Clinical Data Managers are responsible for the collection, validation, and management of data obtained from clinical trials to ensure its accuracy and integrity.
The DMP outlines the procedures and guidelines for data collection, handling, and quality assurance throughout the clinical trial.
The CRF is used to systematically collect data from each participant according to the study protocol.
GCP is an international ethical and scientific quality standard for designing, conducting, and reporting clinical trials involving human subjects, ensuring data integrity and participant safety.
An EDC system is used to capture clinical trial data electronically, improving data accuracy, efficiency, and accessibility compared to paper-based methods.
