Phlebotomist

Elite Clinical Network

Tustin, CAFull-timePosted Mar 28, 2026

40K–60K a year

Behavioral Health Market Context

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Benefits

Paid Time Off

Job Description

th study protocols and regulatory standards.
Key Responsibilities
• Perform venipuncture and collect blood and other biological specimens from research participants according to study protocols
• Properly label, process, and store specimens for laboratory analysis or shipment to central labs
• Maintain accurate and timely documentation of sample collection, handling, and processing activities
• Assist clinical staff in preparing for participant visits and supporting visit procedures
• Monitor and manage lab supply inventory and ensure equipment is clean and properly maintained
• Adhere to all research protocols, HIPAA guidelines, and GCP (Good Clinical Practice) standards
• Collaborate with research coordinators and investigators to ensure smooth study operations
Qualifications
• Certified Phlebotomist (California)
• Previous experience in a clinical or research setting (clinical research experience preferred)
• Familiarity with clinical trial protocols and sample handling procedures
• Strong organizational and documentation skills
• Ability to work with diverse populations in a professional and compassionate manner
• CPR certification (preferred)
• Willingness to be cross‑trained for potential Clinical Research Coordinator responsibilities (a plus)
Job Type

Full‑time
Work Location

In person
Benefits
• Paid time off

Qualifications

  • Certified Phlebotomist (California)
  • Familiarity with clinical trial protocols and sample handling procedures
  • Strong organizational and documentation skills
  • Ability to work with diverse populations in a professional and compassionate manner

Benefits

  • Paid time off

Responsibilities

  • We are seeking a skilled and detail-oriented Phlebotomist to support our clinical research team
  • In this role, you will play a critical part in the collection, processing, and handling of biological samples from study participants
  • Your work will directly support the success of clinical trials by ensuring timely and accurate specimen collection and documentation in accordance with study protocols and regulatory standards
  • Perform venipuncture and collect blood and other biological specimens from research participants according to study protocols
  • Properly label, process, and store specimens for laboratory analysis or shipment to central labs
  • Maintain accurate and timely documentation of sample collection, handling, and processing activities
  • Assist clinical staff in preparing for participant visits and supporting visit procedures
  • Monitor and manage lab supply inventory and ensure equipment is clean and properly maintained
  • Adhere to all research protocols, HIPAA guidelines, and GCP (Good Clinical Practice) standards
  • Collaborate with research coordinators and investigators to ensure smooth study operations


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