SAS Clinical Developer

TechDigital Group; Rahway (NJ); On-site; USD 80,000 - 110,000; Full time

Job summary

TechDigital Group is seeking a Clinical SAS Programmer located in Rahway, New Jersey. The role requires 6-8 years of experience in the clinical domain, with strong expertise in SDTM and SAS programming. You will collaborate with biostatisticians, ensuring regulatory compliance and performing peer reviews.

The ideal candidate has a proven track record in creating SAS macros and utilities, contributing significantly to clinical trials and data processing.

Qualifications

• 6-8 years of experience in the clinical domain.
• Strong knowledge of SDTM and regulatory requirements.
• Extensive programming experience in a clinical trial environment.

Responsibilities

• Serve as the primary programming contact for biostatisticians and study teams.
• Perform peer review of code and documentation.
• Ensure compliance with CDISC standards and regulatory guidelines.

Skills

SDTM

Clinical SAS programming

SAS macros

CDISC standards

Job description

Primary & Secondary Skill: SDTM/Clinical SAS

• 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