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Immunology_Research Associate/Sr. Research Associate/Associate Scientist

GenEditSouth San Francisco, California, United StatesOnsite
This job is no longer open

Research Associate/Sr. Research Associate/Associate Scientist, Immunology


GenEdit is a rapidly growing, early-stage company that is developing a proprietary and novel delivery platform with the potential to transform genetic medicine. Our interdisciplinary team works together across chemistry, payload, formulation, screening, and preclinical groups to develop the next generation of gene therapies. GenEdit fosters an exciting and dynamic environment where we value impactful data and creative solutions to accelerate our progression from a platform technology to a pipeline of therapeutic candidates.

We are seeking talented and motivated individuals to join our team and are expanding across all functions within the organization. Join us in South San Francisco, CA, to be at the forefront of the future of gene therapy.

Job Description


GenEdit is seeking a highly self-motivated, multi-talented and goal-oriented Research Associate/SRA with hands-on experience in performing the cell-based assays using mammalian immune, primary cells and cell lines. The position will be responsible for characterizing GenEdit’s novel polymer nanoparticles across a wide array of cell types to deliver genetic medicines, including mRNA, siRNA, and Cas9. The successful candidate will have experience handling multiple types of mammalian cell cultures, for example Immune cells, PBMC,HSPC, neural cells, and will have experience performing various microplate-based assays, such as viability/toxicity, fluorescence, luminescence, and automated microscopy.

Characterization of payload activity will include molecular biological methods such as the nucleic acid extraction, PCR, RT-qPCR, and immunoassays such as ELISA, ELISpot, Flow cytometry and Western Blot. This position will work cooperatively with multidisciplinary teams, keep detailed and organized lab records, and present results at team meetings.Under the direction of the project leader/immunology manager, this lab-based position will work closely with colleagues on project teams advancing our novel gene delivery system for therapeutic applications in immune-based diseases.

Education and Qualifications:


Bachelor or Master’s degree Immunology, Cell & Molecular Biology, Biotechnology, Biochemistry, Biomedical Engineering, or related subject with 1-2 years (For Technician/RA), 2-3 years (for Senior RA), and 3-4 years (for Associate Scientist) of scientific/pharma/academic research experience>2 years wet lab research experience in ImmunologyWork authorization in the US is required

Desired Skill Sets:


Experience with cell culture/characterization of various immune cells (DC, Macrophages) and primary cells (PBMC, iPSC, HSPC) and neural cells. Experience with multicolor Flow CytometryExperience with molecular and cellular biology techniques such as DNA, RNA and Protein extraction and purification, Electrophoresis, Primer design, PCR, Real Time-qPCR, DNA sequence analysis, ELISA, ELISpot and Western Blot Experience with microplate cell-based assays, in vitro screening, immunocytochemistry, cytotoxicity assay, and quantitative microscopy Experience with Prism and FlowJo for data analysisExcellent written and oral communications skills a plus familiarity with SOP writingExcellent organization and use of network drives Ability to execute on standard operating procedures with accuracy and precisionA creative and proactive approach to problem-solving.

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Life at GenEdit

GenEdit is a next-generation genome editing company. We are developing non-viral delivery technologies for the CRISPR/Cas9 gene editing system that can safely and efficiently correct gene mutations in patients. CRISPR/Cas9 is a powerful genome editing tool that makes therapeutic gene editing possible. It is easier to use, faster, and more accurate than previous gene editing techniques and thus has the potential for a wide range of therapeutic applications. In particular, CRISPR/Cas9 gene editing has the potential to treat a variety of incurable genetic diseases. However, current CRISPR delivery methods rely on viruses and are problematic due to viral-induced toxicity and prolonged Cas9 exposure, increasing off-target effects. A non-viral CRISPR/Cas9 delivery method is needed. In addition, low efficiency levels achieved make it impossible to target certain diseases. GenEdit's novel CRISPR delivery technology has the potential to be a platform delivery system for a broad range of genetic diseases. We also work on engineering of core components of CRISPR/Cas9 genome editing system to increase editing efficiency and enable targeted delivery.
Thrive Here & What We Value1. Dynamic and exciting environment2. Valuing impactful data and creative solutions3. Emphasis on teamwork and collaboration4. Commitment to advancing novel therapies in genetic medicine5. Diversity as a strength6. Inclusive hiring practices
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