Statistical Programmer I

What You Will Be Doing :

• Assisting in the development, validation, and maintenance of statistical programs (SAS, R, or similar) for data manipulation and analysis in clinical trials.
• Collaborating with senior statistical programmers and biostatisticians to understand project requirements and contribute to statistical analysis plans (SAPs).
• Performing data cleaning and preparation tasks to ensure data integrity and accuracy prior to analysis.
• Participating in the preparation of reports and documentation to support regulatory submissions and clinical study reports.
• Learning and applying industry standards, including ICH / GCP guidelines, to programming tasks to ensure compliance.

Your Profile :

Skills Required

Data Management, Programming Language, team environments , Clinical Trials, Integrity