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Responsible for global clinical study delivery, leading cross-functional teams, ensuring study compliance and budget management, overseeing external vendors, and ensuring quality in clinical operations.

Lead statistical programming for multiple clinical development projects, ensuring quality and compliance while collaborating with cross-functional teams and overseeing data analysis.

The Director, Global Regulatory Lead, oversees regulatory strategies for drug development and market access, engages with stakeholders, and ensures compliance with global regulations while mentoring teams.

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.

The Associate Director will lead global marketing initiatives for the BTK CDAC brand, focusing on promotional strategies, omnichannel planning, and market research collaboration with cross-functional teams.

Lead the Central Statistical Monitoring team, ensuring subject safety and data integrity in clinical trials through statistical analysis and collaboration with various stakeholders.

The Senior Clinical Research Associate will oversee clinical study sites, ensuring compliance with regulations, quality of data, and patient safety while mentoring junior staff and supporting study management activities.

The Senior Director, Resource Management oversees global resource and budget management in Clinical Operations, ensuring alignment of resources with portfolio priorities, while driving data-driven decision-making and optimizing operational efficiency.

The Associate Director will design scalable data architectures using Databricks, focusing on performance, governance, and collaboration to enhance data-driven decision-making. Responsibilities include optimizing data processes, integrating systems, and leading rapid proof-of-concept initiatives.

The Senior Manager, Clinical Supply Chain oversees supply planning for clinical studies, manages vendor relationships, and ensures compliance with regulatory requirements while leading process improvements and team staff.