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Statistical Programmer Ii – Clinical Data & Statistical Programming

Syneos Health
Syneos Health
3-5 years
preferred by company
Pune, India
1 May 11, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Statistical Programmer II – Clinical Data & Statistical Programming

Company: Syneos Health
Job Title: Statistical Programmer II
Location: Pune, 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 Pune. This hybrid opportunity is ideal for professionals interested in Clinical Data Programming, Statistical Analysis, SAS Programming, Clinical Research Data Management, and Regulatory-Compliant Reporting.

The selected candidate will contribute to statistical programming activities for clinical trials, supporting clinical data analysis, dataset generation, reporting, and regulatory submission processes while collaborating with global clinical research teams.

This role is suitable for professionals with experience in Clinical Research, Biostatistics, SAS Programming, and Clinical Data Management.


Key Responsibilities

Statistical Programming & Clinical Data Analysis

  • Support statistical programming activities for clinical studies
  • Develop and maintain clinical datasets, tables, listings, and figures (TLFs)
  • Assist in generation of statistical outputs for clinical trial reporting
  • Ensure programming deliverables meet project timelines and quality standards
  • Support regulatory-compliant data analysis and reporting activities

Clinical Research & Data Management Support

  • Collaborate with:
    • Biostatistics teams
    • Clinical Data Management teams
    • Clinical Operations teams
    • Regulatory stakeholders
  • Assist in data validation and quality control activities
  • Maintain accurate and organized programming documentation
  • Support analysis 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 standards
  • Participate in quality review and validation processes

Project Coordination & Team Collaboration

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

Educational Qualification

Candidates with backgrounds in the following areas are preferred:

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

Required Experience

This opportunity is suitable for candidates with experience in:

  • Statistical Programming
  • SAS Programming
  • Clinical Data Management
  • Clinical Research
  • Biostatistics support
  • Regulatory reporting activities

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 standards
  • Knowledge of:
    • SAS Programming
    • Clinical datasets
    • Tables, Listings & Figures (TLFs)
    • Clinical research processes
  • Familiarity with quality control and validation practices

Preferred Soft Skills

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