About the role

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

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JOB OVERVIEW

Experience level

Senior

Location

Alameda, CA

Occupation

Regulatory Affairs Specialists

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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