54 web-programmer-developer "https:" "https:" "https:" "UCL" "UCL" research jobs at University of Kansas Medical Center in United States
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: Professional Staff Job Description Summary: The Clinical Research Assistant in the Department of Internal Medicine, Division of Medical Oncology will work with the Melanoma program. This position will be
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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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proposals or other funding submissions. Professional Development & Mentorship Participate in seminars, workshops, and professional development activities. Develop and follow an Individual Development Plan
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Description: Job Duties Recruit, evaluate, and educate participants regarding clinical trials following established procedures and protocols. Conducts Informed Consent Interviews with participants and where
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opportunities to provide lectures and/or small group teaching. Develop and follow an Individual Development Plan (IDP). Mentor graduate or undergraduate students, interns, or trainees. Present research findings
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professional development activities. Develop and follow an Individual Development Plan (IDP). Mentor graduate or undergraduate students, interns, or trainees. Present research findings at meetings. Compliance
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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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activities. Develop and follow an Individual Development Plan (IDP). Mentor graduate or undergraduate students, interns, or trainees. Present research findings at meetings. Compliance Maintain accurate and up
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. The program also supports professional development through completion of supervised practice hours and preparation for licensure. Qualified fellows may have opportunities to provide teaching and supervision
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) with study setup, participant recruitment efforts, and follow-ups. Prepare and organize research study materials, including participant packets, consent forms, and regulatory documentation. Schedule