Jobs at Novartis

Manage and deliver high-quality medical communications (manuscripts, reviews, abstracts, posters, slide sets, symposia content, reports) on time. Perform QC, manage up to two brands, maintain records and compliance, train colleagues, liaise with customers/vendors, and support publication planning and medical education materials.

Lead GCP compliance for global clinical operations by managing portfolio-wide quality issues, audits, inspection readiness, self-assessments, risk assessments, investigations, and cross-functional compliance governance to protect patient safety and data integrity.

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 global labelling for neuroscience products across lifecycle: develop and maintain core and market labelling, translate clinical and safety data into compliant content, drive cross-functional alignment, support health authority interactions, and implement approved labelling changes ensuring global consistency and traceability.

Lead global labelling content strategy for neuroscience assets, developing core and regional prescribing information. Translate scientific evidence into product claims, partner with regulatory, clinical, safety, medical and commercial teams, negotiate with health authorities, monitor regulatory and competitive changes, and build capability through coaching and quality oversight to ensure compliant, aligned global labelling.

Provide administrative and secretarial support to the marketing team, help prepare basic promotional materials, maintain distributor data, organize reports and marketing samples, support customer satisfaction and compliance activities, and report product complaints or adverse events on time.

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.

Lead clinical data analytics to convert complex trial data into actionable insights. Partner with data quality, central monitoring and data management to enable risk‑based review, drive data quality improvements, implement analytics and visualization (Power BI/Spotfire), support anomaly detection, and accelerate study cycle times while ensuring regulatory data standards and governance.

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.

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.

Manage technical editorial, formatting, and submission-readiness of clinical documents for regulatory filings. Ensure compliance with Health Authority guidelines and GCP, implement standardized templates and strategies, monitor vendors, drive process improvements, support audits/inspections, and act as subject matter expert across global cross-functional teams.

Lead development of production-grade R packages and Shiny applications to support clinical trial analyses and reporting. Collaborate with statisticians and programmers, apply AI responsibly to improve developer productivity, drive tooling rollout, document solutions, and engage with open-source communities to modernize workflows.

Lead development and execution of HEOR and HTA strategies to demonstrate product value for access. Design, oversee and deliver HEOR evidence (cost-effectiveness, budget impact, indirect comparisons, RWE, patient preference studies), integrate access evidence into clinical programs and TPPs, translate evidence into value narratives, and collaborate with global, regional, and cross-functional teams.

Lead development and execution of HEOR and HTA strategies to demonstrate product value and support patient access. Design and oversee HEOR studies, economic models, and evidence synthesis, integrate access evidence into development plans, craft value communications, and collaborate with cross-functional global teams to support reimbursement and market access decisions.

The Associate Director will oversee clinical quality assurance for trials, ensuring compliance with health authority standards and patient safety. Responsibilities include quality risk management, oversight of clinical processes, and collaboration with stakeholders to support audits and inspections and sustain quality improvements.

The Associate Director of Web Analytics will lead the design, implementation, and optimization of GA4, GBQ, and GCP integrations, providing technical expertise and strategic direction for analytics initiatives to drive business impact and efficiency.

The Head of Data Governance will establish data governance frameworks, ensure compliance, and oversee the anonymization of patient data for secondary research, collaborating closely with data management teams.