About this role
We’re looking for a Medical Writer to join our team and help create clinical and regulatory documents that support the development of medicines and medical devices. This is a fully remote position ideal for someone starting their career in medical writing or regulatory communications.
What you’ll do
Your main responsibilities will include:
• Prepare and write clinical and regulatory documents to support drug and device development• Work with guidance from senior team members and subject matter experts as you develop your skills• Help coordinate the review and approval of documents, arranging meetings with team members• Produce documents that meet quality and compliance standards while keeping projects on schedule• Learn about US and international regulatory requirements and guidelines for preparing regulatory documents• Identify issues that arise during the writing process and work with the team to resolve them• Collaborate with leadership and quality assurance teams to support documentation needs
Skills/background needed
We’re looking for someone with:
• A Bachelor’s Degree or higher (scientific discipline preferred, but not required)• Some background in the bio-pharmaceutical, biotech, life science, or healthcare industry (or strong interest in these fields)• Excellent written and oral communication skills• Knowledge of medical and scientific terminology• Ability to read, understand, and work with complex data and scientific information• Experience or familiarity with writing and editing clinical and regulatory documents• Understanding of drug development, clinical research, and basic regulatory requirements• Strong organisational and time management skills• Ability to manage multiple projects and work well with people across different teams
Location
Fully remote – work from home, open to applicants worldwide.
Contract length
Details shared upon application.
Rate
Competitive entry-level pay, details shared upon application.
What we offer
• Full training provided to help you succeed in this role• Flexible remote work arrangement• Comprehensive benefits package• Opportunity to develop expertise in medical writing and regulatory communications• Supportive team environment with mentoring from experienced professionals
Why apply
This is an excellent opportunity to launch a career in medical writing and regulatory communications. You’ll work on meaningful projects that contribute to bringing medicines and medical devices to people who need them, while developing valuable skills in a growing field. No prior medical writing experience is necessary – we provide full training and support as you learn.
Ready to get started? Submit your application below.