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.