Medable is a Decentralized Clinical Trials company founded in 2012 and based in Palo Alto, United States. It has raised $521M in total funding, most recently a Series D in 2021 at a $2.1B valuation.
| Date | Stage | Amount | Valuation | Lead investors |
|---|---|---|---|---|
| Oct 26, 2021 | Series D | $304M | $2.1B | Blackstone Growth, GSR Ventures, Tiger Global |
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Medable's electronic clinical outcome assessment platform captures patient-reported, clinician-reported and observer-reported outcomes on participants' own devices or provisioned hardware. It supports BYOD deployments, wearables and remote patient monitoring data, with localization across 120+ languages and validated migration of legacy paper instruments. The product is a workhorse for sponsors running hybrid and fully decentralized studies and has been deployed in trials reporting 90%+ participant adherence and double-digit reductions in translation timelines.
Total Consent is Medable's electronic informed consent (eConsent) solution, allowing trial participants to review, sign and re-consent on study protocols remotely from any device. It supports multimedia explainers, comprehension checks, multi-language deployments and integrated identity verification, with audit trails designed to meet 21 CFR Part 11, GDPR and ICH GCP requirements. Total Consent is widely used to accelerate site activation, reduce screen-fail rates and broaden geographic recruitment for decentralized and hybrid studies.
Study Studio is Medable's AI-powered, no-code trial build environment that lets sponsors and CROs configure, translate and deploy eCOA, eConsent and televisit experiences in as little as one business day. It replaces the multi-week, vendor-led builds that have historically dominated DCT software with a self-serve toolchain, with reusable templates and automated translation workflows aimed at compressing study start-up costs and timelines for sponsors running large global protocol portfolios.
Medable's Agent Platform is a suite of agentic AI tools for clinical operations, including a Site Monitoring (CRA) Agent, a Trial Master File (TMF) Agent and a PI Summary and Review Agent. The agents automate document review, query generation, monitoring visit prep and TMF reconciliation across the lifecycle of a trial, positioning Medable's stack against new AI-native entrants and incumbent CTMS/eTMF vendors as sponsors look to consolidate spend on AI-driven trial execution.
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