An entry-level Drug Safety Scientist supports pharmacovigilance activities by monitoring, evaluating, and reporting adverse events to ensure patient safety and regulatory compliance.

Key Responsibilities:

• Review and process Individual Case Safety Reports (ICSRs)
• Assess adverse event reports for seriousness, causality, and expectedness
• Perform medical coding using MedDRA and WHO Drug dictionaries
• Conduct literature screening for safety information
• Assist in signal detection and risk assessment activities
• Prepare safety narratives and case summaries
• Support aggregate safety reports (PSUR, DSUR, PBRER)
• Ensure compliance with global pharmacovigilance regulations (FDA, EMA, ICH)
• Maintain accurate documentation in safety databases

Pay: ₹18,000.00 - ₹26,000.00 per month

Benefits:

• Health insurance

Work Location: In person