Senior Statistical Programmer – Hyderabad, India
Location: Hyderabad, India
Job Type: Full-Time
Updated: November 12, 2025
Job ID: 25103268
Company Overview
Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating clinical development and optimizing patient outcomes. With a global workforce of over 29,000 employees across 110 countries, Syneos Health delivers innovative clinical, medical affairs, and commercial solutions, putting patients and customers at the heart of every project.
Why Join Syneos Health
Engage in complex global clinical trials for FDA and EMA-approved drugs
Opportunity to work with a collaborative, innovative, and inclusive team
Exposure to end-to-end statistical programming and advanced SAS programming
Professional growth and mentorship opportunities in a leading biopharma environment
Role Overview
The Senior Statistical Programmer is responsible for developing analysis datasets, tables, listings, and graphs to support clinical trials. You will act as a technical lead, mentor junior programmers, and ensure outputs meet quality and regulatory standards. This is an excellent opportunity to work in a dynamic environment with exposure to high-impact projects.
Key Responsibilities
Develop custom programming code using SAS or other relevant software to generate datasets, tables, listings, and figures per statistical analysis plans
Validate outputs and perform quality control to ensure compliance with project and regulatory requirements
Maintain organized and up-to-date project documentation, testing, and verification/quality control files
Manage multiple projects, adapt to changing priorities, and optimize programming workflows
Serve as lead programmer: review Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs, and SAS database design
Participate in sponsor meetings, kickoffs, and bid defense meetings
Mentor and guide junior programmers, develop training materials, and provide feedback
Perform other project-related tasks as assigned; minimal travel may be required
Qualifications
Undergraduate degree in a scientific or statistical discipline (or equivalent experience)
Extensive experience in SAS or other statistical programming software, preferably in clinical trials
Strong understanding of regulatory guidelines (ICH, GCP) and statistical programming best practices
Excellent written and verbal communication skills in English
Proven ability to manage multiple priorities and meet deadlines efficiently
Impact & Contribution
Develop high-quality statistical outputs that directly support clinical trial success
Optimize programming processes to improve efficiency and productivity
Provide guidance and mentorship to programming team members, building subject matter expertise
Syneos Health Highlights
Supported 94% of all novel FDA-approved drugs and 95% of EMA-authorized products
Managed over 200 clinical studies across 73,000 sites and 675,000+ trial patients
Learn more: syneoshealth.com
How to Apply
This posting is for a potential upcoming opportunity. Interested candidates are encouraged to express interest and join our Talent Network to be considered for future openings.
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