Take ownership of regulatory strategies for in vitro diagnostics, leading cross-functional teams to ensure compliance with U.S. and European regulations while driving successful product submissions and lifecycle management.

Join a dynamic team and lead regulatory strategies for in vitro diagnostics, ensuring compliance and successful submissions while collaborating cross-functionally. Manage project timelines and mentor junior staff in the regulatory process.

Unlock potential by leading regulatory strategies for in vitro diagnostics, ensuring compliance and effective submissions, while collaborating with cross-functional teams to manage product developments and approvals throughout their lifecycle.

Develop strategic partnerships with oncologists and healthcare providers to drive adoption of an innovative AI-powered diagnostic tool for breast cancer treatment, focusing on clinician education and workflow integration.

Advance clinical adoption of an AI-powered assay, educating healthcare providers and fostering key relationships to drive utilization and optimize patient outcomes in early-stage breast cancer treatment.