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Associate Director, Central Monitoring

Jazz Pharmaceuticals
October 2, 2026
Full-time
Remote friendly (Philadelphia, PA)
Worldwide
Clinical Research and Development
Role: Associate Director, Central Monitoring within Jazz's Global Clinical Development Operations, responsible for leading centralized, data-driven oversight of clinical trials. Objectives include defining and interpreting portfolio-level risk indicators and signals, and translating insights into risk-proportionate monitoring strategies. Responsibilities encompass managing the central monitoring team, developing and maintaining KRIs and analytics dashboards, analyzing data trends to inform monitoring adjustments, and ensuring documentation readiness for audits and inspections. The role involves partnering with Trial Risk Management, Site Monitoring, Data Management, and IT teams, while championing technological enhancements, automation, and AI in risk detection. The candidate will also present findings to senior leadership and support strategy development aligned with ICH E6(R2/R3) guidelines. Qualifications: 8-10+ years in clinical operations or research, with extensive experience in risk-based quality management and statistical monitoring; proficiency with analytics platforms, CTMS, and EDC systems; strong data interpretation and stakeholder communication skills; and prior management experience. Preferred qualifications include a relevant advanced degree and experience in biotech or pharma, especially in oncology or neuroscience. The position involves global collaboration and may require international travel.