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Senior Managers of Statistical Programming provide comprehensive programming expertise to clinical project teams to lead statistical programming teams and support the development, regulatory approval and market acceptance of Bristol Myers Squibb products.
$130,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provide functional expertise and leadership to statistical programming and data science colleagues while delivering comprehensive programming expertise to clinical project teams in support of development, regulatory approval, and market acceptance of company’s products.
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Programming Skills - knowledge of statistical programming languages like R, Python, and database query languages like SQL, Hive, Pig is desirable. Proficiency with Python or Scala programming.
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Review key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements.
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What The Role Is As a part of the fundamentals & structuring team, the quant modeler will be responsible for a variety of activities from short and long-term econometric or statistical analysis of power markets and adding quantitative power to fundamental market analysis to assisting structuring and BESS modeling activities and supporting trading/optimization/hedging.
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Solid knowledge of Statistical Analysis System (SAS) programming and knowledge of statistical software (e.g., R, S-Plus, nQuery, EAST). Oversees implementation of statistical analyses, including data monitoring, programming and complex modeling.
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As The Director, Statistical Programming, you will be a champion of Otsuka's culture and values and serve in a leadership role within the Statistical Programming group. Serve as the in-house expert and key advisor to head of the Statistical Programming group on the programming strategy by providing assessment of state-of-art and industry trends in ways of working, efficient coding such as macro library and utility macros, and technology.
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Qualifications & Experience PhD (9+ years experience) or MS (11+ years experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience, Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation.
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Familiarity with at least one software package for statistical analysis (R, Stata) is desired. Strong computer skills, including programming, and grant writing experience are preferred.
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Collecting data from web samplesproficiency with Qualtrics is a priority, and familiarity with HTML/CSS/Javascript/PHP is a plus. Position requires minimum BA or BS degree in Psychology or related social science field or discipline.
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The biostatistician in this role provides study-level statistical expertise in support of the design, analysis, and interpretation of clinical trials through collaboration with other team personnel including clinical research, clinical operations, data management, and programming.
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Two years of experience in managing and coordinating statistical analysis and data processing operations and in performing data analysis by utilizing various types of statistical software packages or programming languages (e.g. SAS, SPSS, or R) is required.
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Represent the biostatistics function in supporting the design, analysis, and interpretation of clinical trials through collaboration with other functions including Clinical Research, Clinical Operations, Data Management, and Programming.
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Four years of experience in managing and coordinating statistical analysis and data processing operations and in performing data analysis by utilizing various types of statistical software packages or programming languages (e.g. SAS, SPSS, or R) is required.
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Minimum 12 years of experience in biostatistics or statistical programming activities in the Pharmaceutical/Biotechnology industry in clinical development with excellent knowledge of CDISC ADaM and SDTM, ICH Statistical and Clinical Report Guidelines and proven experience in the development of processes/tools.
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statistical programming jobs in Princeton, NJ
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