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TG
Tunnell Government Services
Veterinary Medical SME
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What they do
A Medical Writer applies the principles of clinical research in developing clinical trial documents that effectively and clearly describe the research results, product use, and other medical information. Medical writers may also offer writing support to the principal investigators for grant applications and specialized publications.
$78,912 / year median in the U.S.
-2% projected decline
Job Description
Veterinary Medical SME Tunnell Government Services - 3.5 Washington, DC Job Details Full-time 3 hours ago Qualifications Developing medical devices Microsoft Outlook Veterinary medicine Research veterinary medicine Veterinary License Full Job Description 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 Veterinary Medical SME Position Description The successful candidate will serve as a clinical and technical authority to a variety of internal and external stakeholders regarding an array of medical and radiological health products. They will provide scientific, technical, product development, and product validation advice as part of research protocol review, assessment of technical data included in regulatory submissions, as relevant to regulatory review of medical devices. Such submissions include Premarket Notification (510(k)), Premarket Approval Application (PMA), etc. Qualifications The candidate must possess a Doctor of Veterinary Medicine (DVM) degree or equivalent, and an unrestricted license to practice veterinary medicine in a state or territory of the United States. Additional advanced degrees (MS, PhD) or Board certifications in a related/applicable field are strongly preferred. 7 years of experience is required (clinical, academic, and/or industry experience) General knowledge and experience with a variety of medical device development technical disciplines Exceptionally strong written and verbal communication skills 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. Proficiency with Microsoft Office Suite (Outlook, Word, Excel, etc.) Responsibilities The contractor shall provide expert consultant service in the area of Veterinary Medicine and use of animal models as related to Human Medical Device Regulatory Review, consistent with (but not limited to) the following consensus standards: FDA "Guidance for Industry and Food and Drug Administration Staff" documents and webinars, applicable to animal use and/or medical devices, such as General Considerations for Animal Studies for Medical Devices Draft Guidance for 4 Industry and Food and Drug Administration Staff - DRAFT