o Maintains and improves the Agendia QMS [compliance with FDA, IVDR, CLIA, ISO, etc.]. o Ensures applicable standards and regulations pertinent to Agendia are effectively implemented and acts as an advisor to all managers. o Leads development of regulatory submissions. o Provides support to currently marketed products as necessary labeling, product changes/documentation.

Identify, target, educate and manage accounts in the assigned territory including hospitals, pathology groups, oncologists, and surgeons on Agendia's products. Interfaces with current and new collaborations within the oncology field as required Works with managed care in a support role to develop and refine required clinical / medical documentation to support medical poli