Responsibilities &Requirements:
- Understanding of clinical trial objectives, design, endpoints and procedures defined in Protocol and Statistical Analysis.
- Develop programs that convert raw SAS datasets into standard format and improve existing programs by creating standard programs and macros.
- Collaborate with manager and other programmers through participation in formal and ad-hoc meetings.Assist manager through contributions to continuous improvement by developing standard programs and macros that follow CDISC guidelines required for
- Bachelor's degree in computer science, Statistics, Engineering or related field with minimum 4 years of related experience. .
- Create ADS /ADAM datasets from RAW / SDTM datasets according to project / CDISC analysis data model standards; Independently write, test, run, document, maintain and QC SAS programs and macros to generate SAS datasets, spreadsheets, data listings, tables and graphical displays of clinical trials data.
- .Prior experience working with Data Management on edit checks etc is preferred Good knowledge of statistical programming languages. (including SAS)
- SAS/Statistical Programmer: 10+ Years.
- SDTM, ADaM, TLF and oncology trials- 4+ Years.