
1001 - 5000 employees
Founded 2003
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
Jazz Pharmaceuticals is a biopharmaceutical company dedicated to developing innovative medicines that address serious unmet medical needs. With a strong commitment to research and development, Jazz focuses on creating life-changing therapies, emphasizing the importance of collaboration, diversity, and employee engagement in its operations. The company prides itself on transforming patients' lives through its meaningful product offerings and a culture that fosters enthusiasm and flexibility.
🕒 November 6
🇬🇧 United Kingdom – Remote
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🇬🇧 UK Skilled Worker Visa Sponsor
👻 Ghost score 20%
Where this job comes from
Posted on Jazz Pharmaceuticals's careers page ↗, not through a job board
First seen by Remote Rocketship November 6
Still open on Jazz Pharmaceuticals's site. Checked 2 hours ago.

1001 - 5000 employees
Founded 2003
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
Jazz Pharmaceuticals is a biopharmaceutical company dedicated to developing innovative medicines that address serious unmet medical needs. With a strong commitment to research and development, Jazz focuses on creating life-changing therapies, emphasizing the importance of collaboration, diversity, and employee engagement in its operations. The company prides itself on transforming patients' lives through its meaningful product offerings and a culture that fosters enthusiasm and flexibility.
• 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 within IDASP • Serve as internal champion and subject matter expert for self-service analytics, modern visual frameworks, and interactive exploratory tools • Lead architecture, deployment, and enhancement of interactive patient profile viewers, safety signal surveillance interfaces, and cross-study medical monitoring suites • Direct dynamic study monitoring views tracking clinical parameters, adverse events of special interest, laboratory anomalies, query resolution trajectories, and subject disposition • Partner with Study Teams, Clinical Scientists, and Clinical Operations Leads to translate clinical questions into visual solutions • Support study-level data cleaning campaigns and review milestones • Oversee technical strategy, design standards, and lifecycle management for Spotfire, R/Shiny, Tableau, and Power BI environments • Collaborate with statistical programming and clinical data management to ingest, transform, and map EDC, central labs, biomarkers, CDISC SDTM, and ADaM data • Establish standardized visual libraries, reusable templates, and automated data refresh mechanisms • Define SOPs, documentation standards, and user validation frameworks • Evaluate visualization platforms and analytical tools • Oversee external vendors and CRO partners delivering dashboard and analytics assets • Represent IDASP in cross-functional forums, study team reviews, and technology steering committees
• Master’s degree or Ph.D. in Data Science, Health Informatics, Biostatistics, Statistics, Computer Science, or a related quantitative life sciences discipline • 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 • Proven expertise designing and delivering interactive clinical data dashboards and analytics solutions, including TIBCO Spotfire, R/Shiny, Tableau, or Power BI, for medical monitoring, safety reviews, or study execution • Strong proficiency in R, SAS, Python, or SQL • Thorough understanding of clinical trial workflows, Phase I–IV, EDC, eCOA/ePRO, lab data, biomarkers, CDISC SDTM, and ADaM • Demonstrated success 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 • Direct experience implementing centralized clinical trial monitoring dashboards, patient profile viewers, or safety surveillance tools for global clinical trials • Experience with clinical data ingestion platforms, data repositories such as elluminate or Medidata Detect, and validation in GxP environments is highly desirable
• Medical insurance • Dental insurance • Vision insurance • Retirement savings plan • Flexible paid vacation
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💰 $150M Post-IPO Equity on 2022-10
⏰ Full Time
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