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.