Website Katalyst Healthcares & Life Sciences
Katalyst Healthcares & Life Sciences
Company : Katalyst Healthcares & Life Sciences
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.
- Fulfil ad-hoc analysis requests.
- Provide other services.
Requirements:
- Bachelor's 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.