Study Coordinator – Clinical Research (Clinical Operations)

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HR Anew

Study Coordinator – Clinical Research (Clinical Operations)

Dallas/Fort Worth, TX
Full Time
Paid
  • Responsibilities

    Study Coordinator – Clinical Research (Clinical Operations)

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

    Prime Clinical Research is seeking a Study Coordinator 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