Sponsored Research

The primary responsibility of the Office of Sponsored Research is to facilitate the conduct of industry sponsored clinical research studies. Services which are available through this office include:
  • Assistance with the IRB submission process.
  • Preparation of regulatory documents.
  • Participant recruitment.
  • Coordination of study activities.
  • Completion of case report forms and tracking of adverse events.
  • Management of investigational drug products.

Study coordinators and investigational pharmacists are available on a fee-for-service basis to assist investigators.

For more information, contact the Director of Research Administration, 727-767-4813.