Drug Safety Specialist

This is a W2 requirement, Need independent candidates (USC/ GC) only. We are seeking a Drug Safety Specialist with 3–5 years of pharmacovigilance experience and a clinical background (RN, BSN, RPh, or PharmD) to support adverse event case processing for marketed and investigational products. The ideal candidate will manage end-to-end safety case processing, ensure compliance with FDA/ICH/GCP regulations, collaborate with cross-functional teams and CROs, and support clinical safety activities. Experience with Argus, ARISg, or similar safety databases , regulatory safety reporting, and oncology case processing is highly preferred. Required Skills & Qualifications: Clinical degree (RN, BSN, RPh, or PharmD) 3–5 years of Pharmacovigilance/Drug Safety experience Adverse Event (AE/SAE) case processing and safety surveillance FDA, ICH, GCP, and regulatory safety reporting knowledge Experience with Argus, ARISg, Clintrace, or similar safety databases Strong clinical judgment, communication, and organizational skills Oncology pharmacovigilance experience is a plus #J-18808-Ljbffr