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:
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Participant screening
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Obtaining informed consent
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Reporting and tracking adverse events, serious adverse events, and protocol deviations
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Completing case report forms and data entry
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Sample collection, processing, and shipping
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Coordinating sponsor monitor visits
Contact Us:
Phone: 801-587-7514