Phlebotomist
ECN Operating LLC, Long Beach, CA, United States
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)
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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)
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