University Health
Clinical Research Coordinator - Emergency Medicine Administration
University Health, Kansas City, Missouri, United States, 64101
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Clinical Research Coordinator - Emergency Medicine Administration
Job Location: University Health Truman Medical Center, Kansas City, Missouri
Department: Admin ER UHTMC
Position Type: Full time
Work Schedule: 7:00 AM - 5:00 PM
Hours Per Week: 40
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
#J-18808-Ljbffr
Please log into myWORKDAY to search for positions and apply.
Clinical Research Coordinator - Emergency Medicine Administration
Job Location: University Health Truman Medical Center, Kansas City, Missouri
Department: Admin ER UHTMC
Position Type: Full time
Work Schedule: 7:00 AM - 5:00 PM
Hours Per Week: 40
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
#J-18808-Ljbffr