Job Summary
A company is looking for a SAS Programmer.
Key Responsibilities
- Provide comprehensive programming support for clinical trials, including development of programs and analysis datasets
- Manage and deliver programming assignments with high quality and within specified timelines
- Implement programming standards and ensure compliance with regulatory requirements across projects
Required Qualifications
- Bachelor's or Master's Degree in Science, Statistics, Information Technology, or a related field
- 7 years of experience with a Bachelor's or 6 years with a Master's in a pharmaceutical or clinical research setting
- Proficient knowledge of clinical trials, statistical concepts, and regulatory standards
- Expert level programming skills in SAS and knowledge of CDISC based e-submission
- Strong understanding of SDTM and ADaM standards
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