Freelance MedTech Content Writer for Sora Union

Sora Union; United States; On-site; USD 51,400 - 85,500; Full time

Job summary

A professional services company is seeking a Technical Content Writer to support healthcare and life sciences projects. The ideal candidate will have a strong background in medtech, radiology, or clinical trials, and be responsible for writing, editing, and ensuring accuracy across diverse content formats. This temporary role targets mid-senior level writers in the U.S. with a salary range of $51,400 to $85,500.

Qualifications

• 4+ years of experience in technical writing, ideally within medtech or clinical trials.
• Near-native English fluency to cater to U.S. audience.
• Strong portfolio covering technical, regulatory, and digital formats.

Responsibilities

• Collaborate with teams to ensure technical accuracy.
• Translate complex data into understandable narratives.
• Write/edit various healthcare materials like white papers and brochures.

Skills

Technical writing

Understanding of medtech

Editing and proofreading

Research skills

Collaboration

Familiarity with U.S. healthcare terms

Education

Bachelor’s degree in Communications, Journalism, or related field

Advanced degree in healthcare writing or biomedical sciences

Tools

Notion

Google Docs

Job description

Freelance MedTech Content Writer for Sora Union

Talent is everywhere, opportunity is not. Sora Union changes that.

Sora Union is a globally distributed professional services company that specializes in Design, Software Engineering, QA. Our experienced talent comes from communities where there is displacement or risk of displacement due to conflict or climate change. We provide services to global companies and start-ups across various industries, including healthcare, financial services, technology, and education.

We’re looking for a Technical Content Writer with a strong background in medtech, radiology, or clinical trials to support content projects for healthcare and life sciences clients.

This role blends technical precision, storytelling clarity, and editorial excellence. You’ll collaborate closely with designers and brand copywriters, serving as the technical editor and sanity check, ensuring that every piece of content, from long‑form narratives to UI microcopy, is clear, accurate, and appropriate for its audience.

You’ll be responsible for reviewing, editing, and refining content when clinical or technical detail is involved, translating complex information into structured, engaging, and easy‑to‑understand narratives.

Responsibilities

• Collaborate with copywriters and designers to ensure technical accuracy and clarity across all content formats.
• Translate complex clinical data and study outcomes into structured narratives for various stakeholders—clinicians, researchers, patients, and regulators.
• Write and edit a range of healthcare and scientific materials: white papers, abstracts, product manuals, regulatory docs, and articles; patient education materials, brochures, and internal documentation.
• Conduct interviews with medical experts and researchers to validate content and messaging.
• Perform research and literature reviews to support evidence‑based writing.
• Review reports and studies to extract core insights and shape messaging.
• Act as the final editorial checkpoint for content involving medical or technical subject matter.
• Ensure consistency, accuracy, and alignment with brand tone, regulatory standards, and content strategy.
• Maintain organized records, document versioning, and writing guidelines.

Qualifications

• :Bachelor’s degree in Communications, Journalism, English, Life Sciences, or a related field
• dAdvanced degree in healthcare writing, biomedical sciences, or related disciplines is a plus
• sNear‑native fluency in English, with the ability to write and edit content for U.S.-based medical, scientific, and professional audience
• s4+ years of experience in technical or scientific writing, ideally within medtech, radiology, or clinical trial
• sStrong portfolio demonstrating versatility across formats—technical, regulatory, and digital content
• tProven ability to proofread and edit content for clarity, flow, and scientific accuracy
• yFamiliarity with U.S. healthcare terminology, clinical workflows, and regulatory documentation standard
• sComfortable collaborating with designers, marketers, and product teams in cross‑functional environment
• sFamiliarity with tools like Notion, Google Docs, or structured documentation platforms used in content or clinical workflows
• .Sora Union is committed to creating and fostering a diverse team. We encourage people from underrepresented backgrounds and all walks of life to apply. We are committed to providing reasonable accommodations to all applicants throughout the application process

Seniority level

Mid‑Senior level

Employment type

Temporary

Job function

Marketing

Industries

Professional Services

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