Under the direct supervision of the study team, assists in coordinating the details of the study and documentation concerning study protocols, patient scheduling, history work, data collection, data entry, data management, follow-up care, and compliance with federal, state, sponsor and institutional guidelines. Consults with and assists staff in own and other labs in conducting research projects. Performs data entry and manages study database as directed and performs other administrative duties related to the study as assigned. May perform technical duties related to clinical and experimental research as directed and under the supervision of other study personnel. May order materials/supplies and assist with general office work. The hired candidate must be within reasonable driving distance of the Rochester, MN campus. *Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.
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Industry
Hospitals
Education Level
High school or GED