Ophthalmology SME

Tunnell Government Services • Bethesda, MD

31d • Remote

About The Position

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 – Ophthalmology 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, 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 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

• 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
• 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.
• 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.

Nice To Haves

• Sub-specialization in glaucoma and/or retinal disease is strongly preferred
• Familiarity with FDA medical device regulatory processes 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

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree