As a Study Grants Expert, you will manage Grant Plans and FMV assessments for clinical trials, ensuring budget accuracy and operational efficiency while collaborating with various teams to improve cost management and effectiveness.

The Associate Director will optimize Loss of Exclusivity strategies, integrate SharePoint platforms, support workshops, and develop strategies for post-LOE competition.

Lead the development and execution of HEOR strategies to demonstrate product value and support commercialization through research and collaboration with global teams.

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

Lead the Marketing Cloud Intelligence team, designing data solutions, managing stakeholder engagement, and optimizing reporting capabilities to support business goals.

Lead strategic change initiatives within the Integrated Marketing Organization, focusing on enterprise-wide change strategies, stakeholder readiness, and communication plans to enhance business outcomes.

The Director of Data Science Products will lead the development of open-source tools for clinical trial reporting, manage product lifecycles, and foster agile methodologies among product teams.

The Senior Manager People Insights generates and delivers insights for People & Organisation teams, enhancing employee experience and improving organizational performance through data analytics and collaboration.

The Director leads systemic coaching for Global Program Teams to enhance performance, collaboration, and strategic execution. This role involves leveraging team coaching frameworks, supporting leaders, and driving organizational change in complex environments.

The Brand Manager leads brand strategy execution, manages budgets, monitors tactical plans, and collaborates with teams for growth in the pharmaceutical sector.

The Senior Risk Surveillance Lead drives Risk-based Quality Management in clinical trials, overseeing risk surveillance, quality governance, and continuous improvement across trial protocols and teams.

The GPAD will manage global drug development projects, ensuring effective communication and alignment across teams, while maintaining accurate documentation and plans.

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.

Lead a team to analyze market trends, manage scientific events, and collaborate with cross-functional teams to deliver insights and ensure quality compliance.

The Associate Director, Publication Excellence drives high-quality publications and cross-functional collaboration while implementing innovative practices and ensuring compliance with standards.

Lead the strategic planning and delivery of Global Medical Affairs studies, manage cross-functional teams, ensure compliance and operational excellence.

The Senior Manager, Training & Enablement Specialist will manage change initiatives and training programs for the Content Enablement Team, focusing on strategy development, stakeholder engagement, and performance monitoring.

The Senior Manager, Business Analyst Planning coordinates with stakeholders to enhance content processes and drive solutions, while ensuring timely documentation and effective communication across teams.

The Senior Director leads global publications and scientific communications within a therapeutic area, managing a team to ensure high-quality deliverables aligned with regulatory compliance and strategic objectives.

Lead high-impact programs at Novartis, driving commercial excellence, managing cross-functional teams, and championing AI-driven solutions. You will coach teams and build stakeholder relationships to enhance program delivery.