Clinical Education Specialist

Scarlet; City Of London; Remote; GBP 60,000 - 80,000; Full time

Job summary

A healthcare innovation company is looking for a skilled individual to create educational materials for medical device evaluations and regulatory compliance. The role requires strong clinical evaluation experience and the ability to design engaging training resources. You will lead sessions that clarify core concepts and ensure alignment among innovators. The position is remote and offers a competitive salary between £60K and £80K.

Qualifications

• 2+ years of experience in clinical evaluation under EU/UK MDR.
• Knowledge of high-quality clinical data structuring.
• Ability to design training or explain regulatory concepts effectively.

Responsibilities

• Create content to clarify clinical requirements for medical devices.
• Design education-grade materials for various platforms.
• Lead training sessions to align innovators on regulatory standards.
• Collaborate with assessors for consistent regulatory viewpoints.

Skills

Clinical evaluation experience

Understanding of regulatory requirements

Experience with Learning Management Systems

Job description

Location

UK - Remote, London Office

Employment Type

Full time

Location Type

Remote

Department

Product

Compensation

• £60K – £80K • Offers Equity

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.

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

Compensation Range: £60K - £80K