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Research Assistant

External
Labcorp logoLabcorp · Madison, WI
Full-timeOn-site1d ago
AccessibilityComplianceDocumentationGCPLessMove
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Requirements

  • Bachelor's degree in Life Sciences, Chemistry, Biotechnology, or a related field.
  • 6 months or more hands-on experience with LC-MS/MS bioanalysis, including MRM-based quantitation and method execution.
  • 1 or more years of experience with ADME/PK assays such as liver microsomal stability, permeability assays (e.g., MDCK-MDR1), and PK sample processing (plasma, tissue lysates).
  • 1 or more years of exposure to CYP inhibition or Time-Dependent Inhibition (TDI) assays and drug-drug interaction (DDI) studies.
  • 1 or more years of experience assisting in the development or optimization of new bioanalytical methods.
  • Master's degree or other post graduate studies in a relevant life sciences discipline.
  • Additional Job Standards:
  • Proficiency with data acquisition and processing software (Mass Lynx, Mass Hunter, Analyst, or equivalent).
  • Proficiency with ELN documentation, word processing, spreadsheet, and specialized analytical software.
  • Strong attention to detail with demonstrated ability to generate reproducible, high-quality bioanalytical data.
  • Familiarity with Orbitrap platforms or other high-resolution mass spectrometry systems.
  • Knowledge of regulatory guidelines including FDA, EMA, and ICH bioanalytical method validation guidance.
  • Experience working in a GLP/GCP-regulated environment (CRO or pharmaceutical/biotech industry).
  • Excellent written and verbal communication skills.
  • Proven ability to prioritize workloads and manage time effectively in a fast-paced laboratory environment.
  • Labcorp is proud to be an Equal Opportunity Employer:
  • We encourage all to apply

Additional Information

Labcorp is seeking an Research Assistant to join our Metabolism team in Madison, WI. Work Schedule: Monday - Friday 8:00 am - 5:00 pm Job Responsibilities Organize and independently perform routine to moderate-level method validation activities in compliance with SOPs and regulatory guidelines (GLP/GCP). Execute advanced method validation tasks with guidance from a Lead Scientist. Apply intermediate data interpretation and analytical instrumentation skills to resolve procedural and scientific problems with minimal assistance. Assist in the review of reports, methods, protocols, and SOPs; maintain complete and audit-ready study documentation. Communicate problems, deviations, and corrective actions to Lead Scientist and/or management in a timely manner. Manage assigned project work, coordinating activities with team members to deliver high-quality data to internal clients on schedule. Collaborate effectively with colleagues across the Bioanalytical site and support cross-functional communications with external clients. Train and mentor less experienced laboratory staff. Contribute to process improvement initiatives and participate in department-wide quality initiatives. Maintain a clean, safe, and organized laboratory environment.


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