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 in-person and remote clinical support for implementation and adoption of the Edison System. Support live procedures, site launches, physician onboarding, workflow optimization, and cross-functional collaboration to drive procedural utilization and clinical excellence.