Transform complex clinical data into intelligent, actionable insights that inform decision-making across Clinical Trial Teams
Drive collaboration across Data Quality Teams to enhance data strategy, data quality, site experience, and patient safety utilizing the Disease Area, Data Standards & Protocol Knowledge.
Partner with Central Monitoring (CM) and Data Management) Leads to promote risk-based data review approaches within CDO.
Leverage data analytics and visualisation tools such as Power BI and Spotfire to uncover trends, patterns, and emerging risks
Contribute to advanced data quality initiatives such as anomaly detection and continuous improvement of insight generation capabilities
Drive risk‑based analytics by proactively identifying Critical-to-Quality (CtQ) risks and prioritizing data review through advanced analytical approaches.
Implement operational interventions that enhance data quality and accelerate study cycle times.
Essential Requirements:
Extensive experience in clinical data operations within clinical trials, with strong understanding of clinical trial delivery. Ideally a minimum of 10-12 years working experience in a Life Sciences environment with extensive exposure to Clinical Trials and Clinical Operations
Proven track record in driving operational excellence within pharmaceutical or clinical research environments
Proven industry-based experience in clinical data management, clinical programming, RbQM, analytics, and technology transformation.
Strong ability to generate intelligent, data-driven insights and influence decision-making across clinical teams
Experience using data visualisation tools such as Power BI, Spotfire, or similar platforms to uncover trends and insights
Demonstrated capability in data storytelling, translating complex data into clear, impactful narratives for stakeholders
Knowledge of technology transformation, including automation, cloud platforms, and business intelligence tools, with awareness of programming languages such as SAS, R, or Python
Fluent written and verbal English essential
Skills Desired
Benefits
Remote work options
Additional Information
Job Description Summary
#LI-Hybrid
This role can also be offered on a remote working basis for UK, subject to eligibility criteria.
Location: Westworks, London, United Kingdom
Other Locations: Dublin, Ireland
This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible. Novartis cannot sponsor visas for these locations.
This role is also available in Dublin, Ireland. Please apply to the advertisement for this location. For London we offer a Hybrid working arrangement with an expectation of 12 days per month onsite. Remote working arrangement can be considered, subject to eligibility criteria. If your location is only suitable for remote work this can be discussed during the interview process.
Step into a role where your insight can directly improve the way clinical trials are understood, managed, and advanced. As Clinical Data Analytics Lead, you will turn complex clinical trial data into clear, meaningful stories that help teams act earlier, think smarter, and raise the quality of decisions across Clinical Data Operations. Working at the intersection of analytics, data quality, and trial execution, you will help uncover patterns, trends, and opportunities that strengthen study oversight, support risk-based approaches, and bring fresh, actionable insight to the teams shaping patient outcomes.
Job Description
Novartis · London (the Westworks)