Senior Cardiologist — Cardiac Safety & Endpoint Strategy Lead

Clario

United States

On-site

USD 180,000 - 240,000

Full time

14 days+

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Benefits offered by this job

Competitive compensation
Comprehensive health and retirement_BE
Global clinical program exposure
Collaboration with leading scientists
Ongoing professional development

Job summary

Clario, a part of Thermo Fisher Scientific, is seeking a Senior Cardiologist to provide scientific and medical leadership across cardiac safety, cardiac efficacy, and digital physiology solutions. You will partner with pharmaceutical sponsors, contribute to regulatory strategy, and advance endpoint development.

You will educate internal stakeholders, support regulatory decision-making, and help accelerate therapies that improve patient lives worldwide.

Qualifications

  • MD licensed cardiologist with board certifications.
  • Experience in early-phase pharmaceutical development.
  • Strong knowledge of cardiac safety endpoints and QT risk assessment.
  • Familiarity with ICH E14 guidance and concentration–effect modeling.

Responsibilities

  • Provide cardiology expertise across protocol design, cardiac safety and efficacy strategies, and regulatory representation.
  • Lead cross-functional teams and liaise with pharmaceutical sponsors.
  • Support digital physiology endpoints and cross‑unit opportunities.
  • Contribute to ECG core lab procedures and data interpretation.

Skills

Cardiology expertise
ECG interpretation
Clinical research in pharma
Regulatory strategy familiarity
Scientific leadership

Education

MD degree
ABIM Board Certification
Board certification in Cardiovascular Diseases
Clinical Cardiac Electrophysiology training

Job description

Clario, a part of Thermo Fisher Scientific, is seeking a Senior Cardiologist to provide scientific and medical leadership across cardiac safety, cardiac efficacy, and digital physiology solutions. You will partner with pharmaceutical sponsors, contribute to regulatory strategy, and advance endpoint development.

You will educate internal stakeholders, support regulatory decision-making, and help accelerate therapies that improve patient lives worldwide.

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