- Design and implement a sophisticated physician education program for a novel energy modality (pulsed field ablation) and unique cardiovascular catheter design in support of rapid global commercialization. - Design and implement an internal education program for EMEA and APAC regions and certify specialists for product launches.- Multifaceted KOL management from inclusion as FARAPULSE Academy Sites, periodic assessment of sites for consistency with labeling and best practices, site launch execution, and customer feedback collection. - Develop collaborative physician peer-to-peer education to widen breadth and accessibility of content for future customers. - Collaborate effectively with global medical education teams (EMEA and APAC) to develop detailed and rigorous locally-led-and-managed internal training programs to support aggressive commercial launch.- Content creator and reviewer for online modules, in-service training deck, in-person group workshops, academy visits for internal and peer-to-peer physician training. - Ensure adherence to FARAPULSE ‘launch ticket’ concept - to drive sustainable and aggressive product adoption - increasing sales, shortening the learning curve, and ensuring consistent procedural outcomes.- Collaborate with global marketing and R&D teams to communicate voice of customer and device feedback- Develop and execute high-visibility physician programs to showcase commercial device and capture market interest

- Lead preclinical engineering team in pioneering the use of pulsed field ablation (electroporation) in the cardiac space - supporting US and European regulatory filings with several independent class III devices integrated into one system. - Manage several active preclinical sites and execution of multiple device’s protocols in support of early stage device development and regulatory submissions. - Manage planning, protocol development, and execution of biocompatibility testing for several class III medical devices per ISO 10993 guidelines - Manage team of engineers to meet high level company objectives while facilitating professional growth within company objectives.- Draft submissions for CE and FDA and work collaboratively to incorporate regulatory feedback into study design. Familiar with breakthrough pathway designation. - Create internal protocols and reports for preclinical testing in acute and chronic models consistent with GLP standards (21 CFR Part 58) in cardiac space.- Catheter manipulation and treatment as primary interventionalist in cardiac procedures in over 400 subjects.- Provide physician training and field clinical engineering support of three concurrent clinical trials.

- Managed design and execution of device dosing project to show control of energy source through complete spectrum of input conditions in support of FDA submissions.• Scheduled, executed, and processed data for several simultaneous preclinical protocols and locations. • Manipulated both catheter and system components during preclinical studies in over 300 subjects.• Built and managed database of preclinical data to improve device efficacy. • Compiled data as feedback to system robotic software engineers to drive algorithm improvements, and test improvements implemented. • Performed detailed subgross tissue sectioning overlaid with system energy monitoring data to build current dose model. - Trained clinical field engineers on device manipulation and system software manipulation in benchtop and preclinical settings. - Acted as interdisciplinary liaison between R&D, Clinical, Systems, and Software departments to ensure feature or usability requests from each department are communicated effectively and tracked. - Managed relationships between multiple active preclinical sites – coordinating with staff and submitting IACUC protocols and interleaving R&D objectives. - Managed acoustics test engineers’ throughput and yield, and perform scheduled retrospective analysis to catch potential irregularities early to ensure devices in development met all design requirements.

- Developed strong relationships between preclinical vendors and VytronUS – executed existing protocols at multiple preclinical sites. - Managed acoustic team testing and manufacturing schedule and kept team off of critical path including one test engineer and multiple interns. - Wrote and executed design verification on disposables and system-level specifications leading to multiple successful product releases and clinical trials under the ISO13485 standard. - Compiled a database of measurable device properties and for retrospective analysis feeding future process and design improvements. - Performed COGS analysis on critical device components and determined areas of potential improvement. - Redesigned and process developed hydrophilic coating procedures enabling transfer of processes from engineering to manufacturing