About the role:
We’re looking for a detail-oriented Content Writer to join our clinical communications team. You’ll create clear, accurate, and compliant written materials that support clinical research and help people understand important health information. This is a fully remote position perfect for someone starting or building a career in medical and scientific writing.
No prior experience in this field is required—we provide full training and work closely with you to develop your skills. You’ll gain hands-on experience in document design, authoring, editing, and review processes while learning industry best practices.
What you’ll do:
• Write and edit high-quality clinical and regulatory documents with attention to accuracy and clarity
• Collaborate with cross-functional teams to plan, review, and finalize documents
• Learn and apply principles of clear health communication and plain language writing
• Manage multiple projects in a deadline-driven environment
• Identify solutions to writing and process challenges and communicate progress to team leads
• Develop knowledge of clinical research, regulatory requirements, and relevant disease areas
• Participate in process improvement initiatives
• Work with shared document systems and writing tools
Skills/background needed:
• Bachelor’s degree (preferably in a health, scientific, or life sciences field)
• Strong written and oral communication skills
• Excellent attention to detail and analytical thinking
• Ability to manage multiple projects and work to tight deadlines
• Comfortable working both independently and as part of a team
• Proficiency with Microsoft Word, Microsoft Excel, and Google Docs
• Familiarity with shared document systems like Google Drive or similar platforms
• Willingness to learn new tools and adapt to emerging technology
• Problem-solving skills and ability to think logically through complex information
Nice to have:
• Familiarity with clinical research, clinical trial design, or basic statistics
• Experience with clinical regulatory documents, protocol registrations, or medical publications
• Knowledge of regulations around clinical trial registration and disclosure
What we offer:
• Fully remote work—no office required
• Comprehensive training and career development support
• Collaborative, supportive team environment
• Opportunities to grow your expertise in medical writing
• Standard benefits package including healthcare, retirement, and paid time off
Rate: Competitive entry-level pay, details shared upon application.
Contract length: Regular, full-time
Location: Open to applicants worldwide. Work from home.
We are committed to creating an inclusive hiring process and welcome applicants from all backgrounds and experiences. We believe diverse perspectives strengthen our work and encourage you to apply if you meet the core requirements, even if you don’t check every box.
Ready to get started? Submit your application below.