263 master-"https:" "https:" "https:" "https:" "UCL" positions at University of Kansas Medical Center
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the Institution. However, the position’s primary goal will be to ensure adequate support to faculty, including overseeing the management of extramural funds while providing various services and technical support to
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-edge clinical trials and world class research. Job Description: Job Responsibilities Under the direction of the principal investigator, recruit and educate potential patients for and evaluate potential
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with a 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
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with sponsor, KUMC IRB, and subjects. Provide written and verbal reports to the Principal Investigator and Project Manager, as required. This job description is not designed to cover or contain a
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Operations Manager, this position is responsible for providing comprehensive operational and administrative support to a large and still growing clinical research program. The primary function
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primary contact for The University of Kansas Cancer Center (KUCC) Clinical Trials Organization (CTO), the Program Coordinator will serve as the liaison between the KUCC CTO, Sponsors, and Vendors. Will
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procedures, investigational product accountability, regulatory and Trial Master File documentation, and correlative laboratory collection and shipment records. Oversee clinical trial data collection to confirm
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, primary/secondary electrical control systems, pneumatic valves. Water treatment testing and proper record keeping/documentation. Operation and maintenance of a three-tier domestic water treatment system
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tasks assigned by the principal investigator and other faculty members in the laboratory. Handle pancreatic cancer mouse models by following laboratory protocols. Perform molecular and cell biology
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the direction of the principal investigator. Maintain source documents and submit case report forms (CRFs) as required for clinical trials. Recognize and report adverse events/serious adverse events