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The Associate Central Monitor supports the quality and integrity of data in clinical trials under Risk-Based Monitoring. Responsibilities include setting up risk-monitoring systems, defining key risk indicators, reviewing data, and ensuring compliance with regulations and procedures. The role aids in communication with stakeholders and maintains data quality throughout the trial process.

The Senior Manager, Global Labeling Lead is responsible for the development and execution of global labeling strategies, managing the labeling process for pharmaceutical products, and leading cross-functional teams. This role involves authoring labeling content, negotiating with regulatory agencies, and guiding strategic initiatives in the oncology pipeline.

The Oncology Research Project Leader will lead discovery and clinical-stage portfolio research project teams, develop project strategies for cancer treatment, and mentor junior project leaders. This role involves risk management, regulatory strategy contributions, and collaboration with research and commercial teams.