Clinical Specialist - TAVR - AU

The role

The Clinical Specialist will support the execution of clinical trials and advance clinical evidence for TAVR technologies. This role involves providing procedural and clinical trial case support, contributing to trial enrolment, and educating heart team members.

What you will do

• Complete the Anteris internal training programme
• Interface with clinical trial sites for technical TAVI clinical case support, training, and education
• Provide DurAVR THV case support including valve preparation, loading, delivery, and implantation
• Perform pre-case planning and CT analysis
• Support Clinical and Regulatory Operations with site communications and data compliance
• Attend assigned clinical cases and support the heart team
• Provide education to physicians and site personnel regarding study participant identification
• Track patient screening pathway activity and provide site-level metrics
• Identify operational improvement opportunities to accelerate enrolment
• Maintain accurate documentation of case support and site activity

Required qualifications

• Bachelor’s degree in health sciences, nursing, life sciences or another relevant discipline, or an equivalent combination of education and clinical experience
• Minimum of three years of medical device clinical support experience, including experience in a cardiac catheterisation laboratory or operating theatre
• Minimum of two years of direct structural heart TAVI procedural or device implantation experience
• 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
• Current Australian driver’s license
• Ability to meet applicable hospital credentialling requirements
• Full and ongoing working rights in Australia

Nice to have

• Current registration with the Australian Health Practitioner Regulation Agency
• Experience supporting medical device clinical trials conducted in accordance with Good Clinical Practice and applicable Australian regulatory requirements
• Strong communication and organisational skills
• Ability to adapt to shifting priorities and manage competing clinical and operational demands
• Creative resourcefulness and strong problem-solving and decision-making capabilities
• Ability to work independently and confidently lead training
• Excellent interpersonal skills
• Entrepreneurial mindset, strong work ethic and commitment to achieving clinical and organisational goals

Benefits

• Base salary, superannuation, short-term incentive eligibility and equity participation
• Career development opportunities
• Annual leave
• Personal/carer’s leave
• Compassionate leave
• Public holiday entitlements

Before you apply

• Full and ongoing working rights in Australia required
• Anteris is unable to provide employer-sponsored visa support
• May require proof of COVID-19 vaccination to comply with health institutions, state, local municipality, and/or travel regulations

About the company

Anteris Technologies is a global structural heart company dedicated to revolutionizing cardiac care. The company seeks to restore healthy blood flow patterns by creating the world’s first biomimetic TAVR valve, DurAVR THV.