Senior Statistical Programmer (R)

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Remote, 12-month, renewable contract (long-term potential)

Senior Statistical Programmer (R)

Summary
Clinical statistical programmer with hands-on ADaM/TLF production and validation experience in R, supporting clinical study reporting alongside existing SAS workflows.

Responsibilities

• Develop and validate ADaM datasets and TLFs in R for clinical study reports and regulatory submissions
• Perform independent QC/double programming of SAS and R outputs
• Build reusable R code for data visualization, exploratory analysis, and statistical summaries
• Collaborate with biostatisticians and study teams on SAPs, specs, and timelines
• Support the team’s R infrastructure and reproducible programming practices

Requirements

• BS/MS in Statistics, Biostatistics, Mathematics, or related field
• 5+ years of statistical programming experience in pharma/biotech
• Strong R programming skills, including tidyverse, RMarkdown/Quarto, and Git/GitHub
• Experience producing ADaM datasets and TLFs in R, ideally with pharmaverse packages (admiral, rtables/tern)
• Applied experience with CDISC SDTM/ADaM
• SAS experience, to work alongside existing SAS code

Additional skills

• Shiny app development a plus, including user access control (e.g., rAccess, shinymanager, Posit Connect) and app deployment
• R package development, GxP validation, and Linux/shell scripting experience a plus

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