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