Clinical Research Scientist - Medical Affairs

About Skin Analytics

Skin Analytics is an award-winning health tech company revolutionizing skin cancer diagnosis through AI-powered medical devices. Following a £15M Series B funding round, regulatory milestones, and expansion from 50 to 100 employees in 2025, the company is scaling internationally to transform dermatology and oncology care globally.

The company's flagship product, DERM, is a Class III CE-marked AI medical device—the only AI system approved to make clinical decisions autonomously in the cancer space. DERM is also the first to receive a NICE recommendation for use across NHS organizations, currently deployed at more than 28 NHS facilities. The mission is clear: build a future where no one dies from skin cancer.

The Role

As a Clinical Research Scientist in Medical Affairs, you will drive the clinical evaluation and evidence generation for AI medical devices throughout their lifecycle. This is a strategic position combining regulatory expertise, scientific rigor, and clinical investigation design to support product development and global market expansion.

This role is ideal for postdoctoral researchers, medical doctors, and professionals with experience evaluating AI medical devices. The position offers flexibility for those seeking fellowship opportunities or fixed-term contracts.

Key Responsibilities

• Evidence Generation: Design and execute evidence generation activities to address identified research questions and build the clinical evidence base for new and updated AI medical devices.
• Clinical Investigation Management: Contribute to strategic delivery of clinical investigations from conception through dissemination, ensuring timely and high-quality execution.
• Literature Review & Meta-Analysis: Conduct comprehensive State-of-the-Art (SOTA) literature reviews and meta-analyses to contextualize product safety, efficacy, and performance in the broader clinical landscape.
• Regulatory Documentation: Support development of Clinical Evaluation Plans (CEPs) and Clinical Study Reports (CSRs) for regulatory submissions across Europe, the US, and other geographies.
• Regulatory Compliance: Write and maintain Clinical Evaluation Reports (CERs) in accordance with EU MDR and global regulatory frameworks to ensure compliance and support market authorization.
• Cross-functional Collaboration: Work closely with Regulatory and Product teams to provide timely scientific input and support regulatory strategy.
• Scientific Communication: Disseminate research findings through publications, presentations, and scientific communications to advance the field and establish thought leadership.

Who You Are

You bring strong credentials in clinical research, regulatory science, or medical device evaluation. Experience with AI/machine learning medical devices is highly valued. You are detail-oriented, capable of managing complex evidence generation projects, and comfortable navigating international regulatory requirements. Strong scientific writing and communication skills are essential.

Location & Work Arrangement

This role is remote with office presence required. Candidates should ideally be based in or around London and commit to visiting the London office 3 times per week. If based outside London, candidates must be prepared for frequent office travel. Remote work arrangements may be available for exceptional candidates willing to travel regularly.

Why Join Skin Analytics

You'll work at the forefront of AI in healthcare, contributing to life-saving technology that's already improving patient outcomes across the NHS and beyond. The company's recent growth and Series B success create exciting opportunities for career development. You'll be part of a mission-driven team building the future of dermatology—where innovation directly impacts patient care and saves lives.

💰 Compensation not publicly listed. Market estimate for similar roles: from $80K, varying by experience and location.