Medical Writer

Posted Aug 27

This is a fully remote position, open to applicants in United States, +2 more countries.

📋 Description

• Take charge of processes for producing and verifying high-quality synthetic clinical trial data.

• Compose comprehensive sections of clinical study reports (CSRs).

• Develop prompts, ideal outputs, and assessment criteria to measure AI-agent performance.

• Engage in projects aimed at training and improving AI systems.

• Partner with prominent researchers and AI laboratories.


⛳️ Requirements

• Location: United States, Canada, or France.

• A minimum of 5 years of experience is necessary; 10 to 25 years is preferred.

• A PhD or an equivalent qualification is required.

• Must be available for at least 20 to 25 hours per week; 30+ hours is preferred.

• Experience with pre-market (Phases 1-3) clinical trial data is essential.

• Proven experience in authoring clinical trial reports and comprehensive CSR sections.

• Ability to create prompts, ideal outputs, and evaluation rubrics for AI agents.

• Comfortable with extensive document authorship over long periods.

• Must operate as an independent contractor.

• H1-B and STEM OPT candidates are not eligible.


🏝️ Benefits

• Fully remote position with flexible scheduling options.

• Weekly payments processed through Stripe or Wise.

• Competitive compensation.

• Opportunity to collaborate with leading researchers.

• Chance to contribute to the development of next-generation AI systems.

• Referral bonus of up to $600 for each successful referral.

• Reasonable accommodations available upon request.

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