The Solution Design Associate Director will translate business challenges into innovative solutions, lead technical teams, and enhance business operations through strategic design and project management.

The role manages and enhances project and pipeline data, develops actionable reports for decision-making, and ensures data accuracy and accessibility. It requires collaboration with teams to optimize performance and ensure compliance with governance standards.

The Senior Clinical Development Director leads clinical programs, ensuring strategic planning and execution of clinical deliverables, involving regulatory documents and trial data oversight, while supporting safety and training for stakeholders.

Develop and maintain R packages for clinical trial data workflows, build Shiny applications, and promote data science best practices within the organization.

Lead global recruitment marketing strategies, develop employer branding, and enhance candidate engagement to attract diverse talent for Novartis.

The Clinical Development Director leads clinical programs, ensuring delivery of clinical goals, collaborating across teams, managing trial data, and contributing to regulatory documents amidst a focus on patient safety.

The Global Head of Recruitment R&D leads a team, develops innovative talent strategies, drives global recruitment efforts, and collaborates with various stakeholders to enhance hiring outcomes.

The Global Monitoring Functional Excellence Director leads field monitoring strategies at Novartis, enhancing operational efficiency and ensuring compliance with regulations through innovation and process improvements.

The Functional Excellence Lead drives operational advancement in monitoring practices, ensuring alignment with RBQM principles, and optimizing trial efficiency through innovative techniques and stakeholder collaboration.

The Director - Genetic Toxicology Expert will oversee genetic toxicology studies, provide expert insights for drug development, and ensure regulatory compliance while leading cross-functional teams.

The Associate Director, Statistical Programming leads statistical programming for clinical trials, ensuring collaboration, quality, and compliance while mentoring teams and overseeing resource allocation.

The Clinical Quality Assurance Program Lead provides oversight for clinical trials ensuring compliance with regulations, quality strategy implementation, and risk management while leading QA initiatives and collaborating with global teams.

Manage TMF documentation for M&A projects, oversee transitions, develop processes, and ensure compliance in clinical document management.

The Manager of GMA Study Management Excellence oversees demand forecasting, resource planning, and budget management for clinical studies, driving process improvements and ensuring compliance.

The Risk Surveillance Lead ensures RBQM practices, oversees quality risk governance in clinical trials, and collaborates cross-functionally to enhance trial quality.