I will compile, write, and edit medical writing deliverables covering all phases of clinical research for submission to regulatory agencies. will help in writing studies for submissions to the FDA. The writing is also used in publications or medical journals, or for internal company use. Some of the things they write include comprehensive clinical study reports, study protocols, annual reports, investigator brochures, risk/benefit analysis, and integrated summaries from raw data. All deliverables are written in accordance with regulations, standards, and guidelines. The regulatory documents will meet ICH, GLPs, and GCPs guidelines, a writing style guide, or a client template. The end result will comply with the levels of evidence required to achieve regulatory, marketing, and regulatory goals.