Clinical Study Manager

Alignerr Corp.; Birmingham; Remote; GBP 55,000 - 96,000; Part time

Benefits offered by this job

Fully remote

Freelance autonomy

Job summary

Alignerr is seeking aClinical Study Manager to oversee the operational execution of AI training-related clinical trials. This fully remote, hourly contract role offers flexible scheduling (10–40 hours/week) and the opportunity to shape how healthcare data informs world-class AI models.

You will manage timelines, budgets, and CRO/vendor relationships across multiple sites, while maintaining data quality and stakeholder alignment.

Qualifications

• Experience leading clinical trials from start to close.
• Strong budgeting, forecasting, and cost-tracking skills.
• Proven ability to manage CROs, vendors and external partners.
• Excellent communication and cross-functional coordination.

Responsibilities

• Manage clinical trial timelines, milestones, and deliverables to keep studies on track.
• Oversee study budgets, forecasting, and cost tracking across vendors.
• Coordinate with CROs, investigative sites, and internal teams for high-quality execution.
• Identify operational risks early and resolve issues affecting timelines and data quality.
• Keep stakeholders aligned and informed throughout the trial lifecycle.
• Work independently and asynchronously.

Skills

Clinical trial mgmt

Budget forecasting

Vendor management

Stakeholder comms

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 models understand healthcare and medical research? We're looking for experienced Clinical Study Managers to oversee the operational execution of clinical trials - and in doing so, help train the AI systems that will define the future of medicine.

This is a fully remote, flexible contract role built for seasoned clinical operations professionals who want to do meaningful work on their own terms.

• 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 studies on track
• 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, high-quality study execution
• Identify operational risks early and resolve issues before they impact timelines or data quality
• Keep all stakeholders aligned and informed throughout the full trial lifecycle
• Work independently and asynchronously — fully on your own schedule

Who You Are

• Experienced clinical trial project manager with a strong command of study budgets and timelines
• Proven track record managing CROs, vendor relationships, and external research partners
• Skilled at coordinating multiple workstreams simultaneously without losing sight of the details
• Decisive, proactive, and calm under pressure when operational challenges arise
• Clear, concise communicator who keeps cross-functional teams aligned and accountable

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation systems
• Familiarity with AI tools or technology platforms used in clinical research
• Exposure to decentralized or virtual clinical trial models
• Background spanning multiple therapeutic areas or study phases

Why Join Us

• Work on cutting-edge AI and healthcare research projects alongside world-leading research labs
• Fully remote and flexible — structure your hours around your life, not the other way around
• Freelance autonomy with the substance of meaningful, high-impact work
• Gain rare exposure to advanced large language models and how real-world clinical data shapes AI training
• Potential for ongoing work and contract extension as new projects launch