IQVIA Holdings Is Hiring A Pharmacovigilance Specialist

Join our team as a Safety Data Analyst and contribute to the critical process of managing safety data across multiple service lines in a multilingual environment. 🌍

About the Role

In this role, you will review, assess, and process safety data from diverse sources, ensuring accurate distribution of reports and data to internal teams and external partners. You'll operate under established SOPs, regulations, and guidelines, with support from senior team members. Fluency in English, Spanish, and German (or French) is essential for success in this trilingual position.

Main Responsibilities

• Process safety data according to applicable regulations, guidelines, SOPs, and project-specific requirements.
• Perform pharmacovigilance activities: collecting and tracking adverse events (AEs) and endpoint information, determining the status of incoming events, database entry, coding AEs and products, writing narratives, and managing literature-related activities.
• Ensure compliance with quality, productivity, and delivery standards aligned with project needs.
• Collaborate with cross-functional teams and healthcare professionals to address project-related issues effectively.

Qualifications

• Bachelor's degree in Life Sciences or a related field (mandatory)
• Fluency in English and German or French (mandatory); proficiency in a third language at B2 level is acceptable if you can achieve a minimum C1 in English (assessment will be conducted)
• Up to 3 years of clinical experience (preferred)
• 1 year of pharmacovigilance experience is highly valued (preferred)

What We Offer To You 🚀

• OSDE 310
• Annual performance-based bonus
• Salary adjustments throughout the year aligned with inflation
• 21 vacation days
• Work flexibility
• 🔒 100% remote role — work from anywhere!