In this role you will design, implement, and validate SAS programs to support statistical analyses in clinical trials. You will work closely with biostatisticians to shape analysis plans and ensure outputs meet scientific and regulatory standards. You will perform thorough quality checks and help prepare statistical reports and regulatory submissions. You will look for opportunities to improve programming processes and contribute to team innovation. This is an opportunity to impact integral clinical development within a diverse, collaborative culture at ICON.
Compensaciones / Beneficios
- Annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
Responsabilidades
- Design, develop, and validate SAS programs for clinical trial data analysis
- Collaborate with biostatisticians to shape analysis plans and methodologies
- Conduct comprehensive quality control checks on statistical outputs
- Contribute to statistical reports, presentations, and regulatory submission documentation
- Identify enhancements to programming processes and drive continuous improvement
Requisitos principales
- Proven experience in statistical programming, ideally in clinical research or pharmaceutical industry
- Strong command of SAS programming and solid understanding of statistical concepts and clinical data analysis
- Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or related discipline
- Excellent analytical and problem-solving abilities with meticulous attention to detail
- Effective communicator with strong teamwork skills and ability to translate complex analyses into clear insights
- Effective communication
- Team collaboration
- Attention to detail
- SAS programming
- Statistical analysis of clinical trial data
- Quality control and validation processes