Sample Management Specialist

2 weeks ago


New Haven, Connecticut, United States Randstad Life Sciences Full time
Job Overview

We are seeking a dedicated Sample Management Specialist to join our team at Randstad Life Sciences. This role is crucial in ensuring the integrity and compliance of specimens throughout the drug trial process.

Key Responsibilities
  • Process, store, and ship samples acquired during drug trials while maintaining specimen integrity.
  • Review queried reports to ensure quality control in sample processing and report any significant protocol deviations to the Operations Director.
  • Support the verification of specimen compliance and manage daily requirements for study sample processing.
  • Maintain an accurate inventory of items necessary for the processing and storage of clinical trial samples.
  • Oversee the requisition and transport of outsourced safety samples.
  • Perform duties as the Laboratory Study Co-lead.
  • Prepare the daily schedule by printing and distributing the Dashboard schedule and summarizing activities on the whiteboard.
  • Conduct regular reviews of sample processing logs for compliance and document any discrepancies electronically.
  • Ensure that the laboratory is adequately staffed with trained personnel to support sample processing tasks.
  • Record and enter send-out results as required.
  • Exemplify a strong work ethic by maintaining a busy environment and ensuring that new staff are supported.
Qualifications

Education: High School Diploma required; Associate's degree preferred.

Skills Required
  • Proven experience in Sample and Specimen Processing, including logging and accuracy review.
  • Knowledge of Quality Control and Compliance standards.
  • Experience in Inventory Maintenance.
Preferred Skills
  • Familiarity with Cerner Lab systems.
Company Overview

Randstad Life Sciences is a reputable organization known for its innovative contributions to the industry. We are committed to making a significant impact through our work.



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