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Proficiency in quantitative and qualitative research methods, data analysis, and statistical software (e.g., SAS, SPSS, STATA, NVivo). Collect, manage, and analyze quantitative and qualitative data using appropriate statistical methods and software.
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The Crime Analyst performs a variety of functions involved in analyzing and reporting findings on criminal activity, crime trends, patterns and series, and other related statistical data and information in support of crime prevention and suppression efforts.
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Research and advise management on needs and requirements related to statistical data processing information systems and tools and the retention of appropriate data. Review, analyze, investigate, and integrate statistical information; identify and make conclusions regarding crime series, patterns, trends, hot spots, changes in criminal activity, suspects, etc.
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Use relationship management software, geospatial mapping software, open data platforms, statistical analysis applications, data integration tools, and manipulation techniques. Experience with data mining and statistical software visualization.
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Office administrative tasks such as answering phones, maintaining office organization, managing leads, reporting statistical activity to center manager, scheduling appointments, collecting copays, and handling all medical records in compliance with HIPAA.
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Are you an experienced Statistical Programmer with deep knowledge of clinical drug development? As a Statistical Programming Strategy Lead, Director, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives and join us on an exciting journey to pioneer the future of healthcare.
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Demonstrated experience (preferred) with: Statistical software (e.g., SAS, Stata, or SPSS) and Qualitative data analysis software (e.g., NVivo) Bachelor's degree in public health, communications or social sciences and 8+ years of experience OR Master's degree in public health, communications, or the social sciences and 4+ years of experience in social science research qualitative or mixed methods social science research.
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The Head of Biopharma Biostatistics serves as a leader within the global biostatistics department responsible for strategic and operational oversight of the biostatistics and statistical programming activities for Emmes' biopharma portfolio in key therapeutic areas such as vaccine and infectious diseases, ophthalmology, CNS, rare disease and cell and gene therapy among others.
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3+ years experience with a wide range of advanced statistical techniques and major statistical software (SAS, SPSS, STATA) The sampling statistician will develop survey designs and sampling strategies for household-based surveys and health facility surveys working with host-country partners and will also participate in capacity strengthening activities for national statistical organizations and other data collection partners through training and mentoring.
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Able to independently solve sophisticated problems using tools such as: engineering modeling and simulation tools, design and prototyping tools, statistical analysis, benchtop experiments and analysis, usability engineering tools, design for manufacturability/assembly techniques and design for six sigma.
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Westat is seeking a Principal Research Associate with expertise in qualitative data collection and analysis, learning systems/learning collaboratives, and technical assistance to lead tasks and/or projects for government clients in various health services research areas such as alternative payment models, patient safety, patient experience and engagement, program evaluation, policymaking, health care quality, survey research and statistical analysis.
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You will also support internal Risk Adjustment Data Validation (RADV) monitoring programs and audits, interpret statistical analyses to enhance quality and population health, and collaborate with provider leadership to maintain and enhance risk adjustment accuracy.
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Demonstrated experience in statistical analysis, Six Sigma, Lean Manufacturing, or formal continuous improvement programs. Uses engineering principles, team facilitation skills, and statistical process control tools to measure and improve key processes integral to the manufacturing of printed and unprinted laminated packaging materials for the pharmaceutical and medical packaging industry.
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Experience with industry data standards, including CDISC, SDTM, CDASH, ADAM, and their implementation in statistical programming. R, regression analysis, Hypothesis testing, SAS, Clinical Research, biostatistics, statistical programming.
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Work at the forefront of statistical programming and bioinformatics. Conducting and validating statistical analyses for complex clinical trials. Lead critical statistical analysis for Phase I-IV clinical trials.
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statistical job in Germantown, MD
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