Clinical Study Manager
Alignerr · Cambridge, England
CONTRACT
Posted Sep 7, 2026
Job Description
Clinical Study Manager (AI Training)
About The Role
What if your expertise in clinical trial operations could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and to bring that real-world knowledge to the frontier of AI development.
This is a fully remote, flexible contract role built for seasoned clinical research 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, investigative sites, and internal teams to ensure smooth, compliant study execution
- Identify operational risks early, resolve issues proactively, and keep stakeholders aligned throughout the trial lifecycle
- Apply your clinical research expertise to evaluate and improve AI-generated content in healthcare and life sciences contexts
Who You Are
- Experienced clinical trial project manager with a strong command of budgets, timelines, and trial logistics
- Skilled at managing CROs, vendors, or external research partners across complex multi-site studies
- Able to coordinate multiple workstreams simultaneously without losing sight of the details
- Methodical, organized, and confident operating independently in a remote environment
- Clear written communicator who can document findings and feedback with precision
Nice to Have
- Prior experience with data annotation, data quality review, or evaluation workflows
- Familiarity with AI tools or clinical data platforms
- Background spanning multiple therapeutic areas or study phases
- Experience contributing to regulatory submissions or audit-ready documentation
Why Join Us
- Work alongside world-leading AI research teams on projects at the intersection of healthcare and technology
- Fully remote and flexible — set your own hours and work from anywhere
- Freelance autonomy with the structure of meaningful, task-based assignments
- Gain direct exposure to how advanced AI models are trained using real-world clinical expertise
- Potential for ongoing work and contract extension as new projects launch
About The Role
What if your expertise in clinical trial operations could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and to bring that real-world knowledge to the frontier of AI development.
This is a fully remote, flexible contract role built for seasoned clinical research 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, investigative sites, and internal teams to ensure smooth, compliant study execution
- Identify operational risks early, resolve issues proactively, and keep stakeholders aligned throughout the trial lifecycle
- Apply your clinical research expertise to evaluate and improve AI-generated content in healthcare and life sciences contexts
Who You Are
- Experienced clinical trial project manager with a strong command of budgets, timelines, and trial logistics
- Skilled at managing CROs, vendors, or external research partners across complex multi-site studies
- Able to coordinate multiple workstreams simultaneously without losing sight of the details
- Methodical, organized, and confident operating independently in a remote environment
- Clear written communicator who can document findings and feedback with precision
Nice to Have
- Prior experience with data annotation, data quality review, or evaluation workflows
- Familiarity with AI tools or clinical data platforms
- Background spanning multiple therapeutic areas or study phases
- Experience contributing to regulatory submissions or audit-ready documentation
Why Join Us
- Work alongside world-leading AI research teams on projects at the intersection of healthcare and technology
- Fully remote and flexible — set your own hours and work from anywhere
- Freelance autonomy with the structure of meaningful, task-based assignments
- Gain direct exposure to how advanced AI models are trained using real-world clinical expertise
- Potential for ongoing work and contract extension as new projects launch
Additional Details
- City
- Cambridge
- State
- England
- Country
- GB
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