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About the Company
• Cencora is a global healthcare solutions organization specializing in Pharmacovigilance, regulatory compliance, and patient safety services
• Works with leading pharmaceutical and life science companies across international markets
About the Role & Responsibilities
• Perform medical review and clinical assessment of Individual Case Safety Reports (ICSRs)
• Evaluate narratives, seriousness criteria, MedDRA coding, and causality
• Review and prepare PSURs, PBRERs, and Risk Management Plans (RMPs)
• Conduct literature screening and medical triage
• Support signal detection and risk evaluation activities
• Ensure compliance with ICH, GVP, and regulatory guidelines
• Provide medical oversight and mentor PV associates
Qualification
• MBBS (Postgraduate qualification preferred)
Skills
• Strong knowledge of pharmacovigilance regulations
• Expertise in ICSR medical review and aggregate report writing
• MedDRA coding and causality assessment
• Risk management and signal detection understanding
• Excellent communication and documentation skills
Experience
• Minimum 3+ years in Pharmacovigilance / Drug Safety
Salary
• Competitive salary package
Benefits
• Global pharmacovigilance project exposure
• Leadership and career advancement opportunities
• Continuous learning and professional development