808 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "University of Waterloo" positions at University of Colorado
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Journeyman Plumbers license or better. o Assist with equipment data entry within WebTMA. § (5%) Snow & Ice Mitigation o Operate snow removal equipment and apply de-icing materials as needed. o Ensure
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payroll distributions · Work with Department Administrators on Payroll distributions and PETs Assist PASS Core/PIs with other support (OS) and progress report (RPPR) information – 10% · Maintain
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, healthcare administration, public administration, communications, information systems, or a directly related field from an accredited institution. Three (3) years of professional experience in higher education
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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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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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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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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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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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essential information and determine response level. Dispatch appropriate services (police, fire, ambulance, rescue, facilities, security, parking, etc.) using a Computer Aided Dispatching (CAD) system
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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