40 algorithm-development-"Multiple"-"Simons-Foundation"-"Prof"-"UNIS" positions at University of Kansas Medical Center
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Investigator and Clinical Research Coordinator, as required. Recruit, evaluate, and educate patients regarding clinical trials following established procedures and protocols. Conducts Informed Consent Interviews
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assignments and develop plans for research experiments. Make minor modifications to existing laboratory procedures and techniques to meet the needs of the equipment as required. Review laboratory methods manual
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: Extensive programming experience in multiple scripting languages, especially with a biological background Job Duties Outlined: Use programming knowledge to help shape the scientific environment and
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will engage in developing models and finding therapeutic approaches addressing the late effects of radiation therapy. A broad range of skills including tissue culture, animal models of oral cancer
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Clinical Research Coordinators (CRCs) with study setup, participant recruitment efforts, and follow-ups. Prepare and organize research study materials, including participant packets, consent forms, and
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seminars, reviews, and prepare related agendas, reports, and documentation. Support onboarding and training of new lab members, including introducing lab protocols and standard operating procedures. Support
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such as ELISA and Luminex-based multiplex assays using various biological samples, including rodent and human plasma, serum, nasal fluid, and cell culture media. Prepare data summaries for communication
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kidney diseases. The candidate will be expected to contribute with research staff in the laboratory and develop leadership skills. More information about Dr. Sharma's lab is available at: https
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. This is a part-time limited-term position at 20 hours a week ending on 6/5/2026. Job Description: Help develop and implement new and revised policies and procedures affecting tobacco treatment services
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efforts, and follow-ups. Prepare and organize research study materials, including participant packets, consent forms, and regulatory documentation. Schedule study-related appointments and coordinate