Clinical Research Coordinator

2 days ago


Salt Lake, Utah, United States University of Utah Full time
Job Summary

We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team at the University of Utah. The successful candidate will be responsible for coordinating the implementation, quality control, and completion of research studies, while assisting Principal Investigators and ensuring compliance with governing agency guidelines.

Key Responsibilities
  1. Oversee compliance to protocol, manage quality control, and prepare reports for organizations and agencies.
  2. Monitor enrollment goals, initiate strategies to promote enrollment and participant compliance, and coordinate research participant activities.
  3. Recognize, track, and report adverse events and protocol deviations.
  4. Prepare for and coordinate site visits made by sponsors or federal agencies.
  5. Represent the research program at meetings and national/international research consortia.
  6. Prepare, submit, and maintain regulatory documents and research correspondence.
  7. Contribute to developing educational materials and educate the community and research professionals regarding studies and related research issues.
  8. Supervise, mentor, and train new or junior research staff.
  9. Coordinate with referring physicians to provide information regarding available research projects.
  10. Develop and maintain patient databases, investigational logs, and records of drugs administered, medical devices monitored, and/or procedures followed.
  11. Assist the Principal Investigator in the development of study protocols.
Requirements

The ideal candidate will possess a Bachelor's degree in a health sciences or related field, with two years of professional research experience and completion of University RATS Clinical Certification within one year of hire. Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills are also required.

Knowledge of Good Clinical Practices, FDA, HIPAA, and IRB regulations; an understanding of research procedures; and the ability to function independently are preferred.

This position is patient-sensitive and requires the incumbent to be immunized according to CDC standards and hospital policy.



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