Teams at HistoSonics

Lead and coordinate concurrent preclinical programs: oversee study execution (in vivo/ex vivo/in vitro), manage CROs and vendors, coordinate KOLs and labs, support regulatory/clinical/marketing inputs, and maintain timelines, trackers, and cross-functional alignment to advance medical-device preclinical development.

Designs, analyzes, and interprets clinical trial, RWE, and observational data for a medical device. Develops statistical plans, predictive models, and ensures data quality, regulatory compliance, and traceability. Collaborates with clinical, regulatory, and data teams, supports submissions and publications, mentors interns, and represents the company externally.

Provide procedural and clinical support for implementation and adoption of the Edison histotripsy system. Support live cases, site launches, physician onboarding, and workflow optimization. Collaborate with account managers, commercial, clinical, and R&D teams to drive utilization and procedural growth. Maintain clinical excellence, adherence to safety and compliance standards, and strong relationships with clinicians and staff. Travel within the assigned territory up to 75% for on-site support.