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

5+ years
Not Disclosed
10 Sept. 23, 2025
Job Description
Job Type: Full Time 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: Gurugram, India (Hybrid)
Job ID: 25101677
Updated: September 12, 2025
Company: Syneos Health®


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions company dedicated to accelerating customer success. We combine clinical, medical affairs, and commercial insights to deliver outcomes in an evolving market.

  • 29,000 employees across 110 countries

  • Worked on 94% of FDA novel drug approvals in the past 5 years

  • Supported 95% of EMA authorized products

  • Over 200 studies, 73,000 sites, and 675,000+ patients

Why Work Here

  • Career development and progression opportunities

  • Supportive and engaged line management

  • Technical and therapeutic training

  • Peer recognition and rewards program

  • Inclusive Total Self culture – be authentic, feel valued

  • Diverse workplace encouraging collaboration and belonging


Role Summary (P23 Level)

This position involves developing statistical programs, supporting statisticians, and managing multi-study projects. As a P23-level individual contributor, you will be a subject matter expert, contributing to critical programming processes and guiding junior team members.

Core Focus Areas

  • Develop programs and provide statistical programming support

  • Source, organize, and interpret complex datasets

  • Create analysis datasets, statistical tables, listings, and figures

  • Evaluate and improve programming processes to enhance productivity

  • Manage/contribute to cross-functional projects and programs

  • Mentor/direct lower-level professionals

  • Apply advanced expertise to design, implement, and deliver programming solutions


Key Responsibilities

  • Develop and validate statistical analysis datasets, tables, listings, and graphs

  • Provide statistical programming support for clinical trials (Phases I–IV)

  • Lead and manage multiple studies simultaneously

  • Collaborate with cross-functional teams across clinical development

  • Contribute to process optimization and quality improvements


Required Skills & Experience

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

  • Technical Skills:

    • R programming & package development

    • SQL expertise

    • Python (preferred, but not mandatory)

    • TIBCO Spotfire or similar visualization tools (desirable)

  • Domain Knowledge:

    • Clinical trial processes (Phases I–IV)

    • Clinical Data Management

  • Leadership:

    • Prior experience as study lead

    • Ability to manage multiple projects/studies

  • Other Skills:

    • Strong written and verbal communication


Impact & Contribution

  • Deliver expert programming solutions that influence related business areas

  • Drive measurable improvements in departmental productivity and efficiency

  • Shape processes, policies, and projects through advanced technical expertise

  • Support organizational goals by contributing to the success of clinical development programs


Additional Information

  • Responsibilities may evolve at the company’s discretion

  • Equivalent skills, experience, or education may be considered

  • Compliant with ADA (reasonable accommodations provided) and EU Equality Directive

  • No employment contract implied


Application

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