255 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Univ" positions at University of Kansas Medical Center
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monitoring (RBM) or source data verification (SDV) monitoring. Ensure the protection of clinical trial participants by reviewing and verifying the informed consent process, subject eligibility and enrollment
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employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time
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. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time
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retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time
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of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type
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retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time
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breast cancer research. This position will assist in entry level clinical research activities including collecting information from patients/study participants and ensuring study activities are performed
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participating in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Monitor participants’ progress including documenting and reporting
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and families. Data Utilization Ensure the timely completion of necessary paperwork including developmental assessments, lesson plans, parent information, incident/accident report, attendance, USDA meal
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collaboration with the School of Health Professions. Support faculty and staff in meeting ACOTE accreditation requirements, including data collection, documentation, surveys, and departmental reporting. Oversee