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Editas is seeking a computational biologist to join the team. In this role, you will develop, implement, and run algorithms for our genome editing platform based on CRISPR/CAS9 and CPF1. You will work closely with biologists and our informatics group to build robust pipelines and conduct analyses that span a broad range of Next Gen Sequencing (NGS) methodologies as well as other data-intensive methods. The position requires strong fundamentals in engineering, genetics/genomics, and biology. Excellent written and verbal communication skills are crucial.

We are seeking an experienced and highly motivated cell and molecular biologist with expertise in induced pluripotent stem cells (iPSCs) and genetic engineering. The successful candidate will join a multidisciplinary team dedicated to building an iPSC platform for the development of novel engineered cell products for oncology. The individual will be responsible for leading the optimization of the platform for the rapid and robust generation of genetically engineered iPSC lines to support internal programs and external collaborations. The ideal candidate must have exceptional organizational skills and be comfortable leading in a matrix organization. In addition, in depth knowledge of iPSC derivation and characterization are required. This is an excellent opportunity to build, optimize and scale a cutting-edge platform and be a leader in engineered cell medicines by combining the potential of the iPSC platform and CRISPR-based gene editing.

The successful candidate will work as part of the Editas platform team to aid in developing novel CRISPR/Cas9 technologies as therapeutics for the treatment of genetic diseases. The candidate will help to develop techniques and processes for the successful translation of this technology into the clinic. The ideal candidate is a motivated self-starter capable of a high degree of independence and conducting research experiments with minimal supervision. The position requires flexibility, creativity, the ability to work effectively in a multi-disciplinary team, excellent written and verbal communication skills, and a capacity for creativity and innovation.

Minimum Requirements
• B.S./B.A. in cell biology, molecular biology, or a related field with 8+ years of experience or M.S./M.A. with a minimum of 4 years of experience
• Extensive molecular biology expertise including primer design, PCR, cloning, gel electrophoresis, DNA and RNA purification, qPCR, RT-qPCR, ELISAs, and/or Western blots
• Experience in mammalian cell culture, transfections, and cell-based assays
• An ability to work in a fast-paced, team-oriented, multidisciplinary environment
• Excellent attention to detail

Additionally Desired
• Experience working with engineered nucleases for genome editing (TALEN, ZFN and/ or CRISPR)
• Experience working with adeno-associated virus and/or lentivirus
• Experience with fluorescence microscopy, immunostaining, and FACS
• Familiarity with DNA analysis software such as Vector NTI, Geneious, Benchling

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize trans-formative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

This Contract role on the Editas Manufacturing team provides a unique opportunity to contribute to the clinical translation of CRISPR technology by managing efforts that support the development and operationalization of Editas’ clinical programs.

Location: Cambridge, MA
Req Number: 1040

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

This new role on the Analytical Development team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to perform analytical characterization of complex biomolecules, such as the nuclease protein and guide RNA/protein complexes, using HPLC based assays, static and dynamic light scattering and other biophysical techniques. The successful candidate will work as part of a larger analytical development group to generate and interpret analytical data from key techniques in support of the process development group and release assays. Analytical techniques will also be used to design and support developability studies and report findings to group and project teams.

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize trans-formative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

Job Description
Editas Medicine is seeking an experienced and innovative scientist to lead histopathology group. This group is an integral part of department of Biological Development, supporting multiple projects across ophthalmology, oncology, neurology and hematology therapeutic areas, primarily focused on activities ranging from early drug discovery to early development. The qualified candidate will serve as a program pathologist and lead in providing the pathology aspect of the design, conduct, and interpretation of nonclinical studies.

Location – Cambridge, MA
Requisition Number: 1045

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize trans-formative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

This new role on the Chemistry, Manufacturing, and Controls (CMC) team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to perform experiments that generate data to guide development of processing methods and standard operating procedures (SOPs) for the preparation of cellular therapies for translational clinical studies. This individual will also assist in the development and execution of isolation and cryopreservation procedures for various cell types (PBMCs, T cells, CD34+, etc.). Candidate must be experienced with aseptic technique and be versatile to assist in the development and execution of processes for normal donor cellular products derived from different lineages of cells. Candidate must be experienced with aseptic technique and be versatile to assist in the development of processes for autologous or normal donor cellular products derived from different lineages of cells (T cells, HSCs, etc.).

