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Outstanding candidates will possess the above plus quantitative coursework (e.g. math, statistics, informatics, computer programming), proficiency in statistical programming skills (such as STATA, SAS, or R) and experience in using GIS software such as ArcGIS/ArcGISPro.
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Demonstrated statistical/programming experience and/or applied experience with STATA required, and R is required. Provide statistical analysis and design for reports and presentations.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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In addition, the Principal Statistical Programmer works with management to delegate tasks appropriately, track progress, and provide expert technical support to team members. The Principal Statistical Programmer is a designated member of clinical sub-teams in the role of project lead Statistical Programmer.
Full-timeRemoteExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Sr. Statistical Programmer will create specifications and develop SAS programs for data tabulation, analysis and reporting that comply with regulatory requirements (CDISC SDTM and ADaM), SOPs/ SAP, and lead junior level programming personnel.
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Excellent understanding of the drug development process with relevant experience in statistics and statistical programming is a must-meet criteria. Excellent understanding of the drug development process with relevant experience in statistics and statistical programming is a must-meet criteria.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Reporting to the Lead of Clinical Data Programming, Data Management, the clinical programmer works in varied therapeutic areas, develops and validates SAS/SQL programs and macros, performs data and programming quality checks, generates validation documentation, performs data reconciliation/integration, and liaises with internal teams/external vendor/partners to resolve issues.
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In this role you will be responsible for leading a team of FTEs in Data Management, Statistical Programming, and Biostatistics. You must be able to ensure rigorous statistical input, review, and quality control to uphold proper statistical methods, meet or surpass industry and company data quality standards, and ensure accurate data interpretation both internally and externally.
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Provide statistical input into and perform review of SAPs, table shells, programming and table specifications, TLFS, and statistical sections for integrated reports, statistical sections of CSRs, database design, validation checks and critical data, and data review.
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Demonstrated problem-solving, analytical, and multitasking skills with a good understanding of clinical research, statistical programming and CDISC standards. A technical and innovative role that partners with statistical programming, clinical analytics, data standards, statistical sciences, data sciences and information technology experts to implement next generation clinical data analysis ecosystem.
RemoteExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Good knowledge of statistical programming languages (e.g., SAS, R, Python, etc. Minimum 12-14 years of clinical data management and/or database or statistical programming experience in pharmaceutical industry or health related field.
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Has a demonstrated understanding of clinical data capture/management systems, clinical databases, data flow, and related infrastructure, with experience in/around EDC, EHR, eCOA, IRT, CDR, MDR, SCE and adjacent systems.
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Interest in pediatric environmental health disparities and/or climate change and spatial/GIS research+ Outstanding candidates will possess the above plus quantitative coursework (e.g. math, statistics, informatics, computer programming), proficiency in statistical programming skills (such as STATA, SAS, or R) and experience in using GIS software such as ArcGIS/ArcGISPro.
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Desirable technical expertise (e.g., Windows NT and UNIX operating systems) and familiarity with common software products and technologies used in conjunction with SAS, familiarity with Rave and/or Veeva.
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5+ years of experience in statistical programming/analyses (e.g., SAS, SPSS, Stata, Python, R, or MATLAB) Provide guidance and assist clients in study design, statistical methods, analysis plan, and interpretation.
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Thorough knowledge and understanding of standards development processes, focused on clinical data with a strong knowledge of CDISC, HL7, OMOP, ICH, ISO standards and an understanding of global privacy regulations.
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statistical programming jobs in Woburn, MA
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