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About the role
<div class="content-intro"><p>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.</p>
<p>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.</p></div><p><span data-contrast="none">The </span><strong><span data-contrast="none">Senior Clinical Research Scientist</span></strong><span data-contrast="none"> will provide scientific, clinical, and operational expertise to support Anteris’ global clinical studies and ensure scientific objectives are achieved. This individual will work cross-functionally on the design, execution, monitoring, interpretation, and communication of clinical trial data to help advance patient outcomes through Anteris’ breakthrough structural heart technologies.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></p>
<p><span data-contrast="none">This position reports to the Senior Manager, Clinical Research and collaborates closely with the broader clinical and cross-functional teams to support ongoing clinical studies, clinical documentation, and the dissemination of clinical data through publications and congress activities. This is a highly visible role with the opportunity to make a significant impact at Anteris Technologies.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></p>
<p><span data-contrast="none">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.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></p>
<p><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span><strong><span data-contrast="none">Primary Duties and Responsibilities</span></strong><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></p>
<ul>
<li><span data-contrast="none">Represent Anteris as an industry leader within scientific, clinical research, and industry organizations</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Serve as a Scientific Lead and Subject Matter Expert for Anteris-sponsored clinical studies</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Partner cross-functionally to support the scientific objectives of Anteris-sponsored clinical studies and advance the company’s mission as a science-driven organization</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Lead execution of the subject selection process to ensure accurate and timely review of subject eligibility criteria, with oversight from clinical leadership</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Oversee external vendor performance and drive effective cross-functional collaboration</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Contribute to clinical trial design, protocol development, protocol revisions, and reports supporting regulatory submissions, with guidance from clinical leadership</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Participate in publication planning activities in collaboration with cross-functional stakeholders</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Support charter development for clinical studies in partnership with external vendors and study leadership, with oversight from clinical leadership</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Perform data analysis and interpretation in collaboration with external biostatisticians and internal data management teams</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Deliver timely study updates to clinical and cross-functional leadership through clear, well-structured presentations and data summaries</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Develop, maintain, and review clinical study reports and related documentation</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Contribute to root cause analyses, corrective and preventive actions, and effectiveness monitoring, with oversight from clinical leadership</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Collaborate with internal and external stakeholders, including study sites, vendors, and committees, to support clinical trial objectives and appropriately escalate issues when needed</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Build and maintain strong relationships with study investigators and key opinion leaders</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Contribute to Medical Legal Review (MLR) activities as a clinical subject matter expert for external data releases, ensuring scientific accuracy and appropriate clinical interpretation prior to publication or disclosure</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Assist in compiling clinical documentation and data for regulatory submissions</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Provide cross-functional clinical training and education support</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
</ul>
<p><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span><strong><span data-contrast="none">Required Education & Experience</span></strong><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></p>
<ul>
<li><span data-contrast="none">Advanced degree in Life Sciences required; MD or PhD preferred</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">5+ years of Clinical Science or Clinical Research experience within cardiology, cardiovascular, or medical device environments</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Experience contributing scientifically to medical device clinical trials</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Proficiency in medical terminology and medical writing, including experience working within ICMJE guidelines</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Knowledge of healthcare ethics and compliance regulations</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Strong work ethic, self-motivation, collaboration skills, and excellent written and verbal English communication skills</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
</ul>
<p><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span><strong><span data-contrast="auto">Preferred Skills, Knowledge, Experience & Qualifications:</span></strong><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></p>
<ul>
<li><span data-contrast="none">TAVR clinical research experience strongly preferred</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Extensive clinical or scientific experience with advanced training in research, study design, and statistics (MSN, PhD, MS, or equivalent)</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Experience with imaging modalities, including echocardiography, CT, and CMR interpretation</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Experience supporting international, multi-center, randomized clinical trials</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="none">Experience with statistical software programs such as Matlab, SPSS, or SAS is a strong plus</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
</ul>
<p><strong><span data-contrast="auto">What We Offer:</span></strong><span data-ccp-props="{}"> </span></p>
<ul>
<li><span data-contrast="none">Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Collaborative and dynamic work environment with a culture of innovation and excellence.</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Competitive compensation package, including salary, performance-based bonuses, and stock options.</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Career development opportunities and a chance to be part of a growing company that values its employees.</span><span data-ccp-props="{}"> </span></li>
</ul>
<p><strong><span data-contrast="auto">Health and Wellness Offerings:</span></strong><span data-ccp-props="{}"> </span></p>
<ul>
<li><span data-contrast="none">Medical, Dental, and Vision Plans</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Flexible Spending Account (FSA)</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">401k + Company Match</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Life, AD&D, Short-Term and Long-Term Disability Insurance</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Bonus Plan Eligibility</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Employee Stock Option Plan</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Paid Holidays & Vacation</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Employee Assistance Program</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="none">Inclusive Team Environment</span><span data-ccp-props="{}"> </span></li>
</ul><div class="content-pay-transparency"><div class="pay-input"><div class="description"><p><em>This is the national market pay scale.</em></p></div><div class="title">Salary Range</div><div class="pay-range"><span>$130,000</span><span class="divider">—</span><span>$160,000 USD</span></div></div></div><div class="content-conclusion"><p> </p>
<p>Note: We may require proof of COVID-19 vaccination to comply with health institutions, state, local municipality, and/or travel regulations.</p>
<p><em>Anteris Technologies recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.</em></p>
<p> </p></div>
Perks & benefits
- 401k
- Vision Insurance
- Paid Time Off
- Pension Matching
- Equity Compensation
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