Clinical SAS Developer

Cynet Systems • Rahway, NJ

4d

About The Position

We are seeking experienced Clinical SAS Developers with in-depth knowledge of SAS programming, specifically focusing on SDTM standards. The role involves creating advanced SAS macros, templates, and utilities to ensure efficient data processing within clinical trials. You will serve as the main programming contact for biostatisticians and study teams, conduct peer reviews of code and documentation, and review CRF annotations and data specifications. A key aspect of this role is ensuring compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines.

Requirements

• 6-8 years of experience in the clinical domain.
• Strong knowledge of SDTM.
• 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.

Responsibilities

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: No Education Listed