- Perform end-to-end ICSR case processing (Spontaneous / Clinical Trial / Literature cases)
- Execute accurate data entry activities as part of core responsibilities (initial phase)
- Handle case workflows including triage, data entry, coding, narrative writing, and submission readiness
- Ensure compliance with global pharmacovigilance guidelines, SOPs, and regulatory requirements
- Perform quality checks (QC) on processed cases based on experience and performance.
📌 Drug Safety Specialist I / II (Hyderabad)
🏢 Syneos Health
📍 Hyderabad
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