1. Design CRF based on study protocol and prepare the CRF completion guideline.
2. Generate data management plan and data validation plan.
3. Clinical Data Management / Clinical data management status report.
4. Provide training to the site personnel and reporting agencies on proper data collection processes.
5. Coordinate with clinical monitoring activities to help provide prompt feedback to sites on data quality.
6. Establish data quality standards and works with reporting agencies to ensure standards are met.
7. Generate and close queries or apply self evident corrections to the data according to the relevant guidelines.