Clinical Study Manager

Alignerr Corp.

Vancouver

Remote

CAD 83,000 - 124,000

Part time

5 days ago
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Job summary

Alignerr is seeking an experienced Clinical Study Manager to oversee operational execution of clinical trials for AI training initiatives. This fully remote hourly contract role is designed for senior professionals who want to contribute clinical science expertise to cutting-edge AI projects in development.

You will manage timelines, budgets, CROs and sites across multiple studies, identify risks early, and ensure high-quality study operations while working independently in a flexible,

Qualifications

  • Experienced clinical trial project manager with a strong track record managing budgets, timelines, and deliverables.
  • Skilled at coordinating vendors, CROs, and external research partners across multiple concurrent workstreams.
  • Detail-oriented and systematic — you catch problems before they elevate and keep complex studies running smoothly.
  • Clear, confident communicator who can align stakeholders at every level.
  • Self-motivated and comfortable working independently in a remote, asynchronous environment.

Responsibilities

  • Manage clinical trial timelines, milestones, and deliverables to ensure projects stay on track and on budget.
  • 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, high-quality study operations.
  • Identify risks early, resolve operational issues decisively, and keep all stakeholders aligned throughout the trial lifecycle.
  • Apply your clinical research expertise to evaluate and improve AI-generated content related to clinical trial methodology and operations.

Skills

Clinical trial management
Budget & timelines
Vendor coordination
Remote work
Communication

Job description

Clinical Study Manager (AI Training)
About The Role

What if your expertise in clinical trial operations could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and bring real-world domain knowledge to some of the most advanced AI projects in development today.

This is a fully remote, flexible contract role built for seasoned clinical research professionals who want to contribute their expertise to a frontier field. If you know how to keep complex studies on track, this is your opportunity to do it at the intersection of clinical science and AI.

  • 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 projects stay on track and on budget
  • 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, high-quality study operations
  • Identify risks early, resolve operational issues decisively, and keep all stakeholders aligned throughout the trial lifecycle
  • Apply your clinical research expertise to evaluate and improve AI-generated content related to clinical trial methodology and operations
Who You Are
  • Experienced clinical trial project manager with a strong track record managing budgets, timelines, and deliverables
  • Skilled at coordinating vendors, CROs, and external research partners across multiple concurrent workstreams
  • Detail-oriented and systematic — you catch problems before they elevate and keep complex studies running smoothly
  • Clear, confident communicator who can align stakeholders at every level
  • Self-motivated and comfortable working independently in a remote, asynchronous environment
Nice to Have
  • Prior experience with data annotation, data quality review, or evaluation systems
  • Familiarity with AI tools or content evaluation platforms
  • Background working across multiple therapeutic areas or global study sites
  • Experience with regulatory submissions or ICH-GCP compliance
Why Join Us
  • Work on cutting-edge AI and healthcare research projects alongside leading research labs
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, project-based work
  • Gain direct exposure to advanced AI models and how real-world clinical data shapes their development
  • Potential for ongoing work and contract extension as new projects launch
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