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processes, including automation of current manual processes, leveraging the system to automate analysis and identifying other current technology which may provide efficiencies. Support the Central Budget
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staff involved in training, workforce, and continuous improvement activities. Oversee the collection, analysis, and reporting of training, workforce, and continuous improvement activities associated with
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: Develop systems to collect, process, and display CGM and BGM (blood glucose meter) data as structured numerical and graphical elements within the Epic EHR system. Create and maintain note templates and EHR
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resources (Ex: is pathology cancer staging data contained and codified with the clinical data repository; when REDCap might be an appropriate tool). They will conduct analysis and design input/content with
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clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitors study participants’ progress
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, documentation, and analysis of clinical research data. This Clinical Research Coordinator monitors participants' progress including documenting and reporting adverse events. This role participates in periodic
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activities involved in the collection, compilation, documentation, and analysis of clinical research data. Participates in periodic quality assurance audits of protocols. Supports the development of study
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complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitor participants’ progress including documenting and reporting adverse events
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of complex clinical research. Will conduct a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitors participants’ progress
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clinical research. This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical