Jobs at Novartis

The Clinical Development Director leads clinical development programs, ensures execution of clinical trials, manages teams, and collaborates on regulatory submissions and data quality.

Lead global regulatory process transformation and continuous improvement initiatives. Design and maintain process documentation and metrics, assess regulatory impacts, implement system and technology improvements, and support change management, training, governance, risk management, and compliance across Regulatory Affairs.

Manage and enforce data governance frameworks, standards, and lifecycle controls across enterprise data platforms. Coordinate between business and technical teams to ensure data quality, access controls, lineage, reusability, and compliance in a regulated environment.

Lead the development of global labelling strategies for innovative medicines, ensuring compliance with regulatory requirements and alignment with product strategy, collaborating with cross-functional teams.

The Senior Scientific Writer II develops and delivers scientific materials, ensuring accuracy and compliance, while collaborating with cross-functional teams on content strategies.

Lead a newly created cross-process SME role to harmonize and strengthen global financial controls. Drive collaboration across process SMEs, IT application controls, auditors and methodology teams to enable system-enabled controls, S/4HANA transformations, automation, remediation and consistent control design, while managing projects, stakeholders and change.

Lead omnichannel content activation and customer journey orchestration across CRM and marketing platforms. Drive implementation of ICE, IpEx, and DRO frameworks, ensure launch readiness and execution excellence, manage events and budgets, enable AI-driven field force planning, enforce compliance and KPI tracking, and partner cross-functionally to optimize patient and payer engagement.

Lead planning, coordination, and execution of medical and scientific engagement activities (advisory boards, congresses, EEEs, meetings, education). Translate strategy into operational plans, manage vendors/logistics, ensure compliance and audit-ready documentation, track performance, and drive process standardization and cross-functional collaboration.

Lead regulatory intelligence to inform portfolio and regulatory strategy by monitoring global regulatory developments, producing strategic analyses, maintaining trackers and dashboards, driving AI-enabled tools adoption, partnering cross-functionally to escalate risks/opportunities, and representing Regulatory Intelligence in leadership forums.

Lead the legal strategy for Value & Access in international markets, advising on pricing, reimbursement, HTA, and public procurement while managing regulatory and access risks.

As Senior Counsel Antitrust, you will provide strategic antitrust advice, assist in M&A transactions, manage compliance, and monitor global antitrust developments.

The Senior Director Epidemiologist will lead global epidemiology strategies for oncology programs, inform benefit-risk decisions, and engage with health authorities while mentoring junior team members.

Lead a new cross-process SME role to harmonize and strengthen global financial controls. Drive collaboration with process owners, IT, auditors and operations to improve control design, enable system- and S/4HANA-driven controls, manage cross-process projects, and identify opportunities for automation and monitoring improvements.

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.

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.

Partner with Commercial and Value & Access teams to translate business strategy into actionable analytics questions. Lead primary and secondary market research, synthesize internal and external data, support forecasting, generate payer/access insights, and deliver dashboards and data-driven storytelling to senior stakeholders. Coordinate delivery across Data, Analytics & Platforms and external partners to ensure aligned insights and assumptions.

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.