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volunteer intake process under the supervision of OBB staff. Coordinate paperwork and logistics for PEI and OBB volunteers and other program guests, including background checks and requirements of the Dept
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of the clinical trials research process. Supervises staff and functions under the Principal Investigator's medical license and cannot perform any tasks that by state or local law require a medical license to
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, or Python -Excellent organizational and problem-solving skills -Demonstrated success working in interdisciplinary teams Preferred Qualifications: -EEG signal processing -Experience writing IRB protocols and
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% Manages research workflow components, collects, prepares, processes, and submits participant data and samples to appropriate entities, adhering to research protocols 15% Serves as an initial point
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processing participant payments and mileage reimbursement. The Clinical Research Study Coordinator will also cross-train on other clinical studies in the Carlsson group and serve as a back-up coordinator for
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/certification, such as collecting vital signs, obtaining weight, and performing phlebotomy 20% Manages research workflow components, collects, prepares, processes, and submits participant data and samples