Drug Safety Specialist III — Argus & SAE Expert
Exelixis
Exelixis in the United States is seeking a Drug Safety expert responsible for managing SAEs and ensuring high-quality safety documentation in the Argus system. You will lead case processing, MedDRA coding, QA reviews, and coordination with Clinical Development, Regulatory Affairs, and Data Management, with oversight of study operations from start-up to close-out. The role also includes training staff, scheduling submissions, and contributing to safety study plans, with a comprehensive benefits #J-18808-Ljbffr Exelixis
Vacancy posted 8 hours ago
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