Senior Statistical Programmer

JD FOR R Programmer

• Develop and validate R programs to support CDISC dataset and statistical graph

• Create Markdown and Shiny appy for generating statistical

  tables and listings.

• Automate and streamline

  data wrangling, transformation, and visualization

  of clinical datasets using R and associated packages.

• Create and maintain

  Shiny apps,

  R Markdown reports, and

  automated pipelines

  for exploratory and statistical analyses.

• Collaborate with biostatisticians, data managers, and clinical teams to interpret clinical data and support study objectives.

• Contribute to

  statistical analysis plans (SAPs)

  and documentation for regulatory submissions (e.g., FDA, EMA).

• Ensure compliance with

  GxP,

  21 CFR Part 11, and company SOPs in statistical programming deliverables.

Required Qualifications:

• Bachelor's or Master's degree in Statistics, Biostatistics, Computer Science, Engineering or Quantitative field.

• 5+ years of experience in R programming within a

  clinical trials or pharmaceutical

  environment.

• Proficient in R packages such as tidyverse, haven, ggplot2, shiny, TEAL ,

  knitr, and data.table.

• Knowledge of

  CDISC standards (SDTM, ADaM)

  and regulatory submission requirements.

• Experience with clinical data standards and regulatory documentation.

• Excellent attention to detail, problem-solving skills, and communication abilities.

What We Offer:

• Opportunity to work on cutting-edge drug development programs.

• Career growth and access to global clinical research networks.

• Competitive salary and comprehensive benefits package.