283 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Fraunhofer Gesellschaft" positions at University of Kansas Medical Center
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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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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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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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breast cancer research. This position will assist in entry level clinical research activities including collecting information from patients/study participants and ensuring study activities are performed
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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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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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. 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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Department: SOM KC Cancer Center Clinical Trials ----- Clinical Research - Temps Position Title: Clinical Data Coordinator (Temporary, Part-Time) - Cancer Center Job Family Group: Professional Staff
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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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, collection, compilation, documentation and analysis of clinical research data. The Clinical Research Coordinator will monitor participants’ progress including documenting and reporting adverse events and