SAS/ Statistical Programmer

at  Katalyst Healthcares Life Sciences

Responsibilities:

• 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.

Requirements:

• SAS/Statistical Programmer: 10+ Years.
• Bachelor’s degree in Computer Science, Statistics, Engineering or related field with minimum 6 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).

• 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