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Develop and validate SAS, R, and Python programs supporting clinical-trial data analysis and reporting at ICON plc. Partner with biostatistics and clinical teams on regulatory documentation and treatment-development activities.
विवरण
- Create, validate, and maintain SAS, R, or comparable statistical programs for clinical-trial data processing, analysis, and reporting
- Work with biostatisticians and clinical teams to clarify project needs and implement statistical analyses accurately
- Draft and review statistical analysis plans and programming specifications in line with regulatory expectations
- Maintain data quality and comply with applicable industry standards, including ICH/GCP guidelines, throughout programming activities
- Contribute to clinical study reports and other materials submitted to regulatory authorities
- Produce high-quality statistical programming deliverables in collaboration with project stakeholders and colleagues
आवश्यकताएँ
- Bachelor’s degree in statistics, computer science, mathematics, or a related field
- Demonstrated clinical-research experience as a statistical programmer, including a strong understanding of statistical methods
- Working knowledge of SAS, R, or Python and experience with clinical data management systems
- Strong analytical and problem-solving abilities, careful attention to detail, and the capacity to work independently or collaboratively
- Clear communication skills, including the ability to explain complex statistical topics to non-technical stakeholders
- Legal authorization to work in the country where the position is located
लाभ
- Base salary with performance-based incentives
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable
- Retirement and pension programs
- Life assurance and disability coverage
- Employee assistance programs and wellbeing resources
- Professional development through structured training and career progression pathways
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