Exelixis is seeking a Drug Safety Specialist to provide pharmacovigilance expertise and ensure high-quality safety documentation for SAEs within the Argus system. This role oversees vendor interactions and ensures compliance with global regulations and internal procedures.
Responsibilities include: SAE processing from receipt to closure, MedDRA coding, and quality reviews with the Drug Safety Physician. Collaboration with Clinical Development, Data Management, Regulatory Affairs, and Project

Matching similar jobs

Level

Senior L5

Location

Alameda, CA

Occupation

Regulatory Affairs Specialists

Industry

Pharmaceutical Preparation Manufacturing

Posted

2 days ago

APPLY NOW