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Clinical Research Coordinator

Overview
DJL is a growing Investigative Site Network, based in Charlotte, NC. Join our dynamic clinical research team as a Clinical Research Coordinator and play a pivotal role in advancing innovative medical studies. In this energetic and vital position, you will oversee the coordination and management of clinical trials, ensuring compliance with regulatory standards while supporting research teams and participants alike. Your dedication will help accelerate the development of groundbreaking therapies, making a real difference in patient care. This paid position offers an exciting opportunity to grow your expertise in clinical development within a collaborative, fast-paced environment.

Responsibilities

  • Coordinate all aspects of clinical trial activities, including participant recruitment, scheduling, and follow-up to ensure smooth trial operations.
  • Monitor patient progress by reviewing vital signs, blood sampling procedures, and overall health status, ensuring adherence to study protocols.
  • Review and verify clinical documentation for accuracy, completeness, and compliance with FDA regulations and ICH Good Clinical Practice (GCP) standards.
  • Manage data collection and entry using electronic medical record (EMR) systems and ensure data integrity according to CDISC standards.
  • Oversee laboratory procedures related to clinical trials, including blood sampling, phlebotomy, and sample processing within clinical laboratory settings.
  • Ensure all activities comply with HIPAA regulations to protect patient privacy and confidentiality at all times.

Experience

  • Proven supervising experience in a clinical research or healthcare setting.
  • Extensive knowledge of clinical trials management, including familiarity with FDA regulations and ICH GCP guidelines.
  • Strong understanding of medical terminology, clinical laboratory procedures, and data management practices.
  • Experience with EMR systems, statistical software, and analysis skills for research data interpretation.
  • Background in nursing or related healthcare fields is highly desirable; certification such as an ICH GCP certificate from a recognized issuer is preferred.
  • Demonstrated ability to review complex documentation accurately while maintaining meticulous attention to detail.

Pay: From $22.00 per hour

Benefits:

  • 401(k)
  • Dental insurance
  • Flexible schedule
  • Health insurance
  • Paid time off

Work Location: In person

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