Clinical Research Coordinator

5 days ago


Omaha, Nebraska, United States University of Nebraska Medical Center Full time

Job Summary

As a Clinical Study Coordinator at the University of Nebraska Medical Center, you will play a crucial role in the success of our clinical research activities. We are seeking a highly organized and detail-oriented individual to coordinate diabetes and endocrine studies, recruit patients, and maintain required consents and documentation.

Key Responsibilities

  • Coordinate clinical research studies, including recruiting patients and obtaining informed consent
  • Maintain accurate and up-to-date records and documentation
  • Ensure compliance with study protocols and Institutional Review Board (IRB) regulations
  • Provide administrative support to the research team, including data entry and management
  • Collaborate with healthcare professionals to ensure smooth study execution

Requirements

  • Bachelor's degree in a related field (e.g., healthcare, biology, chemistry)
  • 2 years of experience in clinical research or a related field
  • Excellent communication and organizational skills
  • Ability to work independently and as part of a team
  • Attention to detail and ability to maintain confidentiality

Preferred Qualifications

  • Phlebotomy certification or willingness to obtain
  • Experience with electronic health records and laboratory data management
  • Knowledge of study protocols and IRB regulations


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