Senior SDTM SAS Programmer - Clinical Data Expert

Katalyst CRO

North Wales (Montgomery County)

On-site

USD 120,000 - 160,000

Full time

7 days ago
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Job summary

Katalyst CRO is seeking an experienced SDTM expert with deep SAS programming skills to lead data processing and macro development for clinical trials. You will collaborate with biostatisticians and study teams, review CDISC-compliant specifications, and ensure accuracy and traceability across documentation.

This role requires 10+ years in the clinical domain, strong SDTM knowledge, and proficiency in SAS/Base, SAS/STAT, and SAS/MACRO. Regulatory standards and templates will guide daily work.

Qualifications

  • Extensive SAS programming experience in a clinical trial environment.
  • SAS macros, templates, and utilities for efficient data processing.
  • Deep knowledge of SDTM and CDISC standards for regulatory submissions.
  • Familiarity with FDA/ICH guidelines and data specifications.
  • Ability to act as programming point of contact for biostatisticians and study teams.
  • Peer review of code and documentation for accuracy and traceability.

Responsibilities

  • Act as the primary programming contact for biostatisticians and study teams.
  • Create and maintain SAS macros, templates, and utilities for data processing.
  • Review CRF annotations and data specifications for CDISC compliance.
  • Perform peer review of code and documentation for accuracy and traceability.
  • Ensure compliance with CDISC SDTM/ADaM and FDA/ICH guidelines.

Skills

SAS programming
SDTM knowledge
CDISC standards
SAS macros
Clinical data analysis

Tools

SAS/Base
SAS/STAT
SAS/MACRO

Job description

Katalyst CRO is seeking an experienced SDTM expert with deep SAS programming skills to lead data processing and macro development for clinical trials. You will collaborate with biostatisticians and study teams, review CDISC-compliant specifications, and ensure accuracy and traceability across documentation.

This role requires 10+ years in the clinical domain, strong SDTM knowledge, and proficiency in SAS/Base, SAS/STAT, and SAS/MACRO. Regulatory standards and templates will guide daily work.

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