A New Jersey-based biotech company is actively seeking a new Associate Director of Global Drug Safety & Pharmacovigilance Data Management to join its growing team. About the Opportunity: Schedule: Full-time Hours: Standard business Setting: Hybrid (at least 2 days a week onsite) Responsibilities: Triaging and reviewing Argus configuration requests Conducting strategic UAT, including test planning and execution Ensuring compliance with ICH E2B(R2) and (R3) conventions Managing communication with