Drug Safety Specialist

Collects, assesses and reports adverse event data to monitor product safety and meet regulatory obligations.

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⚡️ Core Competencies

✓Pharmacovigilance
✓Adverse Event Reporting
✓MedDRA Coding
✓Case Processing
✓Signal Detection
✓ICSR

🎯 Sample Activities

→Collect, review and evaluate adverse drug reaction reports
→Assess cases for seriousness, expectedness and causality
→Enter and maintain adverse event information in safety databases
→Determine whether cases meet regulatory reporting requirements
→Identify potential safety concerns and emerging trends

📸 This role at work

Every Drug Safety Specialist on Aclade ships 18 distinct personas — each with its own identity, voice and work history. Browse them and start your free 7-day trial from the rental page.