Position Summary The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning writing editing/formatting and performing QC review. Develops documents in compliance with Precision MW Style Guide Precision SOPs applicable regulatory guidelines (ie ICH FDA GCP) and eCTD requirements. The successful candidate has a clear understanding of content requirements for key clinical documents based on regulatory requirements for all phases of development and will complete MW activities with impeccable attention to detail. Essential functions of the job include but are not limited to Planning writing editing formatting and QC review of timely and high-quality clinical documents including clinical study protocols IBs ICF templates DSURs … Sign In to View