Advise on legal issues associated with global Phase 1 through Phase 4 clinical studies, registries and related development activities, including clinical trial conduct, informed consent, data privacy and the collection, use, disclosure and transfer of clinical, patient and research data, research activities and interactions with clinical research organizations, investigators, hospitals, universities and other research partners. This role will independently advise R&D leaders and cross-functional teams on legal matters arising throughout the development lifecycle, including research activities, global clinical trials, clinical operations, data privacy and the collection, use and sharing of clinical and research data, collaborations and contracting matters.