What are the responsibilities and job description for the SAS Clinical Trial Programmer - TXITSP position at NavitsPartners?
SAS Clinical Trial Programmer
Position Summary:
- 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.
