SME-Biostats & Stats Prog

About the role

This hybrid role as a subject matter expert in biostatistics and statistical programming focuses on designing programming and validating clinical study analyses using SAS and Base SAS. The professional will support global teams by transforming complex clinical and observational data into reliable statistical outputs that drive regulatory submissions healthcare decisions and innovative therapies ensuring high quality and compliance in every deliverable.

What you'll do

• Transform complex clinical trial and observational datasets into well structured analysis datasets using SAS and Base SAS to enable robust statistical evaluation of…
• Develop maintain and optimize reusable SAS programs and macros that streamline recurring statistical programming tasks and improve efficiency across multiple clinical…
• Create accurate tables listings and figures from clinical data using SAS procedures and data step programming to support study reports and regulatory documentation
• Validate programming outputs through independent code review and rigorous comparison against specifications to ensure consistency traceability and regulatory grade…
• Collaborate closely with biostatistics and data management teams to interpret statistical analysis plans and translate them into detailed programming specifications and…

What you need

• 2–4 yrs of experience
• SAS
• Clinical research
• Data structures
• VBA
• Regulatory affairs
• Any graduate