Senior Oncology Statistical Programmer Sas
Connect Life Sciences
Lead clinical trial programming with SAS, CDISC, SDTM, and ADaM expertise in oncology statistical programming. Prepare submission-ready data and outputs.This senior statistical programmer supports all statistical programming activities for clinical data. The work includes conversions, analysis datasets, study TFLs, and programming specifications. You will also contribute to best practices, implementation guides, and customer requirements.Key Responsibilities:
Prepare clinical data for submission using CDISC or customized standardsDevelop SAS programs for conversions and analysis datasetsProgram study TFLs from SAPs and shellsReview data conversions, datasets, outputs, and programmingCreate programming specifications for SDTM, ADaM, and derived dataRequirements:
Bachelor’s degree in statistics, computer, or life scienceMinimum eight years programming on clinical trialsGood knowledge of TFL programmingExperience with CDISC SDTM and ADaM standardsExperience preparing Reviewer’s Guide and Define.Xml documentsApply senior SAS programming expertise to oncology clinical trials, CDISC standards, TFLs, and submission-focused statistical programming.
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Prepare clinical data for submission using CDISC or customized standardsDevelop SAS programs for conversions and analysis datasetsProgram study TFLs from SAPs and shellsReview data conversions, datasets, outputs, and programmingCreate programming specifications for SDTM, ADaM, and derived dataRequirements:
Bachelor’s degree in statistics, computer, or life scienceMinimum eight years programming on clinical trialsGood knowledge of TFL programmingExperience with CDISC SDTM and ADaM standardsExperience preparing Reviewer’s Guide and Define.Xml documentsApply senior SAS programming expertise to oncology clinical trials, CDISC standards, TFLs, and submission-focused statistical programming.
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Vacancy posted 1 hour ago
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