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Clinical Research Coordinator - Emergency Medicine Administration

University Health
United States, Missouri, Kansas City
2301 Holmes Street (Show on map)
Oct 14, 2025

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Clinical Research Coordinator - Emergency Medicine Administration 101 Truman Medical Center Job LocationUniversity Health Truman Medical Center Kansas City, Missouri
Department
Admin ER UHTMC
Position Type
Full time
Work Schedule
7:00AM - 5:00PM
Hours Per Week
40
Job Description
Be Part of Breakthroughs That Change Lives Are you ready to play a key role in advancing medicine and improving patient care through clinical research? As a Clinical Research Coordinator I, you'll help bring innovative treatments from the lab to real people - coordinating and managing research studies that make a real difference. Working closely with our investigators, sponsors, and study participants, you'll ensure every detail - from patient enrollment to regulatory documentation - meets the highest standards of ethics, accuracy, and care. What You'll Do
  • Coordinate every phase of clinical studies - from start-up and recruitment to completion - ensuring all activities follow Good Clinical Practice (GCP) and institutional policies.
  • Serve as a key liaison among investigators, sponsors, IRB, and study participants.
  • Manage research documentation, including regulatory files, informed consents, and case report forms.
  • Partner with investigators to prepare and submit protocols and amendments to the IRB.
  • Support the financial and administrative aspects of each study, working with leadership to ensure appropriate funding and compliance.
  • Maintain subject confidentiality and safety in accordance with HIPAA and research regulations.
  • Collaborate across departments to successfully launch new studies and support recruitment efforts.
  • Stay up to date on research ethics, regulatory changes, and institutional requirements.
What You Bring Minimum Qualifications:
  • Bachelor's degree in an allied health or related field
  • Strong organization and time management skills with the ability to manage multiple projects
  • Excellent written and verbal communication skills
  • Attention to detail and ability to work independently
  • Proficiency with computer systems and documentation tools
Preferred Qualifications:
  • One year of clinical research experience
  • Clinical Research Coordinator Certification (ACRP or SoCRA)
  • Working knowledge of GCP, FDA, and DHHS regulations, ICH Guidelines, and HIPAA
You'll Thrive Here If You...
  • Love being part of a mission-driven team advancing healthcare innovation
  • Are naturally organized and thrive in a fast-paced, regulated environment
  • Take pride in accuracy, integrity, and collaboration
  • Want to make an impact on patients' lives while growing your research career
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