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- Tasks: Review and rate AI-generated outputs for medical device criteria.
- Company: Join Medcase, a leader in healthcare AI research.
- Benefits: Fully remote work with flexible hours and a clear project scope.
- Why this job: Shape the future of AI in healthcare and make a real impact.
- Qualifications: UK-based regulatory professional with SaMD experience and strong knowledge of UK/EU frameworks.
- Other info: Collaborate with global experts in a structured, research-driven environment.
The predicted salary is between 13 - 16 £ per hour.
Medcase is partnering with a leading client on a high-impact research initiative focused on generative AI and Software as a Medical Device (SaMD)—and we're looking for UK-based health regulatory specialists to contribute their expertise.
About the Project
- Goal: Evaluate and classify AI-generated outputs to assess whether they meet medical device criteria, supporting the responsible development of healthcare AI.
- Scope: Structured review of model-generated responses following established regulatory evaluation guidelines.
- Time commitment: Approximately 24–32 total hours, including onboarding, calibration, and evaluation work.
- Start date: Upcoming start (onboarding begins once selected).
- Location: Fully remote with flexible, asynchronous participation.
What You'll Do
- Review and rate AI-generated responses using health regulatory criteria.
- Apply SaMD and AI regulatory frameworks to diverse scenarios.
- Ensure consistency and quality across evaluations.
- Participate in calibration and feedback discussions as needed.
Who You Are
- UK-based health regulatory professional with SaMD experience.
- Background in Regulatory Affairs, Health Sciences, Medicine, or a related field.
- Strong knowledge of UK and/or EU regulatory frameworks (MHRA experience is a plus).
- Comfortable working independently in a structured, research-driven environment.
Why Join Medcase?
- Contribute to the responsible development of AI in healthcare.
- Apply your regulatory expertise beyond traditional submissions.
- Collaborate with a global network of health and technology experts.
- Flexible, remote work with a clearly defined scope.
Interested? Apply now and help shape how AI-powered medical technologies are evaluated and regulated for the future.
UK Health Regulatory Specialist – AI & Software as a Medical Device (SaMD) in Hull employer: Medcase
Contact Detail:
Medcase Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land UK Health Regulatory Specialist – AI & Software as a Medical Device (SaMD) in Hull
✨Tip Number 1
Network like a pro! Reach out to professionals in the health regulatory field, especially those with SaMD experience. Use platforms like LinkedIn to connect and engage with them—ask questions, share insights, and show your enthusiasm for the industry.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK and EU regulatory frameworks. Be ready to discuss how you would apply these frameworks to AI-generated outputs. We want to see your expertise shine through!
✨Tip Number 3
Showcase your skills in a practical way! If you have examples of past evaluations or projects related to SaMD, be sure to highlight them during discussions. This will demonstrate your hands-on experience and understanding of the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our mission to shape the future of healthcare AI.
We think you need these skills to ace UK Health Regulatory Specialist – AI & Software as a Medical Device (SaMD) in Hull
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience with SaMD and regulatory frameworks. We want to see how your background aligns with the role, so don’t hold back on showcasing your relevant skills!
Showcase Your Expertise: In your application, emphasise your knowledge of UK and EU regulatory guidelines. We’re looking for someone who can confidently navigate these frameworks, so let us know about any specific experiences you’ve had in this area.
Be Clear and Concise: When writing your application, keep it straightforward and to the point. We appreciate clarity, so avoid jargon and make sure your key points stand out. This will help us quickly see why you’re a great fit!
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Medcase
✨Know Your Regulatory Frameworks
Make sure you brush up on the UK and EU regulatory frameworks, especially those related to SaMD. Being able to discuss specific guidelines and how they apply to AI-generated outputs will show your expertise and confidence.
✨Prepare for Scenario-Based Questions
Expect to be asked about diverse scenarios involving AI and medical devices. Think through examples from your past experience where you applied regulatory criteria, and be ready to explain your thought process clearly.
✨Showcase Your Independent Working Skills
Since this role involves working independently in a structured environment, be prepared to discuss how you manage your time and ensure quality in your evaluations. Share any tools or methods you use to stay organised and efficient.
✨Engage in Calibration Discussions
Demonstrate your willingness to participate in calibration and feedback discussions. Highlight any previous experiences where you collaborated with teams to ensure consistency and quality in evaluations, as this is key for the role.
