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Common questions about this position
A Ph.D. in cell biology, molecular biology, biochemistry or a related field, or equivalent industry experience with 5+ years is required. Key experiences include primary endothelial cell isolation and functional characterization, working with mouse models of endothelial cell function, and transgenic manipulation of endothelial cells ex vivo or in vivo.
Responsibilities include developing functional assays and pre-clinical models for endothelial cell function, collaborating with Functional Genomics and Predictive Modeling teams, measuring impacts of mRNA reprogramming medicines, engineering in vivo nucleic acid delivery methods, and analyzing data for pre-clinical decisions.
Preferred experiences include contributing to drug development programs at pre-clinical or clinical stages, leading pre-clinical studies in mouse models, single cell genomics methods, and pooled screening approaches like CRISPR fitness screens or Perturb/CROP-seq.
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Medicines for healthspan extension via epigenetics
NewLimit develops medicines aimed at extending human healthspan by reprogramming aging cells' epigenomes. This involves changing the chemical modifications on DNA and histone proteins to restore youthful functions in old cells, focusing initially on rejuvenating the immune system and liver. The company uses advanced technologies like single-cell genomics and machine learning to identify aging markers and create interventions that reverse these changes. Unlike competitors, NewLimit's approach is centered on epigenetic reprogramming, targeting age-related diseases with the goal of creating a new class of medicines that enhance health during aging. The company serves the healthcare market, working with pharmaceutical companies and healthcare providers, and aims to transform aging by developing effective treatments.