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    Principal Scientist, CRISPR Platform and Vector Design - Alameda, CA, United States - American Society of Gene & Cell Therapy

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    Description

    Scribe Therapeutics is a molecular engineering company focused on creating best-in-class in vivo therapies that permanently treat the underlying cause of disease. Founded by CRISPR inventors and leading molecular engineers Benjamin Oakes, Brett Staahl, David Savage, and Jennifer Doudna, Scribe is overcoming the limitations of current genome editing technologies by developing custom engineered enzymes and delivery modalities as part of a proprietary, evergreen CRISPR by DesignTM platform for CRISPR-based genetic medicine.

    We are seeking a creative, passionate, and motivated individual to join us in our quest to develop the next generation of CRISPR-based therapeutics. The current role is for a Principal Scientist to lead our Molecular Engineering - Cargo team. The successful candidate will plan and lead engineering campaigns on our CRISPR system expression constructs - with a focus primarily on mRNA delivery. In addition, they will be thought leaders on our CRISPR platform buildout, including assay development for CRISPR expression and localization in vitro and in vivo. As a manager of several scientists and research specialists, the candidate should bring leadership and mentorship around scientific careers in industry.

    The candidate will have numerous opportunities for professional growth in a rapidly growing biotechnology start-up.

    Responsibilities:

    • Lead a research team to optimize and be the experts in our CRISPR delivery constructs, including mRNA and AAV transgenes
    • Oversee and develop assays for characterizing CRISPR delivery constructs, including delivery, expression, and localization within cells and in vivo
    • Collaborate across research teams in biology, process science, NGS and automation to drive effective processes and collaborative initiatives
    • Develop strategy for the selection and optimization of CRISPR components for our therapeutic programs
    • Manage CROs for production and external research activities
    • Critically evaluate results and communicate scientific findings both internal and externally
    • Mentor and manage a motivated group of scientists and research associates
    • Foster a driven, fast-paced, dynamic environment in which to do rigorous science

    Required Skills and Background:

    • A PhD in Bioengineering, Biochemistry, Biophysics, Synthetic Biology, Genetics or related discipline
    • At least 3 years of experience working in an industry setting, with a proven track record of expertise in molecular engineering, designing reporter systems, screening in human cells, and readouts by FACS and NGS.
    • Experience in managing and leading scientific teams of at least 3
    • Expertise in molecular biology, RNA and protein analysis (e.g. qPCR, RT-qPCR, Western, etc.)
    • Demonstrated scientific productivity and drive as evidenced by a strong publication record in top journals
    Preferred Skills and Background:
    • Experience with CRISPR therapeutic approaches and delivery systems.
    • Experience in AAV optimization, production, and characterization
    • Experience with functional genomics or next-generation sequencing approaches.
    • Experience with computational tools for analysis of biological data.

    Salary will be commensurate with experience. We will provide an intellectually stimulating, collegial and fast-paced environment. If you are ready to engineer the future of therapeutics, then we are excited to hear from you Visit us at

    We are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

    At the time of posting, the base pay wage range for this role is $150,000-$190,000 per year. The offered pay range will depend on internal equity and the candidate's relevant skills, experience, qualifications, training, and market data. Additional incentives are provided as part of the complete package in addition to comprehensive medical and other benefits.

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