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Scientist, Cell and Gene Therapy; AI Research

Job in Chicago, Cook County, Illinois, 60601, USA
Listing for: RecruitSeq
Full Time position Listed on 2026-11-12
Job specializations:
Salary/Wage Range or Industry Benchmark: 140000 - 180000 USD Yearly USD 140000.00 180000.00 YEAR

Job Description & How to Apply Below

Position: Scientist, Cell and Gene Therapy (AI Research)

Scientist, Cell and Gene Therapy (AI Research)

San Francisco or remote

* Full-time (W2 position with benefits + equity)

* $140k-180k on-target earnings (base + performance bonus)

Our client is a team that researches and grades how AI performs when scientists ask it to recommend the next step in a drug program. The team is looking for a Scientist who has worked on a cell therapy, gene therapy, or genetic medicine drug program and can explain how the experimental results shaped what happened next.

What You Would Do:

  • Create case studies drawn from cell therapy, gene therapy, or other genetic medicine programs. Examples might include choosing a cell source, comparing vector designs, or selecting an RNA therapeutic for further testing.
  • Use experimental results to frame decisions scientists face in development, such as whether a potency advantage outweighs a safety concern or which experiment would resolve conflicting findings.
  • Work with scientists and engineers to evaluate how AI agents approach those decisions. Identify evidence an agent overlooked, assumptions it made, and whether its proposed next step would answer the scientific question.
  • Write concise assessments explaining which recommendations the data support, where uncertainty remains, and what evidence would change your judgment.

Your Background:

  • You have an MS, PhD, or comparable professional experience, working directly on a therapeutic program involving cell therapies, viral vectors, genome editors, or RNA drugs such as ASOs, siRNAs, or mRNA.
  • You’ve personally designed constructs, screened drug candidates, improved delivery, or planned studies for an IND. You can walk through a result that changed which candidate, dose, or experiment your team chose.
  • You can interpret the evidence that matters for your modality, whether that’s editing specificity, tissue exposure, immune response, or a safety finding. Experience contributing to a nonclinical regulatory package is valuable.
  • You are familiar with using AI agents for your research, and can explain in writing where a recommendation holds up, where the reasoning breaks down, and what evidence would change your view.
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