Lead Biomarker Method Development Scientist

The Steely Group

Kansas City (MO)

On-site

USD 120,000 - 170,000

Full time

5 days ago
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Job summary

The Steely Group is seeking a Sr Scientist in biomarker method development to lead design, optimization, and troubleshooting of ligand binding assays for biomarkers across PK and immunogenicity studies.

You will work in state-of-the-art sterile labs, mentor junior staff, and collaborate with internal and client teams to translate scientific objectives into robust, regulated bioanalytical workflows.

Qualifications

  • PhD/Masters/Bachelors in biology-related field with 5+ years in a bioanalytical lab.
  • Deep biomarker method development experience including assay development and troubleshooting.
  • Hands-on with LBA platforms (ELISA, MSD, immunoassays).
  • Ability to design experiments, evaluate performance, and optimize assay conditions.

Responsibilities

  • Lead design, development, optimization, and troubleshooting of ligand binding assays for biomarkers.
  • Design experiments and independently evaluate assay performance to ensure robust methods.
  • Develop assay conditions, reagents, controls, and workflows to address challenges.
  • Apply scientific judgment to evaluate precision, accuracy, sensitivity, selectivity, and robustness.
  • Troubleshoot issues, identify root causes, and implement solutions.
  • Support method qualification, validation, and transfer activities as appropriate.
  • Collaborate with PK/immunogenicity teams on related biomarker work.
  • Mentor junior scientists and provide technical training and guidance.

Skills

Biomarker method dev
Ligand binding assays
ELISA
MSD
Bioanalytical lab

Education

Bachelor’s/Master’s/PhD in Biology/Biochemistry/Immunology

Job description

The Steely Group is seeking a Sr Scientist in biomarker method development to lead design, optimization, and troubleshooting of ligand binding assays for biomarkers across PK and immunogenicity studies.

You will work in state-of-the-art sterile labs, mentor junior staff, and collaborate with internal and client teams to translate scientific objectives into robust, regulated bioanalytical workflows.

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