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Medical Student Internship - Regulatory & Clinical Documentation

Healthtech Company (Primary Care)

London
Internship
Clinical Operations
Posted 15 Apr 2026

Job Description

Duration: 2–4 Weeks | Setting: In-Person (London) | Ideal for: Medical Students | Start date: Immediate

About the Company

They are one of the UK's leading provider of remote GP resources, partnering with healthcare providers across the country to improve patient access to high-quality primary care while driving down cost. Their mission is to enable modern primary care, supporting the NHS and aligned providers with a qualified, remote clinical workforce that delivers better outcomes for patients and actively supports the UK Government's three big shifts in healthcare delivery.

They are developing a digital health platform toward formal medical device status and are looking for motivated medical students to join them for a focused, hands-on internship supporting the regulatory documentation journey.

The Opportunity

This internship offers a rare insight into the regulatory and clinical evidence processes required to bring a digital health product to market as a medical device under UK and EU frameworks. You will work directly the clinical and regulatory team, contributing meaningfully to real documentation that will support our regulatory submissions.

What They're Looking For

Current medical student, ideally in clinical years or above Genuine interest in digital health, health technology, or the regulatory environment for medical devices Strong written communication skills and attention to detail, regulatory documentation demands precision Ability to critically appraise clinical literature and synthesise findings clearly Self-motivated, organised, and a willingness to learn

What You'll Gain

Practical experience in medical device regulation, a highly sought-after skill set in clinical academia, industry, and health policy Exposure to a fast-growing digital health company at the forefront of primary care transformation Mentorship from experienced clinical and regulatory professionals A tangible contribution to a real regulatory submission, excellent for portfolios, foundation applications, and academic references

Duration & Logistics

Duration: 2–4 weeks, with immediate start date Location: In-person, Office based in London

Interested in this role?

Apply now through OffScript — upload your CV and we'll add you to the candidate pool for this role. We'll be in touch!