54 web-programmer-developer "https:" "https:" "https:" "U.S" research jobs at University of Kansas Medical Center
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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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efforts, and follow-ups. Prepare and organize research study materials, including participant packets, consent forms, and regulatory documentation. Schedule study-related appointments and coordinate
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Recruit and educate patients for clinical trials. Evaluate potential patient eligibility for clinical trials. Maintain source documents and case report forms (CRF's) for clinical trials. Perform subject
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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 Employee Type: Regular Time
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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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is available after 12 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
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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 Employee Type
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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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. 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 Employee Type
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educate patients for clinical trials. Evaluate potential patient eligibility for clinical trials. Maintain source documents and case report forms (CRF's) for clinical trials. Perform subject visits