Bunkerhill Health is a Sequoia-backed company on a mission to facilitate and streamline the AI development efforts of academic researchers and to increase the adoption of AI in healthcare in order to help doctors catch deadly diseases earlier.
We have built a consortium of research institutions (Stanford, Johns Hopkins, UCSF, Harvard, etc.) whose researchers develop and validate AI algorithms seamlessly under our legal umbrella (weeks of setup time for a new project when using the Bunkerhill consortium, versus a year or more for projects outside the consortium). Bunkerhill then manages the FDA clearance and commercial sales process for the algorithms that these institutions develop and validate through the consortium.
We’ve signed commercial contracts and deployed algorithms with some of the world’s leading health systems — UCSF, Mayo Clinic, Georgetown/MedStar, and several others. These algorithms help doctors identify patients earlier than has otherwise been possible, leading to better treatment outcomes (early clinical screening for heart disease, pancreatic cancer, etc.).
We’re backed by world-class investors, including Sequoia, Max Levchin (co-founder of PayPal and Affirm), and Y Combinator.
We’re looking for a strong candidate to be responsible for the design and execution of regulatory strategies for AI algorithm development and commercialization. This individual will build sustainable processes and execute the work to ensure the timely and effective completion of regulatory submissions, with a particular emphasis on securing FDA clearance for a steady pipeline of software as a medical device (SaMD) applications through the 510(k) process. As Bunkerhill’s algorithms are not developed in-house and are instead sourced from the broader research community, this role will offer an opportunity to engage with an unparalleled variety and quantity of AI-based SaMD.
Offer will include base salary and equity.
Skills and qualifications:
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