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Director Crispr Genome Editing Jobs (NOW HIRING)

The project integrates mouse and iPSC models, CRISPR genome editing, molecular biology, flow cytometry, and single-cell multi-omics to dissect disease mechanisms. We are committed to mentoring the ...

Postdoctoral Fellow

Baltimore, MD · On-site

$48K - $66K/yr

Description The Cho Laboratory directed by Sangkyun Cho, PhD, at Johns Hopkins University seeks 1-2 ... CRISPR genome editing, CRISPRa/i * Animal work and rodent surgeries * Machine learning / artificial ...

Showing results 21-40

Director Crispr Genome Editing information

What does a director CRISPR genome editing do?

A Director of CRISPR Genome Editing leads and oversees research teams focused on using CRISPR technology to edit genomes for various applications, such as disease treatment, agriculture, or biotechnology. They are responsible for setting strategic scientific goals, designing and supervising experiments, ensuring compliance with ethical and regulatory guidelines, and managing budgets and collaborations. This role typically requires advanced expertise in molecular biology, genetics, and genome editing technologies, as well as strong leadership and communication skills.

What are the key skills and qualifications needed to thrive as a director CRISPR genome editing?

To thrive as a Director of CRISPR Genome Editing, you need deep expertise in molecular biology, genetics, and genome editing technologies, typically supported by a PhD in a relevant field and significant research experience. Proficiency with CRISPR-Cas systems, next-generation sequencing platforms, and bioinformatics tools is essential, along with familiarity with regulatory compliance standards. Outstanding leadership, strategic thinking, and communication skills set apart those who can lead multidisciplinary teams and drive innovation. These skills ensure effective oversight of complex research programs, successful project execution, and advancement of cutting-edge genomic therapies.

What are some common challenges faced by a director CRISPR genome editing when leading multidisciplinary teams?

A Director of CRISPR Genome Editing often manages teams comprising molecular biologists, bioinformaticians, and regulatory experts. One common challenge is ensuring clear communication across these diverse specialties to align on project goals, timelines, and regulatory requirements. Additionally, staying updated with rapidly evolving CRISPR technologies and integrating new methods into existing workflows can be demanding. Directors also need to balance ambitious research objectives with compliance and ethical considerations, fostering innovation while maintaining rigorous standards.

What is the difference between Director Crispr Genome Editing vs Senior Genome Editing Scientist?

AspectDirector Crispr Genome EditingSenior Genome Editing Scientist
CredentialsAdvanced degrees (PhD), leadership experiencePhD or Master’s, specialized technical expertise
Work EnvironmentLeadership roles, project oversight, strategic planningLaboratory research, experimental design, data analysis
Industry UsageUsed in biotech companies, research institutions, pharmaCommonly in research labs, biotech firms, academia

The main difference is that the Director Crispr Genome Editing oversees projects and teams, focusing on strategy and management, while the Senior Genome Editing Scientist conducts hands-on research and experimental work. Both roles require strong technical skills, but the director position emphasizes leadership and planning.

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Infographic showing various Director Crispr Genome Editing job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% In-person job distribution.

Scientist II - Viral Vector

Dawar Consulting

South San Francisco, CA • On-site

$82.66 - $96.43/hr

Other

Medical, Dental, Vision, Retirement

Posted 29 days ago


Job description

Scientist II - Viral Vector

South San Francisco, United States | Posted on 07/24/2026

Our client, a world leader in biotechnology and life sciences, is looking for a “ Scientist II - Viral Vector ” based out of South San Francisco, CA (Hybrid).

Rate: $65/hr on W2 (DOE)

Job Duration: Long-Term Contract (Possibility Of Extension)

Company Benefits: Medical, Dental, Vision, Paid Sick Leave, 401K

Summary:

We are seeking a highly motivatedViral Vector Research Associate/Scientistwith5–10 years of laboratory research experienceto support ourViral Vector Coreand gene therapy research programs. The ideal candidate will have hands-on experience inviral vector production, mammalian cell culture, molecular biology, and CRISPR genome editing technologies. This role involves the production and characterization oflentiviral and AAV vectors, supporting next-generation viral vector engineering, maintaining viral inventories, and collaborating with cross-functional research teams to advance innovative gene therapy platforms.

Key Responsibilities
  • Produce, purify, and characterizelentiviral librariesandAdeno-associated virus (AAV)vectors to support research and preclinical studies.
  • Perform viral vector analytics using molecular biology techniques includingPCR, qPCR, ddPCR/dPCR, Western blot, and related assays.
  • Maintain and manage viral vector inventory, sample tracking, and documentation usingelectronic laboratory notebooks (ELN)and digital informatics systems.
  • Support the engineering, optimization, and development ofnext-generation viral vectorsand emerging viral-based therapeutic modalities.
  • Performmammalian cell culture, transient plasmid transfection, cloning, and other molecular biology techniques.
  • Participate inCRISPR/Cas9 genome editingexperiments for bothin vitro and in vivoapplications.
  • Operate laboratory instrumentation includingflow cytometersand support data collection, analysis, and interpretation.
  • Maintain accurate laboratory documentation, experimental records, and inventory following established laboratory procedures.
  • Collaborate with multidisciplinary research teams to support gene therapy, virology, and genome engineering projects.
  • Analyze experimental data, troubleshoot protocols, and contribute to continuous process improvements.
Required Qualifications
  • MS or PhDinCell Biology, Molecular Biology, Virology, Biochemistry, Bioengineering, Genetics, or a related scientific discipline.
  • 5–10 yearsof laboratory research experience in molecular biology, virology, or gene therapy.
  • Hands-on experience withlentiviral vector productionand/orAAV production.
  • Strong experience withmammalian cell cultureand transient plasmid transfection.
  • Experience with molecular biology techniques including:
    • PCR
    • qPCR
    • ddPCR / dPCR
    • Western Blot
  • Experience withCRISPR/Cas9 genome editingtechnologies.
  • Strong organizational, analytical, troubleshooting, and communication skills.
Preferred Qualifications
  • Experience withviral vector engineeringand next-generation viral modalities.
  • Experience operatingflow cytometers.
  • Familiarity withelectronic laboratory notebooks (ELN)and digital sample management systems.
  • Experience withdata analysis, computational programming, and bioinformatics tools.
  • Previous experience supportinggene therapy,viral vector core facilities, or translational research programs.
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