Location: Cambridge, MA
Requisition Number: 1063

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

We have an immediate need for a Senior Research Associate, Cellular and Molecular Analytical Development to join our team. This new role on the Analytical Development team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to perform analytical characterization of complex biomolecules, such as the nuclease protein and guide RNA/protein complexes, using cell, immunological, and molecular methods. The successful candidate will work as part of larger analytical development group to generate and interpret analytical data from key techniques in support of the process development group and development of release assays. Analytical techniques will also be used to design and support developability studies and report findings to group and project teams.

Location: Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

Editas Medicine is seeking a Patent Counsel who will play a key role in developing its growing patent portfolio. This position offers a broad range of responsibilities, including identifying patentable inventions, performing patentability and freedom-to-operate analyses, drafting and prosecuting patent applications, counseling internal clients on IP matters, and conducting IP due diligence analyses for various internal projects. This individual will work closely with other members of the legal group as well as scientists and other internal stakeholders. Strong interpersonal and communication skills required. Must be a team player.

Location: Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

Editas Medicine is seeking an experienced Patent Agent who will play a key role in developing its growing patent portfolio. This position offers a broad range of responsibilities, including assisting the IP group in identifying patentable inventions, prior art searches, helping draft and prosecute patent applications, and supporting IP due diligence efforts for various internal projects. This individual will work closely with other members of the legal group as well as scientists and other internal stakeholders. Strong interpersonal and communication skills required. Must be a team player.

Location: Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

Editas is seeking a highly motivated Research Associate I or II to join our Platform Screening Team. In this role, you will employ medium-thoughput laboratory automation to establish and execute cell-based assays, with the goal of identifying Cas9/guideRNA combinations and progressing them to therapies. Experience with cellular assay development, automated liquid handlers, cell culture, molecular biology, AAV gene therapy, and/or data management are desired.

Location: Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.
We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

Job Summary

• Responsible for developing clinical supply strategies that ensure on time delivery and continuous supply of investigational products to patients. This includes selection/setup and management of distribution vendors, depots, logistic vendor, and import/export system.
• Responsible for defining the clinical supply chain risk management plan that ensures that management knows costs to reduce risks and the risk they are taking.
• Oversee Editas’ demand management activities including working with clinical operations to forecast demand, manage changes to clinical program, and manage IRT settings to ensure adequate and timely supply to sites
• Oversee Editas’ labeling/kitting/packaging, distribution, and destruction plans by coordination between CMC, clinical operations, and packaging/labeling vendors.
• Manage global clinical drug supply activities including
o Label creation with CMOs, CROs, Regulatory and translation vendors as necessary
o Depot activations and regulatory approvals necessary to ship to country
o Distribution timeline and coordination or product shipment with distributor, depots, and sites.
• Work with quality assurance to establish Editas cold chain and temperature sensitive product shipment risk management and shipping lane plans.
• Establish Editas’ system for packaging, collection, tracking and cold chain delivery for ATMPs. This includes cradle to grave traceability of identity, chain of custody documentation, and appropriate temperature documentation.
• Lead for triaging product complaint originating from logistics or distribution suppliers.
• Manage cold chain and other temperature sensitive shipments.
• Create a system to control and manage temperature sensitive shipments, site and shipment excursions.
• Maintain files for US Customs Compliance and proactively remit duties in a timely manner as required.

Location – Cambridge, MA
What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.
This new role on the Analytical Development team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to lead development of in process and release cellular analytical assays, including molecular and flow cytometry based assays. Candidate must be experienced with molecular immunology and be versatile to assist in the development and transfer of qualified assays for autologous or allogeneic gene edited cellular products derived from different lineages of cells (T cells, HSCs, etc.).

