Clinical Specialist – TAVR

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

📋 Description

• Successfully complete the internal training program, ensuring competence in CT and echo imaging, internal IFU, best practices, marketing messaging, clinical evidence, and competitive insights.

• Engage with clinical trial sites, showcasing expertise and key skills in all technical aspects of TAVI clinical case support, training and education, customer service, and communication abilities.

• Exhibit proficiency and expertise in all procedural elements, including valve loading and preparation, as well as device delivery and implantation, in accordance with established best practices, complication mitigation, and troubleshooting techniques for DurAVR THV.

• Demonstrate a thorough understanding of all components of the approved DurAVR clinical trial protocol, including inclusion and exclusion criteria, while accurately obtaining any necessary imaging and pre- and post-procedural data.

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

• Possess extensive knowledge and understanding of existing DurAVR clinical data.

• Provide support to the Clinical & Regulatory Operations team by assisting with site communications, data compliance activities, screening review efficiency, and site submission efficiency.

• Attend clinical cases, aiding the heart team with device preparation and the loading of the DurAVR valve in each assigned case.

• Offer education and guidance to physicians and site staff in identifying suitable study patients and assist the site in ensuring complete patient screening and enrollment information.

• Monitor all patient pathway screening process activities, regularly supplying metrics per site on screening and enrollment progress.

• Identify opportunities for operational improvements at the site level and suggest programs for accelerating enrollment, enhancing efficiency, and advancing appropriate therapy tools and strategies.

• Adhere to the company AORTIC values: Accountability, Objectivity, Respect, Teamwork, Integrity, and Courage.

⛳️ Requirements

• Bachelor of Science in health sciences, nursing, or life sciences.

• At least three years of medical device support experience in the sterile environment of a cath lab or operating room is required.

• YOU MUST HAVE a minimum of 2+ years' experience in Structural Heart TAVR procedural/device implantation.

• Clinical expertise in interventional cardiology and TAVI Structural Heart is essential for consideration.

• Willingness to travel 50-70% of the time, as necessary.

🏝️ Benefits

• 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