SDTM, Clinical SAS Programmer

Katalyst HealthCares and Life Sciences

• $110K — $130K *
North Wales, PA 19454In-Person
Pharmaceuticals & Biotech
8 - 10 years of experience
Today
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Job Overview by Ladders

Qualifications

  • 10+ years of experience in the clinical domain
  • In-depth knowledge of CDISC standards
  • Extensive programming experience in a clinical trial environment (CRO/Pharma)
  • Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO
  • Strong knowledge of SDTM

Responsibilities

  • Develop advanced SAS macros, templates, and utilities for data processing
  • Act as the primary programming point of contact for biostatisticians and study teams
  • Perform peer review of code and documentation for accuracy
  • Review Case Report Form (CRF) annotations and data specifications
  • Ensure compliance with CDISC standards and FDA/ICH guidelines

Benefits

  • Opportunities for professional development and training
  • Collaborative environment with cross-functional teams
  • Contributions impact real-world clinical outcomes
  • Access to cutting-edge technology and tools
Full Job Description
Job Description:
  • Looking for SDTM experts having in-depth knowledge of SAS programming(macro's).
  • Must have 10 yrs of exp in clinical domain.
  • Strong knowledge of SDTM.
  • Create advanced SAS macros, templates, and utilities for efficient data processing.
  • ct 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.
* Ladders Estimates

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