This group within ORC drafts, reviews, negotiates and approves agreements related to Duke conducting research as a site in industry-funded clinical trials, including interventional and observational studies, registries, subcontracts, consortia agreements, and confidentiality agreements associated with such projects.   This group is the primary ORC interface with research funders, faculty members, research staff, the Duke Office of Clinical Research (“DOCR”) , the Clinical Research Units (“CRUs”), and the Office of Research Administration (“ORA”) on issues related to those agreements.

For further information regarding Duke Site Based Research Agreements, please refer to Duke myRESEARCHpath available within myRESEARCHhome or at https://myresearchpath.duke.edu.