Senior Nonclinical Editor

Job Summary

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