Urvi Sadariya

I’m a life sciences professional with an M.Sc in Biotechnology and an Advanced PG Diploma in Clinical Research, bringing 2 years of experience in quality control and compliance-focused pharmaceutical operations at Cadila Pharmaceuticals. I focus on accurate, audit-ready documentation while supporting pharmacovigilance and drug safety needs.

In regulated environments, I’ve strengthened my ability to perform detailed data review and verification, support deviation handling and CAPA activities, and apply strong data integrity habits to safety workflows. I’m hands-on with One PV safety database, eTMF, EDC systems, and MedDRA coding basics, and I’m comfortable working within global pharmacovigilance regulations (ICH and GVP). I’m currently seeking remote opportunities across Pharmacovigilance, Medical Writing, Drug Safety, and Regulatory Affairs.