Location – Cambridge, MA
Requistion Number: 1097

Editas Medicine is a transformative genome editing company with a mission to translate its genome editing technology into a novel class of human therapeutics that enable precise and corrective genome level molecular modification to treat the underlying cause of a broad range of diseases.

This new role on the Chemistry, Manufacturing, and Controls (CMC) team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to perform experiments that generate data to guide development of processing methods and standard operating procedures (SOPs) for the preparation of cellular therapies for translational clinical studies. This individual will develop and execute of isolation and cryopreservation procedures for various cell types (PBMCs, T cells, CD34+, etc.). Candidate must be experienced with aseptic technique and be versatile to assist in the development of processes for autologous or normal donor cellular products derived from different lineages of cells (T cells, HSCs, etc.).

Location: Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

Editas is seeking a highly motivated Research Associate I/II to join our Screening Team. In this role, you will contribute to the pre-clinal development of gene-edited cell products. An ideal candidate should have a strong background in cell and molecular biology. Demonstrated culture experience with both IPSC or primary cell lines and a strong interest in genome editing. Experience and interest with lab automation and liquid handling robots, Biomek Fx / I7 or similar, is a plus.

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

This is a highly visible role reporting directly to the VP of Information Technology. You will be responsible for supporting our R&D systems including Quality, Regulatory, Clinical and Manufacturing. This role will provide IT systems leadership and partner with the business to build capabilities in support our corporate objectives. You will be responsible for our R&D application architecture, management of related budgets, and oversight for vendors or managed service providers.

Location: Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

Editas is seeking a Principal Research Associate/Scientist with a focus on research and development of CRISPR-based in vivo therapies. The candidate will be part of the neuroscience group, will interact effectively with the research and platform groups, as well as external collaborators. The individual will provide scientific expertise and guidance for target selection, early research to candidate selection, and transition to early clinical development.

Location: Cambridge, MA

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world?  If the answer is yes, then Editas Medicine is the place for you.

Job Description

Editas is seeking a highly motivated Research Associate to join our neuroscience group. The candidate will be responsible for conducting cell biology studies to support the development of gene-editing based therapies in neurological diseases. The successful candidate will be part of a dynamic team and will interact with the discovery, platform, process development groups, as well as contract research organizations. The successful candidate should demonstrate strong work ethics and ability to work in a fast-paced and highly demanding work environment.

Scientist I – Pharmacology

Location – Cambridge, MA

Company Summary:

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize trans-formative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world?  If the answer is yes, then Editas Medicine is the place for you.

Primary Responsibilities:

The main responsibilities of the candidate are to assist with the strategy, planning and execution of activities related to pre-clinical pharmacology. Activities include:

• Strategy for and oversight of animal model development and characterization in the area of oncology and cell therapies
• Design experiments and develop assays critical to understand in-vivo therapeutic activity, efficacy, and PK/PD properties
• Suggest refinements and optimization to in-life procedures, based on study requests from project teams
• Perform pre-clinical proof-of-concept and interact with clinical development team to design and supervise IND-enabling studies
• Experience managing studies remotely through CRO collaborators
• Documentation of assay development and animal study results
• Responsible for write-up or review of pre-clinical pharmacology-related section of IND

Director / Senior Director of IT Operations

Location – Cambridge, MA

Company Summary:

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize trans-formative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world.  If the answer is yes, then Editas Medicine is the place for you.

Primary Responsibilities:

• Day to day operations of Editas’s network, storage, security and telephony infrastructure
• Oversee the deployment, monitoring, maintenance, development, upgrade, and support of security systems, servers, desktop devices, IT Operations applications, networks and the service desk

• Responsibility for system configurations, Software installations, updates, & upgrades to Windows servers, applications, and other infrastructure systems.
• Monitoring system performance/availability & taking appropriate proactive steps to maximize uptime

• Manage and mature the IT service desk and ensure mutually defined SLA’s are managed and achieved
• Manage Editas’s IT infrastructure vendors, SaaS providers and hosting partners
• Develop capacity plans and budgets that meet the growth, scale and changing needs of the business
• Maintain a high level of infrastructure uptime in a fast-paced environment
• Develop and test disaster recovery and business continuity plans
• Develop, implement and maintain IT policies, procedures, and associated plans for security, data center, desktops and infrastructure based on industry-standard best practices, SOX and FDA requirements
• Develop and mature end user training on our growing portfolio of applications and tools

