Remote Pharmacovigilance ICSR Consultant II
Tailored Management
Tailored Management is seeking an experienced Clinical Trial Consultant II to support pharmacovigilance operations. The role focuses on processing and QC of ICSRs from trials and post-marketing sources, ensuring accurate documentation and timely regulatory reporting. The candidate should have hands-on pharmacovigilance case processing experience, knowledge of MedDRA coding, and familiarity with safety databases like Argus, ArisG, or Veeva. #J-18808-Ljbffr
Vacancy posted 2 days ago
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