The Technical Writer as Subject Matter Expert (SME) will be engaged in developing reading material in Clinical Research, Drug Safety, SAS Functional and Healthcare Programs. Develop student learning materials as presentation, quiz and exercise modules for student learnings. Follow Company SOPs to develop online programs access thru Qtech-Sol learning management system (LMS). Enhance student reading material with latest news and updates on current regulatory, scientific and therapeutic information followed to meet US FDA, European, Canada and Asia Pacific standards on Clinical Trial, Pharmacovigilance (PV) and Healthcare domains. Expand the current training programs by developing new training modules as add-ons. Develop scientific training related manuals, brochures, scientific newsletters and subject related frequently asked questions in LMS. Illustrate with sketches specified materials for module story board development or assembly sequence on documents prepared and make it available to web developers for phase-wise LMS course material development. Gather open source clinical publications, pub-med and technical books by observing, receiving, and otherwise obtaining information from all relevant sources. Use MS Office to prepare the study materials, Maintain records and files of work and revisions.
:Must have Bachelorís degree in Medicine, Clinical Research or closely related.