Clinical Trial CSR AI Training Writer

About OpenTrain

OpenTrain AI is hiring a Clinical Trial CSR AI Training Writer for specialized work at the intersection of medical writing and artificial intelligence. OpenTrain helps people find and build careers in AI training and data labeling, giving contributors a place to develop a credible professional profile and apply for projects in minutes.

This is contract work supporting OpenTrain's AI training portfolio. Creating an OpenTrain account is free.

• Remote contract opportunity
• Part-time schedule with a default 40-hour weekly commitment
• Pay of $90-$150 per hour
• Work focused on clinical trial documentation and AI evaluation

About AI Training and Clinical Documentation

AI training is the human side of building modern artificial intelligence. Specialists create, review, and evaluate examples that help AI systems produce more accurate and useful work. In this role, your clinical writing expertise will help define what high-quality clinical reporting looks like for an AI agent.

You will contribute source materials, realistic prompts, reference answers, and scoring criteria for clinical reporting tasks. This is an opportunity to apply advanced medical documentation judgment to cutting-edge AI development.

• Create expert examples that guide AI system performance
• Translate professional judgment into measurable evaluation standards
• Support long-form, full-document clinical reporting workflows

The Clinical Trial CSR AI Training Writer Role

OpenTrain is recruiting an experienced clinical writer to support AI training workflows involving synthetic clinical trial data and Clinical Study Report authorship. You will produce high-quality source materials and define the prompts, golden outputs, and rubrics used to measure an AI agent's ability to complete comparable clinical writing assignments.

The role involves detailed, sustained work across complete documents and is suited to someone comfortable maintaining accuracy, consistency, and completeness throughout long-form clinical reporting workflows.

• Work with pre-market Phase 1-3 clinical trial data
• Author complete Clinical Study Report sections
• Evaluate clinical writing quality and reporting performance
• Apply consistent judgment across full-document assignments

What You'll Do

You will combine clinical writing expertise with structured evaluation judgment. Your work will help establish reliable training and assessment materials for AI systems handling clinical trial reporting.

• Generate and validate high-quality synthetic clinical trial data for AI training
• Author complete sections of Clinical Study Reports based on pre-market clinical trial work
• Design prompts representing realistic clinical writing tasks and expected outputs
• Create golden outputs that provide reliable quality references for AI-generated work
• Develop rubrics measuring the accuracy, completeness, and quality of AI clinical reporting
• Manage detailed, long-form medical documentation across sustained workflows
• Maintain consistent standards across complete clinical reporting assignments

Required Qualifications

This position requires advanced medical writing expertise and direct experience with clinical trial documentation. The role listing calls for at least five years of relevant professional experience, with ten to twenty-five years preferred.

Candidates should be able to make expert judgments about clinical writing quality and convert those judgments into practical prompts, golden outputs, and rubrics for AI evaluation.

• At least five years of relevant professional experience
• Ten to twenty-five years of relevant experience preferred
• Direct experience with pre-market Phase 1-3 clinical trial data
• Demonstrated experience authoring clinical trial reports and complete CSR sections
• PhD or equivalent advanced qualification
• Ability to generate and validate synthetic clinical trial data
• Ability to design AI evaluation prompts, golden outputs, and rubrics
• Strong attention to clinical accuracy, document completeness, and evaluation criteria

Schedule, Location, and Pay

This is a remote contract role with part-time and contractor engagement options. The role description identifies candidates in the United States or Canada, while the listing's eligible-country data also includes the locations listed below. Availability of at least 20-25 hours per week is required, 30 or more hours is preferred, and the default commitment is 40 hours per week.

• Pay: $90-$150 per hour
• Minimum availability: 20-25 hours per week
• Preferred availability: 30 or more hours per week
• Default commitment: 40 hours per week
• Role type: Remote contract, part-time
• Eligible locations listed: Canada, United States, Denmark, Estonia, Finland, Ireland, Latvia, Lithuania, Norway, Sweden, Austria, Belgium, France, Germany, Netherlands, Switzerland, United Kingdom, Albania, Bosnia and Herzegovina, Croatia, Greece, Italy, Malta, Portugal, Serbia, Slovenia, Spain, Bul

Build Your AI Training Career

AI training and data labeling are growing fields where people help shape how modern AI systems behave. OpenTrain gives contributors a place to discover relevant opportunities, build a profile around credible experience, and develop a long-term portfolio of specialized AI training work.

For an experienced clinical writer, this role offers a way to extend medical documentation expertise into synthetic data creation, generative AI evaluation, and structured quality measurement.

• Apply clinical writing expertise to state-of-the-art AI development
• Build experience in prompts, golden outputs, and evaluation rubrics
• Develop a professional profile for future AI training opportunities
• Work remotely with flexible part-time availability