• Act as a primary database architect for client clinical databases using Medidata Rave, OmniComm TrialMaster, or other database applications as needed for Clinical Trials • Create database entry screens based on approved case report form (CRF) casebook • Perform internal testing of entry screens prior to user acceptance testing • Work with lead CP or Study Clinical Data Manager to implement system edits on built entry screens • Program validation procedures, in conjunction with the Sr. CP or CP II, for clinical studies and other billable projects. • Maintain necessary study build documentation as required by CTI SOPs • Meet all project deadlines on time and on budget • Ensure accuracy of clinical databases as compared to the CRF; perform user acceptance testing (UAT) of database and provide feedback to study team regarding any discrepancies • Perform UAT on programmed edits in the clinical database; ensure accuracy of edits in database as compared to edit specifications documents; provide feedback to study team on functioning of edits. • Perform review and issue queries for CRF data, based on automated edit checks, manual review, post-hoc data listings, and sponsor requirements