- Location
- Durham, NC
- Workplace
- Onsite
- Type
- Full-time
- Department
- Research & Development
- Experience
- 3+ years
- Source
- Lever
Description
The Clinical Laboratory Specialist V is responsible for advanced post-analytical review activities supporting high-throughput clinical genomics testing within a regulated CLIA/CAP laboratory environment. This role focuses on comprehensive review of assay and bioinformatics-generated data following completion of laboratory and computational workflows to ensure accuracy, integrity, and quality of patient results prior to report release.
The individual performs detailed technical assessments of sequencing and assay performance metrics, evaluates data quality trends, investigates discrepancies, and supports timely and compliant report release activities. The role requires strong molecular biology and next-generation sequencing (NGS) knowledge, excellent analytical skills, and the ability to independently assess complex laboratory data within established quality and regulatory standards.
This position operates as an individual contributor within the clinical laboratory and plays a critical role in ensuring high-confidence patient reporting through rigorous data review and quality oversight.
This position works on-site full-time at our office located in Durham, NC
