Tunnell Government Services, Inc.
Radiologist (Breast Imaging)
Provide expert consulting services to assist the FDA Center for Devices and Radiological Health (CDRH) with regulatory responsibilities. Duties include supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, pre-submissions), participating in meetings and teleconferences, coordinating meetings with internal and external stakeholders, developing written reviews and correspondence, performing research, conducting data analysis, writing detailed documents and reports, and executing other administrative office tasks related to CDRH's projects.
Key Responsibilities
- • Provide expert consulting services to assist the CDRH with their regulatory responsibilities.
- • Provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, pre-submissions)
- • Participate in meetings and teleconferences
- • Coordinate meetings with internal and external stakeholders
- • Develop written reviews and correspondence
- • Perform research
- • Conduct data analysis
- • Write detailed documents and reports
- • Execute other administrative office tasks related to CDRH's projects
Required
- • The candidate must possess a Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States
- • In addition, 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
- • Fellowship or equivalent training in breast imaging and substantial professional experience in breast imaging
- • Certification from a U.S. relevant specialty board organization (e.g., American Board of Radiology); current qualification through the Mammography Quality Standards Act (MQSA)
- • Thorough understanding of current clinical practices in radiology, including diagnosis and treatment, use of software to aid the radiologist, and current/emerging trends in practice
- • Proficient in all aspects of breast imaging, including mammography, ultrasound, MRI and image-guided procedures
- • Expert in function and utilization of medical devices commonly used as part of breast imaging radiology (e.g., imaging systems, image-guided intervention devices, localization devices, breast tissue marker devices, contrast agents, AI and advanced imaging software, etc.)
- • Ability to communicate well with others using excellent written and verbal communication skills
- • Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel
- • This candidate should possess specific expertise and training in clinical medicine and breast imaging radiology, as relevant to medical devices.
- • Must be a US Citizen or full Green Card holder.
Preferred
- • Experience in clinical trial evaluation preferred: evaluating clinical trial designs, identification of appropriate study endpoints, review of study results is preferred
- • Familiarity with FDA medical device regulatory processes, regulations (e.g., 21 CFR Part 900 – Mammography, 21 CFR Part 892 – Radiology Devices), and guidances is preferred
Tunnell Government Services, Inc., is comprised of the industry’s leading scientists, medical and technical experts, and human capital and organizational development professionals. We approach all projects as a team and are committed to helping our clients transform and quickly achieve strategic goals. If you are interested in joining an employee-owned company that develops and implements innovative, integrated and differentiated solutions, please click on the links below to find the job that is right for you and contact us.
FDA CDRH – Medical Officer (Breast Imaging Radiologist) SME Position Description
The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote the public health. CDRH assures that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.
Tunnell Government Services is providing professional and scientific services to the CDRH with expert consultants with scientific expertise in the regulation and approval and of medical devices. In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, pre-submissions); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; perform research; conduct data analysis; write detailed documents and reports; and execute other administrative office tasks related to CDRH’s projects.
Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities. This candidate should possess specific expertise and training in clinical medicine and breast imaging radiology, as relevant to medical devices.
Requirements And Qualifications
Must be a US Citizen or full Green Card holder.
Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.
FDA CDRH – Medical Officer (Breast Imaging Radiologist) SME Position Description
The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote the public health. CDRH assures that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.
Tunnell Government Services is providing professional and scientific services to the CDRH with expert consultants with scientific expertise in the regulation and approval and of medical devices. In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, pre-submissions); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; perform research; conduct data analysis; write detailed documents and reports; and execute other administrative office tasks related to CDRH’s projects.
Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities. This candidate should possess specific expertise and training in clinical medicine and breast imaging radiology, as relevant to medical devices.
Requirements And Qualifications
- The candidate must possess a Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States
- In addition, 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
- Fellowship or equivalent training in breast imaging and substantial professional experience in breast imaging
- Certification from a U.S. relevant specialty board organization (e.g., American Board of Radiology); current qualification through the Mammography Quality Standards Act (MQSA)
- Thorough understanding of current clinical practices in radiology, including diagnosis and treatment, use of software to aid the radiologist, and current/emerging trends in practice
- Proficient in all aspects of breast imaging, including mammography, ultrasound, MRI and image-guided procedures
- Expert in function and utilization of medical devices commonly used as part of breast imaging radiology (e.g., imaging systems, image-guided intervention devices, localization devices, breast tissue marker devices, contrast agents, AI and advanced imaging software, etc.)
- Experience in clinical trial evaluation preferred: evaluating clinical trial designs, identification of appropriate study endpoints, review of study results is preferred
- Familiarity with FDA medical device regulatory processes, regulations (e.g., 21 CFR Part 900 – Mammography, 21 CFR Part 892 – Radiology Devices), and guidances is preferred
- Ability to communicate well with others using excellent written and verbal communication skills
- Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel
Must be a US Citizen or full Green Card holder.
Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.
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