Senior SAS Programmer (Onsite)

We are currently seeking a Senior SAS Programmer, Clinical Data Scientist to join our Joint Replacement Division , this is an O nsite 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/R

• Validation study summary report using SAS or R

• Participate 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 discipline

• 2+ 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 field

• M.S. in health/science-related field

• Industry experience in medical technology or pharma

• 2+ 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.