Senior Biotech Program Leader
Editas Medicine is seeking a seasoned Program Leader to advance EDIT-401 by coordinating strategy, governance, and cross-functional execution. This senior role requires balancing scientific ambition with operational delivery and budget management on a high‐v…
Global Medical Affairs Strategy Leader
Editas Medicine is seeking a Senior Director, Medical Affairs to lead medical strategy and execution for our lead in vivo program EDIT-401, a potential one-time therapy for LDL cholesterol. You will shape medical communications and engage with key opinion lead…
Senior Director, Medical Affairs
At Editas Medicine, we are pioneeringthe possible. Our mission and commitmentsto translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around th…
Senior Specialist, Quality Systems Management
Why Choose Editas?At Editas Medicine, we're a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed…
Senior Quality Systems Manager: GMP, QMS & Supplier Audits
Editas Medicine is seeking a Senior Specialist, Quality Systems Management to advance our in vivo program and oversee quality systems supporting GMP documentation and vendor management. The role sits within a collaborative QA team focused on continuous improve…
Senior Medical Director, Clinical Development
At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases aroun…
Vice President, Regulatory Affairs
At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases aroun…
Head of Regulatory Affairs, Gene Editing
Editas Medicine is seeking a Vice President, Regulatory Affairs to lead the global regulatory function for in vivo gene editing therapies. You will implement strategy, manage submissions, and act as the primary regulatory advisor to executives and partners.Rep…
Medical Director, Gene Editing Clinical Development
Editas Medicine is seeking a Senior Medical Director, Clinical Development to provide medical leadership for gene-editing clinical programs (EDIT-401) across early development. You will design trials, oversee execution, and drive cross-functional collaboration…
Lead Lipid Process Chemistry – GMP & CDMO Collaboration
Editas Medicine seeks an Associate Director of Lipid Process Chemistry to lead GMP manufacturing scale-up of novel lipid components for our LNP therapeutic pipeline. You will act as the primary CMC liaison with CDMOs, drive tech transfer, and ensure regulatory…