Receives the Confidentiality Disclosure Agreement (CDA) from Pfizer., Gathers documents for the Office of Sponsored Programs for proposal routing., Completes the Human Subject module in Insight for study approval., Completes the Emory Clinical Research Office (ECRO) eForm for a coverage analysis and budget development., Receives electronic Notice of Award (eNOA)., Recruit potential subjects., Register subjects in OnCore CTMS and link the Epic timeline., Track study activities with the Site in OnCore CTMS and the Case Report Forms (CRFs) with the Sponsor for Invoicing., Provide the study closeout letter in OnCore CTMS., Store paper documents off-site according to the Contractual Trial Agreement (CTA)..

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