Program Coordinator, Regulatory Information Manager

This role will be coordinating work across 2 major initiatives. One set of work will be tied to approach to IDMP (Identification of Medicinal Products), and the activities specifically tied to the introduction of the European Medical Agency (EMA) introduction of underlying infrastructure services, called SPOR. This near term activity will be engaging across groups, primarily within R&D, and largely regulatory to complete the data review of the provided controlled vocabularies for accuracy as industry, and from a  perspective, as well as managing the feedback on changes required back to EMA services.