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Postdoctoral Scientist - Neurodegeneration

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: BioSpace
Full Time position
Listed on 2026-07-26
Job specializations:
  • Research/Development
  • IT/Tech
Salary/Wage Range or Industry Benchmark: 58000 - 123200 USD Yearly USD 58000.00 123200.00 YEAR
Job Description & How to Apply Below

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve.

This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Job Title

Postdoctoral Scientist — Neurodegeneration

Organization Overview

Lilly Neuroscience NGTx is a pre-clinical development team based at the Seaport Innovation Center in Boston alongside Lilly's Boston Neurodegeneration group. The team develops and applies human iPSC-derived in vitro platforms to evaluate compound safety, potency, and efficacy across CNS therapeutic modalities. These platforms are a critical node in Lilly's neuroscience pre-clinical pipeline, supporting high-priority programs targeting amyloid forming proteins across Alzheimer's disease, Parkinson's disease, and other neurodegenerative conditions.

This postdoctoral position will extend the established tri-culture system into disease-relevant pathological contexts, creating a pharmacologically responsive platform for compound assessment in neurodegeneration.

Responsibilities
  • Establish seed and preformed fibril (PFF)-based pathology models in the iPSC tri-culture system for multiple amyloid forming proteins, characterizing seeding efficiency, aggregate formation, and timing parameters for each.
  • Perform systematic mono- vs. co- vs. tri-culture comparisons to quantify the multicellular gain in neurotoxicity and neuroinflammatory responses across culture configurations.
  • Characterize microglial activation and cytokine release profiles (multiplex MSD cytokine profiling) and neurotoxicity in response to pathological insults.
  • Execute a systematic species-ranking study comparing aggregate forms of amyloid forming proteins (monomers, oligomers, and fibrillar preparations) for neurotoxic and neuroinflammatory potency in the human multicellular context.
  • Evaluate publishable tool compounds (siRNAs, antibodies) and internal proprietary compounds for potency, cellular uptake, and safety in healthy vs. pathological tri-culture.
  • Generate paired healthy vs. disease-context datasets to directly compare compound behavior, providing decision-support data for LRL neurodegeneration programs.
  • Publish as first author and present findings at internal and external forums.
Basic Requirements
  • PhD in Neuroscience, Cell Biology, Molecular Biology, or a closely related field.
  • Demonstrated hands-on experience with iPSC culture and/or primary neuron culture systems.
  • Prior experience with in vitro neurodegenerative disease modeling, including PFF seeding, protein aggregation assays, or amyloid forming protein biology.
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
Additional Skills/Preferences
  • Experience with neuronal co- or tri-culture systems incorporating glia (astrocytes and/or microglia).
  • Proficiency in high-content imaging, immunofluorescence (ICC-IF), and image analysis pipelines.
  • Prior work with neuroinflammation assays, including multiplex cytokine profiling (e.g., MSD, Luminex).
  • Experience with CNS therapeutic modality assessment (siRNAs, antibodies, or small molecules in cell-based assays).
  • Proven ability to independently design, execute, and troubleshoot multi-parametric cell-based experiments.
  • Demonstrated scientific productivity, including peer-reviewed publications.
  • Strong collaborative instincts and interest in translational drug discovery in an industry setting.

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