Job Overview
Location
United States Remote
Job Type
Full-time
Category
Data Science
Date Posted
May 7, 2026
Full Job Description
📋 Description
- • A senior medical leadership role providing cardiology expertise to support cardiac safety and efficacy solutions in clinical trials, driving measurable business results through scientific leadership and cross-functional collaboration.
- • Represent Clario as a subject-matter expert in cardiology and digital physiology, advising pharmaceutical sponsors on protocol design, cardiac safety strategies, statistical analysis, and regulatory submissions while supporting internal teams in Science, Marketing, Product, Clinical Data Operations, and Business Development.
- • Work within Clario, a global leader in endpoint technology solutions for clinical trials and part of Thermo Fisher Scientific, contributing to high-impact research and regulatory-ready deliverables across therapeutic areas.
- • Develop deep expertise in cardiac safety, digital physiology, and clinical trial innovation while influencing scientific strategy, mentoring teams, and advancing industry standards through research and regulatory engagement.
🎯 Requirements
- • MD degree required
- • ABIM Board Certification in Cardiovascular Diseases required for U.S.-based candidates
- • Minimum of three years’ experience in the pharmaceutical industry as an employed cardiologist or consultant, particularly in early-phase development
🏖️ Benefits
- • 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
Skills & Technologies
Senior
Remote
Degree Required
About Clario
Clario is a global healthcare technology and services company that provides endpoint data solutions for clinical trials. It delivers imaging, cardiac safety, respiratory, eCOA, and precision motion technologies, supported by scientific and regulatory expertise, to help biopharmaceutical sponsors generate high-quality evidence and accelerate drug development.
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