Clinical Study Manager
Alignerr · Seattle, WA
CONTRACT
Posted Sep 7, 2026
Job Description
Clinical Study Manager (AI Training)
About The Role
What if your clinical trial expertise could directly shape how the world's most advanced AI systems understand healthcare and medical research? We're looking for experienced Clinical Study Managers to bring real-world operational rigor to AI projects that sit at the intersection of clinical science and cutting-edge technology.
This is a fully remote, flexible contract role. You'll apply your clinical operations background to meaningful work — helping ensure AI models are trained on accurate, high-quality, and expertly evaluated clinical data.
- 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 complex projects on track
- Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and partners
- Coordinate with CROs, research sites, and internal teams to ensure smooth operational execution
- Identify risks early, resolve operational issues, and keep stakeholders aligned throughout the trial lifecycle
- Apply your clinical expertise to evaluate and quality-check AI-generated content in healthcare and research contexts
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Experienced in clinical trial project management, with a strong command of budgets, timelines, and vendor oversight
- Proven track record coordinating with CROs, external research partners, or multi-site study teams
- Skilled at managing multiple complex workstreams simultaneously without losing quality or momentum
- Detail-oriented and systematic — you catch problems before they become crises
- Clear and effective communicator, comfortable working cross-functionally in distributed environments
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
- Experience working in biotech, pharma, or academic research settings
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, high-impact work
- Gain direct exposure to advanced AI systems and how they're trained using real-world clinical data
- Contribute to projects that sit at the forefront of healthcare AI development
- Potential for ongoing work and contract extension as new projects launch
About The Role
What if your clinical trial expertise could directly shape how the world's most advanced AI systems understand healthcare and medical research? We're looking for experienced Clinical Study Managers to bring real-world operational rigor to AI projects that sit at the intersection of clinical science and cutting-edge technology.
This is a fully remote, flexible contract role. You'll apply your clinical operations background to meaningful work — helping ensure AI models are trained on accurate, high-quality, and expertly evaluated clinical data.
- 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 complex projects on track
- Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and partners
- Coordinate with CROs, research sites, and internal teams to ensure smooth operational execution
- Identify risks early, resolve operational issues, and keep stakeholders aligned throughout the trial lifecycle
- Apply your clinical expertise to evaluate and quality-check AI-generated content in healthcare and research contexts
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Experienced in clinical trial project management, with a strong command of budgets, timelines, and vendor oversight
- Proven track record coordinating with CROs, external research partners, or multi-site study teams
- Skilled at managing multiple complex workstreams simultaneously without losing quality or momentum
- Detail-oriented and systematic — you catch problems before they become crises
- Clear and effective communicator, comfortable working cross-functionally in distributed environments
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
- Experience working in biotech, pharma, or academic research settings
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, high-impact work
- Gain direct exposure to advanced AI systems and how they're trained using real-world clinical data
- Contribute to projects that sit at the forefront of healthcare AI development
- Potential for ongoing work and contract extension as new projects launch
Additional Details
- City
- Seattle
- State
- Washington
- Country
- US
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