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procedures. Maintain trial regulatory documentation files including correspondence with sponsor, KUMC IRB, and subjects. Assist faculty in preparation of IRB submissions and NIH human subjects research
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FDA CFR. Work closely with the Research Institute and Human Research Protection Program and have a working knowledge of KUMC policies and procedures. Attend continuing education, research and training
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://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time
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, improvise, and remain flexible to changing or competing requirements, schedules, priorities, and efforts. Communicate and act in a professional, clear, and understandable manner through written and verbal
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/human-resources/benefits.html Employee Type: Regular Time Type: Full time
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://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time Rate Type: Hourly Compensation Statement: The pay range listed for this position is determined by our compensation program