Study Lead Programmer

As a Senior Statistical Programmer at ICON, you will drive statistical programming tasks with technical depth, focusing on quality and continuous improvement. You will work closely with biostatisticians to shape analysis plans and ensure accurate reporting for trials. The role includes programming, QC of outputs, and contributing to regulatory submissions, while advancing more efficient methodologies. This is a chance to impact medicine development at a global, values-driven organization.

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

• Developing and validating programs for statistical analysis and reporting of clinical trial data using SAS and R
• Collaborating with biostatisticians to define analysis plans and methods
• Performing quality control checks on statistical outputs and ensuring reporting accuracy
• 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

• Bachelor degree in statistics, computer science, mathematics, or a related discipline
• Experience in statistical programming in a clinical research or pharmaceutical setting
• Strong proficiency in SAS and R with solid understanding of statistical concepts
• Excellent analytical and problem-solving skills with keen attention to detail
• Strong communication and teamwork abilities
• Legal right to work in the country where the role is based

• collaboration
• attention to detail
• strong communication
• SAS
• R
• statistical analysis