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KCAS Bio

GLP/GCP bioanalytical & biomarker CRO services

Senior Scientist - LC-MS/MS Bioanalysis, Sample Analysis

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeKansas City, MO, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's, master's, or PhD in Chemistry, Biochemistry, or a related field, with at least 5 years of experience in a bioanalytical laboratory environment.
  • Extensive hands-on experience working in a GLP-regulated laboratory environment is required.
  • Strong experience with bioanalytical sample preparation and quantitative LC-MS/MS workflows.
  • Experience executing regulated studies, including data review, reporting, and audit support.
  • Demonstrated ability to troubleshoot technical and operational issues in a production environment.
  • Experience interacting with Quality Assurance and supporting audits and inspections.

Responsibilities

  • Execute and oversee all phases of assigned studies, including sample preparation, LC-MS/MS analysis, data review, and report generation in a regulated environment.
  • Act as lead scientist on studies by providing work direction, technical guidance, and training to junior scientific staff.
  • Manage all client communication related to study conduct and data delivery.
  • Interact with Quality Assurance to resolve audit findings, deviations, and compliance-related issues.
  • Have final authority for sample identification, including resolving discrepancies with clinical sites or clients.
  • Be accountable for study timelines and deliverables, and communicate status to management and clients.
  • Ensure all study activities comply with study protocols, standard operating procedures, and GLP regulatory requirements.
  • Review data and ensure its accuracy, completeness, and integrity before reporting.
  • Support audit readiness and participate in client and regulatory inspections as needed.
  • Serve as a technical resource for troubleshooting assay performance and operational challenges within a production environment.

Desired Qualifications

  • Prior experience acting as a study lead or in a Principal Investigator-type role.

About the Company

KCAS Bio

GLP/GCP bioanalytical & biomarker CRO services

KCAS Bio is a full-service bioanalytical and biomarker contract research organization (CRO) that supports pharmaceutical, biotechnology, and academic clients by delivering GLP- and GCP-compliant development services for drugs, biologics, and cell/gene therapies. The company operates on a contract-based model, providing flexible, expert teams and scalable capacity to meet each project’s needs. Its workflow involves conducting bioanalytical assays and biomarker work within regulated frameworks, acting as an extension of clients’ laboratories to enable rapid, scientifically rigorous research. KCAS Bio differentiates itself through a collaborative culture, continuous learning, and a commitment to speed and adaptability, focusing on delivering high-quality results efficiently. The company’s goal is to help clients advance time-critical research and bring new therapies through development and regulatory stages quickly and confidently.

Company size
201-500
Company stage
Seed
Total funding
$250K
Headquarters
Olathe, KS
Founded
1979

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