Minimum Qualifications:

• A minimum of 10 years of Information Technology experience, and 6 years of management experience

• Demonstrated ability to work on diverse projects simultaneously, requiring detailed analysis, creative/practical problem solving, time management, and sound judgment
• Ability to self-motivate while operating effectively in a team-oriented and collaborative environment
• Experience supporting a 100+ end user environment
• Experience in small company or start up environments (Life sciences preferred)
• Experience in vendor management, computer operations, network management, technical management and end user support
• Experience implementing and/or managing one or more of the following processes: IT incident/service request management, IT configuration management, computer system validation
• Experience with SaaS and hosted applications including Okta and Office 365
• Ability to work on a small, fast-paced IT team
• Strong communication and interpersonal skills
• Budget management experience
• Ability to manage multiple projects, activities and tasks simultaneously

Key Capabilities:

• Creative and strategic thinker with ability to adapt quickly to a high-growth, fast paced environment
• Able to communicate complex issues in a simple way, to orchestrate plans to resolve issues, and mitigate risks
• Willingness to roll-up sleeves and be hands-on
• Excellent interpersonal skills with the ability to develop important relationships with key internal and external stakeholders
• The ability to work cooperatively with others; the genuine desire to be a part of a team and contribute to organizational and team goals

Location – Cambridge, MA

Company Summary:

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize trans-formative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world.  If the answer is yes, then Editas Medicine is the place for you.

Primary Responsibilities:

• Develop and execute the company’s investor relations strategy
• Develop written materials including press releases, conference call scripts, slide presentations, and Q&A documents; to prepare for quarterly calls, conference presentations, and other investor events
• Plan, manage, and oversee external events including conferences, analyst days, and non-deal roadshows
• Collaborate with leadership team and key stakeholders to define strategic communications delivered to investors and analysts
• Maintain comprehensive, current knowledge of Editas’ research and development approaches and business strategies to better inform IR strategy
• Develop and manage relationships and maintain regular communication with investors and analysts, to provide up-to-date information

Location: Cambridge, MA

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world?  If the answer is yes, then Editas Medicine is the place for you.

We are looking for an enthusiastic, innovative and experienced scientist to join Biological Development group to support research activities across multiple programs for cell therapy. The potential candidate would be expected to lead the path from the discovery research through early clinical development to evaluate the pharmacology of novel therapeutic approaches. Collaborative interactions with therapeutic area research, preclinical safety, biomarker (imaging or biochemical) and clinical development teams are critical to success in the role.

Location: Cambridge, MA

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world?  If the answer is yes, then Editas Medicine is the place for you.

We are growing our informatics team to build a platform that spans a wide range of our needs ranging from LIMS development, lab automation, and data pipeline design and management. To support our platform, Editas is seeking to hire an informatics developer with proven expertise in designing and implementing a LIMS to handle a variety of lab functions and experiments (NGS, etc.). They should also have knowledge and experience managing scientific data and processes, building automation, and interacting with scientists and researchers.

Experience with modern, agile development practices, Tableau, Java and web services development and cloud computing is highly desirable. You should be familiar with terms like JAXB, JSON, GIT, Jersey, AWS (Batch, Lambda, EC2, Athena, etc.), Swagger, web services, serverless and HTML5.

Location: Boulder, CO

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world?  If the answer is yes, then Editas Medicine is the place for you.

We are currently building an informatics platform that spans a wide range of our needs ranging from LIMS development, lab automation, and data pipeline management.  To support our platform, Editas is seeking to hire an informatics developer with proven expertise in designing and implementing a LIMS to handle a variety of lab functions and experiments (NGS, etc.).  They should also have knowledge and experience managing scientific data and processes, building automation, and interacting with scientists and researchers.  Experience with modern development practices, Tableau, web and web services development and cloud computing is highly desirable as well.

