Surgical Oncologist - FDA

Tunnell Government Services • Bethesda, MD

4d • Remote

About The Position

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, Inc. 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 surgical oncology, as relevant to medical devices.

Requirements

• Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States.
• 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 (10) years of relevant clinical experience
• Certification from a U.S. relevant specialty board organization, e.g., the American Board of Surgery (ABS), Society of Surgical Oncology (SSO), etc.
• Thorough understanding of current clinical practices in surgical oncology, including diagnosis and treatment, and current/emerging trends in practice.
• Expert in function and utilization of medical devices commonly used as part of surgical oncology (e.g., advanced energy and resection devices [electrosurgical units, ultrasonic scalpels, argon beam coagulators], minimally invasive and robotic platforms [robotic-assisted surgery systems, laparoscopes and thoracoscopes], localization and navigation devices [tumor localization seeds, intraoperative ultrasound], tumor ablation systems [radiofrequency ablation and microwave ablation, cryoablation systems, irreversible electroporation], lymph node mapping systems [gamma probes, near-infrared fluorescence imaging], intraoperative therapy devices [hyperthermic intraperitoneal chemotherapy pumps, intraoperative radiation therapy systems]).
• 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 a Full Green Card holder.

Nice To Haves

• Familiarity with relevant FDA medical device regulatory processes, regulations (e.g., 21 CFR Part 878 – General and Plastic Surgery Devices), and guidances is preferred.

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

What This Job Offers

• Career Level: Senior
• Education Level: Ph.D. or professional degree