The Drug Regulatory Affairs (DRA) Global Project Leader is a multi-faceted clinical regulatory role with differing levels of responsibilities from global leader to partner role based on region/country in which the leader is employed and the region/country in which the assigned work is located. Responsibilities include but are not limited to: Global Role: Define and provide optimal global regulatory strategies to support the development and approval of new drugs as well as product life-cycle management activities for assigned product(s) Lead creation of regulatory function plans, including identification and critical assessment of regulatory issues Provide consolidated interpretation of releva