A company is looking for a Principal Statistical Programmer to manage and coordinate statistical programming activities for cardiac safety trials.
Key ResponsibilitiesProduce and maintain submission-ready datasets in support of cardiac safety trialsManage statistical programming staff, including work allocation and professional developmentDevelop and implement data standards and processes for cardiac research and regulatory submissionsRequired Qualifications and EducationPh.
D. with 5+ years of related industry experience or MS with 7+ years of related industry experienceMinimum of 9 years' experience in SAS products and procedures in a pharmaceutical or life sciences settingExperience with CDISC SDTM and ADaM standardsUnderstanding of the pharmaceutical drug development process, with at least two years in the industryExperience in clinical trials within a CRO or pharmaceutical research organization
Principal Statistical Programmer
A company is looking for a Principal Statistical Programmer to manage and coordinate statistical programming activities for cardiac safety trials. ...
Principal Statistical Programmer
Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming.Generating and validating SDTM and Adam datasets/analysis files, and tables, listings, and figures (TLFs).Production and QC / validation programming.Abilit...
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