Safety Data Lead I
HybridNo visa sponsorship
Core
Analysis and interpretation of adverse event (AE) reports for investigational and marketed products in compliance with regulatory requirements.
Role type
Safety Data Lead (Pharmacovigilance)
Builds
Adverse event case management activities
Domain
Life Sciences / Pharmacovigilance
Required skills
Clinical Data Management, Data Processing, Data Review, Data Validation, Pharmacovigilance
Preferred skills
Drug Research, Japanese to English Translation
Technologies
None stated
Responsibilities
Performing analysis, interpretation, and data entry of adverse event reports from various sources; Collaborating with internal and external stakeholders to resolve issues and ensure compliance; Supporting simplification and optimization of case management activities.
Seniority
Individual Contributor (Lead level)
