Phlebotomist

ECN Operating LLC; Pasadena (CA); On-site; USD 35,000 - 50,000; Full time

Job summary

ECN Operating LLC, based in Pasadena, California, is seeking a skilled Phlebotomist to join our clinical research team. The role focuses on specimen collection, ensuring compliance with study protocols while maintaining accurate documentation.

The ideal candidate will have previous clinical experience, strong organizational skills, and the ability to work compassionately with diverse populations. In this vital position, you will help ensure the success of clinical trials through precise sample handling.

Qualifications

• Previous experience in a clinical or research setting is preferred.
• Familiarity with clinical trial protocols and sample handling procedures.
• CPR certification is a plus.

Responsibilities

• Perform venipuncture and collect blood and biological specimens.
• Maintain accurate documentation of sample collection and handling.
• Collaborate with coordinators and investigators to ensure smooth operations.

Skills

Organizational skills

Documentation skills

Ability to work with diverse populations

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)