Reviewing all types of content with an eye for detail, ensuring correct spelling, grammar, and usability of digital assets
Making minor edits to deliverables including editing storyboards
Functional testing of digital assets
Working with Lead ID to ensure there is consistency across deliverables
Ensuring accuracy and adherence to client and agency style for a variety of deliverable types
Fact-checking all relevant information, ensuring that sources cited are appropriate and content accurately reflects information in sources
Substantively editing materials to improve language usage and information flow
Assisting in linking assets as part of MLR review

8-12 years of experience working as an editor or QC Specialist
Proven experience editing in the pharmaceutical/medical field highly preferred
Degree in Communication, Writing, English, Journalism, or Education or equivalent experience
Attention to detail and accuracy; high level of commitment to exceptional work quality
Balances speed with accuracy in a high-volume review environment
Experience with Articulate 360 and Microsoft Office products including Word, PowerPoint, Excel, and Teams
Familiar with medical-legal-regulatory processes (e.g., Veeva, AMA guidelines)
Able to proactively raise concerns
Ability to follow APA Style for referencing deliverables as well as PDG style guides
Passion for learning and working in a fast-paced, innovative, and creative environment
Able to share a portfolio of relevant writing or instructional design samples
Experience validating clinical references

Performance Development Group

Open Positions (1)