Clinical Trials Coordinator

2 weeks ago


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

About the Role

The University of Iowa Institute for Clinical and Translational Science (ICTS) Clinical Research Unit (CRU) is seeking a highly skilled Clinical Research Nurse to serve as a clinical research expert and administrative liaison. This individual will be responsible for maintaining equilibrium between care of the research participant and fidelity to the research protocol.

Key Responsibilities

  • Clinically assess the participant's health status by gathering information and identifying actual and potential health problems.
  • Acquire working knowledge of all current and proposed research projects.
  • Collect accurate data as specified per protocol.
  • Monitor compliance of regulatory guidelines.
  • Manage safety of participants.
  • Provide supervision over functional support staff.

About ICTS

The Institute for Clinical and Translational Science (ICTS) at the University of Iowa was approved by the Iowa Board of Regents in 2007 to support the work of investigators involved in clinical and translational science. Our mission is to accelerate translational science through programs to develop the translational workforce, to promote engagement of community members and other stakeholders, to promote research integration across the lifespan, and to catalyze innovative clinical and translational research.

Requirements

  • Graduation from an accredited RN Program, with a Master's degree in nursing, preferred, supplemented by one or more years of progressively responsible nursing experience or an equivalent combination of education and experience.
  • A current license to practice professional nursing in the state of Iowa is required by the date of hire.
  • 1-3 years recent experience (within the past 5 years) caring for patients in an acute care setting. Strong clinical nursing skills including IV insertion, phlebotomy, and assessment is required.
  • General computer skills are required including MS Word and Outlook.
  • Excellent written and verbal communication skills are required including positive interpersonal skills as demonstrated through written and verbal interactions. Ability to work independently. Excellent time-management skills and the ability to accurately perform detail-oriented work.

Desirable Qualifications

  • Working knowledge of Good Clinical Practice (GCP).
  • Minimum of 1-year chemotherapy infusions experience.
  • Knowledge of clinical research process.
  • Experience with Epic.


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