Jobs at Jazz Pharmaceuticals, Inc

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.

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.

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.

Oversee US corporate tax operations, including ASC 740 tax accounting, federal and state compliance, audit defense, tax planning, international tax matters, M&A support, and tax governance. Lead external tax advisors, manage cross-functional projects, support acquisitions and integrations, maintain SOX controls, and provide technical guidance on complex US, Canadian, and Japanese tax issues.

Establish and mature a global FP&A Planning Excellence capability, including planning governance, forecasting methodologies, budgeting and rolling forecast cadence, accrual and actuals controls, and continuous improvement. The role leads Oracle EPM adoption, planning process standardization, automation, stakeholder alignment, and SOX-related governance. It also manages and develops approximately ten finance professionals, builds succession capability, and implements a sustainable operating model across Global Finance during a 12-month fixed-term assignment.

Manages neurology pharmaceutical accounts and territories, builds relationships with healthcare providers and epilepsy centers, executes promotional and market plans, analyzes sales and customer data, collaborates cross-functionally, manages budgets, and supports patient advocacy initiatives while maintaining regulatory compliance.

Analyze pharmaceutical secondary data and support primary market research to generate actionable insights for brand strategy, performance tracking, customer journeys, and business decisions. Develop dashboards, reports, segmentation analyses, and analytical frameworks while validating data quality. Collaborate with Commercial, Medical, Market Access, data strategy, and technology teams to interpret customer, competitive, and market trends across HCP, patient, payer, and other stakeholder groups.

Delivers customer analytics and market research insights supporting pharmaceutical franchise strategy, brand planning, performance tracking, and business decisions. Analyzes claims, EHR/EMR, specialty pharmacy, prescription, CRM, and omnichannel data; develops dashboards and analytical tools; conducts qualitative and quantitative research; and translates findings into actionable recommendations. Collaborates with Commercial, Medical, Market Access, data strategy, and technology teams in a matrixed environment.

The Associate Director leads enterprise leadership development and field skills enablement across medical, market access, sales, operations, and marketing. Responsibilities include creating leadership curricula and competency models, advising executives, designing role-based learning, supporting capability and change initiatives, using data to improve decision-making, measuring learning impact, presenting readiness insights, and mentoring L&D colleagues. The role requires extensive cross-functional collaboration in a regulated pharmaceutical environment and involves 50–60% travel.

Leads EU and international omnichannel campaign orchestration for pharmaceutical brands. Translates customer, brand, and audience strategies into coordinated cross-channel engagement plans, media strategies, sequencing, and next-best-action frameworks. Partners with brand, medical, analytics, field, market access, and CX teams to activate campaigns, monitor performance, manage KPIs, adapt capabilities to regional requirements, and continuously improve customer journeys and engagement outcomes.

Leads global Phase I–IV clinical trials from planning through closeout, overseeing study teams, vendors, timelines, budgets, risks, documentation, compliance, and trial systems. Develops and reviews protocols, consent forms, monitoring plans, and clinical study reports; supports investigator meetings, audits, inspections, and IMP shipment authorization. Provides portfolio-level updates, leads cross-functional working groups, manages escalations, and mentors clinical operations staff while ensuring adherence to GCP, SOPs, and regulatory requirements.

Manages security governance, risk, compliance, and control programs for enterprise SaaS and PaaS platforms. Coordinates security initiatives, control frameworks, audits, assessments, exceptions, vendor risk reviews, and continuous monitoring. Partners with IT, security, compliance, business, IAM, data governance teams, and vendors to improve platform security, access controls, data protection, and compliance maturity. Reports risks, metrics, KRIs, and compliance status to leadership while supporting secure adoption across Workday, Salesforce, Snowflake, ServiceNow, and Microsoft 365.

The Specialty Sales Consultant promotes Jazz Pharmaceuticals' products, develops relationships with specialists, and meets sales targets while complying with regulations and ethical standards.

Lead delivery of advanced analytics models (segmentation, propensity, attribution) to inform omnichannel investment and commercial decisions; productionize reusable pipelines, ensure quality, collaborate with cross-functional teams, and drive measurable business impact.

Lead the Voice of Customer operations to aggregate and synthesize cross-channel feedback (e.g., NPS), drive closed-loop actions, establish enterprise feedback loops, partner with cross-functional teams, prioritize high-impact opportunities, and use insights to improve patient, HCP, and commercial experiences with measurable outcomes.

The Principal will lead data engineering projects, support pipeline development, ensure compliance with regulations, and collaborate with researchers to meet data requirements.

The Senior Compliance Officer will manage compliance risks, provide insights for R&D and Tech Ops, and ensure adherence to relevant laws and regulations. They will coordinate with various departments, develop training materials, and support compliance initiatives globally.

Responsible for leading the oncology pharmacology team from discovery to regulatory approval, managing programs, and designing experiments to evaluate drug efficacy and mechanisms of action.

The Oncology Activation Lead translates brand needs into operational plans, drives adoption of capabilities across teams, and ensures effective execution of marketing strategies within the Oncology franchise.

Manages global CMC regulatory strategy, submissions, and agency responses for biological products across development and commercial lifecycles. Prepares and reviews CTD Modules 2 and 3, coordinates regulatory timelines, performs risk assessments, supports agency and partner meetings, maintains product information, verifies electronic publishing, ensures regulatory compliance, and drives continuous improvement. Requires strong knowledge of CMC regulations, eCTD submissions, FDA, EMA, and ICH guidelines.