Tanshi Bhowmick

About Tanshi Bhowmick

Drug Safety Associate at IQVIA with hands-on experience in pharmacovigilance, specializing in case processing, regulatory submissions, and global safety reporting. Skilled in using the Argus safety database, MedDRA coding, and narrative writing, while ensuring compliance with global PV regulations, including FDA and EMA. Graduated with a Bachelor of Pharmacy from Rajiv Gandhi University of Health Sciences and furthered expertise through a SAS trainee program. Dedicated to contributing to patient safety through accuracy, quality, and timely safety assessments, while fostering collaboration with cross-functional teams. Open to advancing opportunities in pharmacovigilance and regulatory affairs.

Experience

1. Drug Safety Associate

   IQVIA

   Jun 2025 — Present · Bengaluru, IN

   Pharmacovigilance professional with experience in case processing, regulatory submissions, and global safety reporting. • Skilled in Argus safety database, MedDRA coding, narrative writing, and literature review. • Knowledgeable in ICH-GCP guidelines and global PV regulations (FDA, EMA). • Strong expertise in managing adverse event cases and ensuring regulatory compliance. • Experienced in cross-functional collaboration with clinical, project management, and data management teams. • Focused on quality, accuracy, and timely safety assessments. • Open to opportunities in drug safety, pharmacovigilance operations, and regulatory affairs.

Education

• Overseas pharma limited

  Pharma intern

• Rajiv Gandhi University of Health Sciences

  Bachelor of Pharmacy - BPharm

• Bangalore clinical research institute

  Student trainee, SAS