Janet O Email and Phone Number

• Enter and verify clinical trial data in EDC systems with a focus on accuracy andcompleteness.• Conduct data cleaning and validation to ensure data quality and integrity.• Collaborate with clinical research associates and data managers to resolve datadiscrepancies.• Maintain up-to-date knowledge of Good Clinical Practice (GCP) and regulatoryrequirements.• Generate and review data queries to ensure timely resolution and data lock.• Assist in the development and maintenance of data entry guidelines and standardoperating procedures (SOPs).• Follow Case Report Form (CRF) Completion Guidelines (CCG) to ensure dataconsistency• Perform regular quality checks on data entries to identify and correct errors

Supported data entry activities for clinical studies, ensuring adherence to studyprotocols.• Entered patient information, treatment records, and adverse event reports into EDCsystems.• Conducted quality checks to identify and correct data entry errors.• Assisted in the preparation of data reports for review by clinical teams.• Participated in training sessions to stay updated on new data entry tools and bestpractices.• Followed established data entry guidelines and CRF Completion Guidelines (CCG) foraccurate data entry.• Managed and organized source documents to ensure easy access for data verification.• Collaborated with clinical research coordinators to resolve data discrepancies.• Monitored data entry progress to ensure timely completion of tasks.• Provided feedback to the data management team on potential improvements in dataentry processes