We support the structured planning, design, testing, implementation, and documentation of clinical trial databases to help ensure reliable data collection and efficient study execution.
Defining and documenting database requirements based on study objectives and data collection needs.
Supporting database structure, forms, fields, workflows, and data flow planning.
Designing and reviewing CRFs/eCRFs for clear, consistent, and study-specific data collection. Converting existing paper CRFs into structured electronic forms while preserving the original data fields, sections, visit structure, and study requirements.
Developing specifications for automated data validation and consistency checks.
Supporting functional and validation testing of database components before implementation.
Coordinating UAT activities to verify that the database meets defined user requirements.
Testing database functionality using simulated data to identify potential issues before go-live.
Supporting readiness checks and documentation required for database activation.
Maintaining essential database specifications, testing records, and implementation-related documentation.
Providing ongoing support for database-related queries, updates, issue resolution, and maintenance.
