Ophthalmology SME

Ophthalmology SME

Bethesda, MD

Tunnell Government Services, Inc. is providing professional and scientific services to the FDA Center for Devices and Radiological Health (CDRH) with expert consultants with scientific expertise in the regulation and approval 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 ophthalmology, as relevant to medical devices. Specific expertise involving surgical interventions, and sub-specialization in glaucoma and retinal disease is strongly preferred.

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 fifteen (15) years of relevant clinical experience
• Board Certification from the American Board of Ophthalmology
• Sub-specialization in glaucoma and/or retinal disease is strongly preferred
• Thorough understanding of current clinical practices in ophthalmology, including diagnosis and treatment, performance of ocular surgery, and current trends in practice.
• Expert in function and utilization of ophthalmic medical devices, to include specific knowledge of non-invasive devices and instruments used for diagnosis; invasive devices, such as implantable devices, intraocular lenses, glaucoma stents; and surgical systems, such as lasers and phacoemulsification machines.
• Familiarity with FDA medical device regulatory processes 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 United States Citizen or a Full Green Card holder.

This position is 100% telework.

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.