Clinical Education Specialist

Scarlet; London; On-site; GBP 40,000 - 60,000; Full time

Job summary

A healthcare innovation company in London seeks a professional with experience in clinical evaluation and regulatory compliance for Software as a Medical Device. The role involves creating educational content and leading training sessions for medical device innovators. Ideal candidates should have a passion for standardising high-quality documentation and excellent communication skills. Join us to advance healthcare with cutting-edge technology.

Qualifications

• 2+ years of experience contributing to clinical evaluation under EU and/or UK MDR.
• Experience with Learning Management Systems is a plus.
• Motivated to shape high-quality clinical documentation.

Responsibilities

• Create high-quality content for medical device innovators.
• Design education materials including slides and scripts.
• Lead training sessions on regulatory concepts.
• Work with assessors for aligned regulatory publications.

Skills

Clinical evaluation experience

Understanding of clinical data structure

Training design and delivery

Job description

Our mission is to hasten the transition to universally accessible healthcare. We deliver on this mission by enabling innovators to bring cutting-edge software and AI to the healthcare market safely and quickly. We're regulated by the UK Government and European Commission to do so.

Our certification process is optimised for software and AI, facilitating a more efficient time to market, and the frequent releases needed to build great software. This ensures patients safely get the most up-to-date versions of life-changing technology.

Come help us bring the next generation of healthcare to the people who need it.
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.

What the job involves:

• 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.

The Interview Process

• Intro call with Aarzoo
• Round 1: CX team interviews: Interview with Steven and Sandy(2x45 min)
• Round 2: Founder interviews: Interview with James and Jamie (2x30 min)
• Referencing
• Offer