Pharmaceutical Editor @ Aquent Studios | Jobright.ai
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Pharmaceutical Editor jobs in New Jersey, United States
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Aquent Studios · 6 hours ago

Pharmaceutical Editor

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Actively Hiring
Hiring Manager
Becky Morrissey
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Responsibilities

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 understand or quickly learn how to complete tasks in 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.
Proficient with Adobe Acrobat and Commenting Tools.

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

Copy EditingPharmaceutical KnowledgeAMA Style GuideAprimoVeevaFDA GuidanceAdobe AcrobatProofreadingElectronic Editing Tools

Required

BA or BS degree in English or Communications
5-7+ years editing experience within a pharmaceutical 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
Meticulous attention to detail
Solid working knowledge of grammar, punctuation, and composition
Top notch organizational skills
Ability to comprehend feedback from multiple reviewers
Ability to meet deadlines
Ability to ensure consistency within materials
Ability to make decisions and understand when to escalate issues appropriately
Ability to work with autonomy
Ability to manage multiple projects simultaneously with concurrent deadlines
Proficient with Adobe Acrobat and Commenting Tools

Preferred

Working knowledge preferably Aprimo or Veeva and understand or quickly learn how to complete tasks in workflow system

Company

Aquent Studios

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Aquent Studios is a talent pool and recruiting firm.

Funding

Current Stage
Late Stage
Total Funding
unknown
2018-11-08Acquired· undefined
Company data provided by crunchbase
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Orion

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