📊 Drive Clinical Insights: Senior Statistical Programmer - India (Remote/Hybrid)
Join ICON plc as a Senior Statistical Programmer and transform clinical trial data into life-saving evidence. This role puts you at the heart of statistical innovation, where your SAS expertise will directly shape regulatory submissions and advance treatments for patients worldwide.
As a world-leading healthcare intelligence organization, we're seeking an experienced statistical programmer to lead the analysis of groundbreaking clinical trials. If you're passionate about turning complex data into clear insights that drive medical decisions, this is your opportunity to build a meaningful career while working on cutting-edge clinical development programs.
🎯 Your Programming Mission: Key Responsibilities
Statistical Programming Leadership
- Design, develop, and validate sophisticated SAS programs for statistical analysis and reporting of clinical trial data across all study phases
- Create complex statistical outputs including tables, listings, and figures (TLFs) that meet regulatory submission standards
- Implement CDISC standards (SDTM, ADaM) to ensure data consistency and regulatory compliance across global trials
- Perform comprehensive quality control checks and review statistical outputs to guarantee accuracy and adherence to project specifications
Collaborative Analysis & Strategy
- Work closely with biostatisticians to develop robust analysis plans and apply appropriate statistical methodologies
- Contribute to statistical analysis plans, clinical study reports, and regulatory submission documents
- Partner with data management teams to ensure data quality and integrity throughout the trial lifecycle
- Support the preparation of statistical sections for CSRs, publications, and regulatory interactions
Team Development & Knowledge Sharing
- Mentor junior programmers and provide technical guidance on complex programming challenges
- Contribute to team development by sharing best practices, programming standards, and technical knowledge
- Participate in process improvement initiatives to enhance programming efficiency and quality
- Foster a collaborative environment that promotes continuous learning and excellence
⭐ Your Profile: Statistical Programming Expertise
Essential Qualifications
- Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or related field
- 8+ years of end-to-end statistical programming experience in clinical research or pharmaceutical industry
- Expert proficiency in SAS programming with comprehensive knowledge of statistical concepts and methodologies
- Significant efficacy analysis experience with demonstrated ability to handle complex clinical trial data
Technical Mastery
- Advanced expertise in CDISC standards including SDTM and ADaM implementation
- Strong experience creating TLFs (Tables, Listings, Figures) for regulatory submissions
- Solid understanding of statistical analysis methods and clinical trial design principles
- Basic knowledge of R programming with willingness to expand technical capabilities
Professional Competencies
- Exceptional analytical skills with meticulous attention to detail and data accuracy
- Proven ability to manage multiple projects simultaneously while meeting tight deadlines
- Strong problem-solving capabilities for complex programming and statistical challenges
- Excellent communication skills for effective collaboration within multidisciplinary teams
Regulatory Expertise
- Experience supporting regulatory submissions (NDA, BLA, MAA) and agency interactions
- Knowledge of FDA, EMA, and other major health authority requirements
- Understanding of ICH-GCP guidelines and clinical data standards
💫 Why Build Your Programming Career at ICON?
Meaningful Impact Through Data
- Transform clinical trial data into evidence that supports new treatment approvals
- Work on diverse therapeutic areas and contribute to medical breakthroughs
- See your programming work directly impact patient care and healthcare outcomes
- Contribute to ICON's mission of accelerating drug development globally
Technical Growth & Innovation
- Work with cutting-edge statistical methodologies and programming technologies
- Access to continuous training in advanced statistical methods and new programming languages
- Clear pathway to Principal Programmer, Team Lead, and Management roles
- Exposure to complex study designs and innovative trial methodologies
Flexible Work Environment
- Remote and hybrid working options across India
- Modern technology infrastructure for seamless virtual collaboration
- Balance professional growth with personal lifestyle preferences
- Supportive team environment with global networking opportunities
Competitive ICON Benefits
- Attractive salary package with performance-based incentives
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support access
- Generous annual leave entitlements with flexible scheduling
- Retirement planning benefits and life assurance coverage
- Professional development allowance and certification support
- Wellness programs and team-building activities
✨ Ready to Program Medical Breakthroughs?
If you're an experienced statistical programmer with 8+ years of SAS expertise and passion for clinical research, we encourage you to apply. This Senior Statistical Programmer role offers the unique opportunity to advance your career while contributing to meaningful healthcare innovations that improve patient lives worldwide.
Apply Now and transform data into life-changing medical evidence!
