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About the Role
This strategic and functional leadership role within the Integrated Data Analytics and Statistical Programming (IDASP) department is responsible for leading, defining, and driving enterprise-wide clinical data analytics and data visualization capabilities. The primary focus is to transform multi-source clinical trial data into dynamic, intuitive visual intelligence and self-service analytics suites that empower Clinical Development teams.
Responsibilities
- Establish, drive, and execute the functional vision and roadmap for clinical data analytics and data visualization across global development programs.
- Lead, mentor, and cultivate a high-performing team of clinical data analysts and visual analytics programmers.
- Serve as the internal champion and subject matter expert for self-service analytics, modern visual frameworks, and interactive exploratory tools.
- Lead the architecture, deployment, and ongoing enhancement of interactive patient profile viewers, safety signal surveillance interfaces, and cross-study medical monitoring suites.
- Direct the development of dynamic study monitoring views that track real-time clinical parameters, adverse events of special interest, laboratory anomalies, query resolution trajectories, and subject disposition.
- Partner closely with Study Teams, Clinical Scientists, and Clinical Operations Leads to translate complex clinical questions into elegant, reliable, and user-friendly visual solutions.
- Support study-level data cleaning campaigns and review milestones to expedite database locks and preserve continuous inspection readiness.
- Oversee the technical strategy, design standards, and lifecycle management for enterprise visual analytics environments.
- Collaborate with statistical programming peers and clinical data management to ingest, transform, and map disparate data sources into highly performant analytical views.
- Establish standardized visual libraries, reusable templates, and automated data refresh mechanisms.
- Define standard operating procedures, documentation standards, and user validation frameworks for visual analytics deliverables.
- Evaluate emerging visualization platforms and analytical tools; oversee external vendors and CRO partners.
- Represent IDASP in cross-functional forums, study team reviews, and strategic technology steering committees.
Requirements
- Proven expertise designing and delivering interactive clinical data dashboards and analytics solutions tailored for medical monitoring, safety reviews, or study execution.
- Strong proficiency in programming languages and tools used for clinical data wrangling and visualization, such as R, SAS, Python, or SQL.
- Thorough understanding of clinical trial workflows, phases (Phase I–IV), data streams (EDC, eCOA/ePRO, lab data, biomarkers), and foundational clinical data structures (CDISC SDTM and ADaM).
- Demonstrated success in recruiting, developing, and leading technical teams within a biopharmaceutical or clinical research organization.
- Exceptional communication, stakeholder management, and storytelling abilities.
- Thorough knowledge of Good Clinical Practice (GCP), 21 CFR Part 11 requirements, and quality control procedures for analytical and reporting outputs.
- Direct experience implementing centralized clinical trial monitoring dashboards, patient profile viewers, or safety surveillance tools in support of global clinical trials.
- Experience with clinical data ingestion platforms, data repositories, and validation in GxP environments is highly desirable.
Skills
- Clinical Analytics
- Data Visualization
- TIBCO Spotfire
- R/Shiny
- Tableau
- Power BI
- R
- SAS
- Python
- SQL
- Clinical Trial Workflows
- EDC
- eCOA/ePRO
- Biomarker Data
- CDISC SDTM
- CDISC ADaM
- People Leadership
- Stakeholder Management
- Good Clinical Practice (GCP)
- 21 CFR Part 11
- Clinical Data Ingestion Platforms
- Data Repositories
- GxP Environments
Location
- Remote
Work Type
- Full-time
Experience Level
- Director
- Minimum of 10 years of progressive experience in the biotechnology, pharmaceutical, or CRO industry
- At least 5 years in a dedicated people management and functional leadership role within clinical analytics or statistical programming
Education Level
- Master’s degree or Ph.D. in Data Science, Health Informatics, Biostatistics, Statistics, Computer Science, or a related quantitative life sciences discipline.
Salary/Compensations
- $203,200.00 - $304,800.00
Benefits
- Discretionary annual cash bonus or incentive compensation
- Discretionary equity grants
- Medical insurance
- Dental insurance
- Vision insurance
- 401k retirement savings plan
- Flexible paid vacation
About the Company
- Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families.
- We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options.
- We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments.
- Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience.
- Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide.
- Please visit www.jazzpharmaceuticals.com for more information.
Equal Opportunity
- Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.