267 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UNIV" "Univ" "Univ" positions at University of Kansas Medical Center
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, mitigation, response, and recovery – for the University of Kansas Medical Center. Support organizational continuity of operations (COOP) planning relating to the organization’s assets, data, and operations
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responsible for obtaining informed consent from participants, research data collection and entry, maintenance of web-based research database and regulatory paperwork for research studies. Job Description: Job
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. The Research Assistant will contribute to ongoing research by performing experiments, collecting and analyzing data, and assisting with the preparation of reports and publications. This position provides hands
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. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our
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staff effort aligns appropriately with research funding and institutional expectations, integrity of research data and associated electronic databases and safeguarding research‑related physical assets and
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MRI, PET, ECG, lab draws, IV infusions, lumbar punctures, clinical assessments, and dispensation of study medication. Collect and verify accurate medical history and concomitant medication information
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. Communicate with Study Coordinators regarding the status of tissue requests. Perform study-specific ECGs and transmit data to appropriate database as listed in the study protocol schedule of events. Reference
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across projects. Support the implementation/evaluation of telemonitoring and distance education activities. Complete readiness assessments and practice facilitation. Manage data collection, data management
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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 Rate Type: Salary Compensation Statement: The pay range listed
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to the collection, documentation, and analysis of clinical research data. Additionally, the Clinical Research Coordinator monitors participant progress, documents and reports adverse events, and participates in