Strong communications, organizational, time management, and project management skills are required. * Develop regulatory documents for submission to regulatory agencies globally, including Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and Clinical Overviews, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring standards, as applicable, in adherence with study/project timelines and corporate objectives. * Manage medical writing projects, including developing timelines (working with the study/, as necessary) and communication with cross-functional team members to maintain awareness of review cycles and expectations. * Review other documents associated with the assigned project(s) (eg, Protocols and Statistical Analysis Pl
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