Statistical Programmer
Location: Bangalore, Trivandrum, Chennai – India
Work Model: Office-based or Home-based (Hybrid/Flexible)
Employment Type: Full-Time
Application Deadline: May 7, 2026
Job Requisition ID: JR138352
Company: ICON plc
About ICON plc
ICON plc is a globally recognized healthcare intelligence and clinical research organization supporting the development of innovative medicines and medical devices. With a strong global footprint and a commitment to inclusion, quality, and scientific excellence, ICON partners with biopharmaceutical and medical device companies to deliver high-quality clinical development solutions worldwide.
Job Overview
ICON is seeking an experienced Statistical Programmer to join its growing clinical research team in India. In this role, you will be responsible for developing, validating, and maintaining statistical programs that support clinical trial analysis, regulatory submissions, and reporting activities. This position plays a critical role in ensuring data accuracy, regulatory compliance, and timely delivery of clinical research outputs.
Key Responsibilities
Develop, validate, and maintain complex statistical programs using SAS, R, and related tools for clinical trial data analysis and reporting
Collaborate closely with biostatisticians, data management, and cross-functional teams to translate study requirements into accurate programming outputs
Prepare and review statistical analysis plans (SAPs), programming specifications, and derived datasets in compliance with regulatory standards
Ensure data integrity, traceability, and adherence to ICH-GCP and other global regulatory guidelines
Support clinical study reporting activities, including tables, listings, and figures (TLFs)
Mentor junior programmers and contribute to team training and process improvement initiatives
Required Qualifications and Experience
Bachelor’s degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related discipline; a Master’s degree is preferred
Minimum 5 years of experience as a Statistical Programmer within the clinical research or pharmaceutical industry
Strong hands-on expertise in SAS and R; exposure to Python and R Shiny is an advantage
Solid understanding of clinical trial data standards, statistical methodologies, and regulatory submission requirements
Experience working with clinical data management systems and cross-functional global teams
Strong analytical, problem-solving, and communication skills with high attention to detail
What ICON Offers
Competitive salary and country-specific benefits package
Flexible working arrangements supporting work-life balance
Comprehensive health insurance options for employees and families
Retirement and long-term savings plans
Global Employee Assistance Program (TELUS Health) with 24/7 access to professional support
Life assurance and wellness-focused benefits
Structured career development, mentoring, and global growth opportunities
Diversity, Equity, and Inclusion
ICON is committed to building an inclusive workplace that values diversity and equal opportunity. All qualified applicants will receive fair consideration for employment without discrimination based on race, gender, age, disability, religion, sexual orientation, or any other protected status. Reasonable accommodations are available throughout the hiring process.
Next Steps
Qualified candidates are encouraged to apply even if they do not meet every listed requirement. ICON values potential, growth mindset, and diverse experience.
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