
Accomplished professional with expertise in GMP documentation, deviation reporting, and CAPA development. Demonstrates proficiency in pharmacovigilance case processing and safety data review, ensuring regulatory compliance and effective risk-benefit analysis. Skilled in clinical data collection, analysis, and reporting, with a strong foundation in data interpretation and statistics. Adept at drug information researching and maintaining a comprehensive understanding of pharmacovigilance knowledge. Committed to advancing career goals within the pharmaceutical industry by leveraging core competencies to enhance drug safety and efficacy.