Added
11 minutes ago
Type
Full time
Salary
Salary not provided

Related skills

pharmacovigilance ivrs meddra sae susar
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๐Ÿ“‹ 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)

๐ŸŽฏ Requirements

  • Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in
  • 0-1 year of experience in pharmacovigilance, desirable but not required
  • Organization skills, including attention to detail and multitasking
  • Management skills, including time and issue management
  • English - advanced (spoken, written)
  • Advanced literacy (MS Office)

๐ŸŽ Benefits

  • We offer a role with global reach in a patient-centered pharmacovigilance environment
  • Collaborative team culture with focus on flexibility, growth and belonging
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