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Lead global strategic feasibility for clinical studies by integrating internal and external data, advising country/site selection, recruitment and operational strategies, improving feasibility processes and tools, and partnering with program and study teams to optimize study design and execution across early to late-stage programs.

The Associate Director will drive digital tool adoption, develop communication strategies, train users, monitor progress, and oversee AI capabilities in Quality processes.

The Senior Manager, Data Steward (AI) will lead data stewardship initiatives in Pharma R&D, ensuring data quality and governance while mentoring a team and collaborating across departments to enhance data usability for insights and compliance.

The Sr Manager of Clinical Supply Chain oversees drug supply activities, manages relationships with stakeholders, ensures supply continuity, and leads process improvements.

The role involves leading global forecasting and performance management, setting standards, overseeing processes, collaborating with cross-functional teams, and developing a high-performing team in the oncology biotech sector.

The Manager of Clinical Supply Chain oversees drug supply activities, developing supply plans, managing inventory, and ensuring compliance with regulations while collaborating with internal and external stakeholders.

The Corporate Account Director will develop strategic business plans for regional oncology accounts, expand corporate relationships, and ensure patient access to solid tumor products through collaboration with internal partners and cross-functional teams.

The Executive Director will lead global commercial strategies for TEVIMBRA, oversee cross-functional teams, and ensure alignment with business objectives to drive brand growth in oncology/hematology.

Lead and mentor oncology program management teams, develop global product strategies, manage projects, and drive process improvements in drug development.

The GCO Program Lead is responsible for strategic operational planning, program management, and leading clinical operations teams to ensure excellence in clinical trials. This role involves mentorship, resource management, and collaboration with cross-functional teams.