Detail-oriented B.Pharmacy graduate with 6 months of experience as a Drug Safety Associate at IQVIA. Hands-on experience in pharmacovigilance case processing, adverse event reporting, data entry, medical coding, and compliance with regulatory timelines. Strong understanding of ICH-GCP, GVP guidelines, MedDRA, and drug safety workflows. Seeking to contribute to pharmacovigilance and patient safety in a growth-focused organization.
