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The role involves developing global pricing and market access strategies for Solid Tumor pipeline products and ensuring alignment with payer needs through cross-functional collaboration.

The Director will lead digital marketing strategies for Market Access, enhance digital platforms, collaborate across teams, and manage compliance and budgets.

The Manager R&D Data Steward oversees data governance, quality management, and stewardship of R&D data, ensuring compliance and integrity across data products and leading a team to support data management initiatives.

Manage Trial Master File (TMF) operations ensuring quality, compliance, and inspection readiness. Collaborate with study teams and oversee TMF documentation and processes.

The Associate Director, Global Congresses leads planning and execution of major oncology congresses, coordinating cross-functional teams and managing operations, budgets, and stakeholder communications.

Lead the Central Statistical Monitoring team, ensuring subject safety and data integrity in clinical trials through statistical analysis and collaboration with various stakeholders.

Lead statistical analyses for Real-World Data (RWD) and Evidence (RWE) studies, oversee programming deliverables, analyze large datasets, and provide statistical consultation for biostatistics projects.

The intern will support analytical development and QC activities, conduct data analysis, and manage QC documents in a fast-paced, collaborative environment.

Manage and oversee eTMF processes, including system validation, data migration, and process optimization. Collaborate with teams for reporting and improvements while ensuring project deadlines are met.

The Director, Global Regulatory Project Management leads oncology regulatory strategies, ensuring successful global drug submissions, while driving operational excellence and collaboration across teams.