Clinical Study Manager

What if your clinical trial expertise could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to bring real-world operational knowledge to cutting-edge AI projects — helping ensure the models influencing the future of medicine are built on accurate, high-quality clinical foundations.

What if your clinical trial expertise could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to bring real-world operational knowledge to cutting-edge AI projects — helping ensure the models influencing the future of medicine are built on accurate, high-quality clinical foundations.

This is a fully remote, flexible contract role. If you have a strong background in clinical trial operations and know what it takes to keep complex studies running on time and on budget, we want to hear from you.

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

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

• Proven background in clinical trial project management — you understand budgets, timelines, and what it takes to deliver
• Experienced in managing CROs, external vendors, or research partners across complex, multi-workstream studies
• Skilled at keeping moving parts organized without letting anything slip through the cracks
• Clear communicator who can align diverse teams around shared goals and timelines
• Self-motivated and comfortable working independently in a remote, asynchronous environment

• Prior experience with data annotation, data quality assurance, or evaluation workflows
• Familiarity with AI tools or clinical data platforms
• Background in regulatory affairs, clinical operations, or medical research
  
  Experience working across multiple therapeutic areas or trial phases

• Work on cutting-edge AI and healthcare research projects alongside leading AI labs and research teams
• Fully remote and flexible — structure your work around your life, not the other way around
• Freelance autonomy with the substance of meaningful, expert-level work
• Gain rare exposure to how advanced AI models are trained using real-world clinical data
• Contribute to work that sits at the intersection of clinical science and the future of AI
• Potential for ongoing work and contract extension as new projects launch