Remote
•
2d ago
Required Experience & Qualifications: 58 years of hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains Hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains Strong understanding of CSA principles, CSV, and SDLC processes Experience authoring and/or reviewing validation documentation Working knowledge of GxP regulations (e.g., FDA, EMA, ICH) and da
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Contract
Depends on Experience


















