Director, Central Monitoring & RBQM Analytics

Jazz Pharmaceuticals; Philadelphia (Philadelphia County); On-site; USD 165,000 - 247,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

401k retirement savings plan

Flexible paid vacation

Job summary

Jazz Pharmaceuticals is seeking an Associate Director, Central Monitoring to lead our central monitoring capability within Global Clinical Development Operations. You will define and interpret centralized data outputs, KRIs, and signals, translating insights into risk-proportionate monitoring strategies across studies, sites, and CRAs.

You'll partner with Trial Risk Management, Site Monitoring, Data Management, and IT to advance RBQM, develop analytics dashboards, and drive continuous

Qualifications

• Typically 8-10+ years in clinical research/operations with RBQM exposure.
• Experience defining KRIs and translating data signals to monitoring decisions.
• Solid knowledge of ICH E6(R2/R3) and global regulatory requirements.
• Hands-on with central monitoring analytics, CTMS, and EDC systems.

Responsibilities

• Lead and manage central monitoring to provide data-driven oversight across trials.
• Define and maintain KRIs and analytics dashboards at study/site/CRA levels.
• Analyze data trends to adjust monitoring strategies and resource deployment.
• Document risk-based monitoring changes and partner with leadership to operationalize them.
• Support RBQM strategy, monitoring plans, and training in collaboration with senior leaders.

Skills

Clinical research experience

RBQM expertise

Data analytics

Leadership experience

Regulatory knowledge

Communication skills

Travel willingness

Education

Bachelor's degree in life science

Advanced degree preferred (MS/ MPH)

Tools

CTMS

EDC systems

Statistical analytics platforms

Central monitoring platforms

Job description

Jazz Pharmaceuticals is seeking an Associate Director, Central Monitoring to lead our central monitoring capability within Global Clinical Development Operations. You will define and interpret centralized data outputs, KRIs, and signals, translating insights into risk-proportionate monitoring strategies across studies, sites, and CRAs.

You'll partner with Trial Risk Management, Site Monitoring, Data Management, and IT to advance RBQM, develop analytics dashboards, and drive continuous