Job Title:
Senior / Principal Statistical Programmer (SAS / R, SQL)
Company:
Syneos Health®
Location:
Remote – India
Job ID:
25101677
Updated On:
September 12, 2025
About Syneos Health
A global biopharmaceutical solutions company with 29,000 employees across 110 countries.
Partnered with 94% of FDA-approved drugs and 95% of EMA authorized products over the last 5 years.
Provides career development, technical training, peer recognition, and rewards.
Committed to diversity, inclusion, and authenticity through its Total Self culture.
Job Summary
As a Senior / Principal Statistical Programmer (P23 level), you will:
Develop programs and provide statistical programming support to statisticians and clients.
Organize, interpret, and analyze complex data sets.
Deliver statistical tables, listings, and graphs (TLGs).
Lead or contribute to cross-functional projects and processes, ensuring quality and efficiency.
Act as a senior-level technical expert, mentoring junior programmers when needed.
Core Responsibilities
Programming & Data Analysis
Develop and validate programs using SAS, R, and SQL.
Create and maintain analysis datasets, tables, listings, and figures (ADaM/SDTM).
Interpret complex datasets and transform them into meaningful outputs.
Process Improvement
Evaluate current programming processes.
Suggest and implement revisions to increase productivity and efficiency.
Leadership & Collaboration
Provide statistical programming support to statisticians and cross-functional teams.
Lead study-level programming activities and manage multiple studies simultaneously.
May direct lower-level programmers or manage specific programming processes.
Cross-Functional Contribution
Participate in the design, implementation, and delivery of processes, programs, and policies.
Ensure outputs meet sponsor and regulatory requirements.
Collaborate closely with clinical data management and biostatistics teams.
Qualifications
Education: Advanced degree preferred or equivalent experience.
Experience:
5+ years in advanced SAS/R programming and SQL.
Experience in R package development.
Hands-on Python knowledge (preferred).
Familiarity with TIBCO Spotfire (or similar tools) for visualization and reporting.
Strong understanding of clinical research, drug development (Phase I–IV), and clinical data management.
Experience as a study lead with capability to manage multiple studies.
Skills:
Strong communication skills (written & verbal).
Ability to work in a dynamic, matrix environment.
Problem-solving and mentoring skills.
Impact & Contribution
Recognized as a leading expert individual contributor (P23 level).
Directly influences department results and productivity.
Provides high-value input into projects, spanning multiple related areas.
Contributes advanced knowledge to improve programming processes and cross-functional outcomes.
Additional Information
This job description is not exhaustive; responsibilities may change as needed.
Equivalent skills and experience may substitute listed qualifications.
Committed to equal opportunity, ADA compliance, and global recruitment standards.
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