Role & Responsibilities
• Perform medical review of Individual Case Safety Reports (ICSRs) from spontaneous and organized data sources
• Support review of trial-related adverse events and post-marketing adverse drug reactions
• Ensure narrative consistency, seriousness, expectedness, and completeness of clinical information
• Support MedDRA coding of adverse events under guidance
• Assist with causality assessment and labeling evaluation
• Collaborate with senior medical reviewers and team leads to ensure medical accuracy
• Participate in quality checks and identify improvements in case documentation
• Support audit and inspection readiness through compliant documentation
• Contribute to internal trainings, workshops, and knowledge-sharing initiatives
• Stay updated on evolving pharmacovigilance regulations and practices
Qualification
• Medical degree (MBBS or equivalent)
• Valid medical license to practice
Experience
• 1–2 years of clinical experience
• Prior exposure to pharmacovigilance or medical review required
• Interest in drug safety, clinical data, and regulatory science
Skills
• Strong medical judgment and attention to clinical detail
• Understanding of pharmacovigilance processes and ICSR workflows
• Ability to apply MedDRA coding principles
• Strong written and verbal communication skills in English
• Collaborative mindset with ability to work in global teams
• Process-oriented and quality-focused approach
About the Company
• Teva is a global biopharmaceutical company combining innovative medicines with a strong generics portfolio
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