Clinical SAS Programmer Full-time Job

As a Clinical SAS Programmer, you will be responsible for developing, validating, and maintaining SAS programs used for analyzing clinical trial data. This role involves creating and managing datasets, tables, listings, and figures to support clinical research and regulatory submissions. You will work closely with biostatisticians, data managers, and clinical teams to ensure data accuracy and adherence to study protocols. Key responsibilities include designing statistical analysis plans, programming in SAS to meet study requirements, and performing data validation checks. You will also be tasked with troubleshooting and resolving data issues, creating comprehensive documentation, and ensuring compliance with regulatory standards such as FDA and EMEA guidelines. Effective communication skills and the ability to work collaboratively with cross-functional teams are essential. Strong knowledge of clinical trial methodologies and SAS programming best practices are required.