This position plays a role in the authoring, compilation and peer review of Amgen’s Periodic Aggregate Safety Reports (PASR) e.g. Development Safety Update Report (DSUR), Periodic Benefit Risk Evaluation Report (PBRER)/Periodic Safety Update Report (PSUR), Semi Annual Safety Update Report (SSUR), Periodic Adverse Drug Experience Report (PADER/PAER), Device PSUR, and country specific reports e.g. Korea PSUR, Brazil PSUR and Colombia Clinical Research Annual Safety Report Submission and Evaluation form. In compliance with global regulatory requirements. This role supports the end-to-end writing and documentation process and ensures timelines are met.

**Key Responsibilities:**
**Compilation and authoring of PASRs**
• Coordinate and schedule all meetings with cross-functional stakeholders to ensure effective collaboration and alignment
• Drive report timelines and escalate risks or delays to team leads or management
• Collaborate with cross-functional stakeho...