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Vision Scientist

Background

Tunnell has a contract opportunity available supporting the Division of Ophthalmic Devices (DOD) within the Center for Devices and Radiological Health (CDRH) at the Food and Drug Administration. A Vision Scientist is needed to conduct scientific and regulatory reviews to evaluate the safety and effectiveness of new ophthalmic devices. This is a remote position.

DOD serves as the primary source for scientific and medical expertise on ophthalmic medical devices with regard to safety and effectiveness. The Division carries out scientific and end-to-end medical device review evaluation, including coordinating and making premarket review determinations, as well as planning and coordinating post market compliance and enforcement efforts related to medical devices.

Duties of the position

Duties of the Vision Scientist may include but are not limited to:

With guidance and direction from senior scientists and engineers, the reviewer will review total product life-cycle actions (premarket, compliance, and post-market surveillance) related to ophthalmic devices. Actions may include 510(k)s, PMAs, De Novos, IDEs, pre-submissions, submission issue requests, 513(g)s, recalls and complaint submissions. Reviewer will apply his/her technical expertise to determine the adequacy of methodology, protocols and data concerning bench, animal and/or clinical testing and will, as needed, obtain appropriate consultation reviews of methodology, protocols and data that are outside the scope of the reviewer’s expertise. Based on a collective evaluation of the submission, the reviewer will provide a recommendation of submission clearance, approval, disapproval, request additional information or provide scientific and/or regulatory feedback to applicants. For each submission, the reviewer will prepare a comprehensive memo supporting the recommendation and, when required, prepare the appropriate correspondence to the applicant.
Assist with the developing, modifying, and evaluating guidelines concerning data required in medical device actions to be submitted to the Agency. In this capacity, the reviewer participates as a member of a team of experts to develop agency or center-wide guidelines applicable to the regulation of relevant medical devices.
Present reviews, conclusions, opinions, and recommendations to appropriate scientific review panels on PMAs, petitions for reclassification, etc. These presentations will include key issues pertaining to the safety and effectiveness of the medical device(s), outlines of deficiencies, and recommendations for approval or non-approval of the device or the submission.
Enhance professional career development by collaborating with other scientists to better understand medical device problems. Keep abreast of current events and findings and changes in medical device law and regulations through review of scientific and legislative literature, personal contact with relevant authorities, and by attending scientific meetings.

Qualifications

The candidate should have a solid background in basic and/or clinical visual psychophysics, visual optics, and optical instrumentation as evidenced by a record of independent, peer-reviewed published research.

A highly qualified candidate will have research experience with human participants including clinical trial design and management, especially clinical research involving ophthalmic devices (e.g., surgical lasers - cornea and retina), functional and diagnostic imaging devices, diagnostic visual tests, ocular implants such as intraocular lenses and retinal prosthetics). Experience in the manufacture, quality control, validation/ verification testing and measures for prescription of ophthalmic optical devices (e.g., intraocular lenses and contact lenses) is desired. Expertise in critically reviewing scientific documents and skill in clearly communicating review results are essential. Background in the following technical area(s) is highly desirable: