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Senior Research Associate, In Vivo Discovery

Job in Cambridge, Middlesex County, Massachusetts, 02141, USA
Listing for: Pivotal Life Sciences
Full Time position
Listed on 2026-07-01
Job specializations:
  • Research/Development
    Research Scientist
Job Description & How to Apply Below

Senior Research Associate, In Vivo Discovery

Location:

Boston, MA

Reports to:

Principal Scientist

Job Type: Full-Time, Onsite

About Us

We are an innovative, stealth-mode biotech company developing in vivo gene editing therapeutics with a focus on targeted delivery of CRISPR machinery to therapeutically relevant cell types.

Job Summary

The Translational Research team is hiring a Senior Research Associate to lead the cellular and molecular characterization of delivery and editing platforms supporting our preclinical programs. This is a hands-on bench role with significant ownership of experimental design, execution, and data interpretation. The location for this position is onsite, 5 days per week, in our Boston lab.

Responsibilities
  • Design, develop, and qualify molecular assays to measure CRISPR editing outcomes in vitro and in vivo, including amplicon NGS for indel quantification, TIDE/ICE, ddPCR, and orthogonal confirmation methods.
  • Lead cell-based pharmacology assays evaluating delivery efficiency, editing efficiency, and on-target activity of LNP- and antibody-based delivery platforms.
  • Plan and execute in vivo studies in mice evaluating biodistribution, editing efficiency, and pharmacodynamic activity; analyze tissues for nucleic acid and protein endpoints.
  • Extract and purify RNA, DNA, and protein from cultured cells and animal tissues; run downstream analytical workflows (qPCR, RT-qPCR, Sanger and NGS sequencing, ddPCR, Western blot or Jess, ELISA, flow cytometry).
  • Maintain primary and immortalized mammalian cell lines using aseptic technique; perform transfection and electroporation of CRISPR reagents.
  • Analyze experimental data, interpret results in the context of program goals, and present findings in team meetings and written reports.
  • Contribute to study design, protocol development, and SOPs. Mentor junior research associates and support cross-functional collaboration with Delivery, Editing, and Translational teams.
  • Maintain rigorous electronic and paper lab records consistent with reproducibility and data integrity standards.
Qualifications
  • BS with 6+ years or MS with 4+ years of hands-on research experience in molecular and cell biology in industry or academia.
  • Direct experience with CRISPR gene editing, including assay readouts for editing efficiency (amplicon NGS, TIDE/ICE, or equivalent).
  • Demonstrated expertise in mammalian cell culture and design, execution, and troubleshooting of cell-based assays.
  • Strong working knowledge of core molecular and analytical methods: PCR, RT-qPCR, Sanger and NGS sequencing, SDS-PAGE / Western blot (or Jess capillary electrophoresis), ELISA, and flow cytometry.
  • Mammalian cell culture, cell transfection, and sterile techniques.
  • Experience designing and executing in vivo rodent studies, including tissue collection and downstream analysis.
  • Ability to independently scope, plan, and execute experiments with minimal supervision; track record of contributing to project decisions based on data.
  • Clear written and verbal communication; comfortable presenting data to a scientific audience.
  • Authorization to work in the United States without current or future sponsorship required.
Preferred Qualifications
  • Hands-on experience with hematopoietic stem cells (HSCs / HSPCs), including isolation, ex vivo expansion, and multilineage differentiation assays (CFU, erythroid, myeloid).
  • Experience with LNP-based delivery of nucleic acids, including formulation handling, dose preparation, and in vivo administration.
  • Experience with antibody-based or receptor-targeted delivery strategies.
  • Familiarity with bioinformatics tools for amplicon sequencing analysis (e.g., CRISPResso, CRISPRessoBatch).
  • Prior experience supporting IND-enabling or GLP studies.
Benefits
  • Competitive salary, equity, and comprehensive benefits package.
  • Opportunities for professional growth and leadership development.
  • Fast-paced, collaborative, and innovative work environment.
  • We offer an exceptional benefits package to include Medical, Dental, Vision, Life, Disability, a 401k Match of 4%, Paid Time Off and Equity.
Position Requirements
10+ Years work experience
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