Clinical Study Manager

Clinical Study Manager (AI Training)

About the Role

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 oversee the operational execution of clinical trials - ensuring studies run on time, within budget, and to the highest quality standards - while contributing to some of the most advanced AI projects in medicine today.

This is a fully remote, flexible contract role designed for seasoned clinical operations professionals who thrive on keeping complex, multi-workstream studies moving forward without missing a beat.

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

What You'll Do

• Manage clinical trial timelines, milestones, and deliverables to keep projects on track and on schedule
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
• Coordinate with CROs, clinical sites, and internal teams to ensure smooth, seamless study operations
• Identify risks early, resolve operational issues decisively, and keep all stakeholders aligned throughout the full trial lifecycle
• Apply your clinical operations expertise to AI-driven healthcare research projects that are setting new standards in the field

Who You Are

• Experienced in clinical trial project management, with a strong track record managing budgets, timelines, and complex deliverables
• Skilled at managing CROs, vendors, and external research partners to high standards
• Able to coordinate multiple workstreams simultaneously without losing sight of the details
• Proactive, organised, and solutions-oriented - you anticipate problems before they escalate
• Comfortable working independently and asynchronously in a fully remote environment

Nice to Have

• Prior experience with data annotation, data quality assurance, or evaluation systems
• Familiarity with AI tools, healthcare AI applications, or clinical data workflows
• Background in regulatory compliance, GCP, or ICH guidelines

Why Join Us

• Work at the intersection of clinical research and cutting-edge 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 teams and top clinical research organisations
• Gain exposure to advanced large language models and how real-world clinical data shapes AI training
• Potential for ongoing work and contract extension as new projects launch