Clinical Trials Office

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Clinical Trials Office2016-11-08T15:57:47+00:00

We assist both new and experienced investigators with the review, preparation, and conduction of industry-sponsored and investigator initiated clinical research.

Services Offered

  • study feasibility
  • logistical considerations
  • budgetary review and negotiation
  • financial management

Experienced, certified clinical research coordinators are available, both on and off site, to provide complete study coordination or a range of services, such as, IRB preparation and submission, study start-up, regulatory compliance, participant recruitment, and data management.

Krista Garrison, MPH, CCRP
Interim Director, Clinical Trials Office