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CL
Sample Processing Clerk
Clinical Reference LaboratoryUnited 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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