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Clario

Cardiologist

northern, KY

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Job description

Clario, a part of Thermo Fisher Scientific, is a leading provider of endpoint technology solutions for clinical trials. We are seeking a Cardiologist to provide scientific and medical leadership across cardiac safety, cardiac efficacy, and digital physiology solutions. In this highly visible role, you will partner with pharmaceutical sponsors, contribute to regulatory strategy, advance innovative endpoint development, and serve as a trusted cardiology expert internally and externally. Your expertise will help drive high-quality clinical research, support regulatory decision-making, and accelerate the development of therapies that improve patients' lives worldwide.

What We Offer

Competitive compensation aligned to the U.S. market

Comprehensive health, retirement, and wellness benefits

Opportunities to work on global, high‑impact clinical programs

Collaboration with leading scientists, clinicians, and technologists

Ongoing professional development and research engagement

What You’ll Be Doing

Represent Clario by providing cardiology expertise to pharmaceutical sponsors across consulting services, including protocol design and development, cardiac safety and efficacy strategies, statistical analysis plans, expert report writing, and regulatory representation

Serve as a cardiology liaison across internal departments, supporting cardiologist activities, cardiac solutions, safety consulting, and cardiac‑related compliance strategies

Support clinical consulting for Digital Physiology and other Clario endpoints, enabling cross‑business‑unit opportunities and therapeutic area strategies

Participate in client discussions for prospective and ongoing studies requiring cardiac safety or efficacy approaches

Assist Cardiac Solutions Scientific and Medical Affairs leadership in developing, maintaining, and updating policies, procedures, and SOPs, including Cardiology Review Guidelines and expanded digital physiology endpoints

Stay current on scientific advancements in cardiac safety and efficacy and educate internal stakeholders as appropriate

Support generation of endpoint data through interpretation of ECGs, Holters, patch devices, stress tests, blood pressure variability assessments, and related endpoints, including QA and QC activities

Contribute to ECG core lab procedures to enhance interpretation quality, consistency, and operational efficiency

Provide sales support by contributing scientific and clinical expertise as needed

Support system development and validation efforts for EXPERT and other Clario platforms

Participate in meetings and research collaborations with regulatory authorities

Provide leadership in statistical innovation and research, supporting sponsor interactions involving statistical design and analysis and contributing strategically across Clario lines of business

What We Look For

MD degree required

ABIM Board Certification

Clinical Cardiac Electrophysiology training preferred

Experience in clinical cardiology and electrocardiography experience preferred

Prior experience working with or consulting for pharmaceutical sponsors

Demonstrated high ethical standards and commitment to representing Clario with integrity and professionalism

At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Clario Privacy Policy

Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.

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