Yevgenya Zeynalyan

I work at the intersection of pharmacovigilance, regulatory affairs, and pharmaceutical sciences. In my current Associate roles at ClinChoice, I perform case intake, triage, validity assessment, and medical coding for safety reports across spontaneous, literature, clinical trial, and regulatory sources.

I’m responsible for MedDRA coding (adverse events, medical history, and laboratory findings), assessing seriousness and causality, and verifying labeling information in line with pharmacovigilance requirements. I also complete quality review and completion checks in safety databases and screen the literature to identify potential ICSRs.

Alongside this, I prepare and review cosmetic regulatory documentation in compliance with EU/US regulations. I support product registration and market authorization submissions, coordinate with R&D, safety, and marketing teams, and maintain regulatory databases and documentation systems.

Before this industry focus, I trained through pharmacy education and research as a Junior Researcher at the NAS RA Scientific and Technological Center of Organic and Pharmaceutical Chemistry. I designed and synthesized novel small molecules, applied computational drug design (molecular docking, binding interaction analysis, and ADMET prediction), ran SAR analyses, and characterized compounds using IR, NMR, and UV/VIS—then translated those findings into scientific summaries and research reporting.