• Content Review: Review blog posts for accuracy, tone, clarity, and quality before publication - editing for voice and ensuring posts meet our editorial standards. • Expert Perspective: Add personal anecdotes, real-world examples, and subject matter insight to content where relevant, and serve as the listed reviewer across the Kikoff blog. • Content Briefing: Help shape content direction and communicate feedback and priorities to our content partners. • Partner Communication: Serve as the day-to-day point of contact with our content partners - relaying edits, flagging issues, and keeping production running smoothly. • CMS Publishing: Publish finalized posts directly in the Webflow CMS editor, ensuring formatting and structure are consistent across the blog.

• Verify that lists, tables, and general formatting are styled correctly. • Ensure all content is typo-free, including metadata. • Confirm text matches the approved source, checking live pages against AEM staging. • Review translated text to ensure it fits seamlessly within CTAs, headers, and navigation components. • Check that all media (images, videos) display correctly and are visible. • Flag any inconsistencies or errors found between the live site and the AEM page.

Editor - Pharma #210349 Overview Placement Type: Temp to Perm Salary: $75,000-80,000 Salary Start Date: Jun 22, 2026 Join a pioneering global pharmaceutical company dedicated to improving patient lives through innovative healthcare solutions. This organization is at the forefront of medical advancement, committed to delivering high-quality, life-changing therapies to patients worldwide. Are you a meticulous and passionate editor ready to make a significant impact on critical communications within the pharmaceutical industry? We are seeking a talented individual to join our dynamic creative studio, partnering directly with our esteemed client, a leader in global healthcare. In this pivotal role, you will be the guardian of content quality, ensuring clarity, accuracy, and compliance for materials that inform and educate. Your expertise will directly contribute to the integrity and success of vital promotional and non-promotional content, ultimately supporting the delivery of groundbreaking medical solutions. **What You’ll Do:** * Electronically copy edit and proofread print and digital assets for approval within the Medical, Legal, Regulatory (MLR) system, from initial submission through production proof. * Ensure all content strictly adheres to brand, company, and industry guidelines, including AMA style. * Maintain rigorous compliance with established company and brand style guides. * Utilize top-notch organizational skills to manage feedback from multiple reviewers, annotate electronically, meet tight deadlines, and ensure consistency across all materials. * Edit for consistency, provide insightful commentary, and uphold brand style throughout review cycles, taking ownership of brand voice and claims. * Apply working knowledge of electronic workflow systems like Aprimo or Veeva, or quickly adapt to similar platforms. * Participate in on-site and/or live review meetings and interactions requiring in-person contact when necessary. * Exercise sound judgment in decision-making, knowing when to escalate issues to appropriate stakeholders. * Leverage exceptional proofreading, grammar, and punctuation skills to deliver high-quality output. * Work autonomously while managing multiple projects simultaneously with concurrent deadlines. * Stay current with all relevant industry guidelines and standards to remain a subject matter expert. * Contribute to operational efficiencies by demonstrating proficiency with electronic and online editing and review tools. * Exhibit proficiency with Adobe Acrobat and its commenting tools. **What You’ll Bring:** * Bachelor’s degree in English or Communications. * 3-7 years of editing experience within a pharmaceutical company, creative studio/agency environment, or medical publishing company (Senior roles require 10+ years). * Extensive experience and in-depth knowledge of the AMA style guide is essential. * Proven experience reviewing materials using an electronic approval system such as Aprimo or Veeva. * Working knowledge of FDA guidance on pharmaceutical advertising. * Meticulous attention to detail. MUST BE PROFICIENT IN MS OFFICE: WORD, EXCEL AND POWERPOINT. The target hiring compensation for this role is $75-80K. Compensation is based on several factors including, but not limited to education, relevant work experience, relevant certifications, and location. Additional benefits offered may include: medical health insurance and dental insurance, life insurance, and eligibility to participate in 401k plan with company match (if applicable). Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. #LI-JH5 Client Description Aquent Studios is a global creative studio that delivers scale, speed and efficiency to the world’s most recognized brands. We create the work that matters the most to them—work that has a real impact on their business. As an Aquent Studio team member, you’ll have the opportunity to engage with the largest and most influential companies in the world, solving design challenges and extending their brands across tactic types and platforms, including digital design, UI/UX, video, motion, content, print design, web development, and more. If you want to do work that matters in a collaborative setting that values ingenuity and personal growth, you have found the right place!

• Lead daily web content management activities within Drupal CMS environments. • Perform webmaster functions, including content publishing, page updates, metadata management, taxonomy alignment, and content quality reviews. • Coordinate and manage enterprise content update calendars, release schedules, and publishing timelines. • Ensure website content remains accurate, accessible, compliant, and aligned with agency standards and priorities. • Support high-visibility updates, emergency communications, campaigns, and digital initiatives across SAMHSA web properties. • Monitor content workflows and ensure timely completion of customer requests and operational tasks. • Manage and coordinate task assignments for a team of approximately five Content Managers. • Track workload, priorities, deadlines, and deliverables across multiple concurrent initiatives. • Lead internal content team meetings, status reviews, and operational coordination sessions. • Provide mentorship, quality oversight, and guidance to content staff. • Collaborate with developers, designers, QA testers, and program leadership to support integrated web operations. • Lead meetings and coordination sessions with government customers and stakeholders. • Serve as a primary point of contact for content operations and publishing activities. • Translate customer requests into actionable content tasks and priorities. • Provide status updates, publishing schedules, and operational reporting to leadership and stakeholders. • Coordinate cross-functional communication between content, development, UX/UI, analytics, and infrastructure teams. • Ensure compliance with Section 508 accessibility standards, federal web policies, and content governance processes. • Review content for formatting consistency, usability, readability, and adherence to agency branding standards.