Role & Responsibilities
• ICSR case intake and data entry
• MedDRA coding and safety database management
• Case processing and regulatory submissions
• Compliance with global PV regulations (ICH, GVP)
Qualification: B.Pharm / Life Sciences
Experience: 0-1 year (Freshers eligible)
Skills
• Knowledge of Pharmacovigilance operations
• Familiarity with MedDRA coding and safety databases
• Attention to detail and compliance-driven mindset
• Ability to work in rotational shifts
About The Company
• Accenture offers structured learning and growth opportunities in pharmacovigilance.
• The company specializes in life sciences regulatory services and has a strong global presence.
• Accenture works with leading biopharma clients and promotes an inclusive work culture.
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