• Provide case support to physicians within certain territories. • Case support on peripheral and coronary interventional procedures in the pre-market and post-market phases of product development with the Shockwave Medical Intravascular Lithotripsy (IVL) technology. • Play a critical role in clinical studies including device training, case support, and ensuring timely data collection for clinical programs. • Manage key study investigators; foster and maintain strong relationships through direct interactions with medical advisors and clinical leaders. • Partner with other clinical research colleagues to meet business needs in the field including site re-training, data collection for timely database locks and resolution of critical issues. • Administrative activities including training to procedures, manage territory travel, and budgets. • Other duties as assigned.

• Assist in the maintenance and optimization of clinical onboarding modules within the Learning Management System • Ensure training materials reflect current practices, workflows, and platform capabilities • Support provider readiness by monitoring metrics and feedback related to onboarding and training activities. • Monitor designated communication channels to identify, triage, or escalate clinical or technical onboarding issues • Maintain and update clinical documentation and training materials across verticals and clients • Translate clinical workflows, regulatory requirements, and platform updates into clear, user-friendly educational materials • Assist in the development of new training resources related to clinical initiatives, workflow enhancements, or product updates • Support knowledge base management • Support the Sr. Clinical Specialist (NP) in coordinating required and supplemental materials for client launch preparedness • Collaborate with cross-functional teams to ensure clinical readiness for go-live • Participate in regular Clinical Education team meetings to align on priorities, share insights, and address challenges • Collaborate cross-functionally with Clinical Operations and Quality teams to support training and implementation efforts • Contribute to the ongoing refinement of clinical onboarding, training programs, and launch workflows to improve scalability and effectiveness • Identify trends, gaps, or recurring issues in provider education and escalate recommendations • Support quality improvement initiatives related to clinical training and provider performance • Assist with additional duties as assigned

• Administer stroke-specific scales to trial participants • Review and evaluate assessments conducted by other raters • Conduct live interactions with raters to provide feedback • Participate in training, orientation, and calibration sessions • Prepare for rater discussions by reviewing case data • Complete scheduled rater interactions and submit documentation

• Identify and coordinate specimen vendors for complex clinical specimen procurement, aligning their capabilities with study requirements • Manage all necessary documentation, track timelines, order statuses, and deliveries, while maintaining comprehensive records of communications and shipments • Follow SOPs related to specimen handling, chain of custody, and data integrity to ensure full compliance with applicable regulatory requirements (e.g., FDA, IRB policies) • Ensure specimen documentation is complete, properly labeled, and aligned with procurement or collection protocols • Work closely with Clinical Development teams to align specimen inclusion and exclusion criteria, data needed and other specimen requirements • Coordinate with the Biobank/Biorepository teams for timelines and ensure smooth transfer of specimens • Participate in cross-functional meetings and contribute to specimen tracking updates and inventory status reports • Share observations and suggestions for improving workflows and documentation related to prospective specimen collection