Sr. Clinical SAS Programmer
Sr. Clinical SAS Programmer
Posted on :
14-07-2025
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1 Vacancy
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Job Description
Responsibilities:
- Perform data manipulation analysis and reporting of clinical trial data.
- Develop and maintain department/system-level macros.
- Create and review SDTM and ADaM specifications.
- Create and validate SDTM data sets.
- Create and validate analysis data sets.
- Create and validate patient profiles.
- Program and generate tables figures and listings (TFLs).
- Validate and document SAS programs and outputs.
- Fulfill ad-hoc analysis requests.
- Provide other services.
- Bachelors degree or higher preferably in a scientific discipline such as Statistics Mathematics Computer Science or a related applicable field.
- Minimum of ten (10) years SAS programming experience in the pharmaceutical/biotech industry with extensive experience using CDISC standards.
- Ability to create source and validation programs using SAS software for SDTM datasets ADaM datasets and tables figures and listings (TFLs) for multiple studies/products.
- Experience integrating data across multiple studies or drug programs.
- Expertise in developing and using system-level macro programs.
- Experience programming with SAS/GTL.
- Proficiency in Microsoft Word Excel and PowerPoint.
Employment Type
Full-time
Key Skills
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