Clinical Research Associate II i Freeman Lab

Assist PIs to develop study protocols and procedure manualsAssist with institutional review board (IRB) applications, submissions, and updates across multiple sitesEnsure completion of contract requirements and project specificationsScheduling patients and staff for research visits and meetingsRecruit potential research subjects, complete screening and informed consent processes and data collection proceduresTrack recruitment at study site and adherence to procedures/protocols to ensure optimal subject participation rates and accurate data collection and reporting.Develop and maintain timelines in coordination with defined protocolsComplete assigned projects with an emphasis on coordination and communication with research sponsors, investigators and research team membersAssist in training project staff and research assistants who may be helping with data collection and data entryHelp to facilitate project collaborations and team workOther related functions as assigned