Medical Writer (RID00241)

Red Nucleus; Yardley (Bucks County); Sur place; USD 55 000 - 75 000; Plein temps

Résumé du poste

Red Nucleus is seeking an entry-level Medical Writer to develop clear and accurate scientific content for pharma, biotech, and medical device clients. You will work with senior staff and cross-functional teams to deliver high-quality materials, including slides, posters, and manuscripts.

Responsibilities include literature reviews, AMA-style proofreading, and contributing to MLR reviews while growing knowledge in therapeutic areas and industry standards.

Qualifications

• Strong scientific writing and editing abilities.
• Familiarity with AMA style guidelines.
• Excellent attention to detail and time management.
• Proficiency in MS Office and Adobe Acrobat.
• Ability to work independently and in teams.

Responsabilités

• Write, edit, and reference scientific materials including posters, manuscripts, slides, and training content.
• Conduct literature reviews and summarize findings accurately.
• Proofread according to AMA style, client, and internal guidelines.
• Maintain document version control and filing standards.
• Collaborate with cross-functional teams and participate in client meetings.
• Support medical, legal, and regulatory (MLR) review processes and ensure scientific accuracy.

Connaissances

Scientific writing

Editing

AMA style

Time management

Communication

Team collaboration

Video conferencing

Formation

Advanced degree in science

Bachelor's/master's in science

Outils

EndNote

Adobe Acrobat

MS Office Suite

Description du poste

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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