832 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "IFM" "IFM" "IFM" positions at University of Colorado
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, laws, university policies, and business contracts. The position requires the use of a variety of communications and computer database tools to track and convey issues and decisions about invention
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, division, and departments. Responsible for tracking accurate and timely position data and records. Coordinate and attend various career fairs, career and recruitment events, and other events such as the RMDC
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accuracy and timely completion. Participating in advisory sessions to help faculty understand requirements, timelines, and process expectations. Maintaining and updating faculty information across
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on unemployment claims which includes documentation review to determine eligibility, processing, responding to claims, analysis/tracking of data, and management of communications. This role also responds to State
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patient’s potential financial liability directly to the patient prior to medical services being rendered based on insurance verification data and medical cost estimates. Obtain insurance authorization and pre
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recruitment Collect physiological and psychological data from study participants Collaborate with other members of the team Coordinate research participant activities across research sites, including
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. Experience calculating lab results and data using math and analytical skills. Experience with developing reports, spreadsheets and databases using Microsoft Office software. Experience entering data
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Emergency Department Research Provide project management skills (technical and soft skills) that effectively manage the Data Analytics Team. This includes: Successfully managing all current and future work
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topics, functions, and processes with senior management of the School of Medicine and its departments, educational institutions, CME staff, and the public. 40% - CME Data Management and Accreditation
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information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed consent