Principal Statistical Programmer

Overview

Responsible for statistical programming, data review, reporting, and analytics development across clinical studies and projects. Acts as a key collaborator to ensure timely, high-quality, compliant deliverables.

What you'll do

• Lead statistical programming as a Trial Programmer or Lead/Programmer across phase I–IV clinical studies.
• Coordinate internal and external programmers for study/project programming work.
• Review eCRF, discuss data structures, and participate in data review activities.
• Develop and validate datasets and outputs for CSRs, regulatory submissions/interactions, safety reports, and publications/analyses.
• Ensure quality control and audit readiness for statistical programming deliverables.
• Implement reproducibility, documentation, and code quality best practices.

What you'll need

• 7 to 11 years of work experience in a programming role supporting clinical trials or pharma industry.
• Strong statistical programming skills using R, SAS, or Python for development and validation.
• Experience using R packages (e.g., Tidyverse) and R Shiny applications for data visualization.
• Advanced experience contributing to statistical analysis plans and/or constructing technical programming specifications.
• Knowledge of industry standards and CDISC data structures plus standard programs.
• Understanding of regulatory requirements relevant to statistical programming (e.g., GCP).

Details

• Location: Hyderabad (Office)