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Tunnell Government Services

Radiologist - Breast Imaging

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, District of Columbia, the Commonwealth of Puerto Rico, or a territory of the United States.
  • At least ten (7) years of relevant clinical experience is required.
  • Fellowship or equivalent training in breast imaging and substantial professional experience in breast imaging is required.
  • Certification from a relevant U.S. specialty board organization, such as the American Board of Radiology, and current qualification through the Mammography Quality Standards Act (MQSA) are required.
  • A thorough understanding of current clinical practices in radiology, including diagnosis and treatment, use of software to aid the radiologist, and current or emerging trends in practice is required.
  • Proficiency in all aspects of breast imaging, including mammography, ultrasound, MRI, and image-guided procedures is required.
  • Expertise in the function and utilization of medical devices commonly used as part of breast imaging radiology is required, including imaging systems, image-guided intervention devices, localization devices, breast tissue marker devices, contrast agents, artificial intelligence, and advanced imaging software.
  • Ability to communicate effectively with others in writing and verbally is required.
  • Ability to work effectively both independently and within a team of technical personnel is required.
  • Must be a U.S. citizen or full Green Card holder.

Responsibilities

  • Provide consultation supporting medical device reviews, including EUA, 510(k), PME, De Novo marketing applications, and pre-submissions.
  • 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

  • Experience evaluating clinical trial designs, identifying appropriate study endpoints, and reviewing study results is preferred.
  • Familiarity with FDA medical device regulatory processes, regulations such as 21 CFR Part 900—Mammography and 21 CFR Part 892—Radiology Devices, and guidance documents is preferred.

About the Company

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