Job-ID31508345Reference25-04461 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).
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