Gene Editing Scientist

Preventive Medicine

$120K — $180K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years hands-on experience with CRISPR base or prime editors in mammalian systems
  • Proficiency in NGS library preparation and analysis, with knowledge of CRISPResso2 and CRISPR-RGEN tools
  • Strong track record of leading complex projects and securing publications or patents
  • Demonstrated strong work ethic, scientific rigor, and integrity.

Responsibilities

  • Establish the editor-engineering pipeline for ABE/CBE/RT-editing architectures
  • Optimize high-throughput cloning and screening workflows, ensuring efficient data capture
  • Develop quantitative assays for on-target and off-target analysis using advanced sequencing and bioinformatics
  • Drive preclinical translation in relevant cellular and animal models
  • Recruit, mentor, and lead a team of research associates and scientists
  • Communicate program progress through detailed documentation and presentations to stakeholders.

Benefits

  • Competitive salary plus meaningful equity share in the company's upside
  • Comprehensive health, dental, and vision coverage
  • 401(k) with company match
Full Job Description
Preventive Medicine is a venture-backed biotech startup developing next-generation reproductive-genetics platforms to eliminate severe genetic disease before birth.

As one of the first scientific hires, you will help define our technical roadmap, build our R&D culture from the ground up, and influence the long-term direction of the company. We are seeking an entrepreneurial Scientist to design, build, and evaluate advanced adenine & cytosine base editors (ABE, CBE) and RT editors. Partnering directly with the co-founders, you will take new editor concepts from the bench to IND-enabling studies while laying the foundation of our research organization.

Key Responsibilities
  • Establish the editor-engineering pipeline - Optimize ABE/CBE/RT-editing architectures for potency, specificity, and manufacturability
  • High-throughput cloning & screening workflows (automated assembly, pooled libraries, functional reporters) and streamline data capture
  • Develop quantitative assays for on- and off-target analysis using cutting-edge sequencing and bioinformatics platforms.
  • Drive preclinical translation in relevant cell models and preclinical species
  • Recruit, mentor, and lead a small team of research associates and scientists;
  • Communicate program progress through protocols, data packages, and presentations to investors, advisors, and regulatory consultants.

Requirements

Minimum Qualifications
  • 5+ years hands-on experience engineering CRISPR base or prime editors in mammalian systems - demonstrated impact matters more than formal credentials.
  • Proficiency with NGS library preparation & analysis (e.g., CRISPResso2, CRISPR-RGEN Tools) and basic Python/R scripting for data processing.
  • Proven track record of leading complex projects and publishing or patenting influential work.
  • Strong work ethic, scientific rigor, and high integrity.


Preferred qualifications
  • Familiarity with regulatory standards and assays relevant to gene-editing therapeutics
  • Experience generating and using RNPs and mRNA for gene editing, including delivery via electroporation or nanoparticles.
  • Prior startup or small-team experience in fast-moving environments.
  • Comfort with automation (liquid handlers, LIMS) and/or single-cell genotyping/transcriptomics.

Benefits
  • Competitive salary plus meaningful equity-share in the company's upside.
  • Comprehensive health, dental, and vision coverage.
  • 401(k) with company match.

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