2,729 data "https:" "https:" "https:" "https:" "Inter University Center for Japanese Language Studies" positions at Duke University
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of liability/payment. Admit, register and pre-register patients with accurate patient demographic and financial data. Resolve insurance claim rejections/denials and remedy expediently. Evaluate diagnoses
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Health Sciences. The position will be focused primarily on analyzing data from projects related to emergency medical services, focused on stroke care, and climate change implementation science. This role
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clinical data as relates to event reporting. Completes or manages appropriate report and dashboard documents and keeps stakeholders informed. • Report data to Clinical Registry. • Collect and interpret
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• Proficient in chart review and able to assess needs quickly • Strong with the use of computer software tools and data files • Comfortable with continuous change and is self-motivated • Able to help build and
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, register and pre-register patients with accurate patient demographic and financial data. Resolve insurance claim rejections/denials and remedy expediently. Evaluate diagnoses to ensure compliance with
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with accurate patient demographic andfinancial data. Resolve insurance claim rejections/denials and remedy expediently. Calculate and collect cash payments appropriately for all patients. Reconcile daily
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. Check-in patient upon arrival in the practice. Identify correct patient information in Maestro Care. Verify patient demographic data. Edit Maestro Care as needed. Accurately identify the appropriate
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Intensive Care Unit in the Duke University Health System (DUHS). This position will perform physical exams, collect and documents data, conduct diagnostic and therapeutic procedures, order and schedule
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Ability to use sensory and cognitive functions to process and prioritize information, treatment, and follow-up Ability to use fine motor skills Competent in BLS and/or other specialized life support
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, prepares for study monitoring and audit visits. Under supervision, may document some participant-level information for non-complex (e.g., questionnaire, data registry, scripted) studies outside of the EHR