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29 days ago
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Full time
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ms office english pharmacovigilance icsr management

📋 Description

  • Providing support to other activities undertaken by the project team on behalf of the client and
  • Performing activities in the scope of ICSR management unit within agreed extent and timeframe
  • Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable
  • Performing ICSR follow up
  • SAE/SUSAR Management (unblinding, clinical trial reconciliation, protocol review, Safety Management
  • Reconciliation (clinical, partners)

🎯 Requirements

  • Life science / bio medical background – healthcare related degree (chemistry, biology
  • Excellent communication (written and verbal) skills
  • Organization skills, including attention to details and multitasking
  • Delegation skills
  • Planning and time management
  • Technical skills

🎁 Benefits

  • Employee-centric culture built on kindness, flexibility, growth and belonging
  • Opportunity to work in a global pharmacovigilance specialist company
  • Role with real purpose and global reach
  • Chance to keep growing while helping protect patients
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