Sr. Statistical Programmer
Location: India – Remote
Job Type: Full-Time
Job ID: 25104350
Updated: December 22, 2025
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success by transforming clinical, medical affairs, and commercial insights into actionable outcomes. With 29,000 employees across 110 countries, we foster innovation, collaboration, and inclusivity to advance healthcare and improve patient outcomes.
Position Overview
The Sr. Statistical Programmer develops statistical programs, tables, listings, and graphs to support clinical trials and biopharmaceutical projects. This role ensures high-quality outputs, compliance with regulatory requirements, and contributes to efficient data programming processes across multiple projects.
Key Responsibilities
Statistical Programming & Data Management:
Develop SAS or equivalent code to generate summary tables, data listings, graphs, and derived datasets according to Statistical Analysis Plans (SAP) and programming specifications.
Conduct validation programming, quality checks, and resolve discrepancies with statisticians and project teams.
Maintain comprehensive project documentation, ensuring inspection readiness.
Design datasets and outputs of varying complexity, anticipating potential programming challenges.
Project & Team Leadership:
Act as lead statistical programmer, overseeing programming activities of junior team members.
Review SAPs, mock shells, programming specifications, annotated CRFs, and database design.
Provide feedback to team members to optimize efficiency and quality.
Participate in sponsor meetings, kickoff meetings, and bid defense sessions as required.
Process & Communication:
Manage multiple projects, adapting priorities and timelines as required.
Prepare for and conduct internal meetings, distribute information, and follow through on action items.
Mentor junior programmers through training, guidance, and work review.
Compliance & Best Practices:
Ensure adherence to SOPs, Work Instructions (WIs), and ICH/regulatory guidelines.
Maintain thorough knowledge of clinical trial processes and deliverables.
Perform other project-related duties as assigned; minimal travel may be required.
Required Qualifications
Undergraduate degree in a scientific or statistical discipline, or equivalent experience.
Extensive programming experience in SAS or similar software, preferably in a clinical trial environment.
Excellent written and verbal communication skills in English.
Ability to work independently, manage multiple priorities, and meet deadlines.
Why Join Syneos Health
Contribute to global clinical trials and advanced biopharmaceutical projects.
Collaborate with a diverse, inclusive, and supportive professional team.
Access professional development, mentoring, and career growth opportunities.
Work in a highly impactful environment where your contributions support patient care worldwide.
Gujarat :
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Siliguri |Illinois :
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Frank Scottile Blvd |Missouri :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
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China | Quarry Bay |Liaoning :
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Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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Nedlands |Queensland :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Sheffield |Oxfordshire :
Witney |Ontario :
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Auckland |New Zealand :
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Barcelona |Madrid :
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Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hà Nội | Hanoi |Ho Chi Minh :
Ho Chi Minh City |Italy :
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Japan | Saitama |Tokyo :
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Kyiv |Lima Region :
Lima |France :
Lyon | Paris |South Africa :
South Africa | Midrand |Nišava District :
Niš |Bohemia :
Prague |Chile :
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