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University of Arkansas System
University of Arkansas System
ConsultingEducationHealthcare
The University of Arkansas System is a statewide public university system supporting educational access, research, healthcare, and community service across Arkansas. Established in 1871, it brings together universities, community colleges, and specialized institutions that contribute to the state’s economic, educational, and cultural development. The system’s work spans teaching, discovery, administration, and public engagement, guided in part by its Transformation 2025 strategic plan. Its broad network creates opportunities for people interested in contributing to higher education and the many services its institutions provide.
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Clinical Research Nurse I-III - Little Rock, Onsite

Coordinate oncology clinical trials at UAMS, supporting participant care, protocol compliance, research data, and collaboration among investigators, sponsors, and clinical teams.

USUnited StatesOn-siteFull-timeMiddleSeniorEnglish RequiredClinical Research

Description

  • Coordinate participants in cancer clinical trials through the Winthrop P. Rockefeller Cancer Institute Clinical Trials Office
  • Manage screening, consent, enrollment, treatment or observation, and follow-up activities for cancer trial participants
  • Keep physicians and participants on schedule through each treatment phase and prevent protocol deviations
  • Advise the principal investigator on study requirements and data collection procedures
  • Represent the department and investigators at local, regional, and national meetings
  • Coordinate communication among staff, principal investigators, research and clinical professionals, UAMS leaders, and study sponsors
  • Create, implement, and maintain quality assurance plans and standard operating procedures
  • Act as administrator and liaison for the principal investigator, participants, compliance teams, research and clinical professionals, and funding organizations
  • Maintain compliance with regulatory requirements, including serious adverse event reporting
  • Prepare written materials, analyze research data, and develop conclusions
  • Maintain complete clinical records, research documentation, and database information
  • Assess patients for trial eligibility before enrollment
  • Perform clinical reviews and confirm that study procedures meet protocol requirements
  • Educate patients and their caregivers or families while supporting physicians with patient management
  • Monitor participant compliance with study protocols
  • Collect and manage patient information in collaboration with the CRN Team Lead and clinical research associates
  • Supply accurate data for entry and support query resolution, monitoring, and audit visits
  • Train staff members and investigators on relevant study procedures
  • Improve operational processes and contribute to electronic infrastructure development
  • Complete continuing professional training
  • Perform additional duties as assigned

Requirements

  • Registered Nurse with three years of general nursing and/or general research experience for Level I
  • Registered Nurse with three years of general research experience and demonstrated skill in study planning and development, research nursing, and research patient management for Level II
  • Registered Nurse with at least five years of clinical research experience and demonstrated skill in study planning and development, research nursing, and research patient management for Level III
  • Levels I and II must obtain CRS certification within two years of hire
  • Level III requires CCRP, CCRC, or an equivalent professional certification at hire
  • Level III requires CRS certification within two years of hire
  • Bachelor of Science in Nursing preferred
  • Oncology experience preferred
  • Clinical research experience preferred
  • Proof of legal authorization to work in the United States on the first day of employment
  • License or certificate and resume required, along with three professional references
  • Employment is subject to screening that may include criminal background, drug testing, and education verification
  • Ability to organize complex projects, maintain close attention to detail, and communicate effectively
  • Working knowledge of the Code of Federal Regulations and human research code of conduct requirements
  • Ability to lift or carry at least 25 pounds and push or pull at least 50 pounds

Benefits

  • Medical, dental, and vision coverage is available for eligible staff and family members
  • Holiday, vacation, and sick leave
  • Undergraduate education discounts for staff and dependents
  • UAMS matching contributions of up to 10 percent
  • Basic life insurance coverage of up to $50,000
  • Career development, training, and educational opportunities
  • Merchant discounts
  • Concierge prescription delivery at the main campus through the UAMS pharmacy

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