Offer summary
Qualifications:
Fluency in multiple European languages, Minimum 2 years Pharmacovigilance experience, Strong knowledge of Pharmacovigilance practices and regulations, Experience with case processing activities, Proficiency in using Pharmacovigilance databases.
Key responsabilities:
- Review adverse event reports and safety-related information
- Perform case processing, signal detection, and reporting
- Collaborate with cross-functional teams
- Contribute to process improvement and training
- Maintain regulatory compliance and standards