227 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Univ" "Univ" "UNIV" uni jobs at University of Kansas Medical Center
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or without notice. Required Qualifications Education: High school diploma or GED. Work Experience: Experience with computer-based HVAC automated control systems. Experience with chiller/ boiler plant
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training/on-boarding employees. Skills Presentation skills. Computer skills. Communication. Collaborative. Team-oriented. Organization. Time management. Required Documents Resume/CV Cover Letter
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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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. 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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Department: RI Administration ----- Research Informatics Position Title: Data Scientist - Research Administration Job Family Group: Professional Staff Job Description Summary: The Data Scientist
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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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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