Medical Writer (RID00242)

Red Nucleus; Toronto; On-site; CAD 55,000 - 70,000; Full time

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 collaborate with senior staff and cross-functional teams to deliver high-quality materials.

Responsibilities include literature reviews, drafting and editing slide decks, posters, manuscripts, and training materials; proofreading for AMA style; and assisting with literature reference checks and document version control.

Qualifications

• Strong scientific writing, editing, and communication skills.
• Ability to interpret and communicate scientific data accurately.
• Familiarity with AMA style guidelines.

Responsibilities

• Research, write, edit, and reference scientific materials (slides, summaries, posters, manuscripts, training materials).
• Conduct literature reviews and summarize findings accurately.
• Proofread and annotate content according to AMA and internal guidelines.
• Maintain document version control and filing standards.

Skills

Scientific writing

Editing

Communication

AMA style

Time management

Education

Advanced degree in science

BA/MA with experience

Tools

Microsoft Office

Adobe Acrobat

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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