Clinical Research Coordinator - Women's Health Department

Truman Medical Center

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University Health Truman Medical Center Until 9/9/2026 H-1B sponsor history First posted April 29, 2026 Last posted July 11, 2026
Job description

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Clinical Research Coordinator - Women's Health Department

101 Truman Medical Center

Job Location

University Health Truman Medical Center

Kansas City, Missouri

Department

Admin Womens Health UHTMC

Position Type

Full time

Work Schedule

8:00AM - 4:30PM

Hours Per Week

40

Job Description

Responsible for performing diverse administrative and clinical responsibilities requiring some analysis, sound judgment, and a high level of knowledge of specific research study protocols, Good Clinical Practice Guidelines, Federal research regulations, and institutional requirements. Responsible for coordination and management of clinical study protocols and along with the research investigator, manages many aspects of the clinical trial and conducts all research activities within an ethically based framework in accordance with federal, state, and local regulations. Function as a liaison between investigators, subjects and sponsors, the Institution(s), Institutional Review Board (IRB) and Privacy Board.

Minimum Requirements

  • Bachelor’s degree in allied health medical field, another related field or licensed LPN. 

  • Ability to prioritize and complete several tasks/projects simultaneously in strict accordance with regulations, policies, and study protocol.

  • Demonstrated effective verbal/written communication skills, analytical skills, attention to details, and ability to work independently with minimal supervision. 

  • Organization/time management skills and project management skills.

  • Demonstrated intermediate knowledge of personal computer skills.

Preferred Qualifications

  • One year clinical research experience.

  • Clinical Research Coordinator Certification (by either the Association for Clinical Research Professionals or Society of Clinical Research Associates). 

  • Knowledge of Good Clinical Practices, U.S. Department of Health and Human Services Protection of Human Subjects and U.S. Food and Drug Administration regulations, International Conference of Harmonization Guidelines, and the HIPAA Privacy Rule as it impacts clinical research

About this role

Summary

Coordinate and manage clinical studies in women's health, ensuring compliance with regulations.

Job title

Clinical Research Coordinator

Experience level

1+ years

Industry

healthcare

Location requirements

Kansas City, Missouri, onsite; remote not specified.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

research protocolsGood Clinical Practiceregulationscommunicationorganizationcomputer skills

Preferred skills

clinical research experienceCRCC certificationHIPAAinternational conference on harmonization

Specializations

women's healthclinical trial managementresearch protocolsregulations
Locations

Structured locations inferred from the posting.

Kansas City, MO, USA

On-site City