Jobs at Jazz Pharmaceuticals, Inc

Leads the enterprise talent management strategy, including succession planning, talent assessment, performance enablement, career mobility, talent marketplaces, and leadership pipeline development. Partners with executives, HR business partners, People Analytics, HR Technology, and Learning & Development to build future-ready capabilities and implement modern talent systems. Translates talent data into executive recommendations and drives organizational agility, skills-based development, and continuous feedback practices.

Manages day-to-day operations for U.S. FDA-mandated REMS programs, ensuring regulatory compliance, governance, vendor performance, risk mitigation, documentation, and timely delivery. Coordinates cross-functional workstreams, facilitates governance meetings, tracks milestones and action items, supports audits and inspections, and drives process improvements. Requires pharmaceutical industry experience, project or program management experience, strong organizational and communication skills, and proficiency with Microsoft Office.

Leads statistical design, analysis, validation, and documentation for Phase I–IV clinical studies and regulatory filings. Develops statistical strategies, analysis plans, programs, and data displays; interprets results; validates CRO deliverables; supports regulatory agency interactions; and serves as a statistical subject matter expert across clinical development, medical writing, data management, and regulatory teams.

Leads Jazz Pharmaceuticals’ central monitoring function across sponsored clinical trials. Defines KRIs, statistical monitoring analytics, dashboards, and risk signals; translates findings into risk-based monitoring changes; oversees platforms, documentation, inspections, governance, and cross-functional collaboration. Manages and develops central monitoring staff while advancing RBQM methodology, automation, AI, and machine learning applications. Requires substantial pharmaceutical or biotechnology clinical operations experience, people leadership, and expertise with clinical trial data, monitoring systems, and ICH guidance.

Leads global Phase I-IV clinical trials from strategy through closeout, overseeing cross-functional teams, vendors, budgets, timelines, documentation, risks, and regulatory compliance. Acts as a subject matter expert during audits and inspections, ensures GCP and SOP adherence, manages trial systems and the Trial Master File, supports investigator meetings and data queries, and mentors clinical operations staff.

Leads global R&D resource management strategy, operating models, workforce planning, and portfolio analytics across pharmaceutical development. Oversees Planisware algorithm optimization, AI/ML-based FTE forecasting, Named Allocation deployment, dashboards, scenario modeling, and actuals-versus-forecast analysis. Partners with R&D leaders, finance, governance committees, and executives to resolve capacity constraints, prioritize investments, and align resources across the therapeutic portfolio. Directs and develops resource management and analytics teams.

Field-based pharmaceutical account leader responsible for portfolio-level engagement with healthcare stakeholders across access, care pathways, and healthcare systems. Builds relationships with centers of excellence and scientific experts, develops compliant account plans, drives sales performance, identifies market access opportunities, and coordinates Medical, Market Access, Marketing, and commercial teams. Uses CRM data, analytics, KPIs, and omnichannel engagement to optimize territory performance, while supporting national initiatives and capability building.

Lead hands-on development and delivery of end-to-end AI and GenAI solutions (RAG, vector stores, LLM integrations, ML pipelines). Write production-quality code, design architectures, optimize performance and cost, deploy and monitor models, establish MLOps and governance standards, mentor and manage a small AI development team, evaluate vendors, and help shape enterprise AI strategy and responsible AI practices.

Leads portfolio-level key account engagement across access, care pathways, and healthcare systems in Ontario. Builds partnerships with healthcare professionals, thought leaders, and senior stakeholders; develops account plans; drives compliant portfolio promotion, sales performance, and market access initiatives. Uses CRM data, analytics, and KPIs to optimize engagement, collaborates cross-functionally with Medical, Market Access, Marketing, and Scientific teams, and contributes to national projects and capability building.

Leads statistical design, analysis, validation, and reporting for Phase I–IV clinical studies. Develops statistical analysis plans and programs, supports regulatory filings and agency interactions, validates CRO deliverables, and collaborates with clinical, regulatory, medical writing, data management, and programming teams. Oversees external vendor statistics and programming work while applying clinical trial methodology, regulatory requirements, and CDISC standards.

Promotes Jazz Pharmaceuticals oncology products across the Los Angeles territory, including Hawaii, while managing strategic relationships with physicians, healthcare providers, and complex academic and community accounts. Develops account plans, analyzes sales and market data, collaborates with marketing, medical affairs, and market access teams, educates providers on approved therapies, and executes compliant promotional activities. Requires oncology expertise, frequent travel, strong account management, communication, presentation, and business analytics skills.

Leads Jazz Pharmaceuticals’ global corporate communications strategy, advising the C-suite, shaping executive visibility, employee communications, corporate brand, media relations, digital communications, and reputation management. Oversees change communications, agency relationships, measurement, and development of a high-performing communications team. Requires extensive biopharmaceutical communications leadership and experience navigating M&A, crises, and transformation in public-company environments.

Develop and execute Jazz Pharmaceuticals’ global corporate social media strategy across owned channels. Create compliant copy, graphics, video, and short-form content; manage editorial calendars, community engagement, social listening, executive presence, paid campaigns, and crisis support. Partner with Legal, Medical Affairs, HR, Investor Relations, and agency teams to ensure accurate messaging. Define KPIs, report performance, and optimize content and channel strategy while supporting reputation, patient engagement, and talent attraction.

Leads global nonclinical and investigative toxicology for pharmaceutical development programs. Designs and oversees GLP and non-GLP studies at CROs, interprets toxicology and PK/PD data, prepares regulatory submission content, responds to health authority inquiries, and represents toxicology on cross-functional teams. The role requires expertise in drug development toxicology, regulatory strategy, CRO management, scientific writing, and safety assessment for small and large molecules.

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.

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.