
Jhpiego
Data analytics advisor
Overview Jhpiego is an international, non-profit health organization affiliated with The Johns Hopkins University. For 50 years and in over 155 countries, Jhpiego has worked to prevent the needless...

Tunnell Government Services
·17 hours agoTunnell Government Services
·17 hours agoLocation
remote, United States
Commitment
Full Time
Level
Senior (5+ years)
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.
Job Type: Full Time Employee
Schedule: Monday through Friday (no Holidays)
Location: This position is 100% telework
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; write detailed documents and reports; and execute other administrative 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 applicable training in data analysis and computer science, as relevant to medical devices.
The contractor will support FDA CDRH post market surveillance and data modernization initiatives by developing advanced analytical solutions that integrate Medical Device Reports (MDRs), recalls, allegations, Unique Device Identifier (UDI), and registration/listing data into a unified analytical environment. Working closely with CDRH stakeholders, the individual will design and implement data pipelines, interactive dashboards, and signal detection tools that enable reviewers to independently access, visualize, and analyze post-market safety information.
The candidate must possess a Bachelor’s degree (BS) in engineering, computer engineering, or a related field. An advanced degree (MS, PhD) in a related/applicable field is preferred. Minimum 7 years of applicable experience is required. Experience in post market surveillance analytics, adverse event and recall data, UDI systems, advanced analytics, data engineering, dashboard development, and medical device regulatory environments is highly preferred. Strong communication skills and the ability to present technical findings to non-technical stakeholders are essential. Proficiency with Microsoft Office Suite (Outlook, Word, Excel, etc.). Must be a US Citizen or full Green Card holder.
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.

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