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Verified Pay check_circle $120000 - $165000 per year
Hours Full-time
Location Pleasanton, California

About this job

Job Description

Job Description

Position Summary: 

Crystal Bio Solutions is a CRO providing global-standard services in GLP/GCLP bioanalysis and biomarker. Our clients include multinational pharmaceutical companies and biotech companies.

The Bioanalysis & Biomarkers Department specializes in Method Development, Method Validation, GLP/GCLP Bioanalysis for PK, and biomarkers. The team has successfully supported non-GLP, GLP (non-clinical) and GCLP (clinical) projects. The role is responsible for providing bioanalytical support for both pre-clinical and clinical projects and partnering with our clients for project success.

Key Responsibilities: 

  • Independently propose assay design and/or strategy, develop, validate, conduct, and troubleshoot LCMS-based bioanalytical methods for the quantification of small molecule (and its metabolites) and biologics (e.g. ADC, mAB, protein, peptide, oligonucleotide etc) in support of PK, and Biomarker measurement
  • Serve as Subject Matter Expert (SME) for LCMS platform. 
  • Present and interpret data internally and/or externally as needed.
  • Provide oversight of the laboratory, mentor junior staff, and collaborate to keep improving operational excellence.
  • Understand and adhere to corporate standards regarding code of conduct, Environment Health & Safety (EHS), and GLP/GCP/GDP compliance.
  • Perform other related duties as assigned.

Qualifications & Educational Requirements: 

  • Ph.D., M.Sc., M.A., B.A., in Analytical Chemistry, Biochemistryor other related scientific fields required, including a minimum of 0+(Ph.D.), 9+(Master’s) or 12+(Bachelor’s) years of CRO/Pharma/Biotech experience.
  • Hands-on experience, strong expertise in LCMS method development and troubleshooting for small molecules and biologics (e.g. ADC, mAB, protein, peptide, oligonucleotide etc) are required.
  • Established record of independent achievement of objectives and timelines while maintaining high work quality.
  • Effective in team environments co-workers, managers, and clients.
  • Must be goal-oriented, quality-conscientious, compliance-ensured, and client-focused.
  • Effective writing and communication skills, preferred.
  • Experience in GLP/GCLP LCMS method development and validation for PK and/or biomarker analysis is preferred .
  • Functional experience utilizing LIMS and QMS systems for GLP/GCLP bioanalysis is preferred
  • Familiarity with additional bioanalytical platforms (e.g. LBA, PCR, Flow Cytometry) is a plus.
  • Supervisory experience in both project and talent (people) management is a plus.


  • The salary range represents the anticipated base pay for this position. Actual compensation may vary based on factors including, but not limited to, skills, qualifications, experience, education, and location.
  • As part of our recruitment process, we may use technology-assisted tools to support application review and improve efficiency. All hiring decisions are made by our team.

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Posting ID: 1307642296 Posted: 2026-11-07 Job Title: Senior Scientist Associate
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Senior Scientist Associate