Create advanced SAS macros, templates, and utilities for efficient data processing. Skill: Extensive programming experience in a clinical trial environment (CRO/Pharma).
Numbers & Facts
Location
Rahway, NJ
Industry
Medical Devices and Supplies
Company Size
500 to 999 employees
Description
Job Title SAS Consultant 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