Case Processors and Quality Reviewers

Roles & Responsibilities
• Perform end-to-end case processing of Individual Case Safety Reports (ICSRs)
• Conduct medical coding using MedDRA and WHO Drug dictionaries
• Perform case triage, data entry, narrative writing, and quality checks
• Ensure compliance with global pharmacovigilance guidelines and SOPs
• Perform Quality Control (QC) review of processed cases for accuracy and completeness
• Identify discrepancies and provide feedback to case processors
• Maintain regulatory timelines and ensure submission readiness
• Collaborate with cross-functional safety and regulatory teams

Qualification
• B.Pharm / M.Pharm / Pharm.D

Experience
• 2 – 8+ years of Pharmacovigilance experience
• Experience in case processing and/or quality review
• Knowledge of global safety databases preferred

Skills
• Strong understanding of ICH-GCP and global PV regulations
• Hands-on experience with safety databases (Argus/ArisG preferred)
• Proficiency in MedDRA coding and narrative writing
• Attention to detail and accuracy in data review
• Strong analytical and time management skills
• Good written and verbal communication skills

About the Company
The Accenture organization operates within the pharmacovigilance and drug safety domain, supporting global pharmaceutical clients with case processing, safety review, and regulatory compliance services. The company provides structured career growth opportunities and exposure to international drug safety operations in a professional work-from-office environment based in Bengaluru.