RL
SAS Consultant
Resource Logistics, Inc.
🇺🇸 United States
Hybrid
2 months ago
- SAS
- CDISC
- ICH
2 months ago
Location –Upper Gwynedd, PA /Rahway, NJ
Duration: Long Term contract
Role Overview
- Must have 6-8 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
SAS Consultant · Resource Logistics, Inc.