Senior SAS Programmer (Hybrid)
Role details
Job location
Tech stack
Job description
As the Senior SAS Programmer , you will be responsible for implementation of SAS programming in support of clinical trials, including: generation of data tables, listings and reports using SAS; independent validation of statistical programming; assisting in the preparation of statistical analysis plans; contribution to statistical section of clinical trial protocols; generation of real-world evidence from various data sources, and supporting new and ongoing clinical research initiatives. Ensure timely delivery of tables, listing, and summaries requested by users using SAS.
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Ensure timely delivery of tables, listing, and summaries requested by users using SAS.
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Develop SAS programs to generate clinical evidence from Real-world data sources (e.g., national registries, hospital registry, commercial datasets, etc.)
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Periodically review and report on data trends and cleanliness. Do meta-analysis of data across studies to support business needs.
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Provide programming and statistical analysis support for FDA annual/final submission, post marketing study reports, EU MDR submission, ODEP rating submissions, and publication in professional journals.
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Support publications by providing reports and statistical analyses to researchers and Investigators.
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Interface with biostatistician as needed for complex analyses to support publications and reports.
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Provide input and review statistical analysis plan (e.g., specifications of analysis data sets, pooled data sets, listing, summaries, figures, and tables) for Investigational Device Exemption (IDE) clinical studies, post-marketing studies, and other Real-world clinical trials
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Creation study reporting using RAVE reporting functions, BO4, and SAS/R
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Validation study summary report using SAS or R
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Participate in continuous (breakthrough) improvement activity and process reengineering projects in support of Stryker Orthopaedics' continuous improvement and global clinical initiatives.
Requirements
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Bachelor's Degree in a technical and/or scientific discipline
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2+ years of SAS programming experience with 1+ years in a clinical environment
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Demonstrated SAS report programming skills and be able to independently handle in-house SAS related requests
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Comfortable working with AI-enabled tools (e.g., AI-assisted coding, data exploration, or documentation) and willing to adopt new analytical technologies.
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Strong programming fundamentals with the ability to learn and apply additional languages, tools, or platforms as needed.
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Demonstrated working knowledge of statistical methods and principles that are commonly used in clinical trials and be able to assist biostatistician conducting data analysis
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Working knowledge of data processing, database design and organization in clinical data environment
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Basic knowledge of Food and Drug Administration (FDA) regulations and Standard operation procedures (SOP) as they apply to clinical studies
Preferred
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Bachelor's degree in Biostatistics, Statistics, Computer Science, or related field
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M.S. in health/science-related field
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Industry experience in medical technology or pharma
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2+ years of experience in clinical data management supporting device or pharmaceutical clinical trials
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Experience working with cloud-based data platforms such as Snowflake, Databricks, Azure, or AWS
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Experience with additional programming languages such as R and/or Python for statistical analysis, automation, or advanced analytics