Hematology Lab Associate – Clinical Trials

IQVIA

California

On-site

USD 36,000 - 75,000

Full time

14 days+

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Job summary

IQVIA Laboratories in Valencia, CA is hiring a Lab Associate to perform routine hematology testing for clinical trials. You will handle specimen testing, data review, documentation, and support regulatory compliance while contributing to continuous improvement.

Requirements include a High School Diploma or Bachelor's degree with at least 6 months of lab experience, knowledge of GLP and SOPs, and the ability to follow procedures, document results, and collaborate with cross-functional teams.

Qualifications

  • High School Diploma or Bachelor's Degree with 6 months lab experience
  • Knowledge of GLP, SOPs, and regulatory standards
  • Ability to document results and follow procedures with attention to detail

Responsibilities

  • Perform routine analysis of specimens and document results per SOPs and guidelines
  • Evaluate results against lab system algorithms and identify discrepancies
  • Escalate unusual findings to senior personnel
  • Prepare buffers, solutions, and materials for testing
  • Store samples and reagents properly after testing
  • Assist with procedure development and continuous improvement
  • Support housekeeping, safety, and 6S initiatives
  • Communicate with cross-functional stakeholders and notify staff of supply shortages

Skills

GLP knowledge
SOP compliance
Laboratory equipment knowledge
Communication skills
Attention to detail

Education

High School Diploma
Bachelor's Degree in Chemistry/ Biology/ Medical Laboratory Technology

Tools

Laboratory instrumentation
Computer skills

Job description

IQVIA Laboratories in Valencia, CA is hiring a Lab Associate to perform routine hematology testing for clinical trials. You will handle specimen testing, data review, documentation, and support regulatory compliance while contributing to continuous improvement.

Requirements include a High School Diploma or Bachelor's degree with at least 6 months of lab experience, knowledge of GLP and SOPs, and the ability to follow procedures, document results, and collaborate with cross-functional teams.

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