๐งฎ Job Title: Principal Statistical Programmer
๐ Location: India – Remote
๐ Job ID: 25101353
๐
Updated: August 28, 2025
๐น Company Overview – Syneos Health®
Syneos Health® is a fully integrated biopharmaceutical solutions organization built to accelerate customer success. By combining clinical, medical affairs, and commercial capabilities, we deliver data-driven insights and customized strategies for modern market realities.
๐ Global Impact
29,000 employees
Present in 110 countries
Involved in 94% of all novel FDA-approved drugs (last 5 years)
Supported over 200 studies across 73,000 sites and 675,000+ trial patients
๐ Visit our website
๐ง๐ผ Why Join Syneos Health?
Career development and progression opportunities
Supportive leadership and engaged line management
Access to technical and therapeutic training
Total rewards & recognition programs
“Total Self” culture — Be your authentic self
Diverse, inclusive, and collaborative work environment
๐ผ Position Summary
The Principal Statistical Programmer plays a key leadership role in developing statistical programs and ensuring quality and integrity of clinical trial data. As a subject matter expert, you’ll provide technical guidance, lead projects, and mentor team members to drive high-quality statistical outputs in a regulated environment.
๐ง Key Responsibilities
๐ Statistical Programming & Data Management
Develop and maintain programming standards and best practices
Create and validate analysis datasets, tables, figures, and listings (TFLs)
Ensure accuracy, consistency, and integrity of all statistical outputs
Conduct code reviews and ensure deliverables meet quality standards
๐ค Collaboration & Communication
Work closely with statisticians, data managers, and other stakeholders
Translate scientific/statistical requirements into programming solutions
Present programming plans and results to internal teams and clients
๐ Technical Leadership & Innovation
Provide technical expertise across programming projects
Troubleshoot and resolve complex programming issues
Mentor junior team members and contribute to team knowledge-building
Stay updated with industry trends and implement relevant advancements
๐ Process Improvement
Evaluate and improve current processes to increase efficiency
Contribute to the development of automated tools and programming frameworks
๐ Qualifications & Requirements
๐ Education
Advanced degree (Master’s preferred) in:
Statistics
Computer Science
Data Science
Related quantitative field
๐ผ Experience
Extensive experience in statistical programming in:
Clinical research
Pharmaceutical or biotech settings
Proven experience in clinical trial data standards (e.g., CDISC, SDTM, ADaM)
๐ป Technical Skills
Proficiency in:
SAS (Base, Macro, SQL)
R and/or Python
In-depth knowledge of statistical methods and clinical data analysis
๐ Certifications (Preferred)
SAS Certified Advanced Programmer for SAS 9 (or equivalent)
๐ง Core Skills & Competencies
Strong analytical and problem-solving skills
High attention to detail and data accuracy
Ability to work independently and in collaborative teams
Effective communication and interpersonal abilities
Strong organizational and project management capabilities
๐งญ Role Level: P23 – Expert Individual Contributor
Responsibilities at This Level:
Develop and execute statistical programs with minimal supervision
Lead projects, provide expert-level guidance, and oversee deliverables
Contribute to cross-functional initiatives and strategic planning
Mentor junior programmers and drive innovation across teams
Influence programming decisions with significant organizational impact
๐ Additional Information
Duties may evolve based on business needs
Equivalent experience or alternative qualifications will be considered
This job description does not imply a contractual relationship
Committed to compliance with ADA and EU Equality Directive
Reasonable accommodations are available for candidates with disabilities
๐ How to Apply
๐ Apply Now
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