Regulatory Coordinator, Ophthalmology Human Subjects Research

14 hours ago


Iowa City, Iowa, United States University of Iowa Hospitals & Clinics Full time
Job Summary

University of Iowa Hospitals & Clinics is seeking a highly skilled Regulatory Coordinator to join our Ophthalmology Human Subjects Research team. As a key member of our team, you will be responsible for ensuring compliance with regulatory requirements for human subjects research, providing expert guidance to faculty and learners, and developing and implementing training programs to promote regulatory awareness.

Key Responsibilities
  • Manage external standards review processes, including IRB submissions and approvals
  • Develop and implement a triage system for IRB approval requests
  • Provide expert guidance on regulatory compliance and human subjects protection
  • Disseminate information about changes in regulations and processes related to human subjects research
  • Attend meetings with internal and external groups to provide reporting of study updates and educational and training meetings
Requirements
  • Bachelor's degree or equivalent combination of education and experience
  • 1-3 years administrative and/or program experience in clinical research
  • Excellent written, verbal, and interpersonal communication skills
  • Excellent organizational skills
  • Prior experience with Institutional Review Board application materials and processing
  • Experience in coordinating multiple projects and a variety of functions independently
  • Knowledge of regulations, guidelines, and procedures that apply to human research
  • Proficient in computer, software, and database systems
Desired Qualifications
  • 5+ years of experience in clinical trials research
  • Knowledge of ophthalmology and vision research
  • Experience working in an academic clinical research environment
  • Demonstrated completion of GCP (Good Clinical Practice) training
  • Proven ability to utilize medical terminology
  • Experience following specific protocol techniques and management
  • Experience teaching or training others new skills or knowledge
  • Clinical Research Certification (ACRP and/or SOCRA)
  • Experience with VA IR and/or VA-IRB-03
  • Knowledge of University of Iowa policies, procedures, and regulations


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