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 assignments with quality and within timelines, ensuring compliance with regulatory requirements
- Standardize deliverables across study projects and communicate programming deliverables' status and resource gaps
Required Qualifications
- Bachelor's or Master's Degree in Science, Statistics, Information Technology or equivalent
- 7+ years of professional experience in a pharmaceutical or clinical research setting as a programmer
- Proficient knowledge of clinical trials, drug development processes, and statistical concepts
- Strong understanding of SDTM and ADaM standards
- Demonstrated proficiency in using SAS for analysis datasets and TLGs
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