Oversee medical safety activities and processes for assigned products, ensuring continuous assessment of safety profiles and benefit-risk of investigational and marketed compounds. Provide strategic, 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.
Engage in peer-to-peer scientific dialog with healthcare system National Thought Leaders within a defined geography. Conduct critical activities that support advancing science, educating on evolving clinical practices, and transforming science into patient care. Facilitate the development of new research collaborations, capture medical insights, and act as a therapeutic area resource to cross-functional partners aligned with medical strategies.
The Senior CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Phase I-IV Pharma clinical trials within the country. The Senior CRA is responsible to deliver data within timelines and required quality standard, and adherence to monitoring procedures in accordance with ICH/GCP and US CFR and company SOPs. This position will require 80% travel.