Senior Statistical Programmer – Clinical Research
Job Requisition ID: JR142358
Employment Type: Full Time
Work Mode: Office-Based or Remote (Hybrid/Home Office Eligible)
Locations: Bengaluru, Trivandrum, Chennai, India
Experience Required: 7+ Years
Job Overview
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking an experienced Senior Statistical Programmer to support the analysis, reporting, and regulatory submission of clinical trial data. This role plays a key part in delivering high-quality statistical programming outputs that directly contribute to the success of global clinical development programs.
The position requires strong technical expertise in SAS and R, close collaboration with biostatistics teams, and a deep understanding of regulatory standards governing clinical research.
Key Responsibilities
Statistical Programming & Analysis
Develop, validate, and maintain statistical programs using SAS and R for the analysis and reporting of clinical trial data.
Generate and review analysis datasets, tables, listings, and figures (TLFs) in alignment with approved statistical analysis plans.
Ensure programming outputs meet regulatory submission standards and internal quality expectations.
Cross-Functional Collaboration
Work closely with biostatisticians to define and implement statistical methods and analysis strategies.
Support preparation of statistical reports, presentations, and submission-ready deliverables for regulatory authorities.
Quality & Process Excellence
Perform quality control (QC) checks to ensure accuracy, consistency, and data integrity across statistical outputs.
Identify opportunities to improve programming efficiency, standardization, and methodological best practices.
Required Qualifications & Experience
Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, Data Science, or a related discipline.
Minimum 7+ years of hands-on experience in statistical programming within a pharmaceutical, biotechnology, CRO, or clinical research environment.
Strong proficiency in SAS and R programming, with a solid understanding of statistical concepts and clinical trial methodologies.
Demonstrated experience supporting regulatory submissions and compliance with global standards such as ICH, GCP, and CDISC.
Skills & Competencies
Excellent analytical and problem-solving capabilities with strong attention to detail.
Ability to manage complex datasets and multiple deliverables in a regulated environment.
Strong communication and collaboration skills for working effectively with cross-functional teams.
Proven ability to translate complex statistical concepts into clear, actionable outputs.
Why Join ICON
ICON offers a collaborative, inclusive, and performance-driven work environment where employees are supported in building long-term careers. With flexible work options, competitive compensation, and comprehensive benefits, ICON empowers professionals to contribute meaningfully to global clinical research.
ICON is an equal opportunity employer committed to diversity, equity, and inclusion across its global workforce.
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