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- ...Responsibilities: ~Lead all Data Management activities across clinical trials. ~Manage timelines from study setup to database lock and archiving. ~Provide input into protocol, CRF design, SAP, and Clinical Study Reports. ~Oversee data review, cleaning processes, and...Suggéré
- ...cleanings and review tools that will be further provided to DM PROGRAMMERS for development for the allocated trial(s). ~Prepares and archives Data Management trial documentation. ~Organizes, monitors and tracks the testing of data entry screens (eCRF layout), data...Suggéré