Demo

SAS Programmer

Katalyst CRO
Jersey, NJ Full Time
POSTED ON 1/18/2026 CLOSED ON 2/16/2026

What are the responsibilities and job description for the SAS Programmer position at Katalyst CRO?

Responsibilities

  • You'll be at the forefront of developing and validating programs that create datasets conforming to CDISC standards.
  • Your expertise will drive the creation of Tables, Listings, and Figures for analysis purposes.
  • Depending on the complexity of the study, you may lead programming projects, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements.
  • You'll also have the opportunity to mentor junior programmers and represent Statistical Programming in meetings with internal and external clients.
  • Are you prepared to integrate statistical concepts with SAS Programming efficiently and effectively.
  • Support development of technical programming specifications for SDTM, ADS or ADaM standards.
  • Independently develop and/or validate programs that generate SDTM and analysis datasets based on Alexion or ADaM specifications.
  • Support development and validate technical programming specifications for tables, listings, figures/graphs based on Protocol and SAP.
  • Independently develop and validate programs that generate tables, listings, figures/graphs using Alexion specifications.
  • Manage external vendors and contract programmers.
  • Provide project progress updates of programming activities.
  • Review, maintain, and approve protocol-specific documents as necessary.
  • Provide guidance and mentoring to peer, junior-level Programmers and contract staff.
  • Support project leadership ensuring that department standards are implemented in all studies.
  • Contribute ideas and thoughts towards the optimization of standard operating procedures.
  • Lead team meetings when appropriate.
  • Independently and collaboratively resolve problems.

Requirements:

  • Statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.
  • Develop and validate technical specifications and programs for safety and efficacy analysis datasets, tables, listings, and figures/graphs.
  • Clearly communicate processes and standards with management and team members.
  • Competence in using SAS/Base, SAS/Macro, SAS/STAT.
  • Knowledge of SAS/Graph, and SAS/SQL.
  • Knowledge and implementation of.
  • SDTM and ADaM principals.
  • Relational Databases.
  • Good Clinical Practice principals.
  • Good Programming Practice principals.
  • 21CFR Part 11 Standards principals.
  • Integrated Summary Safety/Efficacy Analyses.
  • Safety data and Coding Dictionaries (MedDRA and WHODD).
  • ICH eCTD format.

Salary.com Estimation for SAS Programmer in Jersey, NJ
$96,402 to $119,253
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