
Adverse Event (AE) & ADR Identification, ICSR Case Documentation, Medication Safety Surveillance, Signal Detection &
Literature Screening, FAERS Database Analysis, VigiFlow Safety Reporting, Drug–Drug Interaction Assessment, Clinical
Safety Documentation, GCP & Regulatory Compliance, Medical Literature Review, Microsoft Excel, Word, PowerPoint
Healthcare Data Analysis & Interpretation
Clinical Data Review
Patient Safety & Quality Improvement
Business Insights & Problem Solving
Stakeholder Collaboration
Patient education and counseling
VigiFlow (WHO UMC) – ADR reporting and safety case documentation
FAERS Database – Adverse event data mining and signal detection
OpenVigil – Disproportionality analysis of pharmacovigilance data
MedDRA (Familiarity) – Medical coding for adverse events
Microsoft Excel – Data management and safety data analysis