Tejal Deshmukh

I am experienced pharmacovigilance professional seeking to contribute to a safety-focused organization by applying strong skills in adverse event assessment, regulatory submission, and benefit-risk evaluation, while expanding expertise in global drug safety operations and clinical development.

Drug safety Associate at Tata Consultancy Services (TCS) (2023-12 – Present)

• Process and manage Individual Case Safety Reports (ICSRs) and literature reports including data entry, processing, medical coding, narrative writing, quality review, and follow-up activities in compliance with global PV regulations.
• Performed data entry and case processing into pharmacovigilance tracking systems (Aris G and Lsmv database) with 100% accuracy.
• Experienced in screening and reviewing scientific literature from Embase and PubMed to identify relevant safety information and potential ICSRS.
• Screening of literature for its validity ie whether it meets the established criteria for validity and seriousness. (Literature validity).
• Proficient in adhoc activities such as splitting and uploads creation and documentation.
• Collaborate with Triage, Case processors, Quality reviewers, Medical reviewers, Data management, and cross-functional teams to ensure timely case closure and high-quality deliverables.
• Experienced in Pharmacovigilance tools like Veeva vault, GPRS, Rightfind, PVDB.

B.Pharma in Pharmacy – Savitribai phule pune university,Marathwada mitra mandal college of Pharmacy Thergaon, pune (2023)