Senior Pharma Copywriter - Remote (US/Canada)

Princeton10

United States

Remote

USD 90,000 - 130,000

Full time

2 days ago
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Job summary

Princeton10 is seeking a Senior Copywriter to join a remote-friendly team dedicated to pharmaceutical marketing. You will craft compelling, compliant copy for digital and print campaigns, ensuring alignment with briefs and brand guidelines.

You will collaborate with cross-functional teams, stay current on regulatory direction, and manage multiple projects to meet tight deadlines while maintaining a high standard of quality.

Qualifications

  • Bachelor's degree in marketing, communications, life sciences, or a related field.
  • 4+ years experience in copywriting, preferably in a pharmaceutical setting.
  • In-depth knowledge of pharmaceutical regulations and industry trends.
  • Strong collaboration skills and ability to work across departments.

Responsibilities

  • Develop copy that aligns with briefs, strategy and brand guidelines.
  • Independently write and review copy for pharma marketing materials across digital and print.
  • Manage multiple projects and meet stringent deadlines.
  • Collaborate with art resources to ensure copy/design continuity.
  • Implement tone of voice and brand messaging guidelines.
  • Maintain up-to-date knowledge of medical/regulatory direction for accuracy.
  • Review reference sources, create citations, and reference content as needed.
  • Present copy and deliverables to the internal team.
  • Anticipate and proactively resolve creative challenges.
  • Contribute ideas aligned to the brand's marketing strategies.

Skills

Copywriting
Regulatory knowledge
Collaboration

Education

Bachelor's degree in marketing or life sciences

Job description

Princeton10 is seeking a Senior Copywriter to join a remote-friendly team dedicated to pharmaceutical marketing. You will craft compelling, compliant copy for digital and print campaigns, ensuring alignment with briefs and brand guidelines.

You will collaborate with cross-functional teams, stay current on regulatory direction, and manage multiple projects to meet tight deadlines while maintaining a high standard of quality.

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