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Tunnell Government Services

Interventional Cardiologist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBethesda, MD, USANo salary listed

About the Job

Requirements

  • The candidate must possess a Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States.
  • The candidate must possess a current, active, full, and unrestricted medical license or registration as a Physician to practice medicine in a State, District of Columbia, the Commonwealth of Puerto Rico, or a territory of the United States.
  • The candidate must have at least fifteen years of relevant clinical experience.
  • The candidate must hold certification from a relevant U.S. specialty board organization, such as the American Board of Internal Medicine, American College of Cardiology, or ABIM Interventional Cardiology.
  • The candidate must have completed specialized training and have experience sufficient to serve as a subject matter expert in interventional cardiology, such as an Interventional Cardiology fellowship, clinical practice, and advanced training in minimally invasive, catheter-based procedures including cardiac catheterization, percutaneous coronary intervention, and transcatheter aortic valve repair.
  • The candidate must thoroughly understand current clinical practices in cardiovascular medicine, including diagnosis and treatment, and current and emerging practice trends.
  • The candidate must be an expert in the function and utilization of cardiovascular and/or interventional medical devices, including angioplasty devices, external and internal defibrillators, ablation catheters, pacemakers, prosthetic valves, and stents; this includes knowledge of non-invasive diagnostic devices and instruments, invasive implantable devices, and surgical systems.
  • The candidate must communicate effectively with others using written and verbal communication skills.
  • The candidate must be able to work independently and within a team of technical personnel, including engineers, statisticians, and biologists.
  • The candidate must be a U.S. citizen or full Green Card holder.

Responsibilities

  • Provide consultation to support medical device reviews, including EUA, 510(k), PMA, HDE, and De Novo marketing applications, pre-submissions, Investigational Device Exemptions, and recalls.
  • Participate in meetings and teleconferences.
  • Coordinate meetings with internal and external stakeholders.
  • Develop written reviews and correspondence.
  • Perform research and conduct data analysis.
  • Write detailed documents and reports.
  • Execute administrative office tasks related to CDRH projects.
  • Provide expert consulting services to assist CDRH with its regulatory responsibilities.

Desired Qualifications

  • Familiarity with FDA medical device regulatory processes, regulations such as 21 CFR Part 870 for Cardiovascular Devices, and related guidance.

About the Company

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