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Company Description
Radmetrix is a specialized provider of clinical trial reader recruitment and management, helping sponsors, CROs, and imaging core laboratories efficiently find, vet, contract, and coordinate physician-specialists for centralized imaging and other expert reviews. Founded in 2015 and led by Dr. Ira Smalberg, a seasoned body imaging radiologist and recognized authority on quantitative oncology criteria such as RECIST 1.0/1.1, iRECIST, irRECIST, mRECIST, Deauville, Hallek, Lugano, LYRIC, and RECIL, the company has built a global network of 150+ contracted experts spanning radiology, oncology, pathology, cardiology, ophthalmology, pulmonology, dermatology, gastroenterology, ENT surgery, and more. Radmetrix has supported over 250 clinical trials and facilitated more than 400,000 reads by combining rigorous reviewer selection and qualification with reader-friendly onboarding, efficient contracting, Errors and Omissions insurance coverage, a robust data portal, and monthly billing reconciliation to ensure timely, reliable payments. Its streamlined operating model reduces measurement variability and systemic reader bias, meeting tight timelines while maintaining charter compliance and data integrity. Beyond core reading support, Radmetrix extends its services to consulting, medical writing, training programs, and indications and modality coverage across oncology and non-oncology areas, including AI software validation. Trusted by repeat customers for scalability and direct leadership access, the organization offers lean, proactive processes that free CROs and ICLs from administrative burden and help sponsors accelerate trial execution. For physician-specialists, Radmetrix creates opportunities to apply domain expertise, build supplemental income, deepen clinical trial experience, and contribute to groundbreaking research. Dr. Smalberg, who serves on the executive board of PINTAD and lectures widely on central review challenges and quantitative imaging criteria, continues to guide Radmetrix’s mission to bring greater efficiency and reliability to clinical trial reviewer recruitment and management.
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