Assists investigators as coordinator of basic to complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance. This position also requires rotating overnight on-call duties outside of the essential functions, specifically for the duration of an existing trauma trial. Additional compensation for these overnight on-call duties is provided.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
1,001-5,000 employees