Clinical Study Manager
Alignerr · Glasgow, Scotland
CONTRACT
Posted Sep 7, 2026
Job Description
Clinical Study Manager (AI Training)
About The Role
What if your hard-won expertise in clinical trial operations could directly shape how AI understands one of the most complex and high-stakes fields in science? We're looking for experienced Clinical Study Managers to help train and evaluate AI systems on clinical research workflows — bringing real-world operational knowledge to the frontier of AI development.
This is a fully remote, flexible contract role built for seasoned clinical operations professionals. If you've managed trials end-to-end, wrangled CROs, and kept budgets on track under pressure, your expertise is exactly what's needed here.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
What You'll Do
- Oversee and evaluate clinical trial timelines, milestones, and deliverables to ensure projects stay on track
- Apply deep budget management expertise to assess study forecasting, financial tracking, and vendor spend across multiple trials
- Review and assess coordination between CROs, investigative sites, and internal teams to evaluate operational execution quality
- Identify risks, flag operational gaps, and provide structured expert feedback throughout the trial lifecycle
- Leverage your clinical operations background to evaluate AI-generated content, workflows, and outputs for accuracy and real-world applicability
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Experienced in clinical trial project management, with hands-on expertise in budgets, timelines, and study operations
- Proven track record managing vendors, CROs, or external research partners
- Able to manage multiple complex workstreams simultaneously and keep studies running smoothly
- Sharp eye for operational detail — you catch what others miss
- Clear and structured communicator who can document findings and feedback precisely
- Comfortable working independently without close supervision
Nice to Have
- Prior experience with data annotation, data quality review, or evaluation systems
- Familiarity with AI tools, clinical data platforms, or healthcare technology
- Background spanning multiple therapeutic areas or trial phases
- Experience with regulatory submissions, ICH-GCP compliance, or quality management systems
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 the structure of meaningful, high-impact work
- Gain unique exposure to how advanced AI models are trained using real-world clinical expertise
- Be part of a global community of domain experts shaping the future of AI in healthcare
- Potential for ongoing work and contract extension as new projects launch
About The Role
What if your hard-won expertise in clinical trial operations could directly shape how AI understands one of the most complex and high-stakes fields in science? We're looking for experienced Clinical Study Managers to help train and evaluate AI systems on clinical research workflows — bringing real-world operational knowledge to the frontier of AI development.
This is a fully remote, flexible contract role built for seasoned clinical operations professionals. If you've managed trials end-to-end, wrangled CROs, and kept budgets on track under pressure, your expertise is exactly what's needed here.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
What You'll Do
- Oversee and evaluate clinical trial timelines, milestones, and deliverables to ensure projects stay on track
- Apply deep budget management expertise to assess study forecasting, financial tracking, and vendor spend across multiple trials
- Review and assess coordination between CROs, investigative sites, and internal teams to evaluate operational execution quality
- Identify risks, flag operational gaps, and provide structured expert feedback throughout the trial lifecycle
- Leverage your clinical operations background to evaluate AI-generated content, workflows, and outputs for accuracy and real-world applicability
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Experienced in clinical trial project management, with hands-on expertise in budgets, timelines, and study operations
- Proven track record managing vendors, CROs, or external research partners
- Able to manage multiple complex workstreams simultaneously and keep studies running smoothly
- Sharp eye for operational detail — you catch what others miss
- Clear and structured communicator who can document findings and feedback precisely
- Comfortable working independently without close supervision
Nice to Have
- Prior experience with data annotation, data quality review, or evaluation systems
- Familiarity with AI tools, clinical data platforms, or healthcare technology
- Background spanning multiple therapeutic areas or trial phases
- Experience with regulatory submissions, ICH-GCP compliance, or quality management systems
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 the structure of meaningful, high-impact work
- Gain unique exposure to how advanced AI models are trained using real-world clinical expertise
- Be part of a global community of domain experts shaping the future of AI in healthcare
- Potential for ongoing work and contract extension as new projects launch
Additional Details
- City
- Glasgow
- State
- Scotland
- Country
- GB
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