What if you could repair broken genes? That is the question we ask ourselves every day at Editas Medicine. We’re a clinical stage genome editing company focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cas12a genome editing systems into a robust pipeline of treatments for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.
We are a vibrant company full of hope, possibilities, and a belief that, working together as One Editas, we can truly revolutionize the development of medicines. We are on an important journey to unlock the full potential of genome editing technology. A journey fueled by our distinct culture, expert team of Editas Medicine ‘Editors’, and the patients we aspire to help around the world. Connect with us to hear about the tremendous progress and scientific advancements we’ve already made and the next breakthrough on the horizon. If you are ingenious, passionate and resilient, come join the revolution. Repairing broken genes is only the beginning.
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201-500 employees
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Biotechnology
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11 Hurley St, Cambridge, Massachusetts 02141, US
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2013
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Cancer, Rare Diseases, Genome Editing, Sickle Cell Disease, Genetic Diseases, Immunogenetics, Blood Diseases, Engineered Cell Medicines, In Vivo (In Body) Editing, Ocular Medicines, Hematopoietic Stem Cells
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Gilmore Oneill is the CEO of Editas Medicine. To contact Gilmore Oneill email at [email protected]. Or you may call 7812981632
The decision makers in Editas Medicine are Charlene Stern, Greg Whitehead, Jeff Roncal, etc. Click to Find Editas Medicine decision makers emails.
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