Tests new treatments for safety and effectiveness through clinical trials, aiding drug and device approvals.

Ensures accurate and reliable clinical trial data collection, cleaning, and preparation for regulatory submissions.

Monitors and prevents adverse drug effects during trials and real-world use to ensure long-term medication safety.

Converts healthcare details like diagnoses and procedures into standard codes for documentation and billing purposes.

Manages communication with regulatory bodies to ensure that medical products follow compliance and approval processes.

Uses SAS software for analyzing and reporting clinical trial data, ensuring clean and regulatory-compliant results.

Microsoft tool for visualizing and analyzing clinical data with interactive dashboards and real-time reporting.

Statistical programming language used for data analysis, visualization, and reporting in clinical research.

Focuses on verifying clinical data quality, regulatory compliance, and process consistency through audits and checks.