Summary :
As a Clinical SAS Programmer, you will be responsible for attending multi-disciplinary team meetings to represent the programming function. You will create or review and approve programming plans at study and project levels, providing input on key study-related documents produced by other functions.
Key Responsibilities :
- Developing CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.
- Creating or reviewing software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.
- Assisting statisticians by suggesting algorithms to address client analysis requests.
- Developing software validation procedures and test plans
Requirements :
Minimum years of experience in developing software for clinical trials using the SAS system.Skilled in programming with SAS. Knowledge of additional programming languages a plus.Good knowledge of statistics and drug development process.Experience as a lead programmer for NDAs / BLAs.Experience overseeing the work of internal contractors and external vendors (CROs).