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The Executive Director of Clinical Data Engineering & Analytics leads programming support for clinical studies, focusing on data standards, governance, and innovative technologies like AI and machine learning, ensuring compliance and improving data quality and operational efficiency.

Lead execution of clinical trials, ensure regulatory compliance, oversee clinical data collection, and provide guidance on clinical practices and communications with health authorities. Requires strong leadership skills and extensive experience in drug development and clinical research.

The Director of Biostatistics leads a team to manage statistical data analysis and reporting, oversee technical activities, and ensure regulatory compliance while fostering team development and collaboration.

The Associate Director of HCP Marketing will lead brand strategy and promotional tactics for oncology products, ensuring compliance and collaboration with internal and external stakeholders. Responsibilities include campaign implementation, budget management, and developing relationships to enhance brand advocacy.

The VP, Assistant Controller will lead technical accounting, financial reporting, and controls, ensuring compliance with US GAAP and SEC regulations. Responsibilities include overseeing financial audits, managing SOX compliance, and developing ESG reporting. The role requires strategic partnership with finance leadership and managing a team of 25.

The Sr Director of U.S. Ethics & Compliance will support commercial compliance, develop internal processes, and lead a team while ensuring ethical practices in alignment with legal standards.

The Business Systems Analyst will gather and document business requirements, facilitate User Acceptance Testing, and represent Development Systems in project interactions with stakeholders.

The role entails managing supply chain operations, developing and implementing strategies, supervising team performance, and ensuring compliance with regulatory requirements.

The Director of Biostatistics will lead statistical analysis for oncology trials, collaborate across teams, and ensure compliance in drug development.

The Manager, Global External Manufacturing ensures uninterrupted supply of clinical and commercial products through external manufacturing and compliance with regulations, while managing supplier performance and facilitating process improvements.