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Senior Stat Programmer

0-2 years
Not Disclosed
10 Nov. 27, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Statistical Programmer – Remote (India)

Location: Remote, India
Job Type: Full-Time
Updated: November 13, 2025
Job ID: 25103313

Company Overview

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating clinical development and optimizing patient outcomes. With over 29,000 employees across 110 countries, we deliver innovative solutions spanning clinical development, medical affairs, and commercial functions, placing patients and customers at the center of every project.

Why Join Syneos Health

  • Opportunity to work on cutting-edge clinical trials and FDA/EMA-approved products

  • Exposure to end-to-end statistical programming in global projects

  • Collaborative, inclusive culture fostering growth, innovation, and professional development

  • Work remotely while contributing to high-impact projects across therapeutic areas

Role Overview

As a Senior Statistical Programmer, you will lead programming efforts to create analysis datasets, tables, listings, and graphs, ensuring accuracy and compliance with regulatory requirements. You will mentor junior programmers, manage multiple projects, and act as a key technical resource in statistical programming for clinical trials.

Key Responsibilities

  • Develop custom programming code using SAS (or other software) to generate datasets, tables, listings, and figures as per statistical analysis plans

  • Ensure outputs meet quality standards and project requirements; perform validation and quality control

  • Maintain well-organized project documentation and prepare for inspections/audits

  • Manage multiple projects, set priorities, and adapt to timeline changes

  • Act as lead programmer, guiding other programmers and providing feedback on Statistical Analysis Plans, mock shells, programming specifications, and annotated CRFs

  • Participate in sponsor meetings, kickoffs, and bid defense meetings as a statistical programming representative

  • Mentor junior programming staff through training, code reviews, and guidance

  • Perform other project-related duties as assigned

Qualifications

  • Undergraduate degree in a scientific or statistical discipline, or equivalent combination of education and experience

  • Extensive experience in SAS or similar programming software, preferably in clinical trial settings

  • Strong written and verbal communication skills in English

  • Proven ability to manage multiple projects and meet deadlines efficiently

  • Knowledge of regulatory standards (ICH, GCP) and statistical programming best practices

Impact & Contribution

  • Develop and deliver high-quality statistical programming outputs to support clinical trial success

  • Contribute to process improvements and efficiency in programming workflows

  • Serve as a subject matter expert and mentor within the statistical programming team

About Syneos Health’s Reach

  • Supported 94% of 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

Qualified candidates with extensive SAS programming experience are encouraged to apply. Join our Talent Network to stay connected with additional clinical and statistical programming opportunities.