Jobs at Novartis

The Associate Director leads statistical programming for clinical trials, ensuring collaboration, resource allocation, and compliance while mentoring team members and developing documentation.

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

The Associate Director will oversee quality assurance for clinical trials, ensuring compliance with health authority requirements and internal standards while providing guidance on Good Clinical Practice and managing quality risks.

The Senior Principal Statistical Programmer leads statistical programming for clinical studies, ensures compliance with standards, supervises programmers, and delivers high-quality datasets and outputs.

The Global Regulatory Affairs Associate Director leads regulatory strategies, manages submissions, and collaborates with teams to ensure compliance and facilitate approvals throughout the product lifecycle.

The Associate Director will lead operational planning and management of medical programs, ensure compliance and effective communication, and drive operational excellence with a focus on delivering quality results.

Lead the development of global labelling strategies, ensure compliance with regulatory requirements, and collaborate with cross-functional teams to support product information for innovative medicines.

The role involves developing global labelling strategies, ensuring alignment across teams, analyzing competitor labelling, and supporting regulatory interactions for product information.

The Global Labelling Manager will develop and maintain global labelling documents, ensuring accuracy and compliance, while collaborating with cross-functional teams throughout the product lifecycle.

Provide strategic legal counsel and risk management for CLS Operations, support compliance, manage BD/M&A activities, oversee regulatory materials, drive innovation, and engage with various stakeholders.

The Senior Scientific Engagement & Program Manager manages scientific engagement activities, collaborates cross-functionally, and ensures high-quality delivery of programs in pharmaceutical settings.

The Associate Manager will oversee operational support for compliance in funding activities and contractual agreements, ensuring timely execution and adherence to regulations while facilitating continuous improvements and training.

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

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

The Virtual Analytics Network PhD Graduate Program at Novartis offers recent PhD graduates a 15-month rotation across clinical trial statistics, providing expert support and training in various disease areas.

The program offers a two-year training in Regulatory Affairs with hands-on experience in various RA functions and strategic regulatory input to projects.

The Global Regulatory Affairs Operations Resource Planner ensures effective planning and allocation of submission resources across a global portfolio, collaborating with stakeholders and optimizing resource assignment processes.

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.