The SAS Clinical Trial Programmer supports all phases of clinical trial data analysis, from preparation to final submission, ensuring data accuracy and reliability.
Key Responsibilities :
Develop, validate, and maintain SAS programs for clinical trial analysis.
Support biostatistics teams with efficient, reproducible code.
Contribute to regulatory submission documentation.
Qualifications :
Bachelor’s in a technical field; Master’s preferred.
Minimum of 2 years in clinical programming.
Deep understanding of clinical trial methodologies and SAS programming.