Operation Specialist - Pharmacovigilance (PV)
About the Role
Role & Responsibilities
• Perform end-to-end pharmacovigilance case processing (ICSRs) in line with global regulations
• Handle case intake, data entry, medical coding, quality review, and case lifecycle management
• Work extensively on the Argus Safety Database for safety case processing
• Ensure compliance with ICH-GCP, SOPs, and regulatory timelines
• Maintain high accuracy, data quality, and audit readiness in safety reporting
• Collaborate with cross-functional and global PV teams
• Support timely delivery of pharmacovigilance activities and safety operations
Qualification
• B.Pharm / M.Pharm / Pharm.D
Experience
• 1 to 5 years of relevant pharmacovigilance case processing experience
• Immediate joiners preferred
Skills
• Mandatory hands-on experience with Argus Safety Database
• Strong knowledge of pharmacovigilance regulations and workflows
• High attention to detail and quality orientation
• Good communication and documentation skills
About the Company
• IQVIA is a global leader in clinical research, pharmacovigilance, and healthcare analytics, Supports pharmaceutical and biotech companies with end-to-end drug development services
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