Jobs at Novartis

Lead analytics for clinical trials by converting complex clinical data into actionable insights, partnering with data quality and monitoring teams, using visualization tools, advancing anomaly detection and risk‑based analytics, and implementing interventions to improve data quality and study timelines.

Lead adoption and continuous improvement of Risk-Based Quality Management (RBQM) for assigned clinical trials. Facilitate protocol risk assessments, define QTLs, maintain IQRMP documentation, monitor aggregate study data via RBQM systems, run risk review meetings, support audits/inspections, champion RBQM training and change, and drive cross-functional mitigation and continuous improvement to protect clinical quality (GCP).

Partner with business and talent teams to design, deliver, and govern Early Career programs across UK, Ireland and selected Europe. Build university partnerships, use data and analytics to measure impact, inform workforce planning, and enhance talent experience and capability building (including AI fluency). Drive stakeholder enablement and process excellence for scalable talent pipelines.

Lead the Regulatory Affairs Knowledge Management capability: define strategy and roadmap, drive adoption and change management, oversee product(s), vendor integrations, stakeholder governance, compliance and audit readiness, and ensure high-quality delivery and alignment with enterprise platforms.

Lead GCP compliance oversight for Novartis' EMEA Hub, managing audits, inspections, quality issues, risk monitoring, and CAPA. Coach and develop a high-performing team, partner with senior leaders to strengthen inspection readiness and operational excellence across clinical operations.

The Global Labelling Manager will develop and maintain global labelling documents, ensure compliance, and collaborate with teams for accurate product information.

The Global Labelling Associate Director will develop global labelling strategies, lead discussions, analyze competitor labelling, support regulatory queries, and mentor colleagues.

The role involves developing global labelling strategies, supporting consistent labelling content, and collaborating with cross-functional partners while mentoring colleagues.

The ESG FRA Process & Project Expert coordinates ESG reporting projects, supports governance, ensures compliance with regulations, and enhances non-financial reporting processes.

Lead end-to-end adaptation and localization of centrally developed promotional content for the Italian market. Manage stakeholders, agencies, DAM/MLR workflows, review cycles, timelines, and quality to ensure compliant, on-brand omnichannel customer experiences.

Lead strategic quality oversight for global clinical trials, implementing risk-based quality strategies, managing risk assessments and inspections, partnering across functions to resolve critical quality issues, establishing governance, and driving continuous improvement to ensure compliance, data integrity, and patient safety.

Develop and maintain production-grade R packages and Shiny apps to support clinical trial data engineering, analysis, automation, and reporting. Collaborate with statisticians and product owners, apply responsible AI to developer workflows, drive tooling rollout, document solutions, and engage open-source communities to modernize clinical reporting.

Provide strategic legal counsel for international neuroscience and gene therapy product portfolio. Lead negotiation and management of complex R&D and commercial agreements, mitigate regulatory and compliance risks, support BD and alliance integration, enable compliant communications, and build legal capability across cross-functional teams.

Serve as lead legal partner for the Breast Cancer Therapeutic Area, providing strategic legal guidance across commercial, medical, development, value and access. Draft, negotiate and manage complex R&D and commercial agreements; assess and mitigate regulatory and compliance risks; support business development and alliance management; review promotional and external materials; enable product launches and build legal capability across regions.

Lead statistical design, analysis, and methodology for neuroscience clinical trials. Develop protocols and SAPs, drive innovative methods, collaborate cross-functionally, and engage externally with regulators and scientific partners.

Lead strategic planning, development, and delivery of high‑quality neuroscience scientific content across international markets. Translate medical strategies into content roadmaps, ensure scientific accuracy and compliance, support launch readiness and lifecycle activities, collaborate with cross‑functional teams and vendors, drive content governance and modular approaches, and build team capability and operational excellence.

Lead development and delivery of HEOR and HTA strategies and evidence (cost-effectiveness, budget-impact, RWE, indirect comparisons) to support product access. Design and oversee HEOR studies, integrate access evidence into development plans, translate evidence into value narratives, collaborate across global cross-functional teams, and monitor HTA/payer trends to inform strategy.

Lead development and delivery of HEOR and HTA strategy and evidence (cost-effectiveness, budget impact, RWE, indirect comparisons, utility work) to support product value and access. Design and oversee HEOR studies, integrate access evidence into development plans, translate evidence into value narratives, and partner cross-functionally across global and regional teams while monitoring HTA trends.

Lead planning and operational oversight of therapeutic-area medical programs and budgets. Serve as central connector for Medical Directors and cross-functional partners, consolidate portfolio data and reports, drive operational excellence, manage meetings, track deliverables, mitigate risks, and ensure compliance and process adherence.

Lead end-to-end delivery of large-scale transformation initiatives for Advanced Quantitative Sciences, translating strategy into integrated roadmaps, governance, and measurable outcomes. Drive cross-functional alignment, influence senior stakeholders, implement scalable operating models, and champion change adoption through data-driven insights and capability building.