111 data-"https:" "https:" "https:" "https:" uni jobs at University of Kansas Medical Center
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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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. 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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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
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commitment to excellence and innovation. May participate in relevant committees, task force, or other similar activities. Maintain confidentiality of medical center, employee, and patient information. Handle
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issues identified by the RSC. Ensure information is provided to the investigator and requested changes are made per committee recommendations. Send approval documents to investigator. Function as Chair
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. Perform research and interpretation of experimental results and analysis of data. Prepare manuscripts for publication in scientific journals based on experimental results. Participate in regular
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, collection, compilation, documentation and analysis of clinical research data. The Clinical Research Coordinator will monitor participants’ progress including documenting and reporting adverse events and