Associate Director Pharmacovigilance

argenx

Belgium
**
8-13 years pharmaceutical industry experience
7+ years pharmacovigilance/drug safety expertise
Master's degree in pharmacy or life sciences
** Argenx is seeking an Associate Director of Pharmacovigilance to serve as a scientific expert and resource for pharmacovigilance within the company and its external partners. The ideal candidate will have significant experience in the pharmaceutical industry, particularly in pharmacovigilance, and will help ensure compliance with local and global safety regulations. **

Job Summary

  • This role serves as the scientific expert and primary point of contact for pharmacovigilance within the assigned country or region.
  • The successful candidate will manage safety information intake, ensure regulatory compliance, and lead the preparation of Pharmacovigilance Agreements.
  • The position requires close collaboration with cross-functional teams including regulatory, medical, legal, and quality departments to support patient safety.

Matching Summary

Match Score: 75

** Argenx is seeking an Associate Director of Pharmacovigilance to serve as a scientific expert and resource for pharmacovigilance within the company and its external partners. The ideal candidate will have significant experience in the pharmaceutical industry, particularly in pharmacovigilance, and will help ensure compliance with local and global safety regulations. **

Skills & Requirements

Must-have

  • 8-13 years pharmaceutical industry experience
  • 7+ years pharmacovigilance/drug safety expertise
  • Master's degree in pharmacy or life sciences
  • Knowledge of GVP guidance documents
  • Fluency in written and spoken English

Nice-to-have

  • PharmD or MD degree preferred
  • Experience with neonatal Fc receptor blockers
  • Strong presentation and communication skills
  • Ability to work in a global environment
  • Proficiency with Microsoft Office Suite

Key Requirements

  • Master's degree in pharmacy, nursing, healthcare, or life science
  • Minimum 8-13 years total industry experience
  • At least 7 years specifically in pharmacovigilance or drug safety
  • Working knowledge of local/regional safety regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter