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Senior / Principal Stat Programmer(Sas/ R, Sql)

None years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior / Principal Statistical Programmer (SAS/R, SQL)

Location: Hyderabad, India (Hybrid)
Job ID: 25101677
Updated: September 12, 2025


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating clinical development and improving patient outcomes.

  • Employees: 29,000 across 110 countries

  • Experience: 94% of Novel FDA-approved drugs, 95% EMA-authorized products, 200+ studies, 73,000 sites, 675,000+ trial patients

  • Culture: Total Self culture fostering diversity, authenticity, career growth, and inclusion


Job Overview

The Senior / Principal Statistical Programmer (P23 level) develops advanced statistical programs and provides programming support for statisticians and clients. This role involves interpreting complex datasets, creating analysis datasets, tables, listings, figures, and optimizing programming processes. The professional contributes to projects spanning multiple areas and acts as a key resource for peers.


Key Responsibilities

  • Develop programs to generate analysis datasets, tables, listings, and figures.

  • Source, organize, and interpret complex datasets.

  • Evaluate programming processes and suggest efficiency improvements.

  • Manage or contribute to multi-project programs and processes.

  • Mentor or guide lower-level programmers.

  • Contribute to the design, implementation, and delivery of processes, programs, and policies.

  • Ensure adherence to clinical trial standards, regulatory guidelines, and company SOPs.

  • Act as a subject matter expert in statistical programming and clinical data management.


Required Skills & Qualifications

  • Experience: 5+ years in advanced SAS/R programming and SQL.

  • Programming Expertise:

    • R programming and R package development

    • SQL knowledge

    • Python knowledge is a plus

  • Visualization Tools: Familiarity with TIBCO Spotfire or equivalent (calculated columns, markings, filtering, document properties) is advantageous.

  • Domain Knowledge: Clinical trials, drug development process (Phase I-IV), Clinical Data Management.

  • Leadership: Study lead experience; ability to manage multiple studies.

  • Communication: Excellent written and verbal communication skills.


Additional Information

  • Tasks, duties, and responsibilities may vary at the discretion of the company.

  • Equivalent experience, skills, or education may be considered.

  • Compliance with ADA and diversity/inclusion policies.

  • Expressing interest adds you to Syneos Health’s talent pipeline for upcoming opportunities.