• Assist with CRF review and testing: Support review of case report forms for completeness, clarity, and alignment with the protocol; participate in UAT testing in EDC systems. • Data cleaning support: Run predefined data checks, identify missing or inconsistent data, and help draft or track data queries under supervision. • Data reconciliation activities: Assist with reconciling clinical data against external sources (e.g., device logs, imaging data, or safety data listings). • Database documentation maintenance : Help maintain data management documentation such as data management plans (DMPs), data dictionaries, and data validation specifications. • Clinical systems support: Assist with user access tracking, training documentation, and basic system support for EDC or CTMS platforms. • Data tracking and reporting: Create simple metrics or dashboards (e.g., query rates, data entry timeliness) to support study oversight. • Process improvement and SOP support: Participate in reviewing SOPs or work instructions and help identify opportunities to improve data management workflows.