Clinical SAS Developer

Resource Logistics, Inc.

🇺🇸 United States

Hybrid

2 months ago

SAS
CDISC
ICH

2 months ago

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Clinical SAS Developer
UpperGwynedd, PA /Rahway, NJ

1.Must have 6-8 yrs of exp in clinical domain
2.Strong knowledge of SDTM
3.Create advanced SAS macros, templates, and utilities for efficient data processing
4.Act as the primary programming point of contact for biostatisticians and study teams
5.Perform peer review of code and documentation for accuracy and traceability
6.Review CRF (Case Report Form) annotations and data specifications.
7.Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines
Skill:
1.Extensive programming experience in a clinical trial environment (CRO/Pharma).
2.Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO.
3.In-depth knowledge of CDISC standards and regulatory submission requirements

Clinical SAS Developer · Resource Logistics, Inc.

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