Medical Writer

Benefits:

• 401(k)
• 401(k) matching
• Competitive salary
• Flexible schedule
  
  
  

We are seeking a detail-oriented and skilled Medical Writer to join our team. In this fully remote role, you will translate complex scientific and clinical information into clear, accurate, and engaging content for diverse audiences—including healthcare professionals, regulatory authorities, and patients. The ideal candidate has strong scientific literacy, excellent writing skills, and the ability to manage multiple projects in a fast-paced environment.

Key Responsibilities

• Develop high-quality scientific and medical content, including:
• Manuscripts, literature reviews, abstracts, posters
• Clinical study reports, protocols, investigator brochures
• Regulatory documents (e.g., IND, NDA, EMA submissions)
• Medical education and promotional materials
• Patient-friendly materials and website content
• Analyze and interpret clinical data to ensure accuracy and scientific integrity.
• Conduct literature searches and stay current with scientific developments in relevant therapeutic areas.
• Collaborate with cross-functional teams including medical affairs, regulatory, clinical operations, and subject matter experts.
• Ensure all deliverables comply with industry guidelines, regulatory requirements, and internal quality standards.
• Manage multiple projects, including timelines, revisions, and stakeholder communication.
  
  
  

Qualifications

Required

• Bachelor’s, Master’s, PharmD, PhD, MD, or other advanced degree in a life science or health-related field.
• 2 years of experience as a medical writer (regulatory, clinical, scientific, or medical communications).
• Excellent written and verbal communication skills with demonstrated ability to simplify complex concepts.
• Strong understanding of clinical research, biostatistics, and scientific methodology.
• Proficiency with literature databases (e.g., PubMed), referencing, and citation tools.
• Ability to work independently in a remote environment with minimal supervision.
  
  
  

Preferred

• Prior experience in regulatory writing, medical communications agencies, or pharmaceutical/biotech industries.
• Knowledge of AMA style, ICH guidelines, GxP standards, and regulatory documentation requirements.
• Experience writing for multiple therapeutic areas.
• Familiarity with project management tools (e.g., Asana, Jira, Monday.com).
  
  
  

Key Competencies

• Exceptional attention to detail
• Strong organization and time-management skills
• Critical thinking and data interpretation abilities
• Collaboration and communication across teams
• Adaptability and comfort with ambiguity
  
  
  

What We Offer

• Fully remote, flexible work environment
• Competitive compensation and benefits package
• Opportunities for professional growth and continuing education
• Supportive team culture with collaborative workflows
• Exposure to diverse therapeutic areas and high-impact projects
  
  
  

This is a remote position.