đ Drive Oncology Clinical Trials Through Advanced Statistical Programming
Join ICON plc as a Statistical Programmer II specializing in R and SAS programming with an oncology focus. In this critical role, you'll leverage your statistical expertise to transform complex clinical data into meaningful insights that advance cancer treatment development and improve patient outcomes worldwide.
đŻ Your Impact: Key Responsibilities
Statistical Programming Excellence
- Develop, validate, and maintain complex statistical programs using R and SAS
- Support data manipulation, analysis, and reporting for oncology clinical trials
- Ensure accurate implementation of statistical methodologies
- Create and maintain derived datasets per study requirements
Clinical Trial Analysis & Reporting
- Collaborate with biostatisticians to interpret study requirements
- Prepare and review statistical analysis plans (SAPs) and programming specifications
- Generate tables, listings, and figures for clinical study reports
- Ensure outputs meet regulatory submission standards
Quality & Compliance
- Maintain data integrity throughout the programming process
- Ensure compliance with ICH/GCP guidelines and regulatory requirements
- Validate programming outputs for accuracy and consistency
- Adhere to standard operating procedures and best practices
Team Leadership & Development
- Mentor junior programmers on R and SAS programming techniques
- Share oncology-specific programming knowledge and insights
- Contribute to team training and process improvement
- Provide technical guidance on complex programming challenges
â Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in Statistics, Mathematics, Computer Science, or related field
- 4+ years of end-to-end statistical programming experience in clinical research
- Hands-on experience with R and SASÂ programming
- Oncology therapeutic area background
- Experience with clinical data management systems
Technical Expertise
- Proficiency in statistical programming languages (R, SAS, Python)
- Strong knowledge of statistical methodologies and clinical trial design
- Experience with CDISC standards (SDTM, ADaM)
- Understanding of regulatory submission requirements
Professional Competencies
- Strong analytical and problem-solving abilities
- Keen attention to detail and accuracy
- Excellent communication and collaboration skills
- Ability to convey complex statistical concepts clearly
- Capacity to work independently and in team environments
đŤ Why Join ICON?
Career Advancement
- Specialized role with oncology focus and advanced programming
- Clear pathway to Senior Programmer and Lead positions
- Exposure to cutting-edge statistical methodologies
- Opportunities for professional development and certification
Meaningful Impact
- Contribute to groundbreaking oncology clinical research
- Support development of innovative cancer treatments
- Work with complex datasets that inform treatment decisions
- Ensure data integrity for critical clinical trials
Comprehensive Benefits
- Competitive compensation package
- Flexible work arrangements
- Comprehensive health and wellness programs
- Global employee assistance program
- Professional development support
⨠Ready to Advance Oncology Research Through Statistical Excellence?
If you're an experienced statistical programmer with R/SAS expertise and oncology background, we encourage you to apply. Join us in transforming clinical data into life-changing insights for cancer patients worldwide.
Apply Now & Power Oncology Clinical Development
