Associate Director, Pharmacovigilance Scientist
Job Description: • Supports Drug Safety Physician’s Safety Governance efforts by leading cross-functional Safety Management Team (SMT) • Leads/contributes to signal detection, monitoring, evaluation, interpretation, escalation, and appropriate communication of safety information • Maintains continuous monitoring and updates of safety profiles for assigned investigational and marketed products • Serves as point of contact for and collaborates with colleagues from Clinical Development, Regulatory Affairs, Biostatistics, and Data Management • Performs review of adverse event reports ensuring appropriate interpretation • Generates or assists with input to Analysis of Similar Events • Leads early identification of safety issues that require Safety Governance escalation • Prepares and presents individual case safety report issues and aggregate data analyses Requirements: • Minimum 8+ years of Pharmacovigilance and Risk Management experience required • Prior oncology industry experience preferred • Experience with early phase development preferred • Experience working in a fast-paced dynamic environment • Prior leadership or project management experience strongly preferred Benefits: • 401(k) plan • Medical insurance • Dental insurance • Vision insurance • Life and disability insurances • Flexible paid time off • 11 paid holidays • 80 hours of paid sick time Apply tot his job
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