Senior / Principal Statistical Programmer (SAS / R, SQL)
Location: Gurugram, India (Hybrid)
Job ID: 25101677
Updated: September 12, 2025
Company: Syneos Health®
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions company dedicated to accelerating customer success. We combine clinical, medical affairs, and commercial insights to deliver outcomes in an evolving market.
29,000 employees across 110 countries
Worked on 94% of FDA novel drug approvals in the past 5 years
Supported 95% of EMA authorized products
Over 200 studies, 73,000 sites, and 675,000+ patients
Why Work Here
Career development and progression opportunities
Supportive and engaged line management
Technical and therapeutic training
Peer recognition and rewards program
Inclusive Total Self culture – be authentic, feel valued
Diverse workplace encouraging collaboration and belonging
Role Summary (P23 Level)
This position involves developing statistical programs, supporting statisticians, and managing multi-study projects. As a P23-level individual contributor, you will be a subject matter expert, contributing to critical programming processes and guiding junior team members.
Core Focus Areas
Develop programs and provide statistical programming support
Source, organize, and interpret complex datasets
Create analysis datasets, statistical tables, listings, and figures
Evaluate and improve programming processes to enhance productivity
Manage/contribute to cross-functional projects and programs
Mentor/direct lower-level professionals
Apply advanced expertise to design, implement, and deliver programming solutions
Key Responsibilities
Develop and validate statistical analysis datasets, tables, listings, and graphs
Provide statistical programming support for clinical trials (Phases I–IV)
Lead and manage multiple studies simultaneously
Collaborate with cross-functional teams across clinical development
Contribute to process optimization and quality improvements
Required Skills & Experience
Experience: 5+ years in advanced SAS / R programming and SQL
Technical Skills:
R programming & package development
SQL expertise
Python (preferred, but not mandatory)
TIBCO Spotfire or similar visualization tools (desirable)
Domain Knowledge:
Clinical trial processes (Phases I–IV)
Clinical Data Management
Leadership:
Prior experience as study lead
Ability to manage multiple projects/studies
Other Skills:
Strong written and verbal communication
Impact & Contribution
Deliver expert programming solutions that influence related business areas
Drive measurable improvements in departmental productivity and efficiency
Shape processes, policies, and projects through advanced technical expertise
Support organizational goals by contributing to the success of clinical development programs
Additional Information
Responsibilities may evolve at the company’s discretion
Equivalent skills, experience, or education may be considered
Compliant with ADA (reasonable accommodations provided) and EU Equality Directive
No employment contract implied
Application
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