273 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Dr" "P" positions at University of Kansas Medical Center
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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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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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assisting with various aspects of research, including participant recruitment, data collection, and compliance with regulatory guidelines. They work under the guidance of principal investigators and research
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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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. 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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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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data at the regional and national levels. Serve on hospital, university, and departmental committees as assigned. This job description is not designed to cover or contain a comprehensive listing of
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Problem solving Interpersonal skills Computer skills Required Documents Resume/CV Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health
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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