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Celerion

Global CRO for early-phase development

Laboratory Operations Assistant

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Part-timeLincoln, NE, USA$17 /hr

About the Job

Requirements

  • A high school diploma or GED is required.
  • Strong ability to work independently with minimal supervision is required.
  • Exceptional attention to detail and organizational skills are required.
  • Strong oral and written communication skills are required.
  • The incumbent must be a non-nicotine/tobacco user because nicotine contamination could compromise study integrity.

Responsibilities

  • Prepare, store, inventory, and dispose of laboratory solutions in compliance with EHS standards and applicable standard operating procedures (SOPs).
  • Clean glassware used in solution preparation and maintain general laboratory organization, stocking, and inventory.
  • Adhere to all written instructions, SOPs, and working instructions related to job responsibilities.
  • Receive, check in, and accurately log biological samples upon arrival.
  • Organize and dispose of analytical samples per SOPs and working instructions.
  • Store samples for long-term preservation and rack samples for production.
  • Ensure proper sample organization and freezer placement; maintain transfer and freezer logs.
  • Count and reconcile samples at the conclusion of each study.
  • Conduct real-time review of production documentation.
  • Complete quality-control reviews of production databases and issue audit findings as appropriate.
  • Perform quality control on bioanalytical documents, including BSPs and EDT files.

Desired Qualifications

  • An Associate's degree in a related field is preferred.
  • Post-secondary coursework in science-related disciplines is a plus.
  • Basic knowledge of chemistry is preferred.

About the Company

Celerion

Global CRO for early-phase development

Celerion is a global contract research organization focused on early-phase drug development. It conducts contracted research across clinical trial design, feasibility studies, project management, clinical and medical monitoring, bioanalytical sciences, and regulatory affairs, using High Resolution Mass Spectrometry-based metabolite profiling to inform decisions. Its advantage comes from over 40 years of experience, specialized metabolite profiling, and a global, integrated service model that accelerates development timelines. The goal is to help pharmaceutical and biotech clients bring safe and effective treatments to patients faster through rigorous, high-quality research.

Company size
1,001-5,000
Company stage
Acquired
Total funding
Not listed
Headquarters
Lincoln, NE
Founded
2010

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