Research Nurse Coordinator

Anteris Technologies

2d•$120,000 - $140,000•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. The Research Nurse Coordinator will assist in in-house screening activities for a global, multi-center pivotal trial. This position will play a critical role in patient case planning and eligibility screening, collaborating closely with the clinical team to identify and prepare potential trial participants. This role will work closely with HCPs and the field clinical organization and will consult with cross-functional team members as needed. This position reports to the Senior Manager, Clinical Science and works collaboratively with the broader clinical science and field therapy teams to assist in subject preparation for screening activities. This is a remote position within the United States, and only minimal (10%) travel is required. At Anteris Technologies, you’ll join a mission-driven team dedicated to improving the lives of patients with aortic stenosis through breakthrough structural heart technologies while helping shape the future of structural heart care.

Requirements

Registered Nurse (RN) with current licensure.
Minimum 10 years of direct cardiovascular nursing experience, preferably in CCU, CICU, or structural heart programs.
Proven experience in patient assessment, heart failure management, and critical care.
Requires prior involvement in clinical trials or research-focused nursing; randomized clinical trial experience preferred.
Strong understanding of cardiology terminology and clinical trial endpoints
Exceptional attention to detail and organizational skills.
Excellent communication and collaboration abilities for cross-functional teamwork.
Proficiency with electronic medical records (EMR) systems and clinical documentation.

Responsibilities

Lead the end‑to‑end screening process, ensuring all pre‑procedure assessments (e.g., CT, echo, labs, risk scoring) are completed accurately and on time across participating sites.
Lead scientific and operational evaluation of inclusion/exclusion criteria, providing clear, defensible decisions on subject eligibility in alignment with the protocol and regulatory expectations.
Partner with investigators, coordinators, and field teams to drive screening performance, troubleshoot barriers, and ensure consistent application of screening criteria.
Collaborate with cardiologists, study coordinators, and clinical teams to prioritize potential participants.
Provide clinical insights to support case planning and feasibility discussions.
Ensure compliance with GCP, FDA, and trial protocols during all screening activities.
Lead live screening meetings to review cases and discuss patient eligibility trends.
Ensure completeness, accuracy, and protocol compliance of all screening‑related data; identify trends, gaps, and risks requiring corrective action.