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discretion. Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research. Be available to work in more than one environment, travel to meetings, off
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statistical techniques and to adapt existing code to customize statistical analysis strategies.
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funding processes, procedures and techniques Full knowledge of Federal Acquisition Regulation, Code of Federal Regulations, sponsor specific policies, intellectual property policy, conflict of interest
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with the Code of Practice and Risk Assessments. Assist with the organisation and preparation of sports activities. Use and maintain equipment in the department as trained and report immediately any
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, leveraging data integration, workflow automation, and modern Low Code/No Code development tools. The position requires proven experience in cloud ERP solutions and proficiency in summarizing technical
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malicious code in support of high-impact customers, design and develop new analysis methods and tools, work to identify and address emerging and complex threats, and effectively participate in the broader
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operation and maintenance; performing complex coding and programming to make high fidelity digital twins to support nuclear reactors co-located with large-scale data centers; and preparing progress reports
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needed. Works with Medical Information Management to ensure proper ICD10 and CPT4 coding are performed on each claim. Responsible for identifying trends in denials and providing education to clinical staff
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• Proficiency in R, python or other coding languages for data analyses • Tree species identification skills would be highly advantageous • Proficiency in QGIS, CloudCompare, DJI Terra and other remote
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• Proficiency in R, python or other coding languages for data analyses • Tree species identification skills would be highly advantageous • Proficiency in QGIS, CloudCompare, DJI Terra and other remote