This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
This is a unique opportunity for a competent and passionate editor to join our creative studio dedicated to supporting our Novartis client. The editor is responsible for content quality and must have a solid working knowledge of grammar, punctuation, and composition to ensure clarity and flow. They are comfortable working within a fast-paced review and approval setting, utilizing various software systems to review assets, and collaborating cross-functionally to ensure accuracy, consistency, and timely delivery of all assigned brand work. The editor contributes to a successful review process through meticulous annotation of resources in adherence with compliance and style guideline standards, and in accordance with AMA style.
Job Responsibility:
Electronically copy edit / proofread print and digital assets for approval in the MLR (Medical, Legal, Regulatory) system from submission through production proof
Ensure all content adheres to brand, company, and AMA guidelines
Maintain compliance with company and brand style guides
Top notch organizational skills, with the ability to comprehend feedback from multiple reviewers, annotate electronically, meet deadlines, and ensure consistency within materials
Edit for consistency, commentary, and brand style for successful review cycles. Own the brand and all information related to claims
Working knowledge preferably Aprimo or Veeva and understanding or quickly learning how to complete tasks in the workflow system
Participate in on-site and/or live review meetings and interactions requiring in person contact, when needed
Ability to make decisions and understand when to escalate issues appropriately to the right decision maker
Use proofreading, grammar, and punctuation to provide quality output
Ability to work with autonomy
Manages multiple projects simultaneously with concurrent deadlines
Remain relevant by keeping abreast of all guidelines and standards
Contribute to efficiencies by being proficient with electronic and online editing and review tools
Oversee editorial review and approval processes during launch phases for assigned brands, to ensure timely delivery and adherence to regulatory and brand standards
Requirements:
BA or BS degree in English or Communications
3-7+ years editing experience within a pharmaceutical company, studio/agency environment or medical publishing company
Extensive experience and knowledge of AMA style guide is a must
Experience reviewing materials using an electronic approval system such as Aprimo or Veeva
Working knowledge of FDA guidance on pharmaceutical advertising
Experience serving as the editorial lead, specifically on a pharmaceutical product launch, managing the workflow and review process
Strong familiarity working within Microsoft Office, specifically Word, Excel, and Teams
Proficient with Adobe Acrobat and Commenting Tools
Meticulous attention to detail
Nice to have:
Strong understanding of pharmaceutical promotional and/or non-promotional materials, as well as product labels
What we offer:
medical health insurance and dental insurance
life insurance
eligibility to participate in 401k plan with company match (if applicable)