Company:
Katalyst Healthcares & Life Sciences
Location: South Plainfield
Closing Date: 20/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
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.
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.
Share this job
Useful Links