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Sr Cardiologist

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Onsite

Sr Cardiologist

Clario Inc

Sr Cardiologist

Skills

Product ManagementTesting & QASales OpsBusiness DevelopmentWorkdayCompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Remote, OR 97458, USA

Work mode:

Onsite

Published on:

26 August 2026

What they need


To deliver measurable business results through leadership in Cardiac Solutions consulting and Cardiac operations that meet both market needs and company goals. Assist other Clario departments including Science, Marketing, Product Management, Clinical Data Operations, and Business Development in developing and implementing Cardiac Solutions Strategies across Therapeutic areas. Provide consultation to Clario clients.  Assist sales with client retention and the development of new clients. Oversee other contract resources as assigned.

Clario, a part of Thermo Fisher Scientific, is a leading provider of endpoint technology solutions for clinical trials. We are seeking a Senior Cardiologist to provide scientific and medical leadership across cardiac safety and efficacy solutions, supporting pharmaceutical sponsors, regulatory interactions, and internal innovation. This role represents Clario externally and internally as a subject‑matter expert in cardiology and digital physiology, contributing to high‑quality clinical research and regulatory‑ready deliverables.

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
  • Board certification in Cardiovascular Diseases required for U.S.‑based candidates
  • Clinical Cardiac Electrophysiology training preferred
  • Minimum of three years’ experience in the pharmaceutical industry as an employed cardiologist or consultant, particularly in early‑phase development
  • Five or more years of clinical cardiology and electrocardiography experience preferred
  • Experience with concentration‑effect modeling and strong familiarity with ICH E14 guidance preferred
  • Experience authoring reports for QT waivers and working knowledge of clinical pharmacology desirable
  • Prior experience working with or consulting for pharmaceutical sponsors
  • Demonstrated high ethical standards and commitment to representing Clario with integrity and professionalism.

Clario, a part of Thermo Fisher Scientific, is a leading provider of endpoint technology solutions for clinical trials, transforming lives by accelerating the development of therapies for patients worldwide.

EEO Statement

Clario is an equal opportunity employer.  Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

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