Freelance Medical Writer

Company Description Path-iQ helps pathologists, laboratories, and researchers move from traditional, fragmented workflows to a unified, digital-first environment powered by artificial intelligence. The platform supports AI-assisted analysis of histopathology images, cloud-based case access and collaboration, and scalable, workflow-driven diagnostics. By improving turnaround times for critical cases, Path-iQ aims to make cancer diagnosis faster, more accessible, and more consistent regardless of location. The company is building the infrastructure layer for the future of pathology, where digital workflows and AI-driven insights drive better clinical outcomes.
Role Description This is a remote, contract role for a Freelance Medical Writer. The writer will create clear, accurate, and evidence-based medical and scientific content related to digital pathology, AI-driven diagnostics, and oncology workflows. Daily tasks include researching peer-reviewed literature and clinical guidelines, drafting and refining manuscripts, white papers, case studies, blog posts, and product-related content, and ensuring alignment with regulatory and ethical standards. The role involves collaborating with subject matter experts, product and marketing teams, and reviewing feedback to update and maintain high-quality materials. The writer is expected to manage multiple projects, meet agreed deadlines, and adapt content for different audiences, including clinicians, researchers, and industry stakeholders.
Qualifications
Strong Medical Writing and Medical Communications skills for creating clear, clinically accurate content.
Proficiency in Scientific Writing and Research to synthesize complex data and peer-reviewed literature.
Excellent general Writing skills, including organization, clarity, and attention to detail.
Advanced degree (e.g., MD, DO, PhD, PharmD, or MS in a life science) or equivalent experience in medicine, biomedical sciences, or related field.
Experience with oncology, pathology, or digital health is highly preferred.
Ability to communicate complex technical concepts to both expert and non-expert audiences.
Familiarity with medical publication standards, citation styles, and ethical guidelines (e.g., ICMJE, GPP).
Comfort working independently in a remote setting, with strong time-management and organization skills.
Experience collaborating with cross-functional teams, including clinicians, researchers, and product or marketing stakeholders.
Fluency in English with excellent grammar, style, and consistency.

Work arrangement
No