Princeton10, LLP
Princeton10, LLP
Princeton10, LLP is a healthcare marketing and creative consultancy serving pharmaceutical, biotech, medical device, diagnostics, and health tech organizations. The firm brings together brand strategy, creative development, digital technology, analytics, content, and regulatory-aware communications to support omnichannel marketing and patient-focused programs. Founded in 2017, Princeton10 combines senior hands-on expertise with streamlined processes and a remote-first operating model, working across strategy and execution as an integrated partner for healthcare teams.

Medical Editor - Remote, United States

Edit and fact-check pharmaceutical promotional content for healthcare professionals and patients at P10, a remote creative agency. Apply medical, regulatory, legal, FDA, and brand standards across digital and print campaigns.

Description

  • Edit branded and unbranded healthcare marketing materials for regulatory compliance across digital and print channels.
  • Fact-check and proofread existing copy for adaptation to new audiences and formats.
  • Apply medical, regulatory, and legal expertise to maintain accuracy and consistency with FDA guidance, internal style rules, and brand standards.
  • Copyedit promotional content for grammar, punctuation, spelling, style, flow, and consistency.
  • Review references to confirm they are current and satisfy applicable criteria.
  • Work with project managers, account managers, designers, copywriters, and freelance editors as needed.
  • Maintain alignment with assigned brands and support other editors when required.
  • Coordinate multiple projects in a fast-paced work environment.
  • Report to the Senior Medical Editor.

Requirements

  • Bachelor’s degree in communications, English, journalism, or life sciences, along with at least three years of agency experience editing pharmaceutical promotional materials.
  • Working knowledge of the current AMA style.
  • Experience with medical, regulatory, and legal reviews; familiarity with FDA drug-promotion requirements is preferred.
  • Self-directed, proactive approach with the ability to work independently.
  • Ability to conduct literature searches and understand scientific journals and medical literature.
  • Experience with anchoring or linking in Veeva is a plus.
  • Experience across multiple therapeutic areas and product launches is a plus.
  • Candidates located in the Eastern time zone are preferred.

Benefits

  • Discretionary bonus.
  • Employee benefits.
  • Remote work arrangement.

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