Phlebotomist

ECN Operating LLC; San Jose (CA); On-site; USD 42,000 - 60,000; Full time

Job summary

ECN Operating LLC in San Jose, California seeks a skilled Phlebotomist to support our clinical research team. You will collect blood and other specimens, ensure proper labeling, and maintain compliant documentation according to study protocols and regulatory standards.

Responsibilities include venipuncture, specimen processing, and helping prepare participants for visits while upholding HIPAA and GCP guidelines.

Qualifications

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

Responsibilities

• Perform venipuncture and collect blood and other specimens from participants per study protocols.
• Label, process, and store specimens for analysis or shipment to central labs.
• Maintain accurate documentation of sample collection, handling and processing.

Skills

Phlebotomy

Sample handling

Documentation

HIPAA compliance

Communication

Job description

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Position Overview
We are seeking a skilled and detail-oriented Phlebotomist to support our clinical research team at our site in San Jose, California. 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)