![]() Experience as lead writer for key documents included in major US and/or international regulatory submissions required.At least 5 plus years of experience regulatory writing for pharma or biotechnology required.Bachelor's degree in science, health profession, or journalism required.Select the best option from a set of defined procedures or based on precedence.Encounter problems that are varied but similar and require some factfinding to define problem.(eg, Please Review, document and submission content management platforms, etc.). Demonstrate technical expertise and background in the use of medical writing templates and software.Exhibit excellent and oral communication and presentation skills.Understand regulatory submissions requirements and clinical study report guidelines in host country.Write technical sections of regulatory documents, eg, protocols, clinical study reports, investigator.Schedule and conduct peer and team quality control review for assigned projects.May serve as an active mentor to one or more junior staff members.Lead project teams in drafting report specifications, medical writing, and coordination of data analysis.Provide scientific and medical writing consultancy to clients and internal colleagues at a moderate.Produce clinical documents as required.Act as a lead medical writer on several projects from simple to complex level.Medical Writer you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Manage multiple assignments simultaneously, while working independently and with others.Įdit and re-write technical documents, training materials with content support from other team members.Ĭonduct substantive edits to improve the language and/or organization of written documents, reviews and make recommendations of other documents as needed approach documents, meeting minutes etc.Įdits a wide variety of content including project documents, PowerPoint presentations, handouts, background materials, meeting materials, agendas and other publications.Ĭreate/Review presentation, MOM (Meeting Minutes) and technical documents.Ĭreate training videos and simulations using Adobe Captivate.Ĭreate screen prototype. Must be flexible and have the ability to interact with all levels of the organization.Īdvanced computer skills in Microsoft Word, Excel and power point, Visio,ĭevelop project process documentation for application teams.Ĭreate documentation templates as required. Strong analytical and problem-solving skills.Įxcellent verbal and written communication skills. Preferably experience in Unemployment Insurance domain.ĥ+ years of technical writing experience. ![]() Experience in technical document writing/editing, software manuals, textbooks, product instructions, technical online content, training materials and memorandums.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |