📊 Drive Clinical Insights as Statistical Programmer II
Join ICON plc as a Statistical Programmer II and transform complex clinical data into meaningful insights that advance medical research. This pivotal role offers the opportunity to leverage your statistical programming expertise while contributing to groundbreaking clinical trials that shape the future of healthcare.
🎯 Your Impact: Key Responsibilities
Advanced Statistical Programming
- Develop, validate, and maintain complex statistical programs using SAS, R, or similar languages for clinical trial data manipulation, analysis, and reporting
- Prepare and review statistical analysis plans (SAPs), programming specifications, and derived datasets to meet rigorous regulatory standards
- Ensure data integrity and compliance with ICH/GCP guidelines throughout the programming lifecycle
- Create robust programming solutions for complex statistical methodologies and analysis requirements
Cross-Functional Collaboration
- Collaborate closely with biostatisticians and cross-functional teams to interpret study requirements and ensure accurate implementation of statistical analyses
- Communicate complex statistical concepts effectively to non-technical stakeholders and team members
- Work with data management teams to ensure clean, analysis-ready datasets
- Participate in study team meetings to provide programming insights and recommendations
Quality Assurance & Validation
- Implement comprehensive validation procedures for all statistical programming outputs
- Maintain detailed documentation of programming processes and validation activities
- Ensure all programming deliverables meet quality standards and regulatory requirements
- Support audit readiness through meticulous programming practices and documentation
Team Leadership & Development
- Mentor junior programmers and assist in training team members on advanced programming techniques and best practices
- Share knowledge and expertise to elevate team capabilities and programming standards
- Contribute to the development and improvement of programming processes and methodologies
- Provide technical guidance on complex programming challenges and solutions
⭐ Your Profile: Qualifications & Experience
Educational Foundation
- Bachelor's degree in Statistics, Mathematics, Computer Science, or related field
- Advanced degree (Master's or PhD) is a significant plus
- Strong academic background in statistical theory and methodologies
Technical Expertise
- 5+ years of experience as a statistical programmer within the clinical research industry
- Proficiency in programming languages such as SAS, R, or Python
- Experience with clinical data management systems and CDISC standards (SDTM, ADaM)
- Strong knowledge of statistical methodologies used in clinical trials
Professional Competencies
- Strong analytical and problem-solving skills with keen attention to detail
- Ability to work independently while contributing effectively to team objectives
- Excellent communication skills for conveying complex statistical concepts
- Experience mentoring junior team members and sharing technical knowledge
Regulatory Knowledge
- Understanding of ICH/GCP guidelines and regulatory requirements
- Experience preparing programming deliverables for regulatory submissions
- Knowledge of industry standards and best practices in statistical programming
- Familiarity with FDA, EMA, and other major health authority requirements
💫 Why Join ICON as a Statistical Programmer?
Technical Impact
- Work with cutting-edge statistical methodologies and programming technologies
- Contribute to diverse therapeutic areas and complex study designs
- Develop expertise in regulatory submission requirements and standards
- Access to advanced programming tools and computational resources
Professional Growth
- Clear pathway to Senior Statistical Programmer and Programming Lead roles
- Opportunities for advanced training in specialized programming techniques
- Exposure to global clinical development projects and international teams
- Support for professional certifications and continued education
Collaborative Environment
- Work with world-class biostatisticians and clinical research professionals
- Participate in cross-functional teams across the drug development lifecycle
- Engage in knowledge sharing with global programming community
- Access to mentorship from experienced statistical programming leaders
Meaningful Contribution
- Play vital role in ensuring accurate interpretation of clinical trial data
- Support the development of innovative treatments and therapies
- Contribute to regulatory submissions that bring new medicines to patients
- Ensure data integrity and statistical validity in clinical research
Comprehensive Benefits
- Competitive salary package with performance incentives
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support
- Generous annual leave and work-life balance initiatives
Career Development
- Retirement planning and financial security benefits
- Life assurance coverage
- Professional development funding and training opportunities
- Health and wellness programs
- Flexible work arrangements
✨ Ready to Advance Clinical Research Through Statistical Excellence?
If you're an experienced statistical programmer with passion for clinical research and expertise in SAS/R programming, we encourage you to apply. This Statistical Programmer II role offers the perfect opportunity to grow your career while contributing to meaningful clinical development through statistical programming excellence.
Apply Now & Transform Data into Medical Insights!
ICON is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
We welcome applications from all qualified statistical programmers - your technical expertise and clinical research experience might be exactly what we need at ICON!
