Skills
ICSR Case Processing (Initial & Follow-up) | Safety Narrative Writing | PSUR / DSUR Support | Clinical Data Management (CDM) | Quality Control (QC) | Clinical Trial Operations | Deviation Management | Time Management | Patient Management | Attention to Detail | strong interpersonal skill
About
Pharmacovigilance and Clinical Research Coordinator professional with 3+ years of experience at IQVIA, Strong expertise in ICSR case processing, adverse event and SAE management, MedDRA coding, safety narratives, PSUR/DSUR preparation, and regulatory compliance (ICH-GCP).Background as a Clinical Research Coordinator with hands-on experience in patient management, EDC/CRF handling, and audit-ready documentation. Detail-oriented, quality-driven, and experienced in fast-paced CRO environments.
Profile Photo
