I have extensive experience with various clinical data management systems, including Oracle Clinical, Medidata Rave, and Clintrial. I have successfully managed and processed large datasets, ensuring data integrity and compliance with regulatory standards. My experience includes setting up databases, performing data validation, and generating reports for clinical trials.

I ensure data quality and integrity by implementing rigorous data validation processes, including edit checks, range checks, and consistency checks. I also conduct regular data audits and collaborate with cross-functional teams to resolve any data discrepancies. Additionally, I ensure that all data management activities adhere to Good Clinical Practice (GCP) guidelines.

My approach to managing timelines and deadlines involves detailed planning and proactive communication with all stakeholders. I create comprehensive project timelines, set clear milestones, and regularly monitor progress to ensure timely completion of tasks. I also maintain flexibility to adjust plans as needed to accommodate any changes or challenges that arise during the project.

I handle data privacy and security by strictly adhering to regulatory requirements such as HIPAA and GDPR. I ensure that all data is stored securely and access is restricted to authorized personnel only. I also implement encryption and secure data transfer protocols to protect sensitive information. Regular training and awareness programs are conducted to keep the team updated on the latest security practices.

One challenging issue I faced was a significant data discrepancy in a large-scale clinical trial. I quickly identified the root cause, which was a coding error in the data entry process. I worked closely with the IT team to correct the error and implemented additional validation checks to prevent future occurrences. This proactive approach ensured that the trial could proceed without further disruptions and maintained data integrity.