297 algorithm-"Multiple"-"U"-"Simons-Foundation"-"Prof" positions at University of Arkansas
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on-campus teaching responsibilities at multiple campuses and may include live streaming, webinar and online courses. Candidates must possess a thorough knowledge of the teaching field, a commitment to high
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. This position requires travel with multiple overnight stays each month. Sometimes trip schedules include departures/arrivals after hours or on weekends, e.g., departure on a Sunday afternoon or return on a
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. This position requires travel with multiple overnight stays each month. Sometimes trip schedules include departures/arrivals after hours or on weekends, e.g., departure on a Sunday afternoon or return on a
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supervision Ability to follow oral and/or written instructions Ability to perform multiple tasks and to prioritize assignments Ability to perform repetitive manual work Ability to do required lifting (up to 50
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: This position will fill multiple positions. This position works under supervision and provides comprehensive support for the patient care activities. This position may meet, greet, and assists the public
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: This posting will fill for multiple positions for Access Coordinator II and Access Coordinator III The Access Coordinator II works under supervision and provides comprehensive support for the patient
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Qualifications: Advanced degree (e.g., MS, JD, MPH, MBA with regulatory focus, PhD) Relevant professional certification (e.g., CIP, CPIA, CRA, RAPS) Experience managing multiple compliance domains Demonstrated
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will work with multiple ongoing and developing research programs in pediatric subspecialties, providing collaboration in study design, data analysis, and grant application development. May be called
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of developmental disabilities and support needs. This position requires travel within the state and collaboration with multiple stakeholders to promote best practices in supporting young children with developmental
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for multiple clinical trials. The Regulatory Affairs Specialist will manage regulatory compliance and administrative tasks for cooperative group and investigator-initiated cancer clinical trials. The role