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

5+ 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) – Syneos Health

Location: Gurugram, 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) is a lead-level role responsible for developing advanced statistical programs and supporting statistical analyses for clinical trials and client projects. The role involves creating and validating datasets, tables, listings, figures, and contributing to process improvements across statistical programming activities.


Key Responsibilities

  • Develop programs and provide statistical programming support for statisticians or clients.

  • Source, organize, and interpret complex datasets by creating statistical tables, listings, and graphs.

  • Develop codes to create analysis datasets, tables, and figures.

  • Evaluate programming processes and suggest revisions to improve efficiency and productivity.

  • Manage or contribute to projects, programs, or processes that span multiple areas.

  • Mentor or direct the work of 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 and a valuable resource for peers and project teams.


Required Skills & Qualifications

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

  • Programming: Hands-on experience with R programming, R package development, and SQL; 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 processes (Phase I-IV), and Clinical Data Management.

  • Leadership: Experience as a study lead and capability to manage multiple studies.

  • Communication: Strong 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.