Position will be working remotely to a small informatics team that designs, develops, and deploys the enterprise software systems that support our scientific team. Professional experience developing Java software in biotech required.  You should be familiar with terms like JAXB, JSON, GIT, Jersey, AWS, web services, serverless and HTML5.

Editas Medicine is a transformative genome editing company with a mission to translate its gene editing technology into a novel class of human therapeutics that enable precise and corrective genome level molecular modification to treat the underlying cause of a broad range of diseases.

This new role on the Editas Manufacturing team provides a unique opportunity to contribute to the clinical translation of CRISPR technology by managing efforts that support the development and operationalization of Editas’ clinical programs.

Editas Medicine is a transformative genome editing company with a mission to translate its genome editing technology into a novel class of human therapeutics that enable precise and corrective molecular modification to treat the underlying cause of a broad range of diseases at the genetic level.

Editas is looking for a versatile and highly-motivated individual to contribute to business development activities of a rapidly growing biotech.  Reporting to Vice President of Business Development the Senior Director of Business Development will play a key role in defining and driving Editas’ strategic initiatives, and will be responsible for the identification, evaluation and execution of strategic collaborations.

Location: Cambridge, MA
Req Number: 1016

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world?  If the answer is yes, then Editas Medicine is the place for you.

This role on the Analytical Development team provides a unique opportunity to contribute to Editas efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies.

Location: Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

The immunogenetics team is seeking an experienced and highly motivated molecular biologist/immunologist with expertise in genetic engineering of hematopoietic cells.   We are seeking a thoughtful, organized, and creative scientist who will play a key role in the generation and characterization of novel cell therapy products for cancer.

Location: Cambridge, MA

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world?  If the answer is yes, then Editas Medicine is the place for you.

Editas is seeking a Vice President of Discovery Biology to lead a group of biologists developing CRISPR/Cas9-based therapies for our current ocular disease platform and other new indications diseases for which in vivo gene editing may provide a potentially differentiated therapy.

Location: Cambridge, MA

What if you could repair broken genes?  That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world?  If the answer is yes, then Editas Medicine is the place for you.

The immunogenetics team is seeking a highly motivated immunologist/molecular biologist with expertise in genetic engineering of hematopoietic cells to join our rapidly growing team.  The successful candidate will help build a new class of immuno-oncology products and will test novel engineered effector cell modalities using in vitro and in vivo human tumor models.  Experience with mammalian cell culture, including isolating and propagating human effector cells, a plus.  This is an excellent opportunity to be at the cutting edge of engineered cell medicines by combining the power of immune-oncology and CRISPR-based gene editing.

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

Editas is seeking a highly motivated Research Associate I/II to join our Biological Development group. The candidate will contribute as part of a dynamic team to the development of gene-editing based ex vivo cell therapies in multiple disease areas, including hematology and immune-oncology. In this role, the candidate will be responsible for performing studies to support the efficacy and safety evaluation of gene editing lead molecules. The successful candidate is expected to have proven practical experience in aseptic cell culture. The candidate will be frequently interacting with the discovery, platform and process development groups. Strong communication skills, and the ability to work in a fast-paced and team-oriented environment will also be vital.

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

The Biological Development department at Editas is seeking a motivated scientist to join the biomarker and bioanalytical group for development of analytical assays to support the preclinical and clinical programs in the ocular, hematology and oncology therapeutic areas. The qualified candidate will be responsible to develop the analytical assays for PK/PD, biodistribution, and immunogenicity as well as biomarker discovery and qualification. The responsibility will include assay development, sample testing and technical report generation to support preclinical studies and regulatory submission. This individual is expected to be a great team player, enthusiastic and enjoy working in an innovative, collaborative and fast-pace environment.

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

Editas is seeking a Scientist/Senior Scientist with a focus on research and development of CRISPR-based in vivo therapies. The candidate will be part of the in vivo discovery group that is responsible for discovering potential therapies for ophthalmology and rare diseases. The successful candidate will interact effectively with the research and platform groups, as well as external collaborators. The individual will provide scientific expertise and guidance for target selection, early research to candidate selection, and transition to early clinical development.

