Clinical SAS Programmer (SAS/R)

Company: princeps technologies
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Job Description:

Job Title: Clinical SAS Programmer (SAS/R)

Experience: 8+ Years (SAS) | 3+ Years (R)

Location: UK/USA

Job Overview

We are seeking an experienced Clinical SAS Programmer with strong R expertise to join our growing Early Phase SAS Programming team. In this role, you will be responsible for developing, validating, and maintaining SAS and R programs to support clinical trial reporting, data analysis, and visualization.

You will work closely with biostatisticians and cross-functional teams to deliver high-quality outputs that enhance the efficiency, quality, and success of early-phase clinical trials. This role reports to the Early Phase Programming Lead and requires the ability to work independently with minimal supervision.

Key Responsibilities

  • Develop, validate, and maintain SAS and R programs for clinical trial data analysis
  • Design and build interactive applications using R Shiny
  • Convert and optimize programs between SAS and R environments
  • Generate Tables, Listings, and Figures (TFLs) for early-phase clinical studies
  • Perform oversight and quality control (QC) of vendor deliverables and datasets
  • Apply CDISC standards (SDTM, ADaM) in programming and data handling
  • Generate and review Pinnacle 21 validation reports and data packages
  • Utilize data visualization techniques (R Shiny) to support data-driven decision-making
  • Ensure reproducibility by organizing code, data, and outputs into structured repositories
  • Prepare and maintain technical and process documentation

Required Qualifications

  • 8+ years of experience in Clinical SAS Programming
  • 3+ years of hands-on experience in R programming
  • Strong experience in R Shiny application development
  • In-depth knowledge of CDISC standards (SDTM, ADaM)
  • Experience with Pinnacle 21 validation processes
  • Proven experience in generating TFLs for clinical trials
  • Strong understanding of clinical trial data and regulatory requirements
  • Excellent written and verbal communication skills

Preferred Skills

  • Experience in early-phase (Phase I/II) clinical studies
  • Exposure to data visualization and reporting automation
  • Ability to work in a collaborative, fast-paced environment with minimal supervision

Posted: April 1st, 2026