Position Summary: We are currently seeking a qualified Technical Writer to assist in the development, drafting, review, editing, and finalization of documents used in supporting R&E development activities. Responsibilities: Drafts and edits documents used in supporting R&E development activities Conducts comprehensive literature evaluations, product complaint reviews, and other product specific information to compile evaluation reports. Manages study team participation in the preparation of such documents, including calling/running meetings, developing timelines, and managing the document review and comment adjudication processes. Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials. Education: Bachelor or higher degree preferred; scientific focus desirable. Minimum requirement: University-level technical writing course(s) or equivalent experience in science/technical writing. EXPERIENCE Fulfills one of the following: Experience writing, reviewing, or editing protocols and clinical study reports and literature based clinical evaluations highly preferred. Intermediate to advanced applied knowledge of routine document content preparation. Ability to interpret basic tabular and graphical data presentations. Ability to create basic tables Knowledge of Microsoft software, (i. e. EXCEL, WORD, POWERPOINT) and ADOBE PDF.
Associated topics: content, documentation, excel, file, log, msword, ms office, technical writer, technical writing, writer