Clinical Trial Protocol Specialist

Found in: Talent IN C2 - 2 weeks ago


Bengaluru, India Parexel Full time

When our values align, there's no limit to what we can achieve.
 

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.
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