Senior Pharmacovigilance Associate

Added
20 minutes ago
Type
Full time
Salary
Salary not provided

Related skills

ms office clinical trials pharmacovigilance meddra icsr
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๐Ÿ“‹ Description

  • 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)
  • Personal data protection

๐ŸŽฏ Requirements

  • Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in
  • Minimum 1 year of work experience in pharmacovigilance
  • 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

  • Make a difference by helping to bring safe and effective pharmaceutical treatment to patients
  • Join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and
  • Diverse and inclusive work environment
  • Culture built on kindness, flexibility, growth and belonging
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