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Clinical Study Manager

Job in Elyria, Lorain County, Ohio, 44035, USA
Listing for: Alignerr Corp.
Full Time position
Listed on 2026-10-09
Job specializations:
  • IT/Tech
    AI Evaluation
Salary/Wage Range or Industry Benchmark: 55000 - 96000 USD Yearly USD 55000.00 96000.00 YEAR
Job Description & How to Apply Below
About

The Role

What if your clinical trial expertise could directly shape how AI understands and navigates the complex world of healthcare research? We're looking for experienced Clinical Study Managers to bring real-world operational knowledge to cutting-edge AI projects — helping ensure that AI-generated clinical content, workflows, and data reflect the highest standards of trial management.

Clinical Study Manager (AI Training)

What if your clinical trial expertise could directly shape how AI understands and navigates the complex world of healthcare research? We're looking for experienced Clinical Study Managers to bring real-world operational knowledge to cutting-edge AI projects — helping ensure that AI-generated clinical content, workflows, and data reflect the highest standards of trial management.

  • 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 studies stay on track and meet quality standards
  • Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
  • Coordinate with CROs, clinical sites, and internal teams to support smooth execution of trial operations
  • Identify operational risks early, resolve issues proactively, and keep all stakeholders aligned throughout the trial lifecycle
  • Apply your clinical expertise to evaluate and improve AI-generated content and workflows related to clinical research
Who You Are
  • Experienced in clinical trial project management, with a strong command of budgets, timelines, and milestone tracking
  • Proven track record managing vendors, CROs, or external research partners
  • Skilled at juggling multiple work streams and keeping complex, multi-site studies running smoothly
  • Detail-oriented and systematic — you catch what others miss and document everything clearly
  • Self-directed 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 clinical data platforms
  • Background in regulatory affairs, clinical operations, or healthcare technology
  • Experience contributing to process improvement or quality assurance in a research setting
Why Join Us
  • Work on cutting-edge AI projects alongside leading research labs and AI teams
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with meaningful, expertise-driven work
  • Gain direct exposure to advanced AI models being trained on real-world clinical data
  • Contribute to projects at the frontier of healthcare and artificial intelligence
  • Potential for ongoing work and contract extension as new projects launch
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