Summary: Under general supervision, is responsible for the overall organization, planning and up-keep of clinical regulatory activities and initiatives. Draft and maintains documents for clinical investigations and evaluations globally. Oversees clinical trial activities. Stays abreast of global clinical trial requirements. Liaises with R&D, Marketing/Sales and other key stakeholders on the development of clinical trial strategies in support of product development and/or sustainability.  Key Duties and Responsibilities: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions Liaise with Marketing, R&D, Quality and other key stakeholders i