Added
11 days ago
Type
Full time
Salary
Salary not provided

Related skills

quality assurance pharmacovigilance meddra medical information sae

πŸ“‹ 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

  • Opportunity to make a difference by helping to bring safe and effective pharmaceutical treatment to
  • Join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and
  • Culture built on kindness, flexibility, growth and belonging
  • Values: Quality, Integrity and trust, Drive and passion, Agility and responsiveness, Belonging
  • Global reach and the chance to keep growing while you help protect patients
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