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Looking for a licensed physician (MD or DO) with proven medical writing experience to draft a concise, technically accurate clinical summary (800 to 1200 words) for a medical device regulatory submission 510k-style overview). Requirements: • Active MD or DO license (any country; US, EU, Canada, Australia preferred) • Prior experience writing clinical evaluation reports (CERs), clinical summaries, literature reviews, or regulatory documents • Strong grasp of clinical data interpretation, statistics (p-values, confidence intervals, hazard ratios, Kaplan-Meier, etc.), • Familiarity with MEDLINE/PubMed searching and critical appraisal of RCTs, meta-analyses, and real-world evidence • Fluent in medical English; ability to write in clear, concise, regulatory-grade language (no fluff) Scope (fixed $60): • Review 8–12 provided full-text articles + product IFU • Write a structured clinical summary with sections: Background, Methods of Literature Search, Data Synthesis, Safety & Performance Evaluation, Conclusion • AMA or Vancouver referencing • Delivery in clean Word docx with track changes off • 1 round of minor revisions included To apply, please submit: 1. Your MD/DO degree + license number (can be redacted) 2. 1–2 samples of past medical/regulatory writing (CER, clinical summary, PMC article, etc.) 3. Confirm you are an actual physician (not an agency or non-MD writer) Only physicians with real clinical/regulatory writing experience will be considered. No agencies, no PhDs without MD, no general freelancers. Fixed-price: $60 USD | Deadline: 4 days after hiring Quick turnaround, clear instructions provided.