Statistical Programmer
Job Requisition ID: JR138352
Employment Type: Full Time
Work Mode: Office or Home (Hybrid/Remote)
Locations: Bengaluru, Chennai, Trivandrum – India
Application Deadline: May 7, 2026
Experience Required: 5–8 Years
Job Overview
ICON plc, a globally recognized leader in healthcare intelligence and clinical research, is hiring a Statistical Programmer to support the analysis, reporting, and regulatory submission of clinical trial data. This role is integral to delivering high-quality statistical outputs that ensure data accuracy, regulatory compliance, and successful study outcomes across global clinical programs.
The Statistical Programmer will work closely with biostatistics and cross-functional teams to translate clinical protocols and statistical analysis plans into validated programming solutions.
Key Responsibilities
Statistical Programming & Analysis
Develop, validate, and maintain complex statistical programs using SAS, R, and related tools for clinical trial data analysis and reporting.
Generate derived datasets, tables, listings, and figures (TLFs) in accordance with study specifications and regulatory standards.
Collaboration & Study Support
Partner with biostatisticians and clinical teams to interpret study requirements and accurately implement statistical methodologies.
Support the preparation and review of Statistical Analysis Plans (SAPs) and programming specifications.
Quality & Compliance
Ensure data integrity, traceability, and compliance with ICH-GCP, CDISC, and regulatory guidelines throughout the programming lifecycle.
Perform peer reviews and quality control checks on statistical outputs.
Mentorship & Process Improvement
Mentor junior statistical programmers and support training initiatives to promote best programming practices.
Contribute to process optimization and standardization initiatives to improve programming efficiency and quality.
Required Qualifications & Experience
Bachelor’s degree in Statistics, Mathematics, Computer Science, or a related discipline; a Master’s degree is preferred.
Minimum 5 years of experience as a Statistical Programmer within a clinical research, CRO, or pharmaceutical environment.
Strong understanding of statistical methodologies applied to clinical trials.
Technical Skills
Advanced proficiency in SAS and R for clinical trial programming.
Exposure to Python, R Shiny, and clinical data management systems is an advantage.
Familiarity with CDISC standards such as SDTM and ADaM is preferred.
Core Competencies
Strong analytical and problem-solving skills with exceptional attention to detail.
Ability to work independently while managing multiple deliverables and timelines.
Excellent written and verbal communication skills, with the ability to explain complex statistical concepts to diverse stakeholders.
Why Join ICON
ICON offers a high-performance, inclusive work environment where professionals contribute to innovative clinical research while advancing their careers. Employees benefit from competitive compensation, flexible work arrangements, and comprehensive benefits designed to support well-being and work-life balance.
ICON is an equal opportunity employer committed to fostering diversity, equity, and inclusion. All qualified applicants will receive fair consideration regardless of race, religion, gender, sexual orientation, disability, or veteran status.
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