About OpenTrainOpenTrain AI is the #1 platform for finding and building careers in AI training and data labeling. We help professionals discover specialized projects, build a credible profile, and apply to opportunities that match their expertise.As an OpenTrain contractor, you will contribute your clinical writing knowledge to advanced AI training workflows while developing experience in a rapidly growing area of technology.Free OpenTrain account and profileAccess to specialized AI training opportunitiesRemote contract work managed through OpenTrainAbout AI Training WorkAI training is the human side of building artificial intelligence. Expert contributors create examples, review model outputs, and define quality standards that help AI systems produce more accurate and useful work.In this role, your clinical reporting expertise will help establish realistic source materials and evaluation standards for AI systems working with clinical trial documentation.Create high-quality examples for model trainingEvaluate AI-generated content against expert standardsTranslate professional judgment into clear prompts and rubricsWork remotely with flexible schedulingThe RoleOpenTrain is seeking a Clinical Trial CSR AI Training Writer to support workflows involving synthetic clinical trial data and Clinical Study Report authorship. You will combine advanced medical writing expertise with structured evaluation judgment to produce source materials, golden outputs, prompts, and rubrics for AI training.The work is designed for an experienced clinical writer who can manage detailed, full-document assignments and maintain consistency throughout long-horizon clinical reporting workflows.Role focus: Clinical Study Reports and clinical trial AI trainingWork type: Remote part-time contractLocation:



United States or CanadaPay: $90-$150 per hourWhat You'll DoYou will create and assess the materials used to train and measure an AI agent's ability to perform comparable clinical reporting work. The role combines document authorship, synthetic data generation, and detailed quality evaluation.Generate and validate high-quality synthetic clinical trial data for AI trainingAuthor complete sections of Clinical Study Reports based on pre-market clinical trial workDesign prompts representing realistic clinical writing tasks and expected outputsCreate golden outputs that provide reliable quality references for AI-generated workDevelop rubrics measuring the accuracy, completeness, and quality of clinical reportingApply consistent judgment across long-horizon, full-document authorship workflowsMaintain accuracy and completeness across long-form clinical documentationRequirementsThis role requires advanced medical writing expertise and direct experience with pre-market Phase 1-3 clinical trial data. You should be able to author complete Clinical Study Report sections and evaluate clinical writing using precise, defensible criteria.The listing is marked entry level in the source requirements,



but the role itself requires substantial professional experience and advanced qualifications.At least five years of relevant professional experienceTen to twenty-five years of experience preferredDirect experience working with pre-market Phase 1-3 clinical trial dataDemonstrated experience authoring clinical trial reports and complete CSR sectionsPhD or equivalent advanced qualificationAbility to evaluate clinical writing qualityAbility to turn expert judgment into prompts, golden outputs, and rubricsStrong attention to clinical accuracy, document completeness, and evaluation criteriaSchedule, Location, and PayThis is a remote contract opportunity for candidates located in the United States or Canada. At least 20-25 hours of availability per week is required, while 30 or more hours is preferred. The default commitment is 40 hours per week.Work from home from the United States or CanadaMinimum availability: 20-25 hours per weekPreferred availability: 30 or more hours per weekDefault weekly commitment: 40 hoursHourly pay range: $90-$150 USDWhy This Work MattersEvery major AI system depends on carefully prepared and reviewed human examples. By contributing clinical reporting expertise, you can help shape how AI systems handle complex professional documentation and evaluation tasks.OpenTrain brings together opportunities across AI training and data labeling so you can build a lasting portfolio around your specialized skills. Your profile can help demonstrate credible experience and support future applications for relevant projects.Apply specialized clinical writing expertise to cutting-edge AI developmentHelp define what accurate and complete AI-generated reporting looks likeBuild experience in AI training alongside your professional disciplineDevelop a portfolio of specialized evaluation and authorship work #J-18808-Ljbffr

📌 Clinical Trial Csr Ai Training Writer (Ottawa)
🏢 OpenTrain AI
📍 Ottawa