Required Skills: Clinical Research, Cross-Functional Teamwork, Drug Development, Global Regulatory, Oncology, Regulatory Affairs Management, Regulatory Communications, Regulatory Documents, Regulatory Filings, Regulatory Management, Regulatory Processes, Regulatory Strategies, Regulatory Submissions, Strategic Planning, Strategic Thinking. Represent GRA within our Company's internal committees to provide regulatory advice and approval according to the committee charters (therapeutic area Document Review Committees (DRC), Product Development Team (PDT), Early Development Team (EDT), and labeling teams (LEAD).