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and analysis of clinical research data. Monitor participants’ progress including documenting and reporting adverse events. Participate in periodic quality assurance audits of protocols. Job Description
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collection. Participate in regular communication with the PIs via lab meetings and personal meetings. Gather data and its analysis for the preparation of published papers, as well as assistance on grant
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Python or R for data manipulation and analysis. Preferred Qualifications Education: Master’s degree in biomedical informatics, computer science, data science, or a related field. Education may be
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, and constituent groups of KUMC and TUKHS. Coordination and communication with ZIEL employees related to KUMC, TUKHS, and ZIEL policies and procedures. Additional functional areas that serve across ZIEL
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, the candidate will be involved in developing purposeful, scientifically sound, imaging and analysis approaches for an accurate representation of brain physiology. The lab focuses on identifying the best
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which includes monthly analysis of area forecasts, monitoring of compliance with the budget policies and funding source compliance, budget funding and process improvement consultation with area management
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, documentation, and analysis of clinical research data. The Clinical Research Coordinator monitors participants' progress including documenting and reporting adverse events and participates in periodic quality
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) for scalable data analysis and infrastructure development. Experience in causal inference methods for observational data. Experience and working knowledge of SQL and R. Established track record in teaching and
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captures and uses data about medical students from pre-med through practice and supports daily operations and integrated data analysis for the offices of the SoM, from both custom software and third-party
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analysis of clinical research data. Monitors participants' progress including documenting and reporting adverse events. Participates in periodic quality assurance audits of protocols. This position will be