SAS Developer

Key Responsibilities: Create advanced SAS macros, templates, and utilities for efficient data processingAct as the primary programming point of contact for biostatisticians and study teamsPerform peer review of code and documentation for accuracy and traceabilityReview CRF (Case Report Form) annotations and data specifications.Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines. Skill Requirements: Extensive programming experience in a clinical trial environment (CRO/Pharma).Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO.In-depth knowledge of CDISC standards and regulatory submission requirements.Must have 5-7 yrs of exp in clinical domainStrong knowledge of SDTM.