Regulatory Affairs Engineering Lead, Clinical Evaluation
MISSION
Neko is redefining what prevention means, from treating illness when it arrives, to sustaining health before it's ever at risk. Our mission: make data-driven, preventative care accessible to more people, before symptoms appear.
In a single, non-invasive visit under an hour, proprietary technology and direct clinical care combine to deliver personalised, actionable insights. It's a team that thinks in 10x, not 10%. Every role here plays a part in building a world where prevention is the norm, and where your work genuinely helps people live longer, healthier lives.
ABOUT THE ROLE
We're looking for a regulatory affairs engineer to own the clinical side of Neko's regulatory work. You'd write the clinical evaluation plans and reports, and the clinical documentation behind our submissions to the FDA, the EU and the UK.
Neko generates its own clinical evidence, so this is authored work. You'd plan and support clinical studies and investigations under ISO 14155, appraise the…
Det här jobbet kommer från karriärsidan hos Neko Health. Vi länkar direkt till källan.