Senior Nonclinical Editor

To ensure high-quality standards in document preparation, the full-time Senior Nonclinical Editor will manage the quality control review and submission-ready publishing of nonclinical documents, working remotely or in a hybrid capacity. Key responsibilities Perform internal document quality control reviews to ensure compliance with style guides and submission standards Copyedit, proofread, and format documents for grammar, style, and internal consistency Assist with clinical document quality control and publishing tasks as needed to meet submission timelines Required qualifications Bachelor's degree in English, Basic Science, Business, or a related field, with 4 years of relevant experience in the pharmaceutical industry, or 8+ years in a related discipline Strong knowledge of editorial and publishing activities within Clinical Development Proficiency in Microsoft Word and experience with Adobe PDF tools for document formatting and submission readiness Experience using an electronic document management system (EDMS) such as Veeva Vault or SharePoint Ability to manage multiple tasks effectively in a fast-paced, deadline-driven environment