Clinical Trials Coordinator

7 days ago


Springfield, Missouri, United States QPS, LLC Full time
Job Summary

We are seeking a highly organized and detail-oriented Clinical Sample Specialist to join our team at QPS, LLC. The successful candidate will be responsible for ensuring the smooth operation of clinical study samples throughout their lifecycle.

Key Responsibilities
  • Read and understand study protocols and laboratory manuals to ensure accurate specimen handling and shipping.
  • Order and manage clinical study supplies, including tubes, kits, and other materials.
  • Prepare, label, and ship specimens, including kit preparation and quality control.
  • Collaborate with internal and external stakeholders to ensure timely and accurate shipment of samples.
  • Develop and maintain shipping manifests to meet sponsor requirements.
  • Ensure all procedures and techniques follow internal standard operating procedures and study protocols.
Requirements

To be successful in this role, you will need:

  • A High School Diploma or equivalent.
  • At least 1 year of experience in a fast-paced, detail-oriented environment.
  • Excellent communication and organizational skills.
About QPS, LLC

QPS, LLC is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive work environment that values and respects all employees. If you are a motivated and detail-oriented individual who is passionate about clinical trials, we encourage you to apply for this exciting opportunity.



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