Jobs at Novartis

Plan, coordinate, and execute medical and scientific engagements (advisory boards, congresses, EEEs, standalone meetings, medical education). Translate strategies into operational plans, manage vendors/logistics/budgets, ensure compliance and audit readiness, track metrics, and drive process improvements while collaborating with cross-functional medical affairs teams.

Manages strategy, roadmaps, governance, adoption, optimization, and continuous improvement for commercial learning products. Partners with business, technology, analytics, operations, vendors, and global teams to deliver scalable, data-driven, and AI-enhanced learning experiences. Uses learner feedback, dashboards, surveys, and performance metrics to measure product health and business impact, while driving stakeholder engagement, change enablement, prioritization, and lifecycle management.

Lead strategy, planning, and execution of clinical document migrations (eTMF/eDMS). Partner with stakeholders and vendors, manage governance, incidents, change control, resource forecasting, audits/inspections support, and drive continuous improvement of migration processes and tools.

Lead Corporate Affairs AI strategy and portfolio, deliver enterprise-grade generative AI solutions, build and manage an AI team, own governance, adoption, value realization, and represent Corporate Affairs in enterprise AI governance and executive forums.

Provide clinical and scientific support across clinical study phases, perform patient-level data review and trend analysis, identify and resolve data issues, contribute to data review and quality plans, support CRF development, participate in safety/pharmacovigilance activities, prepare study documents and present data insights to cross-functional teams and oversight committees.

Serve as GA4/GBQ/GCP SME to design, implement, and govern scalable analytics integrations and data pipelines. Lead stakeholder engagement, drive measurable business impact, oversee GA4 configuration, data quality, reporting (Looker Studio), and provide strategic guidance on digital measurement, architecture, and cloud analytics.

The Commercial Portfolio Lead drives portfolio strategy, partnerships, and lifecycle management to maximize value and ensure operational excellence across the product portfolio.

Lead GCP compliance oversight for global clinical development units, manage a team of GCP Compliance Managers, and drive inspection readiness, audits, quality issue resolution, and risk mitigation. Partner with Development Unit leadership and cross-functional stakeholders to strengthen compliance frameworks, ensure regulatory alignment, and translate quality insights into business decisions.

The Sales and Marketing Head for Immunology leads commercial strategies, executes marketing plans, engages customers, and builds high-performing teams to achieve growth in the therapeutic area.

Lead integrated insights and market research for Therapeutic Areas and Value & Access. Translate strategy into analytics, maintain dashboards and forecasting inputs, run primary/secondary research, support market access insights, and enable cross-functional decision-making through data-driven storytelling and KPI frameworks.

Lead development and alignment of global labelling strategy and content for oncology products across lifecycle stages. Drive creation of core and major market labelling documents, present recommendations to governance bodies, anticipate and mitigate labelling risks, support health authority interactions, and mentor colleagues while ensuring inspection readiness and continuous improvement.

Lead development and maintenance of global labelling strategy and content for established medicinal products. Guide cross-functional alignment, prepare regulatory-facing labelling documents and health authority responses, anticipate and mitigate labelling risks, present recommendations to governance bodies, and mentor colleagues to ensure inspection readiness and high-quality, compliant labelling across markets.

Lead clinical data management across multiple trials, define and execute trial-level data strategies, ensure end-to-end data quality and database lock readiness, manage data risks and compliance, influence cross-functional stakeholders, and drive inspection readiness and continuous improvement for clinical trial data delivery.