Senior Clinical Research Scientist

🕒 September 1

❄️ Minnesota – Remote

❄️ Minnesota – Remote

💵 $130k - $160k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 6%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Anteris Technologies

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2006

🏥 Healthcare

🔧 Hardware

Healthcare • Hardware

Anteris Technologies is a medical technology company focused on developing next-generation transcatheter heart valve solutions to treat aortic stenosis. The company’s lead product, the DurAVR® Transcatheter Heart Valve (THV), is a single-piece, native-shaped biomimetic valve designed to mimic healthy aortic valve physiology and restore laminar flow. Anteris emphasizes science-driven, measurable improvements in cardiac outcomes, citing early clinical and retrospective analyses (EMBARK, EFS, PARADIGM and investigator-led studies) reporting favorable hemodynamics, reduced patient-prosthesis mismatch, and promising short-term safety signals. DurAVR® is currently available for investigational use only while the company pursues regulatory approvals and broader clinical evaluation. Anteris also engages with the medical community through presentations, webinars, and investigator-sponsored research to build clinical evidence for its biomimetic TAVR approach.

📋 Description

• Represent Anteris as an industry leader within scientific, clinical research, and industry organizations • Serve as a Scientific Lead and Subject Matter Expert for Anteris-sponsored clinical studies • Partner cross-functionally to support scientific objectives of clinical studies • Lead execution of the subject selection process and review subject eligibility criteria • Oversee external vendor performance and drive cross-functional collaboration • Contribute to clinical trial design, protocol development, revisions, and regulatory submission reports • Participate in publication planning with cross-functional stakeholders • Support charter development for clinical studies with external vendors and study leadership • Perform data analysis and interpretation with external biostatisticians and internal data management teams • Deliver study updates through presentations and data summaries • Develop, maintain, and review clinical study reports and related documentation • Contribute to root cause analyses, corrective and preventive actions, and effectiveness monitoring • Collaborate with study sites, vendors, committees, and other stakeholders; escalate issues as needed • Build and maintain relationships with study investigators and key opinion leaders • Contribute to Medical Legal Review activities for external data releases • Assist in compiling clinical documentation and data for regulatory submissions • Provide cross-functional clinical training and education support

🎯 Requirements

• Advanced degree in Life Sciences required; MD or PhD preferred • 5+ years of Clinical Science or Clinical Research experience within cardiology, cardiovascular, or medical device environments • Experience contributing scientifically to medical device clinical trials • Proficiency in medical terminology and medical writing, including experience working within ICMJE guidelines • Knowledge of healthcare ethics and compliance regulations • Strong work ethic, self-motivation, collaboration skills, and excellent written and verbal English communication skills • TAVR clinical research experience strongly preferred • Extensive clinical or scientific experience with advanced training in research, study design, and statistics (MSN, PhD, MS, or equivalent) preferred • Experience with imaging modalities, including echocardiography, CT, and CMR interpretation preferred • Experience supporting international, multi-center, randomized clinical trials preferred • Experience with statistical software programs such as Matlab, SPSS, or SAS is a strong plus

🏖️ Benefits

• Competitive compensation package including performance-based bonuses and stock options • Career development opportunities • Medical, Dental, and Vision Plans • Flexible Spending Account (FSA) • 401k + Company Match • Life, AD&D, Short-Term and Long-Term Disability Insurance • Bonus Plan Eligibility • Employee Stock Option Plan • Paid Holidays & Vacation • Employee Assistance Program • Inclusive Team Environment • Opportunity to make a significant impact on the healthcare industry • Collaborative and dynamic work environment with a culture of innovation and excellence