I have experience of working with large pharmaceutical companies as well CROs in the capacity of medical writer and medical information manager. I have hands-on experience on researching, writing, and editing clinical study reports, study protocols, case report forms and informed consent documents; preparation of publication manuscripts; SAEs narratives; product monographs and product training manuals. Responsible to looked after all scientific and medical information need for Asia Pacific and Middle-east region in my earlier assignment; My other core responsibility includes: dissemination of medical Information/scientific inputs for preparation of training slides, doctor’s slide, launch slides, medical letters thus contributing in the product launches and brand promotion all across the region.; handling Medical/Product queries from doctors, patients and field force; Performing literature survey and scientific documents compilations; Providing regular new and existing product information on all key products; Handling ADR reporting. Preparing reports, documents and information on the current and possible future clinical research issues within a country or globally; Development of Standard Operating Procedures (SOPs) for the department for its key processes.