Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies. Screens, enrolls, and recruits research participants. Coordinates schedules and monitors research activities and subject participation. Recognizes adverse events, protocol deviations, and other unanticipated problems and reports appropriately. Collects, abstracts, and enters research data. Performs administrative and regulatory duties related to the study as assigned. Some travel may be required. ADDENDUM (if applicable) Protocol Development and Maintenance Activities Responsibilities may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes. Participates in other protocol development activities and executes other assignments as warranted and assigned.
Associates degree or other college certificate or diploma required. Completion of Mayo Clinic competency based assessment program will be required within one year of hire.
Graduate or diploma from a study coordinator training program is preferred. One year clinical research experience preferred. Medical terminology course preferred.
Education, experience and tenure may be considered along with internal equity when job offers are extended. The minimum pay rate is $20.28 per hour.
The unit is open from 7:00 am - 5:00 pm Monday - Thursday and 7:00 am - 4:30 pm Friday. Currently due to COVID-19 coverage of clinical trials the unit is working rotating shifts between the hours of 7 am - 10:30 pm including weekends. When the demand for 24/7 coverage ends, the work unit will return to normal operating hours.
Please see schedule details.
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Clinical Labs and Research
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Equal opportunity employer
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