Clinical Research Contracts Administration



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The Clinical Research Contracts Administration Office is responsible for the negotiation and execution of industry-sponsored clinical trial agreements (CTAs).

Clinical trial agreements handled by the CRCA team have the following characteristics:

  • They involve human subjects or human subject records and require Institutional Review Board review or exemption.
  • They are funded, directly or indirectly, by a for-profit entity.

Submit your requests for CTAs in eSIFTER.

CRCA is also responsible for the negotiation and execution of Confidential Disclosure Agreements (CDAs), also known as Non-Disclosure Agreements (NDAs), preceding human subjects research, such as those for review of a clinical trial protocol.

Research teams can submit CDA requests through the Clinical Trial CDA intake form.