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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 LivesAre 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 BringMinimum Qualifications :
Bachelor's degree in an allied health or related fieldStrong organization and time management skills with the ability to manage multiple projectsExcellent written and verbal communication skillsAttention to detail and ability to work independentlyProficiency with computer systems and documentation toolsPreferred Qualifications :
One year of clinical research experienceClinical Research Coordinator Certification (ACRP or SoCRA)Working knowledge of GCP, FDA, and DHHS regulations, ICH Guidelines, and HIPAAYou'll Thrive Here If You...
Love being part of a mission-driven team advancing healthcare innovationAre naturally organized and thrive in a fast-paced, regulated environmentTake pride in accuracy, integrity, and collaborationWant to make an impact on patients' lives while growing your research career