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Tunnell Government Services

Cardiologist - Heart Failure SME

Physicians & SurgeonsConfirmed 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, the 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 or the American College of Cardiology.
  • The candidate must have specialized qualifications in Advanced Heart Failure and Transplant Cardiology, such as completing an Advanced Heart Failure and Transplant Cardiology fellowship or having clinical practice experience in Advanced Heart Failure or Heart Transplantation.
  • The candidate must thoroughly understand current clinical practices in cardiovascular medicine, including diagnosis, treatment, and current or emerging practice trends.
  • The candidate must be an expert in the function and utilization of cardiovascular or interventional medical devices, including angioplasty devices, external or 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 well with others using written and verbal communication skills.
  • The candidate must effectively 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 expert consulting services to assist the FDA Center for Devices and Radiological Health with its regulatory responsibilities.
  • Provide consultation supporting 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.

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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