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Sample Processing Clerk

Clinical Reference Laboratory
United Statesfull_timeVerifiedPosted 20 Dec 2024

About the role

GENERAL STATEMENT OF RESPONSIBILITY:  Receive, open, code, and prepare toxicology specimens for laboratory analysis.

ESSENTIAL FUNCTONS: 

  • Bring in and scan all incoming bags and boxes of specimens from dock area.        
  • Separate and sort specimens by category.
  • Open individual specimen containers, discard cardboard and remove specimens.
  • Match information from consent form and specimen, then barcode specimen.
  • Complete consent signature and stamp consents.
  • Scan barcodes and consent (paper, bottle, tube) into computer system. 
  • Must meet minimum accessioning requirement as outlined in incentive program.
  • Enter consents in computer system as necessary. 
  • Aliquot urine specimens.
  • Scan in narcotics.
  • Check and verify counts in computer after each page; correct miscounts.
  • Print aliquot and chain of custody sheets to appropriate areas.
  • Clean up work area, dispose of trash.
  • Assist courier coordinator with weighing specimen shipments.
  • Dump negative urine specimens.
  • Barcode blood specimens for laboratory testing.
  • Re-aliquot urine specimens for screening and confirmation testing.
  • Accession confirmation only specimens.
  • Process insurance and clinical trials specimens.
  • Process sweat patch and oral fluid samples.
  • Enter “blind” specimens into computer.
  • Aliquot specimens for reflexed confirmation testing.
  • Maintain and protect the confidentiality of all CRL, CRL subsidiaries, legal entities and client information.
  • Be able to comply with all applicable federal, state, and local safety and health regulations that would apply to this job.

Other duties as assigned.

JOB QUALIFICATIONS:

EDUCATION:  No formal education requirements.<

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Company

Clinical Reference Laboratory

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