Clinical Research Phlebotomist - Specimen Specialist

Elite Clinical Network; Los Angeles (CA); On-site; USD 29,000 - 34,000; Full time

Job summary

Elite Clinical Network in Northridge, CA, is seeking a skilled phlebotomist to support our clinical research team with specimen collection, processing, and documentation.

You will perform venipuncture, label and store samples, maintain accurate records, assist with participant visits, monitor supplies, and ensure compliance with HIPAA and GCP standards, while collaborating with study staff.

Qualifications

• Certified phlebotomist in California.
• Experience in clinical or research settings preferred.
• Familiar with clinical trial protocols and sample handling procedures.
• Strong organizational and documentation skills.
• CPR certification preferred.
• Willingness to cross-train for Clinical Research Coordinator responsibilities (a plus).

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 standards
• Collaborate with research coordinators and investigators to ensure smooth study operations

Skills

Phlebotomy

Clinical research

Documentation

HIPAA/GCP

Communication

Education

Certified Phlebotomist - CA

Job description

Elite Clinical Network in Northridge, CA, is seeking a skilled phlebotomist to support our clinical research team with specimen collection, processing, and documentation.

You will perform venipuncture, label and store samples, maintain accurate records, assist with participant visits, monitor supplies, and ensure compliance with HIPAA and GCP standards, while collaborating with study staff.