Senior / Principal Statistical Programmer (SAS / R, SQL)
📍 Location: Pune, India – Hybrid
🆔 Job ID: 25101677
📅 Updated: September 12, 2025
About Syneos Health
Syneos Health® is a leading fully integrated biopharmaceutical solutions company, combining clinical, medical affairs, and commercial expertise to accelerate customer success.
Global Workforce: 29,000 employees across 110 countries
Impact: Partnered on 94% of FDA-approved novel drugs (past 5 years) and 95% of EMA-authorized products
Clinical Reach: Supported over 200 studies across 73,000 sites and 675,000+ trial patients
💡 Work Here Matters Everywhere
Why Join Us?
Career development and progression opportunities
Supportive and engaged line management
Technical and therapeutic training programs
Peer recognition and rewards
Total Self Culture – a workplace where you can be your authentic self
Inclusive, diverse, and collaborative environment
Role Summary
As a Senior / Principal Statistical Programmer, you will:
Develop and maintain statistical programs to support biostatistical analyses
Create statistical tables, listings, graphs, and analysis datasets
Support statisticians, clients, and business teams with high-quality deliverables
Provide subject matter expertise in programming standards, tools, and clinical data management processes
Lead studies or multiple projects and mentor junior programmers as required
Key Responsibilities
Develop programs using SAS, R, and SQL to generate analysis datasets, tables, listings, and figures
Source, organize, and interpret complex datasets for statistical outputs
Evaluate programming processes and recommend improvements for efficiency and productivity
Support clinical trials across Phase I–IV of drug development
Provide statistical programming support for regulatory submissions and publications
Act as study lead, managing timelines and deliverables across multiple projects
Collaborate with statisticians, data managers, and cross-functional teams
Mentor and guide junior programmers when required
Required Skills & Experience
5+ years of advanced SAS / R programming and SQL experience
Strong hands-on expertise in R programming and R package development
Knowledge of Python (added advantage)
Experience with TIBCO Spotfire (or similar visualization tools) – creating calculated columns, markings, filters, and document properties
Solid understanding of the clinical domain and drug development process (Phase I–IV)
Experience with clinical data management processes
Proven experience as a study lead, managing multiple studies/projects
Strong written and verbal communication skills
Impact & Contribution (P23 Level)
Act as an expert individual contributor recognized as a valuable resource across teams
Manage and contribute to projects/programs spanning multiple related areas
Influence the design, implementation, and delivery of programming processes and policies
Direct or mentor lower-level professionals when needed
Ensure high-quality programming deliverables that impact departmental and business results
Other Information
Tasks and duties may be reassigned at the company’s discretion
Equivalent education/experience may be considered in place of listed qualifications
Committed to diversity, inclusion, and ADA compliance with reasonable accommodations provided
👉 Apply Now or Join our Talent Network to stay connected with upcoming opportunities.
🔗 Learn more: www.syneoshealth.com
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