**The Position**

Are you ready to make a difference in drug safety? As a Senior Triage & Review Specialist, you will be a key expert in adverse event data processing, ensuring accurate and timely handling of safety information from various sources. Your work will directly shape the safety profile of our investigational and marketed drugs, supporting critical regulatory and post-marketing processes.
In this role, you’ll provide guidance to vendors, local PV colleagues, and peers, while collaborating with GPV risk management physicians. Additionally, you’ll have the opportunity to contribute to global safety platform projects or coordinate phase II and III clinical trials.
If you’re passionate about patient safety and thrive in a dynamic, impactful environment, we’d love to hear from you!

**Tasks & responsibilities**

+ You will guide case processing vendors, non-HCPs, peers, and physicians on adverse event intake, processing, and standard medical inquirie...