102 master-"https:" "https:" "https:" "https:" positions at University of Kansas Medical Center
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-edge clinical trials and world class research. Job Description: Job Responsibilities Under the direction of the principal investigator, recruit and educate potential patients for and evaluate potential
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of the principal investigator, recruit and educate potential patients for and evaluate potential patient eligibility for clinical trials. Maintain source documents and submit case report forms (CRFs) as required
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research career. The fellow conducts research under the guidance of a Principal Investigator (PI), engages in professional development activities, and contributes to independent and collaborative research
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intellectual or developmental disabilities, their families, and service providers. The primary responsibility is delivering training on evidence-based practices, including behavior analysis, autism interventions
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benchmarks, and contributes to the credibility and effectiveness of the role within the university community. Certifications/Licenses: Licensed or licensable in the State of Kansas (primary) and Missouri by
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treatment systems. Maintains primary responsibility for clinical radiation therapy equipment operations, including workflow through the department. Identifies and resolves daily operational issues related
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Principal/Co-Investigator. Train and educate students, residents, fellows, and faculty in a research setting. Obtain extramural/internal grant funding to support laboratory/research team. Mentoring and
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written and verbal reports to the Principal Investigator and Research Project Manager, as required. This job description is not designed to cover or contain a comprehensive listing of activities, duties
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as the primary departmental timekeeper, ensuring accuracy and compliance with institutional guidelines. Coordinate Promotion and Tenure (P&T) processes by managing documentation and timelines in
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procedures, investigational product accountability, regulatory and Trial Master File documentation, and correlative laboratory collection and shipment records. Oversee clinical trial data collection to confirm