Senior / Principal Statistical Programmer (SAS / R, SQL)
Location: IND-Remote
Updated: September 12, 2025
Job ID: 25101677
Company Overview
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, accelerating customer success by translating clinical, medical affairs, and commercial insights into impactful outcomes.
Our Clinical Development model places the patient and customer at the center of everything we do.
We continuously simplify and streamline work processes to make Syneos Health easier to work with and for.
Employees collaborate as passionate problem solvers, innovating to help customers achieve goals, and accelerating the delivery of life-changing therapies.
Global Footprint:
29,000 employees across 110 countries
Worked on 94% of all novel FDA-approved drugs and 95% of EMA-authorized products over the past 5 years
Supported 200+ studies across 73,000 sites and 675,000+ trial patients
Learn more: www.syneoshealth.com
Why Work With Us
Career Development: Training, mentorship, peer recognition, and progression opportunities
Total Self Culture: Authenticity, inclusivity, and belonging across global teams
Diversity & Inclusion: Valuing different perspectives to create a workplace everyone feels part of
Role Summary
Level: P23 – Senior / Principal Contributor
Develop programs and provide statistical programming support for statisticians or client/business use
Source, organize, and interpret complex data sets
Create statistical tables, listings, and graphs
Develop analysis datasets, tables, and figures
Evaluate programming processes and suggest improvements to increase productivity
Manage or contribute to multi-project initiatives
Guide or direct lower-level professionals
Apply advanced knowledge to design, implement, and deliver processes, programs, and policies
Impact:
Contributions directly affect departmental and organizational results
Recognized as a subject matter expert within the statistical programming domain
Key Responsibilities
Develop and validate SAS and R programs for clinical trial data analysis
Create analysis datasets, tables, figures, and listings
Implement and optimize statistical programming processes
Collaborate with cross-functional teams including statisticians and data managers
Mentor and guide junior programmers as needed
Support multiple studies, including study lead responsibilities
Required Skills & Qualifications
Experience: 5+ years in advanced SAS/R programming and SQL
Programming: R programming, R package development, SQL
Additional Skills (Value-Added): Python, TIBCO Spotfire or equivalent (visualization, calculated columns, filtering, document properties)
Domain Knowledge: Clinical trials, drug development (Phase I–IV), Clinical Data Management
Project Management: Experience as a study lead or managing multiple studies
Communication: Strong written and verbal communication skills
Additional Information
Tasks and responsibilities are not exhaustive; may be adjusted at the company’s discretion
Equivalent experience, skills, and education will be considered
Compliance with all local employment legislation and accessibility requirements
Not intended to constitute an employment contract
How to Apply
Directly through the Syneos Health careers portal
Not ready to apply? Join our Talent Network to stay connected with future opportunities
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