Phlebotomist

ECN Operating LLC; Los Angeles (CA); On-site; USD 40,000 - 60,000; Full time

Job summary

ECN Operating LLC in Los Angeles is seeking a skilled Phlebotomist to support our clinical research team. You will collect, process, and handle biological samples for clinical trials, ensuring accuracy and compliance with study protocols.

The ideal candidate will have experience in a clinical setting, excellent organizational skills, and a commitment to compassionate patient care. Join a dynamic team dedicated to advancing clinical research.

Qualifications

• Experience in a clinical or research setting preferred.
• Familiarity with clinical trial protocols and sample handling procedures.
• Strong organizational and documentation skills.

Responsibilities

• Perform venipuncture and collect blood from participants.
• Label, process, and store specimens for analysis.
• Maintain documentation of sample collection activities.

Skills

Organizational skills

Documentation skills

Compassionate communication

Job description

Position Overview

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.

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

• Previous experience in a clinical or research setting (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)