The study coordinator team supports the management and coordination of clinical research studies. They perform PI-delegated study protocol activities for both industry-sponsored and investigator-initiated clinical trials and research studies.

The team provides fee-for-service activities, such as:

  • Participant screening

  • Obtaining informed consent

  • Reporting and tracking adverse events, serious adverse events, and protocol deviations

  • Completing case report forms and data entry

  • Sample collection, processing, and shipping

  • Coordinating sponsor monitor visits 

two medical professionals are working together at a desk

Contact Us:

Email: ClinicalTrialsOffice@hsc.utah.edu

Phone: 801-587-7514