking guidance when necessary and completing assigned tasks with minimal supervision.Key Requirements