Clinical Specialist - TAVR

Anteris Tech

54d•$145 - $200•Remote

About The Position

Anteris® Technologies is a global structural heart company dedicated to revolutionizing cardiac care. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team. Our mission is to forge new frontiers in cardiac care by pioneering science-driven and measurable advancements to restore heart valve patients to healthy function. Transcatheter Aortic Valve Replacement (TAVR) technologies were originally designed for older, high-risk patients. Today, younger, more active patients need a better solution that will not just open and close but restore healthy heart function. We seek to restore healthy blood flow patterns by creating the world’s first biomimetic TAVR valve, DurAVR® THV. This cutting-edge valve, incorporating our proprietary ADAPT® anti-calcification technology, is designed to mimic the natural function of a healthy heart valve. We are seeking a Clinical Specialist to play an integral part in clinical trial support and execution, while also advancing clinical evidence and valve science. In this role, the Clinical Specialist will be responsible for TAVI clinical trial case support and procedural expertise, and they will play an active role in driving trial enrollment and identifying ongoing educational opportunities to heart team members and the referring community. This individual will work closely in collaboration with Clinical Affairs, Regulatory, R&D, Quality and Marketing to ensure optimal clinical outcomes and complete enrollment as aligned with corporate goals and strategy. This role may be filled at varying levels, depending on the candidate's previous experience, and will report to the Sr. Director of Pre-Market Therapy Development. This position will require 50-70% travel to support trial-related activities and will start in Q2 of 2026. At Anteris® Technologies, you'll be part of a team dedicated to enhancing the quality of life for patients with aortic stenosis through groundbreaking medical devices. Join us in our mission to revolutionize structural heart solutions.

Requirements

Bachelor of Science in health sciences, nursing, or life sciences.
A minimum of three years of medical device support and experience working in the sterile environment of a cath lab or operating room required.
YOU MUST HAVE 2+ years' Structural Heart TAVR procedural / device implant experience. Clinical expertise, specifically in interventional cardiology and TAVI Structural Heart, are required in order to be considered.
Ability to travel 50-70% of the time, as needed.

Nice To Haves

Outstanding communication, organizational skills, and ability to initiate and manage communication with physicians, research personnel, and internal colleagues.
Ability to identify and adapt to shifting priorities and competing demands.
Demonstrates creative resourcefulness, strong problem-solving and decision-making skills.
Independent, self-directed, and confident in leading trainings, providing clinical recommendations and leadership in case support.
Excellent interpersonal skills, interfacing with multiple constituencies including interventional cardiologists, cath lab staff and site support staff and colleagues.
Entrepreneurial spirit with a competitive drive and strong work ethic geared toward success.

Responsibilities

Successfully complete internal training program, including competency with CT and echo imaging, internal IFU, best practices, marketing messaging, clinical evidence, and competitive
Interface with clinical trial sites, demonstrating expertise and key competencies in all technical aspects of TAVI clinical case support, training & education, customer service and communication skills.
Demonstrate competency and expertise in all procedural aspects, including valve loading & preparation and device delivery and implantation according to established best practices, complication mitigation and troubleshooting techniques for DurAVR THV.
Demonstrate proficiency and understanding of all aspects of the approved DurAVR clinical trial protocol, including inclusion & exclusion criteria, and accuracy in obtaining any required imaging and pre & post procedural data.
Demonstrate proficiency in pre-case planning, CT analysis and pre & post procedure recommendations to ensure optimal clinical outcomes.
In-depth knowledge and understanding of existing DurAVR clinical data.
Support the Clinical & Regulatory Operations team, assisting with site communications, data compliance activity, screening review efficiency and site submission efficiency.
Attend clinical cases, supporting the heart team with device prep and loading of the DurAVR valve in each assigned case.
Provision of education and guidance to physicians and site staff in identifying appropriate study patients and assist site in ensuring complete patient screening and enrollment information.
Track all patient pathway screening process activity, routinely providing metrics per site on screening and progress of enrollment.
Identify operational improvement opportunities at the site level and recommend programs for enrollment acceleration, improved efficiency, and appropriate expanded therapy advancement tools and strategies.
Uphold the company AORTIC values: Accountability, Objectivity, Respect, Teamwork, Integrity, and Courage.

Benefits

Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.
Collaborative and dynamic work environment with a culture of innovation and excellence.
Competitive compensation package, including salary, performance-based bonuses, and stock options.
Career development opportunities and a chance to be part of a growing company that values its employees.
Medical, Dental, and Vision Offerings
Flexible Spending Account (FSA)
401k + Company Match
Life, AD&D, Short Term and Long-Term Disability Insurance
Bonus Plan Eligibility
Employee Equity Program
Paid Holidays & Vacation
Employee Assistance Program
Inclusive Team Environment