More locations: San Francisco, CA, USA | New York, NY, USA
Hybrid work is listed for the ATS locations; remote work may be available depending on the role. Preference is given to candidates open to working closely with the founding team in Boston.
Absentia Labs builds an AI-driven, organism-wide modeling platform that helps biotech and pharmaceutical teams assess drug safety and translational risk early in development. Its core AI-native engine combines biological, chemical, and assay data to simulate how a drug behaves in the body across whole organs, predicting efficacy and safety issues before preclinical tests. By focusing on organ-specific risks like liver, heart, and kidney liabilities, the platform aims to identify problem candidates early and guide which drugs to advance. This approach is designed to reduce late-stage failures and speed up the process of bringing medicines to the clinic, offering a more ethical and cost-effective alternative to traditional animal testing. Absentia Labs positions itself as the intelligence layer for molecular medicine, working with universities and biopharma partners to standardize and accelerate drug discovery and development.
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Headquarters
Somerville, Massachusetts
Founded
2024
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Flexible Work Hours
Hybrid Work Options
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Absentia Labs, a Boston-based biotech startup founded in 2024, has become the first company to have an AI-driven drug development tool accepted into the FDA's qualification programme. The company's Digital Liver Model, designed to predict drug-induced liver injury, entered the FDA's ISTAND pathway—a historic milestone for AI-based safety assessment tools. The startup was co-founded by MIT-trained scientists Farhan Khodaee and Rohola Zandie, alongside Robert Betancort. Their AI platform combines mechanistic biology with drug-response data to help pharmaceutical companies assess liver injury risk before human trials begin. Drug-induced liver injury is a leading cause of clinical trial failure. Absentia's model addresses gaps in traditional animal testing by capturing the complexity of human liver response, including metabolism, genetics and immune factors.