Responsibilities:
The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting
Develop and validate SAS programs to support clinical trial data analysis and reporting
Create, maintain, and document SAS programming standards and procedures
Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met
Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency
The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry