Medical Editor - Medical Communications

2 months ago
Full-time
Mid Level
Technical Writing and Documentation

Precision AQ

Precision AQ is a life sciences commercialization and healthcare consulting company that helps biopharma companies bring therapies to market and improve patient access. It describes itself as a commercialization partner for biopharma innovators, market access teams, and brand strategists, with expertise spanning access strategy, HEOR, medical communications, market access, data and analytics, branding, investor relations, and omnichannel/product solutions.

Business Consulting and Services
1001-5000

Description

  • Lead editorial work for assigned accounts, including medical editing, fact checking, and preparation of pharmaceutical marketing materials for submission.
  • Copy edit projects for spelling, grammar, consistency, tone, balance, creative brief alignment, client style, and accurate referencing.
  • Perform fact checking and clean reads for unbranded claims, core promotional materials, and data-related claims.
  • Review client and medical/legal/regulatory (MLR) changes in the context of the full piece and edit accordingly.
  • Prepare MLR submissions as needed, including tagging and linking materials in the client submission system.
  • Assume lead editing responsibilities across one or more accounts.
  • Represent the department in internal kickoff meetings and status meetings.
  • Ensure pieces comply with each client’s MLR submission process and best practices.
  • Work collaboratively with account teams to identify and suggest improvements to internal routing processes.

Requirements

  • Bachelor’s degree in a related field such as Communications, English, Life Science, or Regulatory.
  • Minimum of 3 years of editing experience in the medical communications, pharmaceutical, and/or healthcare industry.
  • At least 1 year of experience in advertising and/or pharmaceutical marketing preferred.
  • At least 1 year of experience editing publications such as manuscripts or posters preferred.
  • Strong proficiency with Microsoft Word, PowerPoint, and Adobe Acrobat.
  • Familiarity with scientific search engines such as PubMed and Google Scholar.
  • Strong proficiency in American Medical Association (AMA) Style, 11th edition.
  • Familiarity with Medical Legal Regulatory (MLR) requirements and client submission platforms such as Veeva.
  • Strong written and verbal communication skills and mastery of English grammar.
  • Ability to prioritize deadline-sensitive projects and manage competing priorities.
  • High degree of autonomy, attention to detail, and team orientation.
  • Experience with MLR reviews preferred.
  • Knowledge of FDA requirements for pharmaceutical advertising preferred.
  • Familiarity with editing long-form writing such as publications or dossiers preferred.

Benefits

  • Compensation range of $54,400 to $81,600 USD.
  • Eligible for a discretionary annual bonus.
  • Health insurance coverage.
  • Retirement savings benefits.
  • Life insurance and disability benefits.
  • Parental leave.
  • Paid time off for sick leave and vacation.
  • Remote work designation indicated by #LI-REMOTE.

Interested in this position?

Apply directly on the company website

Apply Now

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