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Senior Statistical Programmer (Clinical Pharmacology) – Sas Programming & Clinical Data Analysis

Syneos Health
Syneos Health
5-8 years
preferred by company
Gurugram, India
2 May 11, 2026
Job Description
Job Type: Hybrid Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Senior Statistical Programmer (Clinical Pharmacology) – SAS Programming & Clinical Data Analysis

Company: Syneos Health
Job Title: Senior Statistical Programmer (Clinical Pharmacology)
Location: Gurugram, India
Work Model: Hybrid
Job ID: 25107869
Department: Clinical Solutions / Statistical Programming


About the Role

Syneos Health is hiring a Senior Statistical Programmer (Clinical Pharmacology) for its Clinical Solutions and Biostatistics team in Gurugram. This hybrid opportunity is ideal for professionals experienced in Clinical SAS Programming, Clinical Pharmacology, ADaM Programming, SDTM Implementation, TLF Generation, and Clinical Trial Data Analysis.

The selected candidate will lead end-to-end statistical programming activities across clinical studies, support clinical pharmacology and PK/PD trials, develop regulatory-compliant datasets and outputs, and collaborate with global clinical research and biostatistics teams.

This opportunity is best suited for candidates with 5–8 years of Statistical Programming experience in clinical trial environments.


Key Responsibilities

Clinical SAS Programming & Data Analysis

  • Develop custom programming code using:
    • SAS
    • Other statistical programming tools
  • Generate:
    • Summary tables
    • Data listings
    • Graphs and figures
    • Derived datasets
  • Support statistical outputs according to:
    • Statistical Analysis Plans (SAP)
    • Programming specifications
  • Ensure deliverables meet project quality standards and sponsor requirements

ADaM, SDTM & TLF Programming

  • Develop and validate:
    • ADaM datasets
    • SDTM datasets
    • Tables, Listings & Figures (TLFs)
  • Support end-to-end statistical programming activities
  • Anticipate and resolve programming issues proactively
  • Define datasets and variables according to sponsor and statistical requirements

Clinical Pharmacology & PK/PD Support

  • Support:
    • Early Phase clinical studies
    • Clinical Pharmacology projects
    • PK/PD trials
  • Collaborate with:
    • Biostatisticians
    • Statistical programmers
    • Clinical research teams
  • Ensure high-quality programming support for pharmacokinetic and pharmacodynamic studies

Validation, Quality Control & Compliance

  • Perform validation programming and discrepancy resolution
  • Maintain:
    • Inspection-ready documentation
    • Quality control records
    • Testing and verification documentation
  • Ensure compliance with:
    • ICH Guidelines
    • SOPs
    • Work Instructions (WIs)
    • Regulatory standards