Associate Director Pharmacovigilance

argenx

Belgium
Not specified
8-13 years pharmaceutical industry experience
7+ years pharmacovigilance or drug safety expertise
Master's degree in pharmacy, nursing, or life sciences
Argenx is seeking an Associate Director of Pharmacovigilance to act as a scientific expert and resource for pharmacovigilance activities within Belgium and Switzerland. The role involves ensuring compliance with local and global safety regulations, managing pharmacovigilance systems, and collaborating with cross-functional teams to enhance patient safety processes

Job Summary

  • The role serves as a scientific expert and primary contact for pharmacovigilance within the assigned country or region.
  • Candidates will be responsible for ensuring adherence to local safety regulatory requirements while maintaining consistency with global standards.
  • The position involves leading the preparation of Pharmacovigilance Agreements and collaborating with cross-functional teams to support patient safety.

Matching Summary

Match Score: 85

Argenx is seeking an Associate Director of Pharmacovigilance to act as a scientific expert and resource for pharmacovigilance activities within Belgium and Switzerland. The role involves ensuring compliance with local and global safety regulations, managing pharmacovigilance systems, and collaborating with cross-functional teams to enhance patient safety processes.

Skills & Requirements

Must-have

  • 8-13 years pharmaceutical industry experience
  • 7+ years pharmacovigilance or drug safety expertise
  • Master's degree in pharmacy, nursing, or life sciences
  • Knowledge of GVP guidance documents and local regulations
  • Experience managing adverse event intake and monitoring

Nice-to-have

  • Excellent presentation and communication skills
  • Ability to influence multidisciplinary teams
  • Fluency in English required
  • Experience with health authority interactions
  • Strong problem-solving and critical thinking abilities

Key Requirements

  • Master's degree in pharmacy, nursing, healthcare, or life science
  • At least 8-13 years of total industry experience
  • Minimum 7 years of specific pharmacovigilance/drug safety experience
  • Proficiency with Microsoft Office Suite
  • Working knowledge of GXP quality and compliance requirements

Work Rights

Not specified

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