Clinical Study Manager

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 oversee the operational execution of clinical trials — and help inform the AI systems being built around them.

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 oversee the operational execution of clinical trials — and help inform the AI systems being built around them.

This is a fully remote, flexible contract role designed for seasoned clinical operations professionals who know how to keep complex studies on track. Bring your project management expertise to a unique intersection of clinical research and cutting-edge AI development.

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

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

• Experienced in clinical trial project management, with a strong command of budgets, timelines, and milestones
• Proven track record managing vendors, CROs, or external research partners
• Skilled at coordinating multiple work streams and keeping complex, multi-site studies running smoothly
• Detail-oriented, organized, and comfortable working independently in a remote environment
• A clear communicator who can translate operational complexity into structured, actionable insight

• Prior experience with data annotation, data quality review, or evaluation systems
• Familiarity with AI tools or digital health platforms
• Background spanning multiple therapeutic areas or study phases
• Experience with regulatory submissions or ICH-GCP compliance frameworks

• Work at the intersection of clinical research and some of the most advanced AI development happening today
• Fully remote and flexible — structure your hours around your life
• Freelance autonomy with the substance of meaningful, high-impact work
• Collaborate with leading AI research labs and contribute to projects that push the boundaries of what AI can do in healthcare
• Potential for ongoing engagement and contract extension as new projects launch