Clinical Research Coordinator

in Healthcare + Life Sciences Permanent

Job Detail

  • Experience Level Mid Level
  • Degree Type Bachelor of Science (BS)
  • Employment Full Time
  • Working Type On Site
  • Job Reference 0000010168
  • Salary Type Hourly
  • Industry Pharmaceuticals
  • Selling Points

    Our client offers a compelling work environment for professionals in clinical research. The facility focuses on rheumatology research, providing employees with the opportunity to work on cutting-edge studies in a specialized field.

Job Description

Job Title: Clinical Research Coordinator

About the Role:

We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our client’s thriving Rheumatology Research Facility in the Dallas-Fort Worth area. The ideal candidate will have patient-facing experience and at least one year of experience coordinating clinical trials. Preference will be given to candidates with phlebotomy training, laboratory sample processing experience, and ECG training.

Key Responsibilities:

  • Oversee and coordinate clinical research studies in compliance with protocols, regulations, and institutional policies.
  • Recruit, screen, and enroll eligible study participants while ensuring proper informed consent procedures.
  • Conduct or assist with clinical procedures, including phlebotomy, ECGs, and laboratory sample processing.
  • Accurately collect, record, and maintain study data, ensuring completeness and compliance.
  • Act as a liaison between study sponsors, investigators, and multidisciplinary teams to facilitate smooth study execution.
  • Ensure strict adherence to Good Clinical Practice (GCP) guidelines and all regulatory requirements.
  • Participate in study meetings, training sessions, and audits to support continuous improvement.

Qualifications:

  • Bachelor’s degree in a health-related field or equivalent experience.
  • Minimum 1 year of experience as a Clinical Research Coordinator in a clinical trial setting.
  • Patient-facing experience is required.
  • Strong preference for candidates with:
    • Phlebotomy training/experience
    • Laboratory sample processing skills
    • ECG procedure proficiency
  • Comprehensive knowledge of Good Clinical Practice (GCP) and clinical research regulations.
  • Exceptional communication, organizational, and interpersonal skills.
  • Ability to work independently while thriving in a collaborative team environment.
  • Highly detail-oriented with strong problem-solving capabilities.

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