Jazz Pharmaceuticals, Inc
Jazz Pharmaceuticals, Inc Benefits Overview
Compensation + Benefits
Offers 401(K)
Provides a pension
Offers life insurance
Offers accidental death & dismemberment insurance
Offers company equity
Offers performance bonuses
Offers employee stock purchase plan
Offers dental insurance
Offers health insurance
Offers Flexible Spending Account (FSA)
Offers vision insurance
Provides family medical leave
Offers generous parental leave
Company Culture
Provides commuter benefits
Provides free snacks and drinks
Offers a remote work program
Work-Life Balance + Wellbeing
Offers company-sponsored outings
Offers gym membership
Offers generous PTO
Provides paid sick days
Provides paid holidays
Provides bereavement leave
Career Growth + Development
Provides customized development tracks
Recently posted jobs
Biotech • Pharmaceutical
Leads global clinical trial start-up strategy, country and site activation planning, CRO and vendor oversight, performance analytics, risk mitigation, regulatory readiness, and process improvement. Partners cross-functionally to optimize timelines using historical, predictive, and real-world data. Oversees SSU team development, supports policies and training, and contributes to audit and inspection readiness. Requires 10%–20% US and international travel.
Biotech • Pharmaceutical
Provides scientific leadership and operational management for non-interventional pharmacoepidemiology studies, including post-marketing requirements and commitments. Responsibilities include literature searches, secondary data analysis, regulatory submission support, statistical analysis plans, CRO and data-provider management, budgeting, cross-functional coordination, and communication with regulatory teams. The role also contributes to forecasting, presents research findings, authors publications, and supports clinical development, safety, medical affairs, and regulatory activities.
Biotech • Pharmaceutical
Leads biostatistical strategy, design, analysis, validation, and reporting for Phase I–IV clinical trials and regulatory submissions. Develops statistical analysis plans, programs simulations and analyses, interprets data, and supports integrated reporting. Collaborates with clinical, data management, programming, regulatory, and research teams, including agency interactions. Manages external vendors, contributes to department standards, presents results, and may supervise statisticians and direct reports. Oncology experience, regulatory knowledge, and expertise in SAS, R, and CDISC standards are required.
