Clinical Specialist – TAVR

This is a fully remote position, open to applicants in Australia.

📋 Description

• Successfully complete the internal training program at Anteris, showcasing proficiency in CT and echocardiographic imaging, relevant Instructions for Use, procedural best practices, clinical evidence, authorized product messaging, and the competitive landscape.

• Collaborate with clinical trial sites, exhibiting expertise in all technical aspects of TAVI clinical case support, training and education, customer service, and effective communication.

• Exhibit competence in all procedural elements of DurAVR® THV case support, encompassing valve preparation and loading, device delivery and implantation, complication mitigation, and troubleshooting, in alignment with the clinical trial protocol and established best practices.

• Demonstrate a comprehensive understanding of the approved DurAVR clinical trial protocol, including inclusion and exclusion criteria and the requirements for pre- and post-procedure imaging and clinical data.

• Show proficiency in pre-case planning, CT analysis, and pre- and post-procedure recommendations to facilitate optimal clinical outcomes.

• Maintain extensive knowledge of existing DurAVR clinical data and the evolving landscape of structural heart evidence.

• Assist the Clinical and Regulatory Operations teams with site communications, data compliance activities, screening review efficiency, and requirements for site submissions.

• Attend designated clinical cases and aid the heart team with the preparation and loading of the DurAVR valve.

• Provide education and guidance to physicians and site personnel regarding the selection of suitable study participants, while ensuring complete and accurate patient screening and enrolment documentation.

• Monitor patient screening pathway activities and consistently provide site-level metrics related to screening progress and trial enrolment.

• Identify opportunities for operational improvements at the site level and propose strategies to accelerate enrolment, enhance efficiency, and appropriately advance therapy adoption.

• Maintain precise and timely documentation of case support, site activities, training, and other necessary clinical trial information.

• Adhere to 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

• Bachelor’s degree in health sciences, nursing, life sciences, or another relevant field, or an equivalent combination of education and clinical experience.

• A minimum of three years of clinical support experience in the medical device sector, including experience in the sterile environment of a cardiac catheterisation laboratory or operating theatre.

• At least two years of direct experience in structural heart TAVI procedures or device implantation is essential.

• Proven clinical expertise in interventional cardiology and structural heart therapies.

• Strong comprehension of cardiac anatomy, valvular heart disease, and TAVI procedures.

• Willingness and ability to travel approximately 50–70% of the time, including interstate and occasional international travel as required.

• Flexibility to support clinical procedures outside of standard business hours when necessary.

• Current Australian driver’s license and the ability to meet applicable hospital credentialing requirements.

• Full and ongoing working rights in Australia. Anteris cannot provide employer-sponsored visa support for this position.

🏝️ Benefits

• The chance to significantly impact patient care by advancing innovative structural heart therapies.

• A collaborative and dynamic work environment that fosters a culture of innovation, scientific excellence, and teamwork.

• Competitive compensation package, including base salary, superannuation, eligibility for short-term incentives, and equity participation.

• Opportunities for career development within a rapidly growing global medical device company.

• Annual leave, personal/carer’s leave, compassionate leave, and public holiday entitlements as per the National Employment Standards and company policy.

• An inclusive and supportive team environment.