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Scientist​/Sr. Scientist —Cell, Molecular & Chemical Biology; Taosheng Chen Lab

Job in Memphis, Shelby County, Tennessee, 37544, USA
Listing for: St. Jude Children's Research Hospital, Inc.
Full Time position
Listed on 2026-09-20
Job specializations:
  • Research/Development
    Research Scientist, Drug Discovery, Biomedical Science
Salary/Wage Range or Industry Benchmark: 104000 - 186160 USD Yearly USD 104000.00 186160.00 YEAR
Job Description & How to Apply Below

e Children's Research Hospital, we know what can be achieved when the brightest scientific minds face the fewest barriers. That’s why we provide world-class facilities. State-of-the-art technologies. Extraordinary support. And a collaborative, bench-to-bedside environment where you can see, firsthand, how your science translates into survival for the children we serve. Quite simply, e, we encourage you to dream big and stop at nothing when it comes to finding cures and saving children.

The Taosheng Chen Lab within our Department of Chemical Biology and Therapeutics is seeking a collaborative and innovative Scientist or Senior Scientist with expertise in cell biology, molecular biology, and/or chemical biology to lead research efforts to develop and characterize the mechanisms of action of novel chemical probes - including agonists, antagonists, and degraders - targeting the nuclear receptors PXR and CAR.

The successful candidate will independently design and execute studies, generate high-quality datasets to test scientific hypotheses, and integrate findings across multiple disciplines. The candidate will work closely with in-house structural biologists and medicinal chemists to generate complementary data and advance projects, and will take a leading role in organizing and writing multidisciplinary manuscripts. The Chen Laboratory leverages multidisciplinary approaches to investigate the chemical regulation of nuclear receptors, with the overarching goal of elucidating nuclear receptor-driven transcriptional networks and developing innovative therapeutic strategies to combat drug resistance and tumorigenesis.

Using integrated cellular, molecular, and chemical biology approaches, our research is closely aligned with structural biology and medicinal chemistry, enabling the successful execution of high-impact, collaborative studies. This synergistic framework has led to publications in leading journals, including Nature Communications (2017, 2024, 2025) and PNAS (2023), highlighting our contributions to advancing the understanding and therapeutic targeting of nuclear receptor signaling.

The successful candidate will have a strong track record of high-quality research and publication in peer-reviewed journals.

Relevant Experience
  • DNA: cloning, plasmid construction, and related molecular biology techniques
  • RNA: RNA isolation, gene expression analysis, and transcriptional profiling
  • Proteins:
    Western blotting, protein-compound interactions, protein-protein interactions, and/or proteomic profiling
  • Small molecules: experience evaluating the cellular activity, mechanism of action, and/or pharmacology of small-molecule compounds
  • Structural biology: a basic understanding of protein crystal structures and ligand-protein interactions is essential for effective collaboration with structural biologists
  • Medicinal chemistry: a basic understanding of small-molecule structures and structure-activity relationships is important for meaningful collaboration with medicinal chemists
  • Murine studies experience is a plus
Candidate Profile Priorities
  • Strong cell and molecular biology expertise with exposure to chemical biology
  • Experience evaluating small-molecule mechanisms of action
  • An understanding of structural biology and medicinal chemistry concepts
  • A demonstrated record of impactful publications, particularly in high-quality journals
Research Focus & Key Projects
  • Developing and characterizing novel chemical probes, including agonists, antagonists, and degraders, targeting nuclear receptors
  • Investigating the mechanisms of action of small molecules and protein degraders, including PROTAC-based approaches
  • Defining how chemical modulation of PXR and CAR influences transcriptional networks, drug metabolism, chemotherapy…
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