Our Clinical Operations team offers to help with Identification of potential sites for your clinical trial, including help with selection of the type of site, number of sites and geographic location, a preliminary list of investigators when available, and any other Sponsor’s request;
As a first step of our feasibility preparation process, we suggest scheduling a teleconference with the involved team members in order to discuss the feasibility process and documents.
Once potential investigators are identified, the representative from the selected region will contact site and send the Confidentiality Agreement (CDA). Once CDA is signed by the site, potential PI – country representative will send Site Questionnaires via e-mail or information may be gathered via phone contact. Follow-up calls are made to the sites if no response is received. Information collected form potential site reviewed by the responsible person and prepared in requested format to present to the Sponsor.