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

The Director of Global Commercial Marketing leads brand planning, launch readiness, and competitive positioning for BTK CDAC, collaborating with global teams to ensure marketing excellence.

Lead the oncology program management team, develop global product strategies, manage projects in drug development, ensure stakeholder alignment, and implement project management best practices.

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.

The Director of Clinical Science will lead clinical development programs, ensuring execution aligns with scope, integrity, and timelines, while collaborating across teams and with external partners.

Lead the Central Statistical Monitoring team to oversee statistical design and governance in clinical trials, ensuring data integrity and safety. Develop monitoring indicators, validate models, and communicate findings to cross-functional teams. Provide training and support for audits and inspections, promoting continuous improvement in statistical practices.

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 Director of Global Regulatory Project Management leads oncology regulatory strategies, ensures timely submissions, manages global project teams, and fosters cross-regional collaboration to maintain market access for products.

The Associate Director is responsible for leading global regulatory project management, ensuring successful regulatory submissions, and facilitating cross-functional collaboration to maintain product market access worldwide.

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.