Scientist II, CRISPR-X - Gene Insertion

CRISPR Therapeutics; Boston (MA); On-site; USD 130,000 - 140,000; Full time

Job summary

CRISPR Therapeutics, Inc. in Boston is seeking a Scientist II to grow the CRISPR-X team, advancing next-generation gene editing therapies for human disease.

You will design and execute molecular biology experiments, CAR T cell engineering, and translate findings across in vitro and in vivo systems. The role emphasizes collaboration in a fast-paced, on-site research environment, with opportunities to contribute to a broad clinical portfolio and to develop novel medicines for patients.

Qualifications

• PhD in biology, bioengineering, immunology, or related discipline with 2-5+ years of professional experience.
• Hands-on experience with CAR T cell engineering and gene editing.
• Experience with molecular biology techniques (qPCR, ddPCR, NGS).
• Strong writing, reviewing and presentation skills.
• Ability to work independently and in a team.

Responsibilities

• Lead and optimize research exploring next-generation gene editing strategies (CRISPR-based) and immunology.
• Design, execute and interpret molecular biology experiments (cloning, qPCR, NGS, RNA/DNA analysis, cell culture).
• Guide construct design and target selection using knowledge of immune cell biology.
• Review literature to find novel solutions for gene editing and immunology problems.
• Develop translational assays across in vitro and in vivo systems.

Skills

CAR T cell engineering

Gene editing technologies

Molecular biology techniques

Critical thinking

Education

PhD in biology or related field with 2-5+ years of experience

Non-PhD with 10-12+ years of experience

Tools

qPCR/ddPCR

NGS

Cell culture

Transfection/nucleofection

Viral vectors/particles

Job description

Job Description:

Company Overview

Founded over a decade ago,CRISPR Therapeuticsis a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY®(exagamglogene autotemcel [exa-cel]), the world's first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia.CRISPR Therapeuticsis advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase™ editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact,CRISPR Therapeuticshas established strategic collaborations with leading biopharmaceutical partners, includingVertex Pharmaceuticals.CRISPR Therapeutics AGis headquartered inZug,Switzerland, with its wholly-ownedU.S.subsidiary,CRISPR Therapeutics, Inc., and R&D operations based inBoston, MassachusettsandSan Francisco,California.

Position Summary

Are you passionate about developing next-gen CRISPR therapies? We are seeking a highly motivated and creative Scientist II to grow our diverse, innovation-focused CRISPR-X team that pioneers novel gene editing therapies for human disease. We are part of CRISPR Therapeutics, a leading gene editing company with a broad clinical portfolio. The successful candidate will be an integral part of our team, whose aim is to research, develop and advance the next generation of genome editing modalities and genetic therapies for a wide range of human indications. The position requires enthusiasm, passion, outstanding skills in the art, attention to detail, and a desire to create new medicines for patients

Responsibilities

• Lead, design, and optimize research with the aims of exploring and developing next-generation gene editing strategies, primarily gene insertions, using CRISPR-based tools and beyond, and synthetic immunology.
• Design, execute, and interpret research requiring molecular biology techniques including cloning, qPCR/ddPCR, NGS, RNA and DNA analysis, cell culture, and other cell-based assays.
• Use knowledge of immune cell biology to guide construct design, target selection, and interpretation of phenotypic outcomes of in-vivo CAR T and other immune studies.
• Dissect published literature to find novel solutions to gene editing and immunology problems.
• Develop a deep understanding of the biology underlying new disease indications and design translational assays and experimental strategies to enable evaluation of gene editing and CAR approaches across in vitro and in vivo systems.

Minimum Qualifications

• Prior experience with gene editing, including experience applying and developing next generation gene editing technologies, such as recombinases, retrotransposons or other integration approaches, in an academic and/or industry setting, with a track record demonstrating significant contributions.
• Hands-on experience with chimeric antigen receptor (CAR) T cell engineering, including CAR construct design, gene editing and/or transgene delivery in primary human T cells, and functional characterization of the resulting CAR-T cells.
• Ph.D. in biology, bioengineering, immunology, or related discipline with 2-5+ years of professional experience, or non-PhD and 10-12+ years of progressive, relevant experience.
• Outstanding problem-solving skills and attitude to think outside the box.
• Excellent writing, reviewing, and presentation skills.
• Challenges oneself continuously to enhance scientific capabilities.
• Ability to work independently as well as collaboratively in a results-oriented research team environment.
• Must possess critical thinking and self-reliance to solve tasks independently.
• Self-motivated and scientifically rigorous, with outstanding organization and multitasking capability.
• Entrepreneurial spirit showing resourcefulness, accountability, agility to pivot, transparency, and productivity.

Preferred Qualifications

• Prior experience with protein and/or RNA engineering.
• Prior experience establishing next-generation CAR T cells ex-vivo and/or in-vivo CAR T cells.
• Prior experience with diverse delivery technologies, including transfection/nucleofection, lipid nanoparticles, and viral vectors/particles.
• Prior experience designing and executing in vivo studies, including downstream tissue processing.
• Experience managing and mentoring junior scientists.

Competencies

• Collaborative – Openness, One Team
• Undaunted – Fearless, Can-do attitude
• Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
• Entrepreneurial Spirit – Proactive. Ownership mindset.

Due to the nature of their work, our manufacturing and lab-based positions are located fully on‑site.

Scientist II: Base pay range of $130,000 to $140,000+ bonus, equity and benefits

The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.

CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.

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