Argenx is seeking an Associate Director of Pharmacovigilance to serve as a key scientific expert and resource for pharmacovigilance activities in Belgium and Switzerland. The ideal candidate will have extensive experience in drug safety, strong leadership skills, and the ability to communicate effectively across multidisciplinary teams
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 establishing local PV systems, ensuring compliance with regional regulations, and supporting global harmonization efforts.
The position involves managing adverse event intake, leading Pharmacovigilance Agreements, and collaborating cross-functionally to ensure patient safety.
Matching Summary
Match Score: 85
Argenx is seeking an Associate Director of Pharmacovigilance to serve as a key scientific expert and resource for pharmacovigilance activities in Belgium and Switzerland. The ideal candidate will have extensive experience in drug safety, strong leadership skills, and the ability to communicate effectively across multidisciplinary teams.
Skills & Requirements
Must-have
8-13 years pharmaceutical industry experience
7+ years pharmacovigilance/drug safety expertise
Knowledge of GVP guidance documents
Master's degree in pharmacy or life sciences
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
At least 8-13 years total industry experience
Minimum 7 years in pharmacovigilance or drug safety
Working knowledge of GVP guidance and regulatory requirements