A successful candidate will demonstrate extensive knowledge in molecular and cellular pathways in ophthalmology and rare diseases. Experience with in vivo models is essential. Working experience with gene editing, cellular models, and cell manufacture are desirable but not essential.

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

Editas is seeking a Research Associate/Senior Research Associate with a focus on cell biology, stem cells and related assays. The candidate will be part of the cell biology group that is responsible for discovering potential therapies for ophthalmology and other diseases. The successful candidate will interact effectively with the research and platform groups. The individual will provide support to cell biology, stem cells, differentiation, disease modeling, gene editing and cell-based assays.

A successful candidate will demonstrate extensive knowledge in molecular and cell biology and stem cells. Work experience with gene editing is highly desirable.

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

The Immunogenetics team is looking to add highly talented and motivated candidates to assist in the development of novel immune-oncology therapies for cancer.  The successful candidate will contribute to exploring innovative cell-based anti-tumor strategies for cancer using gene editing and genetic engineering as part of a dynamic, multidisciplinary discovery team dedicated to the development of novel first in class therapeutics. This position will serve a critical function in providing high-level laboratory support to project leads with a focus on cellular and molecular immunology. We are seeking a highly motivated and innovative senior research associate with immunology/cancer biology expertise.

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world. If the answer is yes, then Editas Medicine is the place for you.

Editas Medicine is seeking a highly motivated Research Associate I/II to join our ex vivo Immunogenetics group. In this role, you will contribute to the pre-clinical development of gene-edited cell products for oncology indications. An ideal candidate should have a background in immunology, cancer biology, and a strong interest in genome editing. The successful candidate will be part of a dynamic team and will interact with the discovery, platform, process development groups, as well as contract research organizations. The successful candidate should demonstrate strong work ethics and ability to work in a fast-paced and highly demanding work environment.

Location – Cambridge, MA

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.
Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

This new role on the Chemistry, Manufacturing, and Controls (CMC) team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to perform experiments that generate data to guide development of processing methods and standard operating procedures (SOPs) for the preparation of cellular therapies for translational clinical studies. This individual will develop and execute of isolation and cryopreservation procedures for various cell types (PBMCs, T cells, CD34+, etc.). Candidate must be experienced with aseptic technique and be versatile to assist in the development of processes for autologous or normal donor cellular products derived from different lineages of cells (T cells, HSCs, etc.).

Location: Cambridge, MA
Req Number: 1015

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.

We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

This new role on the Analytical Development team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to develop in process and release cellular analytical assays. Candidate must be experienced with aseptic technique, flow cytometry, and be versatile to assist in the development of qualified assays for autologous or allogeneic gene edited cellular products derived from different lineages of cells (T cells, HSCs, etc.).

Location – Cambridge, MA

Editas Medicine is a transformative genome editing company with a mission to translate its genome editing technology into a novel class of human therapeutics that enable precise and corrective molecular modification to treat the underlying cause of a broad range of diseases at the genetic level.  Editas is seeking a Scientist/Senior Scientist with a focus on research and development of CRISPR/Cas9-based ocular medicines.

The candidate will be part of the ophthalmology discovery group that is responsible for discovering medicines for  both inherited retinal degenerations and genetically treatable ocular diseases. The successful candidate will interact effectively with the pre-clinical and platform groups, as well as external collaborators.  The individual will provide scientific expertise and guidance for target selection, early research candidate selection, and transition into early clinical development.

A successful candidate will demonstrate extensive knowledge in molecular and cellular pathways in ophthalmology.  Experience with cellular and animal models is essential as well as experience with gene editing and molecular skills.

Location – Cambridge, MA
Req Number: 1068

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases.
We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before.

Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

This new role on the Chemistry, Manufacturing, and Controls (CMC) team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to build and manage a team designing and performing experiments that generate data to guide development of methods and standard operating procedures (SOPs) for the preparation of cellular therapies for translational clinical studies. Candidate must be versatile and able to work with research colleagues to develop processes for autologous or normal donor cellular products derived from different lineages of cells (T cells, HSCs etc.).