Work Flexibility: Onsite We are currently seeking a Senior SAS Programmer, Clinical Data Scientist to join our Joint Replacement Division, this is an Onsite position based in Mahwah, New Jersey.

What you will do 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.Ensure timely delivery of tables, listing, and summaries requested by users using SAS.Develop SAS programs to generate clinical evidence from Real-world data sources (e.g., national registries, hospital registry, commercial datasets, etc.)Periodically review and report on data trends and cleanliness.

Do meta-analysis of data across studies to support business needs.

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.

Support publications by providing reports and statistical analyses to researchers and Investigators.

Interface with biostatistician as needed for complex analyses to support publications and reports.

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 Creation study reporting using RAVE reporting functions, BO4, and SAS/RValidation study summary report using SAS or RParticipate in continuous (breakthrough) improvement activity and process reengineering projects in support of Stryker Orthopaedics’ continuous improvement and global clinical initiatives.

What you need Required Bachelor's Degree in a technical and/or scientific discipline2+ years of SAS programming experience with 1+ years in a clinical environment Demonstrated SAS report programming skills and be able to independently handle in-house SAS related requests Demonstrated working knowledge of statistical methods and principles that are commonly used in clinical trials and be able to assist biostatistician conducting data analysis Working knowledge of data processing, database design and organization in clinical data environment Basic knowledge of Food and Drug Administration (FDA) regulations and Standard operation procedures (SOP) as they apply to clinical studies Preferred Bachelor’s degree in Biostatistics, Statistics, Computer Science, or related fieldM.S. in health/science-related field Industry experience in medical technology or pharma2+ years of experience in clinical data management supporting device or pharmaceutical clinical trials**$100,000.00 - $166,600.00** salary plus bonus eligible + benefits.

Individual pay is based on skills, experience, and other relevant factors.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer.

Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.

Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.

However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.