Clinical Study Manager

Alignerr Corp.; Glasgow; Remote; GBP 62,000 - 103,000; Part time

Job summary

Alignerr is seeking an experienced Clinical Study Manager to train and evaluate AI systems on clinical research workflows. This remote, hourly contract role invites seasoned clinical operations professionals to shape AI understanding with real-world expertise.

Manage trials end-to-end, coordinate CROs and vendors, and provide structured feedback while working on your own schedule. If you have hands-on study operations experience, budget control, and a track record of managing multiple trials,

Qualifications

• Experience in clinical trial project management with budgets, timelines and study operations.
• Proven track record managing vendors, CROs, or external research partners.

Responsibilities

• Oversee and evaluate trial timelines, milestones and deliverables.
• Apply budget management expertise to study forecasting and vendor spend.
• Review coordination between CROs, investigative sites, and internal teams to assess execution quality.
• Identify risks, flag operational gaps, and provide structured feedback throughout the trial lifecycle.
• Evaluate AI-generated content, workflows and outputs for accuracy and real-world applicability.
• Work independently and asynchronously on your own schedule.

Skills

Clinical trial management

Budget & forecasting

Vendor coordination

Independent work

Tools

Project management tools

Job description

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.

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