262 data-"https:" "https:" "https:" "https:" "https:" "https:" "SciLifeLab" positions at University of Kansas Medical Center
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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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generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time Rate
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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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months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html
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months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html
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patient simulators, lower technology task trainers, medical equipment, computer hardware/software, recording devices and related multimedia technologies used in the training of healthcare professionals and
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. Assist with recruitment, enrollment, and retention activities of participants. Maintain accurate and detailed participant records through timely documentation and data entry, in compliance with university
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or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time Rate Type: Hourly Compensation Statement: The pay range listed for this position is
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employer contribution and additional voluntary 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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Assistant assists in clinical research activities for the Department of Cardiovascular Research including screening, consenting, and collecting information from patients/study subjects. The Clinical Research