Jobs at Novartis

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.

Partners with Therapeutic Area leaders to support strategic planning, investment decisions, portfolio performance, budgeting, forecasting, and reporting. Translates financial data into actionable recommendations, identifies risks and opportunities, builds cross-functional relationships, improves financial processes, and promotes AI-enabled innovation within Finance.

Leads end-to-end medical safety strategy for global pharmaceutical programs across development and lifecycle management. Identifies and evaluates safety signals, chairs safety management teams, prepares regulatory safety documents and reports, guides benefit-risk assessments, supports health-authority interactions, and embeds safety insights into labeling and lifecycle decisions. The role also ensures compliant governance and mentors colleagues.

Conduct all-source intelligence collection and analysis to identify security, geopolitical, crime, reputational, and disruptive risks. Produce threat assessments, executive briefings, and actionable intelligence supporting executive protection, business continuity, and enterprise risk management. Use AI-enabled capabilities, structured analytical techniques, OSINT, and social media intelligence while supporting AI governance, source evaluation, and analytical standards. Build partnerships with internal stakeholders and external security networks.

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.

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.

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.

Lead GCP compliance for global clinical operations, managing quality issues, audits, inspection readiness, self-assessments, risk assessments, and cross-functional investigations to ensure patient safety, data integrity, and regulatory adherence across a portfolio.

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.

Design, build, and deploy AI and automation solutions to accelerate clinical trial data workflows. Develop scalable document processing, data extraction, and analytical tools, ensure regulatory and data-quality compliance, and provide technical leadership to drive adoption across scientific teams.

Lead customer-centric content and marketing strategy for the renal franchise, translating disease, patient and HCP insights into omnichannel campaigns, congress plans, and measurable engagement. Manage brand-content lifecycle, agencies, budgets, cross-functional stakeholders, and performance optimization to support launches, lifecycle management, and regional commercial execution.

Lead development and execution of data strategy plans for clinical programs, support assessment selection and data collection consistency (especially in Neuroscience), perform early data landscaping using internal/external sources, advise on clinical assessments and risks, and provide downstream data oversight to enable data-driven decisions and smooth handoff to trial teams.

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

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

Lead strategy, planning and end-to-end execution of clinical document migrations across enterprise eDMS platforms. Partner with internal and external stakeholders, oversee vendor activities, manage incident/change management, support audits and CAPAs, and drive migration governance, roadmaps and resource forecasting to enable eTMF consolidation and compliant transfers.

Lead and coordinate statistical programming across complex clinical programs (Phase I-IV). Develop programming strategy, adopt tools (R, Tidyverse, Shiny, Git, AI-enabled), ensure quality, validation, and audit readiness, manage resources and mentor programmers, and represent statistical programming in cross-functional teams and submissions.

Lead statistical programming across clinical studies and programs, coordinate internal/external programmers, develop and validate datasets and regulatory-ready outputs, enforce CDISC and quality standards, implement reproducible Git-based workflows, contribute to analysis plans and programming specifications, and drive adoption of modern tools and automation.

Provide GCP compliance oversight for clinical programs and trials, advise clinical teams on complex regulatory scenarios, lead investigations and root-cause analysis, coordinate inspection readiness and CAPA, monitor portfolio trends, deliver self-assessments, and collaborate cross-functionally to ensure data integrity and quality across global clinical operations.

Provide strategic legal advice to commercial, medical, and market access teams; draft, review and negotiate commercial agreements; advise on pharmaceutical regulation, compliance, disputes, and governance; deliver legal training and improve legal processes and technology.

Lead global regulatory strategy for precision and companion diagnostics, manage submissions and health-authority interactions across lifecycle stages, integrate diagnostics into drug development, ensure regulatory compliance, and support cross-functional training and processes.