Clinical Study Manager (AI Training)
About The Role
What if your clinical trial expertise could directly shape how AI understands and supports the future of healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and in doing so, contribute to training the AI models that will power the next generation of medical research tools.
This is a fully remote, flexible contract role built for seasoned clinical operations professionals who know how to keep complex studies on track. If you've spent time managing timelines, wrangling vendors, and keeping stakeholders aligned across the lifecycle of a trial, this role was built for you.

• Organization: Alignerr
• Type: Hourly Contract
• Location: Remote
• Commitment: 10–40 hours/week
  

What You'll Do

• Manage clinical trial timelines, milestones, and deliverables to ensure studies stay on track and on budget
• Oversee study budgets, forecasting, and financial tracking across multiple vendors and research partners
• Coordinate with CROs, clinical sites, and internal teams to ensure smooth, high-quality study execution
• Identify operational risks early, resolve issues efficiently, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your real-world clinical expertise to help evaluate and improve AI-generated content related to clinical research
  

Who You Are

• Experienced in clinical trial project management — you've owned budgets, timelines, and vendor relationships
• Comfortable managing CROs, external research partners, and cross-functional teams simultaneously
• A natural problem-solver who keeps complex, multi-workstream studies running smoothly under pressure
• Detail-oriented and organized — you notice what others miss and act on it before it becomes a problem
• Self-motivated and reliable when working independently in a remote, asynchronous environment
  

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation systems
• Familiarity with AI tools or clinical data platforms
• Background in regulatory affairs, GCP compliance, or clinical data management
  

Why Join Us

• Work on cutting-edge AI and healthcare research projects alongside world-leading AI labs
• Fully remote and flexible — structure your hours around your life
• Freelance autonomy with meaningful, substantive work that draws on your deepest expertise
• Gain firsthand exposure to how advanced AI models are trained using real-world clinical data
• Potential for ongoing work and contract extension as new projects launch

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