The Medical Monitor will provide input into the design and conduct of clinical trials, reviewing and/or generating key study documents, assessing and interpreting safety data, and contributing to investigator, other site staff and clinical study team training. Responsibilities include reviewing adverse events, ensuring SAE-related activities comply with SOPs and regulations, and managing clinical data collection.

Oversee medical safety activities and processes for assigned products, ensuring continuous assessment of safety profiles and benefit-risk of investigational and marketed compounds. Provide patient-focused leadership for medical safety, support asset strategies, and strengthen medical and scientific innovation. Timely escalation of safety issues to the Takeda Safety Board Chair is required.