Dynamic and results-driven professional with 8 years of experience in case processing and a strong foundation in pharmacovigilance. Proficient in safety databases and well-versed in global regulatory requirements. Demonstrated ability to manage teams effectively while ensuring compliance and data accuracy. Adept at adapting to evolving industry standards and delivering high-quality work in fast-paced environments. A career oriented individual with excellent communication and interpersonal skills with degree of Masters in Pharmacy. ✔️8+ years in pharmacovigilance ICSR case processing (including data entry, quality control, submissions and Mailbox handling). ✔️3+ years of experience in Submissions. ✔️2+ years of experience in risk management and reconciliations/compliance (CAPA) activities. 🔸Detailed knowledge on : ✔️ICSRprocessing ✔️Argus/ArisG/Clinevo ✔️GPV modules ✔️Drug Safety Expert in handling serious and non serious cases including ➡️Clinical trial, literature, Spontaneous, Solicited, E2B L2A, E-fax, safety mail box, Social media, digital platforms screning, MLM, Adisinsight, Pubmed, Health authority, LP/BP Cases, FTA cases, Medical Devices and Neutravigilance, Cosmetovigilance and Legal cases. 🔸Received recognitions for quality, accountability, collaboration & Team Work.