Job Title: Senior / Principal Statistical Programmer (Oncology) – Immediate Joiner
Location: Pune, Maharashtra, India
Job Type: Full-Time | Hybrid
Updated On: October 31, 2025
Job ID: 25102640
Company: Syneos Health®
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization designed to accelerate clinical and commercial success. The company combines clinical, medical affairs, and commercial expertise to deliver high-quality outcomes and transform patient care worldwide.
With over 29,000 employees in 110 countries, Syneos Health partners with 94% of all novel FDA-approved drugs, 95% of EMA-authorized products, and has conducted 200+ studies across 73,000 sites and 675,000+ trial patients.
Work Here Matters Everywhere.
Why Join Syneos Health
🚀 Career Growth: Structured learning, technical training, and leadership development.
💬 Collaborative Culture: Cross-functional teamwork and continuous feedback environment.
🌍 Inclusive Workplace: “Total Self” culture where everyone can be authentic and thrive.
🧠 Knowledge Expansion: Exposure to global trials, therapeutic expertise, and regulatory environments.
🏆 Recognition Programs: Total rewards and peer recognition initiatives.
Position Overview
As a Senior / Principal Statistical Programmer (Oncology), you will develop and validate statistical programs for clinical trials using SAS and related tools. You’ll support Biostatisticians, provide leadership to junior programmers, and ensure accurate and compliant deliverables within timelines.
Key Responsibilities
Develop custom SAS programs (Base/Advanced SAS, ADaM, TLF) for generating statistical outputs including datasets, listings, tables, and graphs.
Validate and review programs to ensure data quality and accuracy per Statistical Analysis Plans (SAPs) and programming specifications.
Collaborate with Biostatisticians, Data Managers, and Clinical Teams to resolve data discrepancies.
Maintain complete and audit-ready documentation for all programming and validation work.
Manage multiple studies simultaneously, ensuring deliverables meet project timelines and regulatory standards.
Anticipate programming challenges and propose effective solutions to enhance efficiency.
Lead programming teams on assigned studies — review project documents (SAP, mock shells, annotated CRFs, specs) and ensure consistency.
Participate in kick-off, sponsor, and bid defense meetings as a programming representative.
Mentor and guide junior programmers through code review, training, and technical supervision.
Support ISS/ISE (Integrated Summary of Safety/Efficacy) programming and oncology-specific data handling.
Ensure adherence to ICH-GCP, company SOPs, and regulatory guidelines.
Qualifications & Skills
Education: Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, Life Sciences, or related field.
Experience: Minimum 5+ years in Clinical SAS Programming.
Technical Skills:
Strong expertise in Base SAS / Advanced SAS, ADaM, and TLF programming.
Experience in Oncology therapeutic areas (mandatory).
Exposure to Safety & Efficacy data handling.
Knowledge of ISS/ISE and R Programming (preferred).
Soft Skills: Excellent communication, problem-solving, and time management skills.
Language Proficiency: Fluent in written and spoken English.
Availability: Immediate joiners preferred.
Additional Information
Minimal travel may be required.
Duties listed are not exhaustive; equivalent combinations of skills and education may be considered.
Syneos Health adheres to global employment and equality regulations, including the EU Equality Directive and the Americans with Disabilities Act (ADA).
Reasonable accommodations are available for applicants or employees as needed.
How to Apply
🔗 Apply Now via Syneos Health Careers
💬 Not ready to apply? Join the Talent Network to receive updates on future opportunities.
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