Alignerr logo

Clinical Study Manager

Alignerr
Department:Project Management
Type:REMOTE
Region:Australia
Location:Sydney, New South Wales, Australia
Experience:Mid-Senior level
Estimated Salary:A$80,000 - A$120,000
Skills:
CLINICAL TRIAL MANAGEMENTBUDGET MANAGEMENTFINANCIAL FORECASTINGVENDOR MANAGEMENTCRO COORDINATIONRISK MANAGEMENTDATA ANNOTATIONREGULATORY AFFAIRS
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Job Description

Posted on: June 24, 2026

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 support the operational execution of clinical trials — while helping to inform how cutting-edge AI models learn from real-world clinical data. This is a fully remote, flexible contract role built for seasoned clinical operations professionals who want meaningful, high-impact work on their own schedule.

  • 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 studies on track and on budget
  • Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
  • Coordinate with CROs, trial sites, and internal teams to ensure seamless execution of study operations
  • Identify risks early, resolve operational issues, and keep all stakeholders aligned across the full trial lifecycle
  • Apply your clinical expertise to support AI training projects grounded in real-world research workflows

Who You Are

  • Experienced clinical trial project manager with a strong track record managing budgets, timelines, and multi-vendor environments
  • Skilled at coordinating across CROs, sites, and cross-functional teams in complex study settings
  • Comfortable managing multiple workstreams simultaneously without losing sight of the details
  • Self-directed and reliable — you deliver quality work without needing hand-holding
  • Strong written communicator who can document findings and decisions clearly

Nice to Have

  • Prior experience with data annotation, data quality review, or evaluation systems
  • Familiarity with AI tools or clinical data platforms
  • Background in regulatory affairs, clinical data management, or medical writing

Why Join Us

  • Work on cutting-edge AI and healthcare research projects alongside leading AI research labs
  • Fully remote and flexible — structure your hours around your life
  • Freelance autonomy with the substance of meaningful, expert-level work
  • Gain direct exposure to how advanced AI models are trained using real-world clinical data
  • Potential for ongoing work and contract extension as new projects launch
Originally posted on LinkedIn

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