Location : Remote – Located United States
Company Overview :
Prytime Medical Devices is committed to revolutionizing the toolset physicians use for patients at risk for bleeding. We design, develop, and commercialize innovative endovascular hemorrhage control devices, including the pREBOA-PRO™, the world’s first and only FDA cleared device indicated for partial balloon occlusion. Our goal is to improve the physician experience and elevate clinical outcomes.
General Description :
The Global Military and OUS Clinical Liasion is a subject matter expert responsible for global deployment, training, and clinical integration of the pREBOA-PRO™ catheter. This role supports strategic program development across U.S. DoD, NATO, and OUS markets, partnering with internal and external stakeholders to establish Early Aortic Intervention (EAI) Programs as a standard of care. The Liasion serves as a critical bridge between commercial, clinical, and operational teams, playing a central role in clinician training, protocol enhancement, data-driven performance tracking, and system-wide adoption initiatives.
The Liasion will report directly to the Vice President, Military Programs and coordinate with Commercial team members to include Medical Education, Data and Science, Training, Clinical Advisory Board and others as required.
Responsibilities :
Program Development & Integration : Lead global implementation of Early Aortic Intervention programs, ensuring consistent adoption across military, NATO, and civilian trauma systems.
Spearhead the launch and refinement of the Transport Index to benchmark aortic control and transport readiness to include Transport Index compliance
Collaborate with regional program development managers and distribution partners to drive integration within hospital systems and forward medical facilities.
Serve as a clinical liaison during program capture and health technology assessment (HTA) engagements with DoD, NATO, and EU health authorities.
Clinical Education & Training : Deliver on-site and virtual training to multidisciplinary clinical teams (ED, Trauma, OB, Anesthesia, ICU, IR, and Prehospital).
Support evaluator sites in training and early deployment of pREBOA-PRO™ and related technologies.
Contribute to the creation of educational content, simulation modules, and standardized training pathways (including ARTI-PRO and EARLI curricula).
Implement adult learning and evidence-based instructional methods to improve clinical competency and retention.
Stakeholder Engagement & Performance Metrics : Collaborate with internal team to integrate emerging evidence, feedback, and key opinion leader (KOL) insights into training content and clinical programs. Leveraging internal resources.
Lead the planning and documentation of case debriefs, ensuring actionable field feedback informs updates to clinical dashboards and protocols.
Track and report clinical performance metrics, including, time to aortic control, training completion rates and survival benchmarks.
Represent Prytime Medical at national and international conferences, trade shows, and clinical symposia.
Qualifications :
Bachelor’s degree in nursing, allied health, or related clinical field required; advanced degree preferred.
Licensed healthcare professional (RN, NP, PA, or MD) with 5+ years of acute care experience in trauma, emergency, critical care, or prehospital domains.
Demonstrated experience in clinical education or device training within hospital or military medicine environments.
Strong understanding of trauma workflows, massive transfusion protocols, and multidisciplinary hospital systems.
Experience with multinational or NATO medical systems strongly preferred.
Proficiency in simulation-based and remote training with adult learning design preferred.
Excellent interpersonal, presentation, and communication skills across diverse stakeholder groups.
Passion for improving survivability in time-sensitive hemorrhage scenarios.
This role supports clinical education and system integration activities. It does not provide direct patient care or clinical decision-making within regulated medical practice. All clinical recommendations and protocols will align with approved regulatory indications and CAB guidance.
Travel : Approximately 50-70%, including domestic and international and military training environments.
Clinical Clinical • United States