Medical Writer (RID00238)

Red Nucleus

Pennsylvania

On-site

USD 55,000 - 75,000

Full time

2 days ago
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Job summary

Red Nucleus is seeking an entry-level Medical Writer to develop clear, accurate scientific content for pharmaceutical, biotechnology, and medical device clients. You will work with senior staff and cross-functional teams to deliver high-quality materials and support literature reviews, editing, and MLR processes.

Ideal candidates have strong scientific writing skills, attention to detail, and familiarity with AMA guidelines, with an advanced degree in a scientific field or relevant experience.

Qualifications

  • Strong scientific writing, editing, and communication skills.
  • Familiarity with AMA style guidelines.
  • Excellent attention to detail, organization, and time management.

Responsibilities

  • Develop clear, accurate scientific content for pharma/biotech/medical device clients.
  • Conduct literature reviews and summarize findings accurately.
  • Proofread and annotate content per AMA and client style guidelines.
  • Maintain document version control and filing standards.
  • Partner with cross-functional teams and participate in client meetings.
  • Support MLR reviews and ensure scientific accuracy of visuals and materials.
  • Build knowledge of therapeutic areas and industry trends.

Skills

Scientific writing
Editing
Communication
Attention to detail
Time management
Independent & collaborative work

Education

Advanced degree in a scientific/healthcare field
Bachelor's or master's with applicable experience

Tools

Microsoft Office
Adobe Acrobat
Virtual collaboration tools

Job description

Job Overview

The Medical Writer is an entry-level role responsible for developing clear, accurate, and engaging scientific content for pharmaceutical, biotechnology, and medical device clients. Working closely with senior scientific staff and cross-functional teams, the Medical Writer supports the delivery of high-quality content that meets client objectives and industry standards.

Content Development
  • Research, write, edit, and reference scientific materials, including slide decks, meeting summaries, posters, manuscripts, training materials, and digital content.
  • Conduct literature reviews and summarize findings accurately.
  • Proofread and annotate content according to AMA, client, and internal style guidelines.
  • Maintain document version control and filing standards.
Collaboration & Communication
  • Partner with scientific, account, design, editorial, and other cross-functional teams.
  • Participate in client meetings and support content-related discussions.
  • Ensure scientific accuracy of visuals and interactive materials.
Quality Assurance
  • Support medical, legal, and regulatory (MLR) review processes and comment resolution.
  • Review content for scientific accuracy, readability, grammar, consistency, and brand alignment.
  • Assist with research, data verification, and reference checks.
Professional Development
  • Build knowledge of therapeutic areas, medical terminology, and industry trends.
  • Manage multiple assignments and deadlines effectively.
  • Seek guidance when needed and contribute positively to team success.
Education
  • Advanced degree in a scientific or healthcare-related field preferred (e.g., MSc, PhD, PharmD, MD).
  • Relevant bachelor's or master's degree with applicable experience may be considered.
Skills & Abilities
  • Strong scientific writing, editing, and communication skills.
  • Ability to interpret and communicate scientific data accurately.
  • Familiarity with AMA style guidelines.
  • Excellent attention to detail, organization, and time management.
  • Proficiency in Microsoft Office, Adobe Acrobat, and virtual collaboration tools.
  • Ability to work independently and collaboratively in a fast-paced environment.

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