151 parallel-processing-bioinformatics positions at University of Kansas Medical Center
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-edge clinical trials and world class research. Job Description: Job Duties : Possess an in-depth knowledge of specimen collection, processing, and shipping requirements for protocols within the Clinical
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the RDO Director, PIs, Co-Is, and partner institutions. Oversee the process of compiling application documentation such as biosketches, letters of support, human subjects section documents, budgets/budget
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to medical and other emergencies, write moving traffic violations and assist other local law enforcement agencies. High school diploma or equivalent. Certified or in process of being certified as a law
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license Work Experience: 2 years of experience with NIH, HRSA, or other federal grant mechanisms. 2 years of experience with IRB processes and clinical research protocols. 1 year of experience with federal
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, eyewash logs, and other required checks. Perform phlebotomy and sample collection, lab processing, handling, and shipping as outlined in study protocols and within KUMC policy. Perform vital signs, height
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champion for process improvements. Reporting directly to the Associate Vice Chancellor Controller, with a dotted reporting line to the Dean of School of Nursing and Dean of Health Professionals, the Director
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for the effective utilization, maintenance, and optimization of the Workday platform. This role ensures data integrity, compliance, and provides technical support to enhance HR processes. The ideal candidate is a
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logs, eyewash logs, and other required checks. Perform phlebotomy and sample collection, lab processing, handling, and shipping as outlined in study protocols and within KUMC policy. Perform vital signs
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families, helping them understand the treatment process and manage any challenges. Participate in research to advance radiation therapy techniques and improve patient outcomes. Teach and train other medical
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clinician/principal investigator. Maintain source documents and submit case report forms as required for clinical trials. Assist clinical staff with sample collection, process, handling, and shipping as