Mayo Clinic
Mayo Clinic
Posted about 23 hours ago
Full Time
Rochester, Minnesota
In Person
Smart Summary
Responsibilities
The coordinator manages non-therapeutic clinical research protocols, including participant recruitment, data collection, and regulatory compliance. They also assist with complex study logistics and ensure all research activities adhere to institutional and federal standards.
Qualifications
You have experience coordinating clinical research protocols, including screening, enrolling, and recruiting participants. You are proficient in collecting and entering research data, recognizing adverse events, and performing administrative and regulatory duties. A background in a clinical setting or related experience is required, with a preference for a study coordinator training program or medical terminology course.
Must Have Skills for ATS
Medical Terminology
Clinical Research
Job Description
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.
During the selection process you may participate in an OnDemand (pre-recorded) interview that you can complete at your convenience. During the OnDemand interview, a question will appear on your screen, and you will have time to consider each question before responding. You will have the opportunity to re-record your answer to each question – Mayo Clinic will only see the final recording. The complete interview will be reviewed by a Mayo Clinic staff member, and you will be notified of next steps.
*Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.
Mayo Clinic
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