Freelance Medical Writer – Ophthalmology, AI-MDSW

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deepeye Medical

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2021

🤖 Artificial Intelligence

⚕️ Healthcare Insurance

🧬 Biotechnology

💰 Seed Round on 2023-11

Artificial Intelligence • Healthcare Insurance • Biotechnology

deepeye Medical is a company focused on empowering ophthalmology with AI-driven therapy planning support for retinal eye diseases. They provide specialized AI tools for ophthalmologists to improve treatment outcomes and adherence, particularly focusing on conditions like Age-related Macular Degeneration (AMD). deepeye also offers a research platform that enhances clinical studies and trials using advanced AI and data management for precision medicine in retinal therapy.

📋 Description

• Lead the preparation, update, and quality control of Clinical Evaluation Plan (CEP) and Clinical Evaluation Report (CER) • Design and document systematic literature searches, appraise clinical evidence, and produce evidence synthesis • Support PMCF planning and reporting, and where applicable, the SSCP • Translate clinical and technical data into scientific manuscripts, research summaries, and white papers • Act as the link between clinical, R&D, and regulatory teams, ensuring clinical evidence is reflected in documentation • Establish project-specific style guidelines and maintain high quality standards

🎯 Requirements

• Suitably qualified evaluator with expertise in the diagnosis and management of the target indication • Reliable freelancer mindset with strong project management • Demonstrated experience drafting and editing scientific manuscripts/abstracts/posters and other clinical/scientific communications in English • Proven track record (5+ years) in medical writing for medical devices (ideally SaMD/AI) • Ability to plan and execute systematic literature searches, critically appraise clinical data, and synthesize evidence • Hands-on experience authoring and/or updating Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER) in accordance with Regulation (EU) 2017/745 (EU MDR)

🏖️ Benefits

• Project-based collaboration • Flexible, fully remote setup • Potential for long-term partnership on upcoming clinical and regulatory projects • Startup culture & a great, international team • High personal responsibility for your project & fast personal growth • Direct impact on improving quality of life for our end users (patients)