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
• Education & Experience:
• 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.
Location: South Plainfield, NJ
Posted: Oct. 13, 2024, 3:34 a.m.
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