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Senior Scientist, Bioanalysis & Biomarkers

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Judo Bio
Full Time position
Listed on 2026-08-28
Job specializations:
  • Research/Development
    Research Scientist, Biotech Research, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 140000 - 200000 USD Yearly USD 140000.00 200000.00 YEAR
Job Description & How to Apply Below

Senior Scientist, Bioanalysis & Biomarkers

Nonclinical Development | Cambridge, MA | Full-Time | Title Commensurate with Experience

About Judo

Judo Bio is pioneering oligonucleotide medicines delivered to the kidney, opening the way for new RNA medicines for systemic and renal diseases. With our STRIKE (Selectively Targeting RNA Into Kidn Ey) platform, we use a proprietary approach that harnesses a natural, endogenous mechanism to target oligonucleotide medicines to the kidney.

Our initial drug programs are ligand-siRNA conjugate drugs designed for receptor-mediated uptake by specific kidney cell types, resulting in gene silencing of disease-modifying target genes for systemic diseases.

Enabled by a network of high caliber experts and internal talent, we are thoughtfully building a team of passionate, innovative, and energetic scientific champions to discover and develop therapeutics that have the potential to change the lives of patients and families.

Role Summary

Judo Bio is seeking a Senior Scientist to lead bioanalytical assay development and biomarker strategy in support of our siRNA discovery and nonclinical development programs. This role is equal parts bench scientist and program-level strategist: you will personally develop and run LC-MS/MS and chromatographic methods for oligonucleotide and small-molecule quantitation, while also managing external CRO relationships that generate GLP-adjacent and GLP bioanalytical data supporting IND-enabling studies.

You will partner closely with DMPK, Pharmacology, Toxicology, and Regulatory to ensure bioanalytical and biomarker data packages are scientifically rigorous and regulatory-ready for first-in-human (FIH) filings.

Title commensurate with experience.

Key Responsibilities
  • Design, develop, optimize, and qualify LC-MS/MS and chromatographic (HPLC/UPLC/FPLC/IEC) assays for quantitation of siRNA oligonucleotides, metabolites/fragments, and small-molecule conjugation partners or linker components in plasma, tissue, and other biological matrices.
  • Lead hands-on bench work including method development, sample preparation, extraction, and instrument operation/troubleshooting on mass spectrometry and chromatography platforms.
  • Develop and implement targeted proteomics or other biomarker assays to support pharmacodynamic (PD) readouts and strengthen PK/PD and exposure-response relationships across nonclinical programs.
  • Serve as primary technical point of contact and day-to-day manager for bioanalytical CROs, including method transfer, protocol review, data review/QC, timeline management, and troubleshooting to ensure high-quality, regulatory-ready data packages.
  • Author and contribute to bioanalytical and biomarker sections of nonclinical regulatory documents (e.g., IND Module 2.4/2.6, study reports, briefing documents) in collaboration with Regulatory Affairs and nonclinical leadership.
  • Partner with DMPK, Toxicology, and Pharmacology teams to design bioanalytical and biomarker strategies for GLP toxicology studies and FIH-enabling packages, including matrix selection, assay validation strategy, and sample logistics planning.
  • Independently analyze, interpret, and present complex analytical data to inform program-level nonclinical decision-making, candidate selection, and study design.
  • Maintain instrumentation (mass spectrometers, HPLC/UPLC systems, fraction collectors) to ensure operational reliability and data integrity; establish and enforce performance-qualification standards internally and at CRO sites.
  • Contribute to the build-out of internal bioanalytical capabilities and SOPs as Judo scales its nonclinical development organization.
Required Qualifications
  • Ph.D. in analytical/bioanalytical chemistry, biochemistry, pharmaceutical sciences, or a related discipline (or M.S. with equivalent hands‑on industry experience).
  • 5+ years of hands‑on bioanalytical experience developing and qualifying LC‑MS/MS assays, with demonstrated expertise across both oligonucleotide (e.g., siRNA, ASO, or other modified nucleic acid) and small‑molecule matrices.
  • Deep hands‑on proficiency with nanoLC‑MS/MS, HRMS, and chromatographic separations (RP‑HPLC, UPLC, FPLC, IEC) including method…
Position Requirements
10+ Years work experience
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