Clinical Specialist – TAVR

Anteris Technologies

Clinical Specialist at Anteris Technologies supporting clinical trials with a focus on TAVI and valve science. Providing procedural support and advancing clinical evidence within the heart care team.

Posted 7/27/2026full-timeRemote • 🇦🇺 AustraliaMid-LevelSenior💰 A$145,000 - A$200,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in TAVI clinical case support, including valve preparation, device delivery, and troubleshooting, while maintaining compliance with clinical trial protocols and Australian regulations. Proficient in pre-case planning, CT analysis, and providing education to clinical teams to ensure optimal patient outcomes.

Highest-signal resume keywords

TAVI Procedural ExperienceInterventional Cardiology ExpertiseClinical Trial Protocol ComplianceCardiac Anatomy KnowledgeMedical Device Clinical Support

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

CT ImagingEchocardiographic ImagingValve PreparationDevice DeliveryComplication MitigationPre-Case PlanningClinical Data AnalysisPatient ScreeningDocumentation ManagementRegulatory Compliance

Soft Skills

Customer ServiceCommunicationTeamworkFlexibilityProblem-Solving

Certifications & Qualifications

Bachelor’s Degree in Health SciencesCurrent Australian Driver’s License

Industry Keywords

DurAVRStructural Heart TherapiesCardiac Catheterisation LaboratoryOperating TheatreClinical Trial RequirementsPatient EnrolmentSterile EnvironmentClinical EvidenceBest PracticesAORTIC Values

About the role

Key responsibilities & impact

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 existing DurAVR clinical data and the evolving structural heart evidence landscape.
Support the Clinical and Regulatory Operations teams with site communications, data compliance activities, screening review efficiency and site submission requirements.
Attend assigned clinical cases and support the heart team with preparation and loading of the DurAVR valve.
Provide education and guidance to physicians and site personnel regarding the identification of appropriate study participants and support complete and accurate patient screening and enrolment documentation.
Track patient screening pathway activity and routinely provide site-level metrics related to screening progress and trial enrolment.
Identify operational improvement opportunities at the site level and recommend strategies to accelerate enrolment, improve efficiency and appropriately advance therapy adoption.
Maintain accurate and timely documentation of case support, site activity, training and other required clinical trial information.
Comply with all applicable Australian regulations, clinical trial requirements, company policies and site-specific procedures.
Uphold the company’s AORTIC values: Accountability, Objectivity, Respect, Teamwork, Integrity and Courage.

Requirements

What you’ll need

Bachelor’s degree in health sciences, nursing, life sciences or another relevant discipline, or an equivalent combination of education and clinical experience.
A minimum of three years of medical device clinical support experience, including experience working within the sterile environment of a cardiac catheterisation laboratory or operating theatre.
A minimum of two years of direct structural heart TAVI procedural or device implantation experience is essential.
Demonstrated clinical expertise in interventional cardiology and structural heart therapies.
Strong understanding of cardiac anatomy, valvular heart disease and TAVI procedures.
Ability and willingness to travel approximately 50–70% of the time, including interstate and occasional international travel, as required.
Flexibility to support clinical procedures outside standard business hours when necessary.
Current Australian driver’s license and the ability to meet applicable hospital credentialling requirements.
Full and ongoing working rights in Australia. Anteris is unable to provide employer-sponsored visa support for this position.

Benefits

Comp & perks

The opportunity to make a meaningful impact on patient care by advancing groundbreaking structural heart therapies.
A collaborative and dynamic working environment with a culture of innovation, scientific excellence and teamwork.
Competitive compensation, including base salary, superannuation, short-term incentive eligibility and equity participation.
Career development opportunities within a growing global medical device company.
Annual leave, personal/carer’s leave, compassionate leave and public holiday entitlements in accordance with the National Employment Standards and company policy.
Inclusive and supportive team environment.