Scarlet is looking for a Clinical Education Specialist to help medical device innovators understand clinical regulatory requirements. Our mission is to hasten the transition to universally accessible healthcare by enabling innovators to bring cutting-edge software and AI to the healthcare market safely and quickly.
What You'll Do
- Create high-quality content that enables medical device innovators to understand the clinical requirements of medical device regulations.
- Design education-grade materials, including slides, diagrams, lesson plans, and voiceover scripts, for use across videos, knowledge base articles, and enablement tools.
- Lead training and enablement sessions that clarify core concepts, surface common pitfalls, and align medical device innovators on what 'good' looks like.
- Work closely with the assessors to ensure that everything we publish reflects a consistent, aligned regulatory view.
What We're Looking For
- 2+ years of experience contributing to clinical evaluation under EU and/or UK MDR, particularly for Software as a Medical Device.
- Understand the characteristics of high-quality clinical data and how to structure a clinical evaluation to comply with regulatory requirements.
Nice to Have
- Experience teaching, designing training, or working with Learning Management Systems, or you may simply find yourself explaining regulatory concepts to others and doing it well.
- Motivated by the opportunity to shape how high-quality clinical documentation is taught, learned, and standardised at scale.
