Contribute to high-quality regulatory submissions for oncology products, collaborating cross-functionally to support timely and strategic regulatory operations. Thrive in a dynamic environment that values proactive team engagement and effective communication.

Contribute to strategic regulatory submissions and enhance oncology product development. Collaborate with cross-functional teams to ensure compliance, manage timelines, and communicate effectively while maintaining high standards for quality and accuracy.

Lead CMC regulatory strategies to support clinical development initiatives, ensuring compliance with global regulations. Collaborate cross-functionally to drive submissions and manage risks while maintaining strategic oversight of quality documentation.