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Clinical SAS Programmer

Company

Katalyst HealthCares & Life Sciences

Location

Raleigh, North Carolina

Posted

July 02, 2026

Position Overview


Responsibilities:
  • Review protocols for CDISC conformance.

  • Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements.

  • Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emmes' SDTM Implementation Guide, project standards, and the study protocol.

  • Create DEFINE specifications for mapping of SDTM and ADaM compliant datasets.

  • Review and QC submission ready SDTM datasets, , and supporting documentation, as appropriate.

  • Provide CDISC training and serve as a subject matter support to project staff.

  • Maintain and coordinate CDISC standards efforts, ensure maximum reuse of applied standards, involvement in ongoing process improvement efforts and working with teams to provide technical and process guidance.

  • Stay current with the evolution of all CDISC standards and be involved in creation and maintenance of process ...
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