With hands-on experience in Pharmacovigilance, I have managed sensitive patient records and ensured accurate documentation of adverse events related to specific drugs. 

I worked with structured forms designed to capture comprehensive patient data, including demographics, medical history, drug exposure details, and reported adverse events. Using these forms, I consolidated and sorted patient information for accurate reporting and analysis.

Key responsibilities included:

• Entering and validating patient records in standardized templates

• Sorting and categorizing data for case processing

• Ensuring completeness, accuracy, and compliance with regulatory requirements

• Maintaining confidentiality of sensitive patient information