38 master-"https:" "https:" "https:" "https:" research jobs at University of Kansas Medical Center
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trials. Maintain trial regulatory documentation files including correspondence with sponsor/CRO, IRB, and subjects. Provide written and verbal reports to the Principal Investigator and Research Project
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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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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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, general paperwork, scheduling, procurement, and correspondence. Assist the Principal Investigator with day-to-day administrative tasks and research coordination. Edit and format grant proposals and
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research studies and interpret data under the mentorship of the Principal Investigator (PI). Work independently and collaboratively on research projects. Participate in the design and execution
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, analyzing, documenting, and drawing preliminary conclusions from experimental results. The research assistant collaborates with the principal investigator to design and perform experiments with a limited
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, document and draw tentative conclusions from experimental results. Confer with principal investigator to review work assignments and develop plans for research experiments; make minor modifications
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: Training, mentorship for team members and study teams. Assigned unit administrative support (inventory, ordering, billing, scheduling). Assist Principal Investigators, physicians and/or nurses with special
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are individuals who have received their terminal degree and who have opted to pursue further training in a postdoctoral appointment. Postdoctoral scholarship is a time-limited appointment, the primary purpose
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sponsored studies. Consults with the study coordinator and /or the principal investigator regarding potential eligibility as appropriate. Conduct Informed Consent Interviews with participants and study