Clinical Study Manager

Alignerr Corp.

Brisbane

À distance

AUD 96 000 - 165 000

Temps partiel

Il y a 3 heures
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Résumé du poste

Alignerr seeks an experienced Clinical Study Manager to support operational execution of clinical research projects and help train AI models built on real-world data. This fully remote hourly contract role targets seasoned clinical operations professionals who can manage CROs, multi-site timelines, and stakeholder alignment.

Responsibilities include overseeing timelines, budgets, CRO coordination, risk management, and contributing to AI training data quality workflows.

Qualifications

  • Minimum 5 years of clinical trial project management.
  • Experience managing budgets, timelines and multi-vendor operations.
  • Strong communication and cross-functional collaboration.

Responsabilités

  • Manage clinical trial timelines, milestones and deliverables.
  • Oversee budgets, forecasting and vendor expenditure.
  • Coordinate with CROs, sites and internal teams for quality study execution.
  • Identify operational risks and resolve issues to keep timelines.
  • Support AI training data quality and evaluation workflows.

Connaissances

Budget management
Multi-vendor coordination
Cross-functional teamwork
Communication

Description du poste

About The Role

What if your clinical trial management expertise could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to support the operational execution of clinical research projects — and in doing so, help train the next generation of AI models built on real-world scientific data.

Clinical Study Manager (AI Training)

What if your clinical trial management expertise could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to support the operational execution of clinical research projects — and in doing so, help train the next generation of AI models built on real-world scientific data.

This is a fully remote, flexible contract role built for seasoned clinical operations professionals who know how to keep complex studies on track. If you've managed CROs, juggled multi-site timelines, and kept stakeholders aligned under pressure, this role was made for you.

  • 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 schedule
  • Oversee study budgets, financial forecasting, and expenditure tracking across multiple vendors and research partners
  • Coordinate with CROs, investigator 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 support AI training data quality and evaluation workflows
Who You Are
  • Experienced clinical trial project manager with a strong track record managing budgets, timelines, and multi-vendor operations
  • Skilled at coordinating across CROs, sites, and cross-functional teams in complex research environments
  • Able to manage multiple workstreams simultaneously without losing sight of quality or deadlines
  • A clear, confident communicator who can align stakeholders and resolve friction efficiently
  • Self-directed and reliable — you deliver without needing to be micromanaged
Nice to Have
  • Experience with data annotation, data quality assurance, or evaluation systems
  • Familiarity with AI tools, clinical data platforms, or digital health research environments
  • Background spanning multiple therapeutic areas or study phases
Why Join Us
  • Work on cutting-edge AI projects alongside world-leading research labs
  • Fully remote and flexible — structure your hours around your life
  • Freelance autonomy with the depth and meaning of high-impact scientific work
  • Gain rare exposure to how advanced AI models are trained using real clinical research data
  • Potential for ongoing work and contract extension as new projects launch
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