Postdoc: Synuclein Biology & Neurodegeneration

BioSpace

Boston (MA)

On-site

USD 58,000 - 123,000

Full time

8 days ago

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Job summary

Lilly’s Neurodegeneration Biology group in Boston seeks a Postdoctoral Scientist to investigate α-synuclein dysfunction and aggregation, using iPSC-derived neuronal models and engineered cell lines to build a mechanistic basis for new therapies in synucleinopathy.

This fixed-term role focuses on quantitative aggregation biochemistry, cell biology, and translational neuroscience within a collaborative drug discovery environment.

Qualifications

  • PhD in cell biology, biochemistry, molecular biology, neuroscience, protein biophysics, or a related field.
  • Hands-on expertise in protein aggregation biochemistry, including ThT-based kinetic assays.
  • Experience generating and engineering mammalian cell lines, including CRISPR editing, lentiviral transduction, or stable line development.
  • Qualified applicants must be authorized to work in the United States on a full-time basis.

Responsibilities

  • Define molecular and cellular mechanisms that drive α-synuclein aggregation and dysfunction.
  • Develop cellular models including engineered cell lines and iPSC-derived neurons.
  • Establish aggregation paradigms and quantify kinetics and misfolding outcomes.
  • Apply Thioflavin T (ThT) assays and biophysical readouts to assess aggregation.
  • Validate findings in neuronal disease models and collaborate with Lilly Boston and external partners.
  • Present results at meetings and contribute to publications; maintain electronic lab notebooks.

Skills

Protein aggregation biochemistry
Cell engineering
Mammalian cell lines
Biochemical/biophysical character
Scientific communication

Education

PhD in life sciences

Tools

Confocal microscopy
iPSC-derived neurons

Job description

Lilly’s Neurodegeneration Biology group in Boston seeks a Postdoctoral Scientist to investigate α-synuclein dysfunction and aggregation, using iPSC-derived neuronal models and engineered cell lines to build a mechanistic basis for new therapies in synucleinopathy.

This fixed-term role focuses on quantitative aggregation biochemistry, cell biology, and translational neuroscience within a collaborative drug discovery environment.

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