OverviewJoin to apply for the Principal Statistical Programmer role at ProPharma.The Principal Statistical Programmer position is responsible for organizing and producing datasets and tables listings and figures for life sciences-related projects including clinical trials.ResponsibilitiesProvide statistical programming and validation for life sciences-related projects including clinical trial datasets and tables, listings, and figures.Coordinate programming activities among the study programmers to achieve timely deliveries.Access and convert data to SAS datasets and other file types from database management system and PC file formats (e.g., Microsoft Excel, text files).Work with external vendors to develop and/or monitor the content and structure of SAS datasets and other files.Oversee programming activities by external vendors (e.g., CROs).Work closely with statisticians and other statistical programmers to generate and validate outputs to ensure accuracy and ensure the quality and soundness of statistical programming algorithms.Provide input to specifications of tabulation and analysis datasets, validation plans, and other related documentsReview data submission packages including define files, and data reviewers guide documents.Mentor less-experienced statistical programmers.Contribute to infrastructure development in the form of macro library and other initiative development.Necessary Skills and AbilitiesIn-depth knowledge of statistical programming within a CRO.Excellent communication and interpersonal skills, with the ability to work collaboratively in cross functional teams and with external partners.Ability to program in SAS and/or R.Educational RequirementsBachelor’s degree in Statistics, Computer Science, Mathematics, or a related discipline, or a combination of other education with 8+ years of relevant work experience.Experience RequirementsOutsourcing industry experience required.Experience with CDISC data structures, such as SDTM and ADaM.Seniority levelMid-Senior levelEmployment typeFull-time
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