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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: Hyderabad, India (Hybrid)
Job ID: 25101677
Updated: September 12, 2025
Company: Syneos Health®


About Syneos Health

Syneos Health® is a leading fully integrated biopharmaceutical solutions company, accelerating customer success through clinical, medical affairs, and commercial insights.

  • 29,000 employees across 110 countries

  • Partnered on 94% of FDA-approved novel drugs in the past 5 years

  • Supported 95% of EMA-authorized products

  • Conducted 200+ studies across 73,000 sites and 675,000+ patients

Why Work Here

  • Career development & progression opportunities

  • Supportive, engaged line management

  • Technical and therapeutic training

  • Peer recognition & rewards program

  • Inclusive Total Self culture – be authentic, feel valued

  • Diverse global workplace fostering collaboration and belonging


Role Summary (P23 Level)

This role involves developing statistical programs, supporting statisticians, and managing cross-functional projects. As a P23-level professional, you will serve as a technical expert and mentor, contributing to programming innovation, process improvements, and high-impact results.

Core Focus

  • Develop programs and provide statistical programming support

  • Source, organize, and interpret complex clinical trial data

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

  • Evaluate programming processes and suggest improvements

  • Manage and contribute to projects spanning multiple related areas

  • Direct and mentor junior programmers

  • Apply advanced knowledge to design and deliver programming solutions


Key Responsibilities

  • Program statistical analysis datasets, tables, listings, and figures (TLFs)

  • Provide programming support across clinical studies (Phases I–IV)

  • Lead and oversee multiple studies simultaneously

  • Collaborate with cross-functional clinical teams

  • Drive programming quality and process optimization


Required Skills & Experience

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

  • Technical Skills:

    • Proficiency in R (including package development)

    • SQL expertise

    • Python knowledge (value-added)

    • Familiarity with TIBCO Spotfire or similar visualization tools (advantageous)

  • Domain Knowledge:

    • Strong understanding of the clinical domain and drug development (Phases I–IV)

    • Clinical Data Management knowledge/experience

  • Leadership:

    • Prior study lead experience

    • Ability to handle multiple projects simultaneously

  • Other Skills:

    • Strong written and verbal communication


Impact & Contribution

  • Deliver programming solutions critical for clinical development

  • Drive measurable productivity and efficiency improvements

  • Influence related business areas with comprehensive technical expertise

  • Support departmental and organizational success through innovation


Additional Information

  • Job duties may evolve at the company’s discretion

  • Equivalent experience, skills, or education may be considered

  • Syneos Health complies with ADA (reasonable accommodations available) and EU Equality Directive

  • No employment contract implied


Application

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