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, provide the real-world knowledge that helps cutting-edge AI models understand how complex research actually works. This is a fully remote, flexible contract role built for seasoned clinical operations professionals who know how to keep trials on track, on budget, and audit-ready.

• 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 from startup through closeout
• Oversee study budgets, forecasting, and financial tracking across multiple vendors and research partners
• Coordinate with CROs, investigator sites, and internal teams to ensure smooth, compliant execution of study operations
• Identify operational risks early, resolve issues proactively, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your hands-on clinical expertise to evaluate and improve AI-generated content related to clinical research workflows

Who You Are

• Experienced clinical trial professional with a strong background in study project management, including budget control and timeline oversight
• Skilled at managing vendors, CROs, and external research partners across multiple concurrent studies
• Able to coordinate complex, multi-workstream projects and keep them running smoothly under pressure
• Naturally detail-oriented and systematic — you catch what others miss
• Clear and confident written communicator who can document findings and decisions effectively
• Self-motivated and reliable when working independently in a remote environment

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation systems
• Familiarity with AI tools or content evaluation workflows
• Background in regulatory compliance, ICH-GCP guidelines, or clinical data management
• Experience working across therapeutic areas or global multi-site trials

Why Join Us

• Work at the intersection of clinical research and cutting-edge AI development alongside leading research labs
• Fully remote and flexible — work when and where it suits you
• Freelance autonomy with the structure of meaningful, task-based project work
• Gain exposure to advanced AI models being trained on real-world clinical research data
• Contribute to meaningful work that improves how AI understands healthcare and clinical science
• Potential for ongoing work and contract extension as new projects launch