Remote Interventional Cardiologist — Regulatory & Device Expert

Tunnell Government Services, Inc.; Bethesda (MD); Remote; USD 250,000 - 420,000; Full time

Job summary

Tunnell Government Services, Inc. seeks an expert interventional cardiologist to provide regulatory consulting to the FDA CDRH Office of Cardiovascular Devices.

The candidate will leverage extensive clinical experience and board certification to support medical device reviews, submissions, and advisory activities for national and federal program clients. This 100% telework position requires US citizenship or permanent resident status, and a deep understanding of cardiovascular medicine, device

Qualifications

• Must possess an MD from an accredited US medical school.
• Current, active medical license to practice in the United States.
• Minimum 15 years of relevant clinical experience.
• ABIM/ACCI Interventional Cardiology certification.
• Specialized training in interventional cardiology and minimally invasive procedures.
• Deep understanding of cardiovascular medicine and device regulation practices.
• Familiarity with FDA medical device regulatory processes.
• Excellent written and verbal communication and teamwork.

Responsibilities

• Provide expert regulatory consulting to assist the CDRH with device reviews and related activities.
• Prepare written reviews and correspondence for regulatory submissions and communications.
• Participate in meetings and teleconferences with internal and external stakeholders.
• Coordinate meetings with engineers, statisticians, biologists, and other technical personnel.
• Ensure compliance with safety protocols and maintain high professional standards.

Skills

Interventional cardiology

Cardiology expertise

Medical license

Regulatory knowledge

Education

Doctor of Medicine (M.D.)

Board certification in Interventional Cardiology

Tools

Cardiac catheterization equipment

FDA regulatory processes familiarity

Job description

Tunnell Government Services, Inc. seeks an expert interventional cardiologist to provide regulatory consulting to the FDA CDRH Office of Cardiovascular Devices.

The candidate will leverage extensive clinical experience and board certification to support medical device reviews, submissions, and advisory activities for national and federal program clients. This 100% telework position requires US citizenship or permanent resident status, and a deep understanding of cardiovascular medicine, device