Study Lead Programmer
ICON · Warsaw, Poland +9 more
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Role summary
A global clinical research organization seeks a Senior Statistical Programmer to lead statistical programming initiatives for clinical trials. The role involves developing and validating SAS and R programs, collaborating with biostatisticians on analysis plans, performing quality control checks, and contributing to process improvements. Candidates need a bachelor's degree in statistics or related field, clinical programming experience, and strong proficiency in SAS and R.
What they're looking for
- Bachelor's degree in statistics, computer science, mathematics, or related field
- Statistical programming experience in clinical research or pharmaceutical settings
- Strong proficiency in SAS and R programming languages
- Solid understanding of statistical concepts and methodologies
- Excellent analytical and problem-solving skills with attention to detail
- Strong communication and collaborative teamwork abilities
- Legal right to work in the country where role is based
What you'll be doing
- Develop and validate programs for statistical analysis and clinical trial data reporting
- Collaborate with biostatisticians to define analysis plans and statistical methods
- Perform quality control checks on statistical outputs for accuracy and consistency
- Assist in preparing statistical reports, presentations, and publications for regulatory submissions
- Identify and contribute to process improvements in programming practices and methodologies
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.