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Senior Statistical 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 – 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.