Job description

Since its founding in 2016, Acumen Medical Communications has served its clients in the pharmaceutical industry with the highest quality medical writing and clinical development expertise. As our reputation for excellence spreads throughout industry, we need talented medical writers and editors who can integrate into our internal culture of collaboration, innovation, and creative thinking to meet the increasing demand for services. We're in search of a full-time Editor II/Senior Regulatory Editor for a remote position. Candidates must be highly proficient in MS Word and English grammar, detail-oriented, be able to work independently, and be flexible to meet often tight, shifting deadlines. At the Editor II level, 1-3 years of in editing scientific data within the pharmaceutical industry as well as proficiency in the use of Style Guides and/or the AMA Manual of Style are required; experience with eCTD publishing is preferred. Our compensation is highly competitive. A full-time in‑house Regulatory Editor II starts at $70,000 per year (plus benefits and bonus); Senior Regulatory Editor starts at $80,000 per year (plus benefits and bonus). Actual salary is dependent on experience.

CORE RESPONSIBILITIES

• Partner with authoring medical writer to align on the scope and specifications of the editorial/quality review
• Line-edit and format documents to ensure cohesiveness and internal consistency
• Align document to pre-set templates, regulatory guidance, or style guide
• Perform data checks against source documents, including tables, listing, and figures
• Update/add references using EndNote or other reference software
• Provide concise and clear editing suggestions to authoring medical writer
• Create submission-ready PDFs with all internal links and bookmarks

If you're interested in joining our team, please send us your resume along with a brief description of your passion for editing.