253 professor-computer-"https:"-"https:"-"https:"-"https:"-"https:"-"Keele-University" positions at University of Oklahoma
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contracts. Experience coordinating a large program. General accounting experience. Proficient in Microsoft Office, specifically Excel. Great attention to detail. Highly organized. Working Conditions: Standard
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. Develops budgets for all grant submissions and may assist key program leadership in the preparation of grants. Works closely and collaboratively with the Director of Post-Award, Office of Research Services
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job opportunity that could be right for you! The Clinical Trials Manager – Regulatory Affairs provides senior administrative management to the clinical trials program by overseeing, training and
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Information Provider (PIP). Assesses community needs and implements appropriate poison prevention strategies; develops evaluation tools to measure program effectiveness. Maintains Oklahoma Poison Center social
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, Psychology, Engineering, Computer Science, Sociology, or a related discipline aligned with the specific area of research or project focus), AND: 1 year of experience supporting research or working in a
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reports and correspondence, distributing information, conducting research and computation, managing office procedures, assisting with budget preparation, and coordinating activities. Serves as a payroll
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, program evaluation, data collection, or support roles in academic or community-based research settings. Knowledge, Skills, & Abilities: Clear and professional written and verbal communication, including
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*Marketing/Communication Coordinator - Job Number: 260456 Organization : Dept of Pediatrics Job Location : Oklahoma-Oklahoma City-Health Sciences Center Schedule : Full-time Work Schedule: M-F 40 hrs per week Work Type: Onsite Salary Range: Targeted salary of $60,400 annually, based on...
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technical and instructional support for the simulation operations. Responsible for operating and maintaining simulation and computer equipment to include but not limited to all hardware and software
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procedures. Enters data and maintains on-going compliance with NCI Clinical Trial Reporting Program requirements. Coordinates schedules, formulates agendas and takes minutes for all PRMS related meetings