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Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.
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2+ years of expertise using database management (e.g., MS-Access) and statistical programming (e.g., SAS) required. The Associate Director, Pharmacoepidemiology position provides epidemiologic, methodological, and analytic support to Daiichi Sankyo products.
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Associate Director, Pharmacoepidemiology. This position independently carries out various functions (e.g., literature reviews, study design, preparation of data for statistical analysis to obtain background rates) for development of safety documents (e.g., RMP), support SMTs, SERM or other safety-related meetings and study protocols.
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Participate in data review along with biostatistics and statistical programming team. The Director, Clinical Data Management (CDM), will provide data management support to clinical studies within the Biometrics function, and would be responsible for all CDM related areas/activities for clinical studies assigned.
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Proficient in statistical programming languages such as Python, R, SAS, or SPSS as well as SQL (incl. As a member of our team, you will report directly to the Associate Director, Display & Video Marketing.
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The Associate Director, Statistical Programming is accountable for program specific statistical programming activities and oversight related activities by vendors in clinical development, maintaining programming infrastructure and ensuring compliance with SOPs to produce quality and timely deliverables.
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The purpose of this job is to provide statistical programming technical support to DSI project teams on all statistical programming deliverables and programming submission.
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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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Proficiency in R programming language and other statistical software, including EAST. Proclinical Staffing is seeking an Associate Director Biostatistics to join a cutting-edge pharmaceutical company.
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Associate Director Biostatistics - Permanent - Remote. Manages CRO statistical and programming support. Consults with Research & Preclinical colleagues on statistical questions in their work.
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Collaborates with Statistical Programmers on summary and analysis of trial data. Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts.
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Develop statistical sections of clinical development plans, protocols, statistical analysis plans, and key specifications for statistical programming implementation of analyses.
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Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation. Provides statistical support and leadership to address health authority request, publication, presentation, and other public release of information.
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The Associate Director for RNA Screening & Assay Development is not just a technical on-site role at our Seaport location but also a strategic one. Use a variety of software packages and write scripts for programming liquid handlers (in-house and third-party tools), designing and viewing DNA sequences, processing data, and performing statistical analysis (Spotfire, Python, JMP) laboratory information management system (LIMS), database management (in-house and third-party tools), and third-party lab instrumentation and automation software.
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Principal / Associate Director, Statistical Programmer - Biotech - California. Partnered with an exciting Biotech seeking a Principal / Associate Director, Statistical Programmer to join their team.
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