Contract role: Senior Clinical SAS Developer at North Wales, PA (Onsite) || W2 Only

• Looking for SDTM experts having in-depth knowledge of SAS programming(macro’s)

• Must have 10+ yrs of exp in clinical domain
• Strong knowledge of SDTM
• Create advanced SAS macros, templates, and utilities for efficient data processing
• Act as the primary programming point of contact for biostatisticians and study teams
• Perform peer review of code and documentation for accuracy and traceability
• Review CRF (Case Report Form) annotations and data specifications.
• Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines

Skill:

• 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