Clinical Study Manager
Clinical Study Manager (AI Training)
About The Role
What if your clinical trial expertise could directly shape how AI understands and advances healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and contribute your real-world knowledge to some of the most ambitious AI projects in medicine today.
This is a fully remote, flexible contract role built for seasoned clinical operations professionals who know how to keep complex studies on track. Bring your expertise in timelines, budgets, and vendor management — and help build the future of AI-powered healthcare.
• 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 remain on track and on budget
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
• Coordinate with CROs, investigative sites, and internal teams to ensure smooth, high-quality study operations
• Identify operational risks early, resolve issues decisively, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your clinical expertise to evaluate and improve AI-generated content related to clinical research processes
Who You Are
• Experienced clinical trial project manager with a strong command of budgets, timelines, and operational delivery
• Skilled at managing vendors, CROs, and external research partners across complex, multi-workstream studies
• Organised, proactive, and comfortable navigating the fast-moving demands of clinical trial operations
• Clear communicator who can keep diverse stakeholders informed and aligned
• Detail-oriented and quality-driven — you hold yourself and your projects to a high standard
Nice to Have
• Prior experience with data annotation, data quality review, or evaluation workflows
• Familiarity with AI tools or clinical data platforms
• Background in regulatory affairs, clinical data management, or medical writing
• Experience working across multiple therapeutic areas or global trial settings
Why Join Us
• Work at the intersection of clinical research and cutting-edge AI development
• Partner with world-leading AI research teams and labs on meaningful, high-impact projects
• Fully remote and flexible — work on your own schedule from anywhere
• Freelance autonomy with the structure of substantive, expertise-driven work
• Gain exposure to advanced AI models being trained on real-world clinical data
• Potential for ongoing work and contract extension as new projects launch
About The Role
What if your clinical trial expertise could directly shape how AI understands and advances healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and contribute your real-world knowledge to some of the most ambitious AI projects in medicine today.
This is a fully remote, flexible contract role built for seasoned clinical operations professionals who know how to keep complex studies on track. Bring your expertise in timelines, budgets, and vendor management — and help build the future of AI-powered healthcare.
• 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 remain on track and on budget
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
• Coordinate with CROs, investigative sites, and internal teams to ensure smooth, high-quality study operations
• Identify operational risks early, resolve issues decisively, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your clinical expertise to evaluate and improve AI-generated content related to clinical research processes
Who You Are
• Experienced clinical trial project manager with a strong command of budgets, timelines, and operational delivery
• Skilled at managing vendors, CROs, and external research partners across complex, multi-workstream studies
• Organised, proactive, and comfortable navigating the fast-moving demands of clinical trial operations
• Clear communicator who can keep diverse stakeholders informed and aligned
• Detail-oriented and quality-driven — you hold yourself and your projects to a high standard
Nice to Have
• Prior experience with data annotation, data quality review, or evaluation workflows
• Familiarity with AI tools or clinical data platforms
• Background in regulatory affairs, clinical data management, or medical writing
• Experience working across multiple therapeutic areas or global trial settings
Why Join Us
• Work at the intersection of clinical research and cutting-edge AI development
• Partner with world-leading AI research teams and labs on meaningful, high-impact projects
• Fully remote and flexible — work on your own schedule from anywhere
• Freelance autonomy with the structure of substantive, expertise-driven work
• Gain exposure to advanced AI models being trained on real-world clinical data
• Potential for ongoing work and contract extension as new projects launch