Full-Time

Clinical Research Assistant

Multiple Teams

Updated on 8/1/2026

University of Kansas Medical Center

University of Kansas Medical Center

Compensation Overview

$22.88 - $33.17/hr

Kansas City, KS, USA

In Person

Category
Medical, Clinical & Veterinary (1)
Biology & Biotech (1)
Required Skills
Epic (EHR)
Inventory Management

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Requirements
  • Two years of experience in health sciences, biology, nursing, or a related field, with education substitutable for experience on a year-for-year basis.
  • Computer skills.
  • Organizational skills.
  • Communication skills.
  • Interpersonal skills.
  • Attention to detail.
  • Multitasking skills.
Responsibilities
  • Assist Clinical Research Coordinators with study setup, participant recruitment efforts, and follow-ups.
  • Prepare and organize research study materials, including participant packets, consent forms, and regulatory documentation.
  • Schedule study-related appointments and coordinate participant visits.
  • Maintain an up-to-date inventory of study supplies and assist in ordering necessary materials.
  • Serve as a point of contact for study participants, providing general study information and answering non-clinical questions.
  • Assist with scheduling and sending reminders for study visits.
  • Provide participants with instructions regarding study expectations, visit logistics, and follow-up care.
  • Escort study participants to different departments or areas for required study procedures.
  • Collect, enter, and maintain research data in electronic and paper-based systems.
  • Ensure proper documentation and organization of study records, regulatory binders, and case report forms.
  • Assist with maintaining compliance with institutional and regulatory guidelines by supporting the Clinical Research Coordinator in Institutional Review Board submissions and protocol updates.
  • Assist in preparing materials for audits, sponsor site visits, and regulatory inspections.
  • Track and report study milestones and participant recruitment status.
  • Maintain study logs and ensure proper filing of all study-related correspondence.
  • Support the Clinical Research Coordinator in coordinating study team meetings, taking meeting minutes, and preparing reports.
Desired Qualifications
  • A bachelor's degree in health sciences, biology, nursing, or a related field.
  • Experience in a research, healthcare, or administrative support role.
  • Experience with research protocols, Institutional Review Board regulations, and data entry procedures.
  • Experience with electronic data capture systems such as REDCap and Epic.
University of Kansas Medical Center

University of Kansas Medical Center

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