Builds and maintains clinical research projects in clinical research management systems, including creating visit and procedure calendars and entering budget and payment information. Supports end users by creating study protocols and related calendars, procedures, visits, forms, and budgets. Collaborates with feasibility coordinators and study teams to establish data requirements and maintain accuracy across studies of varying complexity. Helps with data migration and study-related data entry, resolves issues with relevant teams, and ensures calendars, budgets, and payment terms are accurate and complete for billing compliance, organizational reporting, and revenue capture. May also assist with builds in other clinical research management systems, including eRegulatory, eConsent, RedCap, and Smartsheets.