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Clinical Study Manager

Job in Raleigh, Wake County, North Carolina, 27601, USA
Listing for: Alignerr Corp.
Full Time position
Listed on 2026-10-12
Job specializations:
  • Research/Development
    Clinical Research, 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 deep experience managing clinical trials could directly shape how AI understands and advances healthcare research? We're looking for Clinical Study Managers to bring their operational expertise to a unique intersection of clinical science and artificial intelligence - ensuring complex, real-world study data is handled with the precision and rigor that AI training demands. Clinical Study Manager (AI Training) About

The Role What if your deep experience managing clinical trials could directly shape how AI understands and advances healthcare research? We're looking for Clinical Study Managers to bring their operational expertise to a unique intersection of clinical science and artificial intelligence - ensuring complex, real-world study data is handled with the precision and rigor that AI training demands.
  • Organization:
    Alignerr
  • Type:
    Hourly Contract
  • Location:

    Remote
  • Commitment: 10-40 hours/week
What You'll Do
  • Oversee clinical trial timelines, milestones, and deliverables to keep studies on track and on budget
  • Manage study financials - including forecasting, budget tracking, and vendor reconciliation across multiple partners
  • Coordinate with CROs, investigative 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 clinical operations knowledge to help evaluate and improve AI systems trained on healthcare and research data
Who You Are
  • Experienced in clinical trial project management with a strong command of budgets, timelines, and regulatory expectations
  • Skilled at managing CROs, external vendors, and research partners across complex, multi-workstream studiesA natural problem-solver - you anticipate issues before they escalated and know how to keep things moving
  • Highly organized and detail-oriented with the ability to juggle multiple priorities without dropping the ball
  • A clear communicator who keeps cross-functional teams informed and aligned
Nice to Have
  • Experience with data annotation, data quality review, or evaluation workflows
  • Familiarity with AI tools or clinical data management platforms
  • Background working across therapeutic areas or global multi-site trials
Why Join Us
  • Work at the frontier of AI and clinical research alongside world-leading research labs
  • Fully remote and asynchronous - work on your schedule, from anywhere
  • Freelance autonomy with meaningful, substantive work that draws on your real expertise
  • Gain exposure to cutting-edge large language models and how they're trained using real-world clinical data
  • Potential for ongoing work and contract extension as new projects launch
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