Clinical Study Manager

What if your clinical trial expertise could directly shape how AI understands and communicates healthcare and research concepts to the world? We're looking for experienced Clinical Study Managers to bring their operational know-how to cutting-edge AI research projects - helping ensure that AI models are trained on accurate, high-quality clinical data.

What if your clinical trial expertise could directly shape how AI understands and communicates healthcare and research concepts to the world? We're looking for experienced Clinical Study Managers to bring their operational know-how to cutting-edge AI research projects - helping ensure that AI models are trained on accurate, high-quality clinical data.

This is a fully remote, flexible contract role built for seasoned clinical operations professionals who want to contribute to something genuinely groundbreaking - on their own schedule.

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

• Manage clinical trial timelines, milestones, and deliverables to keep complex studies on track
• Oversee study budgets, forecasting, and financial tracking across multiple vendors and partners
• Coordinate with CROs, investigative sites, and internal teams to ensure smooth operational execution
• Identify risks early, resolve operational issues, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your clinical operations expertise to AI training workflows that demand real-world domain accuracy

• Experienced clinical trial project manager with a strong track record across budgets, timelines, and vendor oversight
• Skilled at managing CROs or external research partners in complex, multi-workstream environments
• Methodical and detail-oriented - you keep studies running smoothly even when things get complicated
• A clear, confident communicator who can align diverse stakeholders without missing a beat
• Self-directed and comfortable working independently in a remote, asynchronous environment

• Prior experience with data annotation, data quality review, or evaluation systems
• Familiarity with AI tools or clinical data platforms
• Background in oncology, rare disease, or other complex therapeutic areas
• Experience contributing to regulatory submissions or audit-ready documentation

• Work at the intersection of clinical research and frontier AI - a genuinely rare opportunity
• Fully remote and flexible - structure your hours around your life, not the other way around
• Freelance autonomy with the substance of meaningful, high-impact project work
• Collaborate with world-leading AI research labs and contribute to how next-generation models understand clinical science
• Potential for ongoing work and contract extension as new projects launch