To draft abstracts, posters, manuscripts,publication alerts, clinical/regulatory documents, informed consent forms. To prepare clinical trial summaries from various data sources like clinical study reports, patient profiles etc. To provide training or educational deliverables for doctors and medical representatives (product monographs, pamphlets,website development etc.) Specialized in writing script for various medical deliverables (print modules, articulates, slide decks and e-modules) To perform quality control/proof reading and data fact checking of above documents to meet customer expectation. Conduct background research and literature reviews to help with document preparation.