Drive quality assurance excellence by leading validation activities across commercial manufacturing operations. Ensure compliance with GMP regulations while fostering collaboration with internal and external partners for successful product lifecycle management.

Lead the charge in statistical leadership and strategy for late-stage clinical development, collaborating with cross-functional teams to design, analyze, and support oncology studies throughout the product life cycle.

Develop and execute comprehensive Global Medical Affairs strategies focusing on asset launch and lifecycle management in the oncology field, specifically GI tumors. Collaborate across functions to communicate and optimize scientific insights effectively.

Champion quality control excellence by overseeing testing at contract labs, ensuring compliance and timely project execution across development and commercial portfolios in a dynamic pharmaceutical environment.

Support GxP compliance by leading audits, managing supplier quality, and collaborating cross-functionally to enhance vendor management processes and ensure regulatory standards are met while driving continuous improvement initiatives.