Medical Affairs Fellow

Please note: this role is office based (Farringdon) for 3 days a week. The role can be done at 0.8FTE, 0.9 FTE or fulltime.

About Skin Analytics
Skin Analytics is an award-winning, health tech company that works with dermatology teams to deploy world-leading skin cancer pathways using AI as a medical device, DERM.

Following our recent £15M series B funding round and regulatory milestones, we're ready to scale internationally, making history for AI in healthcare and the future of dermatology.

We're proud to epitomise AI for good - with a Class III CE mark, DERM is the only AI as a medical device approved to make clinical decisions autonomously in the cancer space, as well as being the first company to receive a NICE recommendation for use across the NHS.*

DERM is deployed at more than 25 NHS organisations where we're supporting dermatology teams to build sustainable services that enable patients to gain quicker access to skin cancer diagnosis. If that's not enough, we also collaborate with some of the largest health insurers to reach patients in their own homes.

We are a team of passionate people on a mission to build a future where no one dies from skin cancer.

The role
This medical fellow supports the clinical evaluation of AI Medical Devices, delivers regulatory and technical documentation across the AI product lifecycle. Finally, you’re also responsible for scientific communication and dissemination.

Responsibilities

• Identify new research questions and help to design strategies to build the evidence base for new and updated AI medical devices.
• Support the development of Clinical Evaluation Plans (CEPs) and Clinical Study Reports (CSRs) to support regulatory submissions in Europe, the US and other geographies.
• Contribute to the strategic and timely delivery of all clinical trial activities, from design to dissemination.

• Write and maintain Clinical Evaluation Reports (CERs) in accordance with EU MDR and global regulatory frameworks.
• Conduct State-of-the-Art (SOTA) systematic literature reviews and meta-analyses to contextualize product safety and performance.
• Collaborate with Regulatory and Product teams to provide timely and accurate technical documentation for pre- and post-market submissions.

• Support publication of clinical trial and real world data in peer-reviewed journals, at international conferences (abstracts, posters, presentations), and in an internal knowledge base.
• Develop evidence summaries, scientific claims documents, and clinical value narratives tailored to clinicians, patients, regulators and payers.

Requirements

• Advanced degree in relevant field - e.g. Medical Doctor, PhD, or Master’s in Life Sciences, Biomedical Engineering, Statistics, or Public Health.
• Experience in medical writing (e.g. CERs, CEPs and CSRs), ideally to support the clinical evaluation of AI medical devices.
• Ability to manage multiple projects with competing deadlines without compromising on standards.
• Excellent communication skills with the ability to communicate complex scientific concepts clearly.
• Strong attention to detail, analytical mindset and a proactive approach to problem-solving.
• Involvement with the conduct and publication of systematic reviews and meta-analyses.
• Proficiency with reference management tools (e.g. EndNote, Mendeley, etc) and document collaboration platforms (e.g. Google Drive).
• Knowledge of statistical methods and principles commonly applied in clinical research and regulatory documentation.

Preferred:

• Ability to use statistical programming and data analysis tools (e.g. R, Python or Stata).
• Familiarity with global regulatory and quality management standards (e.g. EU MDR, FDA, ISO 13485), possibly evidenced by a relevant certification (e.g. RAPS).

Benefits

💰Competitive salary

🏥Private healthcare

🌴25 days annual leave (plus 5 day company shutdown in August + bank holidays)

👪Enhanced parental leave - includes adoption & foster

💻Training budget

💬Weekly catch-ups, monthly meetings to talk about your ambitions and make plans

🎊Lots of fun social activities including company offsite!

Our Values

🌱 Building a Strong Foundation 

🎓 Always Learning 

🏅 Lead from the Front 

💪 Tough and Resilient 

The Real Stuff

Skin Analytics embraces and is committed to diversity and equal opportunities. We are dedicated to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be. If you need any changes made to our application process to accommodate your needs, please get in touch with maarty.ramakers@skinanalytics.co.uk

*The National Institute for Health and Care Excellence has recommended DERM for use within the NHS until May 2028, while further evidence is gathered