What You Will Do:

As a Senior Statistical Programmer I at ICON, you will analyse clinical trial data and support the statistical analysis process to ensure high-quality results.

Key Responsibilities:

• Developing and validating SAS programs for statistical analysis and reporting of clinical trial data.
• Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.
• Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting.
• Assisting in the preparation of statistical reports, presentations, and publications for regulatory submissions.
• Contributing to process improvements by identifying efficiencies in programming practices and methodologies.

Your Profile:

You will have a strong foundation in statistical programming, with the experience to work independently and guide others.

Required Qu...