Statistical Programmer II / Senior Statistical Programmer
Location: Trivandrum, India | Chennai, India
Work Model: Office or Home (Hybrid/Remote)
Employment Type: Full-Time
Job Requisition ID: JR142451
Posted: 10 Days Ago
About ICON plc
ICON plc is a globally recognized healthcare intelligence and clinical research organization, partnering with pharmaceutical, biotechnology, and medical device companies to accelerate the development of innovative therapies. ICON is committed to scientific excellence, regulatory compliance, and building an inclusive, high-performance culture that supports long-term career growth.
Role Overview
ICON is currently hiring Statistical Programmer II and Senior Statistical Programmers to join its growing statistical programming team in India. These roles are critical to the delivery of high-quality statistical programming for clinical trial analysis, reporting, and regulatory submissions.
Depending on experience level, candidates will contribute through hands-on programming, close collaboration with biostatisticians, and a strong focus on data quality, compliance, and continuous improvement across clinical studies.
Key Responsibilities
Develop, validate, and maintain statistical programs to support clinical trial analysis and reporting using R, R Shiny, and SAS
Collaborate closely with biostatisticians to interpret study protocols and statistical analysis plans (SAPs)
Prepare and review programming specifications, derived datasets, and statistical outputs in compliance with regulatory standards
Generate and validate tables, listings, and figures (TLFs) for clinical study reports and regulatory submissions
Perform quality control checks to ensure data accuracy, consistency, and traceability
Support submission deliverables in accordance with ICH, GCP, and regulatory authority requirements
Contribute to process optimization, automation, and programming best practices
For senior-level roles, mentor junior programmers and support team knowledge sharing
Required Qualifications and Experience
Statistical Programmer II
5–7 years of experience in statistical programming within a CRO or pharmaceutical environment
Hands-on expertise in SAS and R, with exposure to R Shiny preferred
Solid understanding of clinical trial data structures and statistical methodologies
Senior Statistical Programmer
7–10+ years of experience in statistical programming supporting global clinical trials
Advanced proficiency in SAS, R, and R Shiny
Demonstrated experience supporting regulatory submissions and leading programming deliverables
For Both Levels
Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field (advanced degree preferred)
Strong knowledge of clinical research processes and regulatory guidelines, including ICH and GCP
High attention to detail with strong analytical and problem-solving skills
Effective communication skills and the ability to collaborate across cross-functional and global teams
What ICON Offers
Competitive salary and performance-based compensation
Comprehensive health insurance plans for employees and dependents
Flexible work arrangements supporting work-life balance
Generous annual leave and holiday entitlements
Retirement and long-term financial planning benefits
Life assurance coverage
Global Employee Assistance Program (TELUS Health) with 24/7 access to wellness professionals
Country-specific benefits including childcare support, wellness initiatives, subsidized travel, and fitness programs
Diversity, Equity, and Inclusion
ICON is an equal opportunity employer committed to creating an inclusive and accessible workplace. All qualified applicants will receive equal consideration regardless of race, color, religion, gender, sexual orientation, gender identity, nationality, disability, or veteran status. Reasonable accommodations are available throughout the recruitment process.
Why Join ICON
This opportunity is open to professionals at different stages of their statistical programming careers and offers a strong platform for skill development, career progression, and contribution to impactful global clinical research.
Current ICON employees are encouraged to apply through the internal career portal.
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