254 cloud-computing-"https:"-"https:"-"https:"-"https:"-"https:"-"BioData" positions at University of Oklahoma
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. Skills: Ability to communicate effectively Ability to prioritize work Basic computer skills Certifications: None Advertised Physical Requirements: Physical: Standing for prolonged periods. Manual dexterity
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, trade shows, meetings, and industry events. Position involves standing or sitting for extended periods during meetings, presentations, or computer work. Environmental: Standard office environment
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that could be right for you! The Clinical Trials Manager in the Clinical Trials Office Tissue Lab provides senior administrative management to the clinical trials program for the Tissue Lab by overseeing
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*Senior Data Specialist - Job Number: 260114 Organization : Medicine Infectious Diseases Job Location : Oklahoma-Oklahoma City-Health Sciences Center Schedule : Full-time Work Schedule: Monday - Friday, 8AM - 5PM Work Type: Onsite Salary Range: Commensurate based on experience Benefits...
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, provides administrative support to a state or national level sponsored grant or contract program by coordinating the program activities, attending meetings, preparing reports, recruiting for the program
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advisement to students regarding their financial aid options, to make informed decisions about their educational expenses. Providing detailed information to a student about the costs of their program and what
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Office (CTO) click here. Duties: Patient Recruitment and Scheduling. Identifies, recruits, and schedules patients who may be eligible to participate in the oncology clinical research program. Assessment
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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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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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patients who may be eligible to participate in a clinical trial or research program, distribute information, act as a clinical resource, manage data, and conduct follow-up care for patients within