Clinical Trial Protocol Specialist

​Clinical Trial Protocol Specialist • The Clinical Trial Protocol Specialist will research, create, and edit clinical trial protocols as well as provide expert support for protocol development. • Operates as a lead medical writer or as a Subject Matter Expert (SME) to support Medical Writers and Clinical Trial Services management, as well as other Parexel functions. • Facilitates process improvement by participating in protocol development initiatives. • The Clinical Trial Protocol Specialist may also support Medical Writing Services management during the sales process by providing client liaison and proposals input. • The writers must have at least 5 years of overall writing experience, specifically Clinical trial protocol writing experience, with at least 5-10 protocols in the last year, and/or protocol design experience.