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Statistical Programmer Ii – Clinical Data & Statistical Programming

Syneos Health
Syneos Health
3-5 years
preferred by company
Hyderabad
1 May 11, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Statistical Programmer II – Clinical Data & Statistical Programming

Company: Syneos Health
Job Title: Statistical Programmer II
Location: Hyderabad, India
Work Model: Hybrid
Job ID: 25107811
Department: Clinical Solutions / Statistical Programming


About the Role

Syneos Health is hiring a Statistical Programmer II for its Clinical Solutions and Biostatistics team in Hyderabad. This hybrid opportunity is ideal for professionals interested in Clinical Data Programming, Statistical Analysis, SAS Programming, Biostatistics, and Clinical Research Data Management.

The selected candidate will support statistical programming activities for clinical trials, helping generate datasets, statistical outputs, and regulatory-compliant reports while collaborating with global clinical research and data management teams.

This opportunity is suitable for professionals with experience in Clinical Research, Statistical Programming, Biostatistics, and Healthcare Data Analysis.


Key Responsibilities

Statistical Programming & Data Analysis

  • Support statistical programming activities for clinical studies
  • Develop and maintain:
    • Clinical datasets
    • Tables, Listings & Figures (TLFs)
    • Statistical outputs
  • Assist in data analysis and reporting for clinical trials
  • Ensure programming deliverables meet quality and timeline expectations
  • Support regulatory-compliant clinical reporting activities

Clinical Research & Data Management Support

  • Collaborate with:
    • Biostatistics teams
    • Clinical Data Management teams
    • Clinical Operations teams
    • Regulatory stakeholders
  • Participate in data validation and quality control activities
  • Maintain accurate and organized programming documentation
  • Support dataset preparation and reporting workflows

Regulatory Compliance & Quality Assurance

  • Ensure compliance with:
    • ICH Guidelines
    • Clinical Research standards
    • Company SOPs and regulatory requirements
  • Support inspection readiness and documentation quality
  • Participate in quality review and validation processes

Project Coordination & Team Collaboration

  • Work collaboratively within global clinical research teams
  • Support project timelines and deliverables
  • Adapt to changing project priorities and operational requirements
  • Contribute to process improvement and operational efficiency initiatives

Educational Qualification

Candidates with backgrounds in the following areas are preferred:

  • Statistics
  • Mathematics
  • Computer Science
  • Biostatistics
  • Life Sciences
  • Clinical Research
  • Related scientific or technical disciplines

Required Experience

This opportunity is suitable for candidates with experience in:

  • Statistical Programming
  • Clinical Data Analysis
  • SAS Programming
  • Clinical Research
  • Biostatistics support
  • Clinical data reporting

Preferred Industry Experience

  • Pharmaceutical Industry
  • Biotechnology Industry
  • Contract Research Organizations (CROs)

Required Technical Skills

  • Understanding of:
    • Statistical programming concepts
    • Clinical trial data workflows
    • Regulatory reporting requirements
  • Knowledge of:
    • SAS Programming
    • Clinical datasets
    • TLF generation
    • Clinical research processes
  • Familiarity with validation and quality control practices

Preferred Soft Skills

  • Strong analytical and problem-solving skills
  • Good communication and teamwork abilities
  • Attention to detail and data accuracy
  • Organizational and multitasking capabilities
  • Ability to work effectively in collaborative environments