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Scarlet seeks medical professionals for short engagements to inform regulatory assessments of medical devices. You will provide targeted clinical insight during reviews and help resolve assessment questions based on your expertise.
You will review evidence, discuss regulatory questions, and advise on clinical performance, safety and benefit for a device’s intended clinical use. Registration and a clinical specialty are required.
Scarlet is authorised to assess and certify medical devices. We combine clinical, technical and regulatory expertise with AI agents and software so rigorous certification can keep pace with product development at the world’s most ambitious technology companies, without lowering the safety bar.
Our customers have cut a year or more from their certification timelines for new AI-enabled medical devices and shortened product-update cycles from months to weeks. You’ll join a team building the infrastructure that makes these outcomes repeatable at scale.
As a member of Scarlet’s expert roster, you’ll be contacted for short engagements (typically a few hours of review or discussion) when your expertise is relevant to a device or assessment question. Your advice will resolve specialist clinical questions so Scarlet can reach sound, evidence-based assessment decisions that help safe devices reach patients sooner.