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ms office english japanese pharmacovigilance meddra
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📋 Description

  • Support PV processes within ICSR management scope
  • Process ICSRs per regulations and timelines
  • Follow up on ICSR activities
  • Manage SAE/SUSAR and reconciliation tasks
  • Handle data protection and QA interactions
  • Contribute to reports and resource management

🎯 Requirements

  • Life science or healthcare qualification
  • 1+ year pharmacovigilance experience
  • Strong organization and multitasking skills
  • Time and issue management capabilities
  • Japanese: Advanced; English: Conversational
  • Advanced MS Office skills

🎁 Benefits

  • Global pharmacovigilance environment
  • Collaborative and inclusive culture
  • Opportunity to grow in PV and regulatory fields
  • Localization to country-specific responsibilities
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