Statistical Programmer Sr

About the role

Experienced Statistical Programmer with expertise in supporting multiple clinical studies through the development, validation, and delivery of high-quality statistical programming outputs. Proficient in SAS (Base SAS, SAS/STAT, and Macro Language) and CDISC standards, including SDTM, ADaM, and TLF development for regulatory submissions.

What you'll do

• Use of R and AI tools to augment, enhance day to day programming is a huge plus
• Develop specifications and SAS programs for SDTM datasets and clinical data analysis deliverables
• Create specifications and SAS programs for ADaM datasets supporting trial-level reporting and integrated safety and efficacy analyses
• Develop, maintain, and validate Tables, Listings, and Graphs (TLGs) based on biostatistical requirements and Statistical Analysis Plans (SAPs)
• Design and maintain reusable SAS macros to support Phase I–IV clinical trial reporting

What you need

• 8–14 years in pharma & medical sales
• SAS
• Clinical research
• R
• Git
• SQL
• Shell scripting
• B.Sc or M.Sc

Good to have

• Regulatory affairs
• VBA
• SOP writing