Clinical Specialist - TAVR - AU

Job Description

We are seeking an experienced TAVI Clinical Specialist to play an integral role in supporting the execution of clinical trials while advancing clinical evidence and valve science. The Clinical Specialist will provide procedural and clinical trial case support, contribute to trial enrolment, and identify ongoing educational opportunities for heart team members and the broader referring community. This individual will collaborate closely with Clinical Affairs, Regulatory Affairs, R&D, Quality and Marketing to support optimal clinical outcomes and achieve enrolment objectives aligned with the company’s goals and strategy.

This position may be appointed at varying levels depending on the successful candidate’s qualifications and experience and will report to the Senior Director of Field Operations. The role requires approximately 50–70% domestic and occasional international travel to support trial-related activities and is expected to commence in Q3 / Q4 2026.

At Anteris® Technologies, you will be part of a team dedicated to improving the quality of life for patients with aortic stenosis through groundbreaking medical devices. Join us in our mission to revolutionise structural heart solutions.

Primary Responsibilities

• Successfully complete the Anteris internal training programme, including demonstrating competency in CT and echocardiographic imaging, the applicable Instructions for Use, procedural best practices, clinical evidence, approved product messaging and the competitive landscape.
• Interface with clinical trial sites, demonstrating expertise in all technical aspects of TAVI clinical case support, training and education, customer service and communication.
• Demonstrate competency in all procedural aspects of DurAVR® THV case support, including valve preparation and loading, device delivery and implantation, complication mitigation and troubleshooting, in accordance with the clinical trial protocol and established best practices.
• Demonstrate a thorough understanding of the approved DurAVR clinical trial protocol, including inclusion and exclusion criteria and requirements for pre- and post-procedure imaging and clinical data.
• Demonstrate proficiency in pre-case planning, CT analysis and pre- and post-procedure recommendations to support optimal clinical outcomes.
• Maintain in-depth knowledge and understanding of relevant clinical data, device technologies, and competitive products.