Associate Director, Clinical Pharmacovigilance
Meet Life Sciences
Associate Director, Clinical Pharmacovigilance Safety – RTP, North Carolina Join a growing biotechnology organization focused on developing innovative therapies for patients with serious and unmet medical needs. As the Associate Director, PV Clinical Safety, you will play a critical leadership role in the oversight of clinical trial safety operations, ensuring rigorous SAE and AESI management while supporting global safety surveillance and benefit-risk management across clinical programs. Why Join Us? Strategic Leadership Opportunity: Lead clinical safety strategy across clinical trials, helping shape safety governance, operational excellence, and regulatory compliance. High-Impact Role: Oversee end-to-end processes, inspection readiness, vendor performance, and continuous process improvements across global programs. Mission-Driven Innovation: Contribute to the development of novel therapies for rare and serious diseases Who We’re Looking For We’re seeking an experienced Pharmacovigilance and Clinical Safety leader with expertise in clinical trial ICSR case management, SAE/AESI oversight, global GCP/GVP regulations and people leadership. Your Role & Impact As the Associate Director, you will: Provide strategic leadership and operational oversight for SAE and AESI across clinical trials Ensure end-to-end clinical trial case processing meets global GCP/GVP regulations, SOPs, Safety Management Plans, and industry standards Lead safety governance, inspection readiness, audit management, root cause analysis, and CAPA activities Drive process improvements in response to evolving regulatory requirements and business needs Lead and develop team members Key Qualifications Clinical Pharmacovigilance expertise 7–12+ years of Pharmacovigilance experience, depending on degree level, with strong end-to-end clinical trial ICSR case processing expertise Clinical trial oversight and vendor management experience Team leadership experience What We Offer Join a bold, purpose-driven biotechnology organization working to provide a brighter future for patients with rare and life-threatening diseases. You’ll have the opportunity to shape clinical safety operations, influence global pharmacovigilance strategy, and collaborate across development programs focused on innovative medicines. #J-18808-Ljbffr Meet Life Sciences
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