Clinical pharmacologists and software engineers with deep roots in oncology research and clinical trial data systems.
CEO, Co-Founder
Former clinical pharmacologist at Dana-Farber Cancer Institute and HMS, where she ran PK/PD modeling for Phase I/II oncology studies for six years. Holds a PhD in pharmaceutical sciences from ETH Zurich and authored 14 peer-reviewed publications on population pharmacokinetic modeling in oncology.
CTO, Co-Founder
Previously led clinical data engineering at Medidata Solutions, where he architected the FHIR R4 migration for Rave EDC integrations. PhD in biomedical engineering from MIT. Built the Bayesian inference engine underpinning the DoseMind platform and holds two patents related to real-time PK estimation in constrained computation environments.
VP Clinical Operations
Eight years in clinical operations at AstraZeneca and Genentech, focused on oncology Phase I/II trial execution across North America and Europe. Led the implementation of TDM programs for three carboplatin re-dosing protocols. Joined DoseMind in early 2024 to lead site onboarding and protocol validation.
Full-time team members
Nationalities represented
Peer-reviewed PK publications among founders
Headquartered in the Longwood Medical Area
We hire people who have spent time at the intersection of clinical pharmacology and software. You do not need to be a PhD, but you do need to understand why the difference between MAP Bayesian and empirical Bayesian estimation matters in a sparse-sampling context.
Everything we ship has to be understood and trusted by an oncologist or CRC under time pressure. We look for people who can explain a model assumption in plain language - not because clinicians cannot handle complexity, but because they should not have to decode jargon to make a decision.