Description

You will manage laboratory data systems and ensure seamless integration between testing and reporting platforms.

Responsibilities

  • Configure IRFs into laboratory computer systems such as ULTRA.
  • Liaise with IT and cross-functional teams to maintain system functionality.
  • Validate test codes and execute end-to-end validation between LIS and reporting systems.
  • Manage multiple projects and deliverables to meet established timelines.
  • Synthesize information from various sources to support laboratory data management.

Required Skills

  • 5+ years of experience in laboratory data management and Lab system Validation.
  • Experience with LIMS, CTMS, and ULTRA/LIS.
  • Knowledge of Corepoint and the ability to read HL7 messages.
  • Familiarity with FDA regulations, specifically 21 CFR Part 11.
  • Proficiency in Microsoft Excel and Word.
  • Strong analytical skills and attention to detail.
  • Ability to work independently and manage competing priorities.

Preferred Skills

  • Experience with end-to-end system validation workflows.

Education

Any Graduate