As a medical writer, you can work on a variety of projects based on your area of specialization, experience, and work setting. Clinical trial documents, such as protocols, informed consent forms, investigator's brochures, clinical study reports, abstracts, posters, and manuscripts are used to support the submission and approval of new drugs, devices, and biologics by regulatory agencies. Regulatory documents provide information about the safety, efficacy, quality, and pharmacology of drugs, devices, and biologics to obtain and maintain authorization and marketing. Educational materials are used to educate healthcare professionals and patients about medical topics such as diseases, treatments, guidelines, or best practices. They also raise awareness for medical research and innovation. Examples include review articles, case reports, newsletters, brochures, slide decks, webinars, podcasts, blogs, and social media posts.