266 engineering-computation-"https:"-"https:"-"https:"-"https:"-"https:"-"BioData"-"BioData" positions at University of Oklahoma
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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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seven professional colleges. This position coordinates a clinical research program by identifying and assessing patients, distributing information, acting as a clinical resource, managing data, conducting
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eligible to participate in a clinical trial or research program, distributes information, acts as a clinical resource, manages data, conducts follow-up care for patients, and attends meetings pertaining
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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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customers. Performs statistical, business research, and routine computations that require knowledge of mathematics. Calculates service costs and issues service contracts for on and off campus vendors. Assesses
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physicians, promoting a team approach to strategic planning and the development of a full continuum specialty program. Knowledge of the regional and national healthcare environment a plus. Highly developed
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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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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