Clinical Research Coordinator (Phlebotomist)

Clinical Research Coordinator (Phlebotomist)
Prime Clinical Research (

Location: On-Site
Employment Type: Full-Time
Department: Clinical Operations

Prime Clinical Research is seeking a Clinical Research Coordinator (Phlebotomist) experience to support the operational execution of clinical trials. This role focuses on participant coordination, visit preparation, specimen collection, and data documentation across active clinical studies.

This position does not include regulatory documentation responsibilities and focuses on the operational coordination of clinical trial visits and participant management.

Candidates with experience as a Clinical Research Coordinator (CRC) or Clinical Trials Coordinator are encouraged to apply.

What You Will Do

Clinical Trial Coordination

• Screen potential research participants according to study eligibility criteria
• Coordinate and schedule participant visits including screening, baseline, and follow-up visits
• Guide participants through the informed consent process

Visit Preparation and Execution

• Prepare charts, documentation, and study materials prior to visits
• Ensure protocol-required procedures and assessments are completed

Clinical Support

• Perform or assist with specimen collection including blood draws
• Process and document samples according to study protocol

Data Management

• Enter study data into Electronic Data Capture (EDC) systems
• Maintain accurate source documentation
• Respond to sponsor data queries and maintain organized study records

Study Operations

• Track participant visits and follow-up schedules
• Support monitoring visits and sponsor requests

Qualifications

Required

• Bachelor's degree in life sciences, healthcare, public health, or related field, or equivalent clinical research experience
• Minimum 2 years of clinical research experience as a Study Coordinator, Clinical Research Coordinator (CRC), or similar role
• Knowledge of ICH-GCP guidelines
• Experience using Electronic Data Capture (EDC) systems
• Strong organizational and documentation skills
• Phlebotomy or specimen collection experience

Preferred

• Clinical research certification (CCRC or CCRP)
• Experience coordinating multiple clinical research studies
• Experience working with pediatric populations

Compensation

Salary Range: $45,000 – $55,000 depending on experience