228 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "IFM" "IFM" "IFM" uni jobs at University of Kansas Medical Center
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Organization Time management Multitasking Interpersonal skills Communication Computer skills Required Documents Resume/CV Cover Letter Comprehensive Benefits Package: Coverage begins on day one for health
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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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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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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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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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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
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in contracts to ensure all agreed upon terms are incorporated Input budget information into the Clinical Trial Management System (CRIS/Velos). This job description is not designed to cover or contain a