287 engineering-computation-"https:"-"https:"-"https:"-"https:"-"https:"-"UCL" positions at University of Oklahoma
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daily operations of the office or program by serving as a staff and resource person. Acts as a liaison with internal and external agencies, compiles data, statistics, and other information. Plans events
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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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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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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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. Proficient with computers including data software and Microsoft Office Suite (Outlook, Excel, and Word) Ability to communicate verbally and in writing Ability to be detail oriented. Ability to collect and
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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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environment. Communicate effectively. Engage in repetitive motion. Use of computer and calculator. Equal Employment Opportunity Statement The University, in compliance with all applicable federal and state laws
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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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CLEET Ability to complete complex administrative paperwork Excellent verbal and written communication skills Ability to operate police equipment, i.e., radar, breath alcohol analyzers, mobile computers
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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