CRISPR Therapeutics
CRISPR Therapeutics is seeking a Research Associate II to design, develop, and optimize lipid nanoparticle (LNP) formulations for non-viral delivery of genome editing therapies. The role involves executing analytical characterization, managing cell culture, and supporting preclinical therapeutic programs with minimal supervision. This position contributes to advancing platform technology and clinical translation within the CRISPR-X division.
Headquarters
Boston, Massachusetts, United States
Company Size
201-500 employees
Founded
2013
CRISPR Therapeutics is a gene-editing company pioneering the development of transformative medicines using CRISPR/Cas9 technology to treat serious diseases. The company has a broad pipeline spanning hemoglobinopathies, immuno-oncology, autoimmune diseases, in vivo editing, and regenerative medicine, including CASGEVY™, the first-ever approved CRISPR-based therapy for sickle cell disease and transfusion-dependent beta thalassemia. CRISPR Therapeutics operates across multiple clinical and preclinical programs in collaboration with partners such as Vertex Pharmaceuticals.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for CRISPR Therapeutics.
31% below the average for this role
CRISPR Therapeutics’ CASGEVY Progress Reframes Growth And Valuation Story
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