Jobs at Novartis

Design and implement the operating model for International Communications & Patient Advocacy. Lead governance, planning, prioritization, process simplification, and adoption of data- and AI-enabled automation. Build performance frameworks and dashboards, manage budgets and headcount, lead vendor strategy, and deliver transformation initiatives across global and country teams.

The Access Strategy Head drives commercial growth by developing pricing, reimbursement, and access strategies while ensuring sustainable patient access and payer engagement. Responsibilities include leading external stakeholder engagement and tracking access performance across brand portfolios.

Lead global regulatory maintenance for complex product portfolios: prepare and submit regulatory deliverables, advise cross-functional teams, liaise with health authorities, respond to queries with scientific justification, identify and mitigate regulatory risks, and mentor junior staff while driving process improvements to ensure compliant, timely approvals.

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.

The Global Program Clinical Head will lead clinical development programs in neuroscience, ensuring compliance and collaboration across teams while engaging with regulators.

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.

Provide clinical and scientific support across clinical study phases, performing patient-level data review, trend analysis, and identifying data quality and safety signals. Develop and execute data review plans, support CRF design, contribute to regulatory documents, and present data insights to study teams and committees. Collaborate cross-functionally to resolve data issues and improve data review processes.

Lead and execute regional and global regulatory strategies for neuroscience programs. Prepare and submit regulatory dossiers and clinical trial/IND applications, manage Health Authority interactions and responses, coordinate cross-functional teams, identify regulatory risks, and ensure compliance to support timely approvals across assigned regions.

Lead statistical work and innovative trial designs in collaboration with clinical teams to enable quantitative decision making across projects.

Lead identification, evaluation, and implementation of technology- and AI-driven innovations across clinical trial portfolios. Drive cross-functional alignment, assess risk/value, integrate solutions into execution plans, and scale operational improvements to accelerate recruitment, access, and patient-centric trial delivery.

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

The Risk Surveillance Lead drives RBQM practices at trial level, overseeing quality risk surveillance, improving clinical trial quality, and facilitating risk assessment and management activities.

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

Lead identification, evaluation, and implementation of operational innovations (especially AI-driven) across clinical trial portfolios. Influence stakeholders, assess value/risk, integrate solutions into execution plans, support trial teams, and scale successful technologies to improve recruitment, access, and trial efficiency.

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

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.

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

The GCP Compliance Manager ensures adherence to Good Clinical Practice in clinical trials, providing guidance, oversight, and managing compliance-related activities across studies.

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