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Proficiency with statistical programming in SAS and/or R. The Associate Director/Director Biostatistics is responsible for providing technical leadership and biostatistical support to Clinical Development through the design and conduct of clinical studies; review and accuracy of clinical data; the evaluation, interpretation, and reporting of study results; and regulatory submissions to the FDA and other regulatory agencies.
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The Real World Statistics Associate Director will perform sophisticated scientific statistical analyses in support of the company's post-marketing areas for Global Medicines Development and Affairs and Commercial and Strategic Management, with minimal guidance on new and complex issues.
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Proficiency with a statistical programming language (preferably R). The Missouri Prevention Science Institute is recruiting for a full-time research associate to assist with the management of data across many large-scale community-, agency-, and school-based studies of social, emotional, behavioral, and educational development of youth, adults, and families.
$42,800 - $56,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Harmony Biosciences is recruiting for an Associate Director, Biostatistics in our Plymouth Meeting, PA location. Strong programming skills in SAS; proficiency with R programming is a plus.
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The Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.
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As a Statistical Project Leader (Associate Director) in our Statistical Innovation Hub, you will provide technical expertise in psychometric analysis to support establishment o novel digital endpoints or re-engineering of existing endpoints from (digital) clinical outcome assessments (COAs.
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Statistical Project Leader (Associate Director) page is loaded. Advanced R programming skills and good understanding of SAS programming. At Sanofi, we have a shared commitment to bring innovation to a broad and diverse portfolio of therapeutics supported by our Biostatistics and Programming department.
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Strong knowledge of fixed income risk and the competitive environmentPhD or master’s degree in financial engineering, Science, Technology, Engineering or MathematicsStrong knowledge of probability theory, statistics, linear algebra, and numerical methodsExperience wor8king with large data sets, statistical data analysis, building multivariate regressions modelsGood programming skills, preferably using the languages Python, C.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Manage CRO statisticians and internal biostatistics team, including junior statistician, contract statistician and programming team in support of biostatistics operational activities. Develop and/or review statistical documents or deliverables for clinical trials including Statistical Analysis Plan (SAP) and integrated summaries of drug efficacy and safety, TFLs, interim analysis plan and others.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Associate director: Experience leading the statistical execution of a clinical trial as a study lead or indication lead. Experience utilizing statistical software for design and analysis of clinical trials (e.g., SAS, R, EAST, FACTS)Proficient R programming skills are required.
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Proficiency in R programming language and other statistical software, including EAST. Manages CRO statistical and programming support. Consults with Research & Preclinical colleagues on statistical questions in their work.
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Managing the technical assistant/associate director(s), psychometrician(s) and research specialist(s), as well as statistical programming at the TIMSS and PIRLS International Study Center.
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Proclinical Staffing is seeking an Associate Director Biostatistics to join a cutting-edge pharmaceutical company. Associate Director Biostatistics - Permanent - Remote. Collaborates with Statistical Programmers on summary and analysis of trial data.
RemoteExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts. Experience programming in SAS. Provides statistical guidance on conduct of ongoing trials.
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Contributes to or prepares statistical analysis plans. Experience with CDISC, including SDTM, ADaM, CDASH. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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