Processing ICSR from all sources in compliance with regulations and PrimeVigilance procedures
Performing ICSR follow-up and SAE/SUSAR management tasks
Reconciliation (clinical, partners) and personal data protection
Product quality complaint handling and interaction with QA
Medical information interaction and MedDRA/WHO coding
Database outputs and reports for monthly client reporting

🎯 Requirements

Life science graduate, pharmacy, nursing, or related PV qualification/experience
Minimum 1 year of work experience in pharmacovigilance
Strong organization, attention to detail, and multitasking
Time and issue management skills
English - advanced (spoken, written)
Advanced literacy (MS Office)

🎁 Benefits

Join a global pharmacovigilance specialist with patient safety at the core
Collaborative culture across Europe, North America, South America, Asia, and Australia
Opportunity to grow and contribute to patient safety with a diverse team

Apply on employer's website

This employer gathers applications via their own applicant tracking system.

You will be redirected to an external application form.

Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Data Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Activate JobCopilot