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The Associate Director GLP Quality Assurance ensures compliance with GLP standards in clinical studies, manages vendor audits, and provides quality assurance recommendations. Responsibilities include developing audit plans, conducting audits, and reviewing compliance of CRO study protocols.

As a Project Coordinator, you will support project goals by collaborating with cross-functional teams, creating project plans, and enhancing program management skills.

This role involves leading the global Quality Management System, ensuring compliance with regulatory standards, and fostering a culture of quality excellence in the organization.

The Director, HEOR/RWE is responsible for executing HEOR plans and generating evidence to demonstrate the value of oncology products, especially for lung cancer, engaging with stakeholders and leading evidence generation initiatives.

The Senior Financial Analyst/Finance Manager will manage clinical trial accruals, financial reporting, and support audits while collaborating with cross-functional teams.

The Manager of Document Management will oversee controlled documents lifecycle, ensuring compliance with regulations and managing change requests across teams.

The Director will oversee stability management, designing, and evaluating studies, and ensuring compliance with ICH and GMP standards in clinical oncology drug development.

The Director, U.S. Forecasting will develop and execute forecasting models for oncology products, manage cross-functional collaborations, and enhance forecasting processes and tools.

Responsible for statistical design, analysis, and reporting of oncology clinical studies, collaborating across functions to ensure timely and accurate deliverables.

The role involves leading Organizational Development to enhance team performance and organizational health, emphasizing leadership effectiveness and strategic growth.