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Lead strategy for customer experience technologies in oncology. Oversee product lifecycle, partner with cross-functional teams, and ensure compliance with regulations.

Oversee and manage clinical development projects, ensuring alignment with strategic goals, tracking progress, and fostering collaboration across teams while driving process improvements.

The Associate Director will enhance risk management, compliance, and security measures. Responsibilities include developing policies, managing third-party risks, and leading GRC implementations across North America & LATAM.

The Associate Director will operationalize and lead BeOne's clinical trial diversity strategy through data-driven insights and collaborations across Clinical Operations, enhancing patient enrollment diversity.

The Associate Director will lead the development of regulatory strategies, manage CMC submissions, and ensure compliance with health authority requirements for small molecules.

Manage regional study delivery, oversee clinical operations, ensure compliance and inspection readiness, and collaborate with stakeholders to meet study goals.

The Associate Director leads and mentors clinical study managers, ensuring alignment with organizational goals and quality standards while managing study performance and resources.

The Senior Clinical Research Associate manages site monitoring to ensure data quality and compliance with clinical study protocols, while training junior CRAs and collaborating with study teams.

The Head of Global Clinical Process Management oversees clinical operations processes, enhances efficiency, and collaborates cross-functionally to implement process improvements in global trials, particularly in oncology.

The Director, Global Regulatory Lead develops and implements regulatory strategies for product development, ensuring market access and oversight in compliance with global standards while leading regulatory affairs teams.