Job Description:Greetings from Cyient. We are looking for candidates with good experience in regulatory medical writing . Experience : 3 to 10 Years. Job Location: Hyderabad. Job Description : Developing Clinical Study Outlines Feasibility analysis for the clinical trials by discussing with specialists in various therapeutic areas Preparing Feasibility questionnaires to support Clinical Operations Timely preparation of new documents or amendments of clinical trial documents (Protocol, CRF, IB, PIS and ICF), IP calculation submission as per schedule Designing protocols Development of creative medical content in the form of articles, slide shows, scripts, case studies, manuscripts, newsletters, SMS etc. as required by the clients. To gather, organize, compile & analyze information on all matters related to medical updates. To undertake necessary reference searches. To develop original content from the available inputs & maintain a database of medical information. To ensure accuracy of information.