Statistical Programmer

About the role

As a Statistical Programmer at ICON, you will play a vital role in the development, validation, and execution of statistical programs to support clinical trial analysis and reporting. Your expertise will contribute to the accurate interpretation of clinical data, helping to ensure the successful delivery of research projects.

What you'll do

• Developing, validating, and maintaining complex statistical programs (SAS, R, or similar) for data manipulation, analysis, and reporting in clinical trials
• Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses
• Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards
• Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process
• Mentoring junior programmers and assisting in training team members on programming techniques and best practices

What you need

• 5–9 years in pharma & medical sales
• Clinical research
• SAS
• Clinical data management
• R
• Python
• Communication
• B.Tech or B.E. or B.Sc or BCA

Good to have

• Two-wheeler