Wilson Jeerge

I am a B.Pharm graduate with focused training in pharmacovigilance, clinical research, and clinical data management. I combine academic knowledge of drug safety with hands-on exposure to adverse event reporting and data handling.

As a program coordinator at Sci-teh series, I organized scientific conferences, managed logistics, handled data extraction and filtering, and supported bulk campaigns, mailing and social media scheduling for events and journal publications.

I have completed a 4-month course in clinical research, pharmacovigilance and related areas at Clini India and hold a Good Clinical Practice certificate from the NIDA clinical trial network. I am familiar with ICH-GCP principles, MedDRA, ICSR/SAE/SUSAR reporting, signal detection, and aggregate reporting (PSUR/DSUR).

I bring strong problem-solving, communication, critical-thinking and project-management skills, and I am committed to continuous learning and maintaining high standards of regulatory compliance and patient safety.