34 developer-"https:" "https:" "https:" research jobs at University of Kansas Medical Center
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requested information and support. Job Description: Job Duties Recruit, evaluate, and educate participants regarding clinical trials following established procedures and protocols. Conduct Informed Consent
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physical activity and nutrition strategies across the lifespan, with attention to individuals with typical and atypical development in both urban and rural settings. The Division has a major research mission
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closely with Dr. Dhawan and the other researchers in her lab at KU Medical Center (KUMC) to assist in the successful development and completion of basic science research studies in pancreatic cancer
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: The Postdoctoral Fellow in the Department of Pathology & Laboratory Medicine (laboratory of Professor Soumen Paul) participates in research investigating stem cell biology and mammalian development, particularly
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Duties Recruit, evaluate, and educate participants regarding clinical trials following established procedures and protocols. Conduct Informed Consent Interviews with participants and when required
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Description: Key Roles and Responsibilities: Research Overview: Develop and perform synthesis of multiple small molecule platforms in collaboration with principal investigators of KUMC, KUCC and from other
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: Under the direction of the Research Project Manager, may assist in recruitment, evaluation, and education of patients regarding clinical trials following established procedures and protocols. Develop and
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. Contribute to the development of study protocols, manuals of procedures, and regulatory documentation. Assist with preparation of grant proposals and scientific manuscripts. Maintain accurate and up-to-date
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, scheduling, procurement, and correspondence. Maintain regulatory paperwork for research studies. Recruit, evaluate, and educate patients regarding clinical trials following established procedures and protocols
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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