Senior Statistical Programmer (R)

Simulstat Inc.
United States
about 1 month ago
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Role details

Contract type
Temporary contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Working hours
Regular working hours
Job source

Tech stack

Data Analysis Data Visualization Linux R (Programming Language) Package Development Process SAS (Software) Shell Script Software Engineering GXP

Job description

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