Clinical Research Nurse Coordinator

4 weeks ago


Iowa City, Iowa, United States The University Of Iowa Full time
Job Summary

The University of Iowa is seeking a highly skilled Clinical Research Nurse Coordinator to support ongoing and new clinical research studies for the Division of Neonatology in the UI Stead Family Department of Pediatrics.

Key Responsibilities
  • Perform skilled clinical and healthcare research activities in the neonatal intensive care unit (NICU).
  • Screen patients for study eligibility and consent for clinical trials.
  • Monitor randomizations into studies and educate patient families on study scope, potential risks, and benefits.
  • Supervise the ordering of study medication, schedule study medication, and monitor adherence to administration per protocol.
  • Oversee the recruitment of subjects and scheduling of trial-related procedures.
  • Prepare study recruitment materials and relay study information to the principal investigator.
  • Obtain and process human blood and tissue samples.
Protocol Development and Study Responsibilities
  • Assist in the design, development, execution, administration, and maintenance of protocols and clinical studies.
  • Assist clinicians and patient families with problems related to protocol.
  • Oversee case report form development, review query reports, and resolve monitoring visit issues.
  • Develop complex study materials and serve as a liaison to local healthcare practitioners, agencies, and sponsors.
  • Attend protocol meetings as required and possess a thorough understanding of the protocols.
Data Collection and Monitoring
  • Participate in the design, development, and testing of clinical research trial data management systems.
  • Validate data and make recommendations for resolution.
  • Revise and implement changes in data collection.
  • Responsible for collecting, assembling, and mailing data forms, bills, specimens, and other protocol-related documents and medical records.
Regulatory Guidelines and Documents
  • Manage and organize regulatory documentation and prepare regulatory submissions.
  • Perform on-site audits of research and clinical data.
  • Maintain regulatory binders/folders for each protocol.
  • Recommend corrective action for reportable events.
  • Communicate with the Research Manager and PI about the status of the research projects.
Education and Experience Requirements
  • A Master's degree in Nursing or an equivalent combination of education and related NICU experience.
  • 1-3 years previous experience working in a Neonatal Intensive Care Unit (NICU).
  • A Current, valid Iowa Registered Nurse license.
  • Proficiency with Microsoft Office and the Internet.
  • Excellent written and verbal communication skills.
  • Experience in a position requiring independent decision-making.
Desired Qualifications
  • More than 5 years clinical experience in the NICU.
  • Experience managing and coordinating multiple tasks simultaneously.
  • Experience communicating with patient families by phone.


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