788 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UCL" "UCL" "UCL" positions at University of Colorado
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communicate and present data to stakeholders Collaborate with Research Services Program Director and Research Administrative Team on various projects including helping monitor study coordinator time/utilization
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and audits. The incumbent is responsible for data entry and resolution, study subject advocacy; and possible management of studies at the local level. Examples of Work Performed by the Clinical
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System Administration . Position Summary: University Information Services (UIS) provides IT services and enterprise applications to the University of Colorado (CU) campuses and the Office of the President
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will provide professional guidance regarding the conduct/flow of the research projects and is critical in the design of research processes. This position will also provide specialized guidance in data
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to begin to maintain their own technology portfolio and work more independently as they progress. The position requires the use of a variety of communications and computer database tools to track, convey
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; sets the tone for a positive experience Checks patients in and out for appointments, schedules follow-up appointments at the time of discharge Verifies patient and insurance information, while accurately
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nationally. The Clinical Research Coordinator is responsible for participant recruiting, consenting, scheduling, performing study visits, processing lab samples, entering data and other study-related duties
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, physiology, and medical terminology. Ability to interpret and master complex research protocol information. Comprehensive understanding of molecular biology, lung physiology, and sterile tissue culture
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programmatic communication and marketing efforts. · Assist the Finance Manager, Business HR Partner and other administrative staff with project support, data gathering, entry and administrative support
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current medication information, review the research protocol inclusion/exclusion criteria, and confirm the eligibility of the subject to participate in the clinical trial Perform the informed consent