Director, Toxicology
Editas MedicineCambridge, Massachusetts, United States
Posted October 10, 2025
220000 - 240000 USD year
Full Time
About the Company
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.
Job Description
Editas Medicine is seeking a highly accomplished Toxicologist to join the DMPK, Nonclinical Safety and Translational Sciences (DSTS) team. The role involves overseeing nonclinical safety assessments for both rodent and non-rodent models, driving the pipeline through development and ensuring regulatory compliance. This is an integral part of the nonclinical leadership team and will build the department to meet the business needs and bring life changing therapies to patients.
Requirements
- PhD in toxicology, pharmacology or related field (preference for DABT certified)
- 10+ years of industry experience
- Core expertise in toxicology, including general toxicology, genotoxicity, developmental and reproductive toxicology
- Track record of advancing programs through nonclinical development
- Familiarity with FDA/EMA/ICH guidelines and health authority interactions
- Experience with gene editing or gene delivery technologies and lipid nanoparticle delivery is highly desired
Benefits
- Blue Cross Blue Shield PPO Medical Plan
- Company-funded Health Savings Account
- Dental and Vision Insurance
- Life and Disability Insurance
- Dependent Care Account
- Tuition Reimbursement
- 401(k) plan with company match
- Employee Stock Purchase Plan
- Employee Assistance Plan
- Wellness Programs
- Flexible Paid Time Off policy
