Clinical Education Specialist
Who you are:
- You have 2+ years of experience contributing to clinical evaluation under EU and/or UK MDR, particularly for Software as a Medical Device.
- You understand the characteristics of high-quality clinical data and how to structure a clinical evaluation to comply with regulatory requirements.
- You 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.
- You're motivated by the opportunity to shape how high-quality clinical documentation is taught, learned, and standardised at scale.
- 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.
- Intro call with Aarzoo
- Round 1: Team interviews: Interview with Steven and Sandy (2x30 min)
- Round 2: Founder interviews: Interview with James and Jamie (2x30 min)
- Referencing
- Offer
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